Garcinia mangostana

Upload a new image!

Details

Description

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Biological Material

Contributors

Collections

Details Top

Internal ID	UUID64401d30a2876791116269
Scientific name	Garcinia mangostana
Authority	L.
First published in	Sp. Pl. : 443 (1753)

Description Top

Suggest a correction or write a new one!

No description added yet. Help us by writing one.

Synonyms Top

Scientific name	Authority	First published in
Mangostana garcinia	Gaertn.	Fruct. Sem. Pl. 2: 105 (1790)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	mangosteen
English	purple mangosteen
Spanish	mangostin
Spanish	jobo de la india
Spanish	mangostan
Spanish	mangostán
Spanish	mangostín
Spanish	mangostino
Spanish	manzana de oro
Arabic	المانجوستين
Arabic	المانغوستين
Arabic	مانجوستين
Arabic	جوز جندم
ban	manggis
bcl	manggosten
Belarusian	Мангастан
Bulgarian	мангостан
Bengali	ম্যাঙ্গোস্টিন
Catalan	mangostà
Catalan	mangostaner
Czech	mangostan
Czech	mangostana lahodná
German	mangostanfrucht
German	mangosteen
German	mangostinbaum
German	mangostane
dv	މަބުސްތާން
Greek	Μαγκοστίν
Esperanto	mangostano
Estonian	mangostan
Basque	mangostan
Persian	پرپل منگوستین
Persian	منگوستانا
Persian	منگوستین
Persian	ترگیل
Finnish	mangostaani
Finnish	mangostee
Finnish	punamangostani
Finnish	mangostani
French	mangoustan
French	mangoustans
French	mangoustanier
Irish	mangóistín
Irish	mangaistín
Irish	crann mangaistíní
Galician	mangostaneiro
Galician	mangostaneira
Hebrew	מנגוסטין
Hindi	बैंगनी मेन्गोस्टीन
Croatian	mangostin
Hungarian	ázsiai mangosztán
Hungarian	fanyar mangosztán
Hungarian	királygyümölcs
Hungarian	mangosteen
Hungarian	mangosztán
Armenian	Մանգոստան
Indonesian	buah manggis
Indonesian	manggis
Italian	mangostano
Japanese	茫栗
Japanese	果物の女王
Japanese	マンゴスチン
jv	manggis
Georgian	მანგუსტანი
Georgian	მანგოსტანი
Kazakh	Мангостан
Khmer	មង្ឃុត
Kannada	ನೇರಳೆ ಗಾರ್ಸಿಯ
Korean	망고 스틴
Korean	망고스틴
koi	Мангостан
kv	Мангостан
lbe	Мангостан
ln	mangusita
ln	mangusitá
Lithuanian	mangostaninė garcinija
Latvian	mangustīns
Latvian	mangostāns
Macedonian	мангостан
Malayalam	mangosteen
Malayalam	മങ്കൊസ്റ്റിൻ
Malayalam	മാംഗോസ്റ്റീൻ
Malayalam	മാങ്കോസ്റ്റീൻ
mrj	Мангостан
Malay	daftar laman yang sedang dialih bahasa
Malay	jus manggis
Malay	pokok manggis
Malay	manggis
Burmese	မင်းကွတ်ပင်
Burmese	မင်းကွတ်သီး
Norwegian Bokmål	mangostantre
nia	bua magi
Dutch	manggis
Dutch	manggistan
Dutch	mangoestan
Dutch	mangostan
Dutch	mangosteen
Dutch	mangistan
Norwegian Nynorsk	mangostan
pam	mangosteen
Polish	mangostan właściwy
Polish	garcynia
Polish	smaczelina
Polish	żółciecz
Polish	żółtopla
Portuguese	mangustin
Portuguese	mangostão
Romanian	mangostan
Romanian	mangustan
Russian	Мангкут
Russian	Мангостана
Russian	Мангостин
Russian	Мангустан
Russian	Мангустин
Russian	Мангостан
sd	منگوسٽين
Slovak	mangostána
Slovenian	mangostan
su	manggu
Swedish	mangostan
Tamil	மங்குசுத்தான்
Telugu	వంగ మామిడి
Thai	มังคุด
Turkish	mangosteen
Turkish	mangostan
udm	Мангостан
Ukrainian	Мангостан
Uzbek	mangustan
Uzbek	mangostan
vep	mangostan
Vietnamese	măng cụt
Chinese	山竹子
Chinese	倒捻子
Chinese	凤果
Chinese	山竺
Chinese	莽吉柿
Chinese	鳳果
Chinese	山竹

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

Name	Authority	First published in
Garcinia mangostana var. malaccensis	(Hook.f.) Nazre	Phytotaxa 373(1): 33. 2018

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
  - Hainan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
- Indo-China
  - Cambodia
  - Laos
  - Myanmar
  - Vietnam
- Malesia
  - Borneo
  - Lesser Sunda Islands
  - Malaya
  - Maluku
  - Philippines
  - Sumatera
- Papuasia
  - Solomon Islands

Australasia click to expand
- Australia
  - Queensland

Southern America click to expand
- Caribbean
  - Trinidad-Tobago

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000694452
UNII	UGD4B7BE1Z
USDA Plants	GAMA10
Tropicos	7800753
INPN	447083
KEW	urn:lsid:ipni.org:names:428073-1
The Plant List	kew-2816978
Missouri Botanical Garden	279214
PFAF	Garcinia mangostana
Open Tree Of Life	766177
NCBI Taxonomy	58228
IPNI	428073-1
iNaturalist	123001
GBIF	3189571
Freebase	/m/01vn4d
EPPO	GANMA
EOL	584879
Elurikkus	209649
USDA GRIN	71011
Wikipedia	Mangosteen
CMAUP	NPO6249

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Pest categorisation of Pyrrhoderma noxium

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL

EFSA J

19-Mar-2024

PMCID:	PMC10949325
doi:	10.2903/j.efsa.2024.8667
PMID:	38505477

Higher Plant-Derived Biostimulants: Mechanisms of Action and Their Role in Mitigating Plant Abiotic Stress

Martínez-Lorente SE, Martí-Guillén JM, Pedreño MÁ, Almagro L, Sabater-Jara AB

Antioxidants (Basel)

06-Mar-2024

PMCID:	PMC10967762
doi:	10.3390/antiox13030318
PMID:	38539851

Quantifying the Impact of Different Dietary Rumen Modulating Strategies on Enteric Methane Emission and Productivity in Ruminant Livestock: A Meta-Analysis

Pepeta BN, Hassen A, Tesfamariam EH

Animals (Basel)

29-Feb-2024

PMCID:	PMC10931330
doi:	10.3390/ani14050763
PMID:	38473148

Magnetic iron oxide-based nanozymes: from synthesis to application

Ghazzy A, Nsairat H, Said R, Sibai OA, AbuRuman A, Shraim AS, Al hunaiti A

Nanoscale Adv

19-Feb-2024

PMCID:	PMC10929596
doi:	10.1039/d3na00903c
PMID:	38482039

Bavachin Rejuvenates Sensitivity of Colistin against Colistin-Resistant Gram-Negative Bacteria

Li J, Han N, He Z, Dai X, Zhao F, Li Y, Xiong W, Zeng Z

Int J Mol Sci

16-Feb-2024

PMCID:	PMC10889384
doi:	10.3390/ijms25042349
PMID:	38397028

Polyherbal Combinations Used by Traditional Health Practitioners against Mental Illnesses in Bamako, Mali, West Africa

Moussavi N, Mounkoro PP, Dembele SM, Ballo NN, Togola A, Diallo D, Sanogo R, Wangensteen H, Paulsen BS

Plants (Basel)

04-Feb-2024

PMCID:	PMC10857219
doi:	10.3390/plants13030454
PMID:	38337987

Can daily consumption of enriched fatty acids diet be effective in improving metabolic syndrome? An attractive paradox for walnut kernel

Samei M, Dowlatkhahi N, Boozari M, Hosseinzadeh H

Food Sci Nutr

28-Jan-2024

PMCID:	PMC11016402
doi:	10.1002/fsn3.3972
PMID:	38628188

A Comprehensive Multispectroscopic and Computational Analysis of the Interaction between Plant-Based Antiplasmodial Compounds and Bovine Serum Albumin

Azeem K, Abdulhameed HT, Hussain A, Amir S, Parveen M, Patel R, Abid M

ACS Omega

28-Jan-2024

PMCID:	PMC10851409
doi:	10.1021/acsomega.3c07630
PMID:	38343956

Natural Deep Eutectic Solvents for the Extraction of Spilanthol from Acmella oleracea (L.) R.K.Jansen

Alperth F, Feistritzer T, Huber M, Kunert O, Bucar F

Molecules

27-Jan-2024

PMCID:	PMC10856685
doi:	10.3390/molecules29030612
PMID:	38338357

Inhibition of Seizure-Like Paroxysms and Toxicity Effects of Securidaca longepedunculata Extracts and Constituents in Zebrafish Danio rerio

Moussavi N, van der Ent W, Diallo D, Sanogo R, Malterud KE, Esguerra CV, Wangensteen H

ACS Chem Neurosci

25-Jan-2024

PMCID:	PMC10853935
doi:	10.1021/acschemneuro.3c00642
PMID:	38270158

The Potential of Wood Vinegar to Replace Antimicrobials Used in Animal Husbandry—A Review

Gama GS, Pimenta AS, Feijó FM, de Azevedo TK, de Melo RR, de Andrade GS

Animals (Basel)

25-Jan-2024

PMCID:	PMC10854697
doi:	10.3390/ani14030381
PMID:	38338024

Extraction and Separation of Natural Products from Microalgae and Other Natural Sources Using Liquefied Dimethyl Ether, a Green Solvent: A Review

Wang T, Zhu L, Mei L, Kanda H

Foods

22-Jan-2024

PMCID:	PMC10815339
doi:	10.3390/foods13020352
PMID:	38275719

Chestnut tannin extract modulates growth performance and fatty acid composition in finishing Tan lambs by regulating blood antioxidant capacity, rumen fermentation, and biohydrogenation

Gao C, Qi M, Zhou Y

BMC Vet Res

10-Jan-2024

PMCID:	PMC10782739
doi:	10.1186/s12917-023-03870-3
PMID:	38200507

In Vitro Activity of Allium cepa Organosulfur Derivatives against Canine Multidrug-Resistant Strains of Staphylococcus spp. and Enterobacteriaceae

Maroto-Tello A, Ayllón T, Aguinaga-Casañas MA, Ariza JJ, Penelo S, Baños A, Ortiz-Díez G

Vet Sci

09-Jan-2024

PMCID:	PMC10820550
doi:	10.3390/vetsci11010026
PMID:	38250932

Preparation and evaluation of a niosomal delivery system containing G. mangostana extract and study of its anti-Acanthamoeba activity

Sangkana S, Eawsakul K, Ongtanasup T, Boonhok R, Mitsuwan W, Chimplee S, Paul AK, Saravanabhavan SS, Mahboob T, Nawaz M, Pereira ML, Wilairatana P, Wiart C, Nissapatorn V

Nanoscale Adv

09-Jan-2024

PMCID:	PMC10898434
doi:	10.1039/d3na01016c
PMID:	38419876

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
(3R)-3-Methyl-5,8-dihydroxy-3,4-dihydro-1H-2-benzopyran-1-one	10442609	Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)O	194.18	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
3,4-Dihydro-5,8-dihydroxy-3-methylisocoumarin	14779567	Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)O	194.18	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
2-Hydroxy-6-methylbenzoic acid	11279	Click to see CC1=C(C(=CC=C1)O)C(=O)O	152.15	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
> Benzenoids / Benzene and substituted derivatives / Benzophenones
2,4,4'-Trimethoxy-3',6-dihydroxybenzophenone	101763992	Click to see COC1=C(C=C(C=C1)C(=O)C2=C(C=C(C=C2OC)OC)O)O	304.29	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.04.032
2,4,6,3',5'-Pentahydroxybenzophenone	19910294	Click to see C1=C(C=C(C=C1O)O)C(=O)C2=C(C=C(C=C2O)O)O	262.21	unknown	https://doi.org/10.1016/J.BMCL.2010.08.061
3,4,5,3'-Tetrahydroxybenzophenone	52948815	Click to see C1=CC(=CC(=C1)O)C(=O)C2=CC(=C(C(=C2)O)O)O	246.21	unknown	https://doi.org/10.1016/J.BMCL.2010.08.061
Maclurin	68213	Click to see C1=CC(=C(C=C1C(=O)C2=C(C=C(C=C2O)O)O)O)O	262.21	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde	240	Click to see C1=CC=C(C=C1)C=O	106.12	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
> Benzenoids / Benzene and substituted derivatives / Phenylacetaldehydes
Phenylacetaldehyde	998	Click to see C1=CC=C(C=C1)CC=O	120.15	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
> Benzenoids / Benzene and substituted derivatives / Toluenes
Toluene	1140	Click to see CC1=CC=CC=C1	92.14	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
> Benzenoids / Benzene and substituted derivatives / Xylenes / m-Xylenes
m-Xylene	7929	Click to see CC1=CC(=CC=C1)C	106.16	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
> Benzenoids / Benzene and substituted derivatives / Xylenes / o-Xylenes
O-Xylene	7237	Click to see CC1=CC=CC=C1C	106.16	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
> Benzenoids / Benzene and substituted derivatives / Xylenes / p-Xylenes
P-Xylene	7809	Click to see CC1=CC=C(C=C1)C	106.16	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Heptane	8900	Click to see CCCCCCC	100.20	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
Octane	356	Click to see CCCCCCCC	114.23	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
> Hydrocarbons / Saturated hydrocarbons / Cycloalkanes
Ethylcyclohexane	15504	Click to see CCC1CCCCC1	112.21	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides
1-(beta-D-Glucopyranosyl)-3-ethyl-4-methyl-1H-pyrrole-2,5-dione	100933901	Click to see CCC1=C(C(=O)N(C1=O)C2C(C(C(C(O2)CO)O)O)O)C	301.29	unknown	https://doi.org/10.1016/0031-9422(96)00276-2
3-Ethyl-4-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]pyrrole-2,5-dione	154791048	Click to see CCC1=C(C(=O)N(C1=O)C2C(C(C(C(O2)CO)O)O)O)C	301.29	unknown	https://doi.org/10.1016/0031-9422(96)00276-2
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexanol	8103	Click to see CCCCCCO	102.17	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
cis-3-Hexen-1-ol	5281167	Click to see CCC=CCCO	100.16	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Taxanes and derivatives
Paclitaxel	36314	Click to see CC1=C2C(C(=O)C3(C(CC4C(C3C(C(C2(C)C)(CC1OC(=O)C(C(C5=CC=CC=C5)NC(=O)C6=CC=CC=C6)O)O)OC(=O)C7=CC=CC=C7)(CO4)OC(=O)C)O)C)OC(=O)C	853.90	unknown	https://doi.org/10.1055/S-2002-35668
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene	441005	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
(+)-gamma-Cadinene	6432404	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene	92042749	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
(E)-alpha-bisabolene	5315468	Click to see CC1=CCC(CC1)C(=CCC=C(C)C)C	204.35	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
(Z)-alpha-Bisabolene	5352653	Click to see CC1=CCC(CC1)C(=CCC=C(C)C)C	204.35	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
Cadina-1(10),4-diene	10223	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
Copaene	19725	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
gamma-Cadinene	15094	Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C	204.35	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
Guaiene	6949	Click to see CC1CCC(=C(C)C)CC2=C1CCC2C	204.35	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
4a,5-Dimethyl-3-(prop-1-en-2-yl)-1,2,3,4,4a,5,6,7-octahydronaphthalene	288227	Click to see CC1CCC=C2C1(CC(CC2)C(=C)C)C	204.35	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
Valencene	9855795	Click to see CC1CCC=C2C1(CC(CC2)C(=C)C)C	204.35	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(2R,3S,4S,5S,6R)-2-[[(1S,4aS,5R,7S,7aS)-5,7-dihydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-1-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	154496125	Click to see CC1(CC(C2C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O	348.34	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
(2S,3S,4R,5R,6S)-2-[(3S,4E,6E,8E,10E,12E,14E,16E,18E,20E,22E,24E)-2-hydroxy-25-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-2,6,10,14,19,23-hexamethylpentacosa-4,6,8,10,12,14,16,18,20,22,24-undecaen-3-yl]oxy-6-methyloxane-3,4,5-triol	162905296	Click to see CC1C(C(C(C(O1)OC(C=CC(=CC=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CC(CC2(C)C)O)C)C)C)C)C(C)(C)O)O)O)O	731.00	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.04.032
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(1S,2S,7R,8R)-7-hydroxy-1,5-dimethyl-8-[2-[(1R,2R,3R,7R,10S,11R,13S,14R)-1-methyl-14-propan-2-yl-12-azapentacyclo[8.6.0.02,13.03,7.07,11]hexadecan-2-yl]ethyl]-6-oxabicyclo[3.2.1]octan-2-yl] acetate	163185813	Click to see CC(C)C1CCC2(C3CCC45C3NC1C2(C4CCC5)CCC6C7(CCC(C6(C(O7)O)C)OC(=O)C)C)C	513.80	unknown	https://doi.org/10.1016/0031-9422(91)84157-N
Betulin	72326	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO	442.70	unknown	https://doi.org/10.1016/0031-9422(91)84157-N
Friedelin	91472	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	426.70	unknown	https://doi.org/10.1016/0031-9422(91)84157-N
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(3R,6S,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol	145925700	Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	426.70	unknown	https://doi.org/10.1016/0031-9422(91)84157-N
(E,6R)-6-[(1S,3R,6S,12S,15R,16R)-6-hydroxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-2-methylhept-2-enoic acid	145999601	Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	456.70	unknown	https://doi.org/10.1016/0031-9422(91)84157-N
(E,6S)-6-[(1S,3R,7S,8R,11S,12S,15R,16R)-7-hydroxy-7,12,16-trimethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]hept-3-en-2-one	162908349	Click to see CC(CC=CC(=O)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCCC5(C)O)C)C	412.60	unknown	https://doi.org/10.1016/0031-9422(91)84157-N
3beta-Hydroxy-27-norcycloarta-23-ene-25-one	21626061	Click to see CC(CC=CC(=O)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	426.70	unknown	via CMAUP database
6-(7-Hydroxy-7,12,16-trimethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl)hept-3-en-2-one	162908348	Click to see CC(CC=CC(=O)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCCC5(C)O)C)C	412.60	unknown	https://doi.org/10.1016/0031-9422(91)84157-N
Cycloartenol	92110	Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	426.70	unknown	https://doi.org/10.1016/0031-9422(91)84157-N
Mangiferadiol	131751908	Click to see CC(CCC=C(C)CO)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	442.70	unknown	https://doi.org/10.1016/0031-9422(91)84157-N
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/0031-9422(91)84157-N
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/0031-9422(91)84157-N
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
Hexyl acetate	8908	Click to see CCCCCCOC(=O)C	144.21	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
> Organic nitrogen compounds / Organonitrogen compounds / Guanidines / Biguanides
Metformin	4091	Click to see CN(C)C(=N)N=C(N)N	129.16	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucosinolates / Alkylglucosinolates
Glucotropaeolin	9548605	Click to see C1=CC=C(C=C1)CC(=NOS(=O)(=O)O)SC2C(C(C(C(O2)CO)O)O)O	409.40	unknown	https://doi.org/10.1016/S0031-9422(02)00142-5
Glucotropeolin	6537197	Click to see C1=CC=C(C=C1)CC(=NOS(=O)(=O)O)SC2C(C(C(C(O2)CO)O)O)O	409.40	unknown	https://doi.org/10.1016/S0031-9422(02)00142-5
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[2,4-dihydroxy-6-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-phenylmethanone	101130544	Click to see C1=CC=C(C=C1)C(=O)C2=C(C=C(C=C2OC3C(C(C(C(O3)CO)O)O)O)O)O	392.40	unknown	https://doi.org/10.1021/NP000583Q
[2,4-Dihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-phenylmethanone	85362951	Click to see C1=CC=C(C=C1)C(=O)C2=C(C=C(C=C2OC3C(C(C(C(O3)CO)O)O)O)O)O	392.40	unknown	https://doi.org/10.1021/NP000583Q
garcimangosone D	11003703	Click to see C1=CC=C(C=C1)C(=O)C2=C(C=C(C=C2OC3C(C(C(C(O3)CO)O)O)O)O)O	392.40	unknown	https://doi.org/10.1021/NP000583Q
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5-Methylfurfural	12097	Click to see CC1=CC=C(O1)C=O	110.11	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
Furfural	7362	Click to see C1=COC(=C1)C=O	96.08	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Nonanal	31289	Click to see CCCCCCCCC=O	142.24	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
2-(4-Oxo-2-pent-2-enylcyclopentyl)acetic acid	162952830	Click to see CCC=CCC1CC(=O)CC1CC(=O)O	210.27	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
Botryosphaerinone	102161310	Click to see CCC=CCC1CC(=O)CC1CC(=O)O	210.27	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
7-hydroxy-1,8a-dimethyl-1H-naphthalene-2,6-dione	75079747	Click to see CC1C(=O)C=CC2=CC(=O)C(=CC12C)O	204.22	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
Botryosphaeridione	44605081	Click to see CC1C(=O)C=CC2=CC(=O)C(=CC12C)O	204.22	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(2S,3S)-2,3,8-trihydroxy-6-methoxy-7-(3-methylbut-2-enyl)-1,2,3,4-tetrahydroxanthen-9-one	163065723	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)CC(C(C3)O)O)OC)C	346.40	unknown	https://doi.org/10.1016/J.FITOTE.2010.02.002
1,3,7-Trihydroxy-2-methoxyxanthone	12133315	Click to see COC1=C(C2=C(C=C1O)OC3=C(C2=O)C=C(C=C3)O)O	274.22	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.04.032
1,4,5,6-Tetrahydroxy-2-(2-methylbut-3-en-2-yl)xanthen-9-one	10426622	Click to see CC(C)(C=C)C1=CC(=C2C(=C1O)C(=O)C3=C(O2)C(=C(C=C3)O)O)O	328.30	unknown	via CMAUP database
2-(1,1-Dimethyl-2-propenyl)-1,4,5-trihydroxy-9H-xanthen-9-one	364825	Click to see CC(C)(C=C)C1=CC(=C2C(=C1O)C(=O)C3=C(O2)C(=CC=C3)O)O	312.30	unknown	via CMAUP database
2,3,5,7-Tetrahydroxyxanthen-9-one	162847405	Click to see C1=C(C=C(C2=C1C(=O)C3=CC(=C(C=C3O2)O)O)O)O	260.20	unknown	https://doi.org/10.1016/J.BMCL.2010.08.061
2,7-Dihydroxyxanthen-9-one	2836049	Click to see C1=CC2=C(C=C1O)C(=O)C3=C(O2)C=CC(=C3)O	228.20	unknown	via CMAUP database
BR-Xanthone B	14034125	Click to see COC1=C(C=C(C2=C1C(=O)C3=C(O2)C(=CC=C3)O)O)O	274.22	unknown	https://doi.org/10.1016/0031-9422(88)80242-5
Euxanthone	5281631	Click to see C1=CC(=C2C(=C1)OC3=C(C2=O)C=C(C=C3)O)O	228.20	unknown	via CMAUP database
Gentisein	5281635	Click to see C1=CC2=C(C=C1O)C(=O)C3=C(C=C(C=C3O2)O)O	244.20	unknown	https://doi.org/10.1016/J.BMCL.2010.08.061
Norathyriol	5281656	Click to see C1=C(C=C2C(=C1O)C(=O)C3=CC(=C(C=C3O2)O)O)O	260.20	unknown	via CMAUP database
Xanthone	7020	Click to see C1=CC=C2C(=C1)C(=O)C3=CC=CC=C3O2	196.20	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 2-prenylated xanthones
(1R,2R)-1,8,10-trihydroxy-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-1,2-dihydrofuro[3,2-a]xanthen-11-one	163186423	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C4=C(C=C3)OC(C4O)C(C)(C)O)O)C	412.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.023
(1S,2S)-1,8,10-trihydroxy-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-1,2-dihydrofuro[3,2-a]xanthen-11-one	154495936	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C4=C(C=C3)OC(C4O)C(C)(C)O)O)C	412.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.023
(2R)-2,6,9,11-tetrahydroxy-3,3-dimethyl-10-(3-methylbut-2-enyl)-1,2-dihydropyrano[3,2-a]xanthen-12-one	163048793	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C4=C(C=C3O)OC(C(C4)O)(C)C)O)C	412.40	unknown	https://doi.org/10.1021/NP000583Q
(2S)-2,6,9,11-tetrahydroxy-3,3-dimethyl-10-(3-methylbut-2-enyl)-1,2-dihydropyrano[3,2-a]xanthen-12-one	163048792	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C4=C(C=C3O)OC(C(C4)O)(C)C)O)C	412.40	unknown	https://doi.org/10.1021/NP000583Q
(2S)-4,8,10-trihydroxy-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-1,2-dihydrofuro[3,2-a]xanthen-11-one	162980002	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C4=C(C(=C3)O)OC(C4)C(C)(C)O)O)C	412.40	unknown	https://doi.org/10.1016/J.FITOTE.2010.02.002
(2S)-4,8,10-trihydroxy-9-(3-methylbut-2-enyl)-2-prop-1-en-2-yl-1,2-dihydrofuro[3,2-a]xanthen-11-one	163031668	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C4=C(C(=C3)O)OC(C4)C(=C)C)O)C	394.40	unknown	https://doi.org/10.1016/J.BMC.2010.07.033
1-Hydroxy-3,6,7-trimethoxy-2-(3-methyl-2-butenyl)-8-(3-hydroxy-3-methyl-1E-butenyl)-xanthone	5319715	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(C(=C(C=C3O2)OC)OC)C=CC(C)(C)O)OC)C	454.50	unknown	https://doi.org/10.1016/S0031-9422(02)00142-5
1-Hydroxy-8-(3-hydroxy-3-methylbut-1-enyl)-3,6,7-trimethoxy-2-(3-methylbut-2-enyl)xanthen-9-one	78385304	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(C(=C(C=C3O2)OC)OC)C=CC(C)(C)O)OC)C	454.50	unknown	https://doi.org/10.1016/S0031-9422(02)00142-5
1,3,7-Trihydroxy-2-prenylxanthone	5495920	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C=C(C=C3)O)O)C	312.30	unknown	https://doi.org/10.1016/J.FITOTE.2010.02.002
1,5-Dihydroxy-3-methoxy-2-prenylxanthone	10449043	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C(=CC=C3)O)OC)C	326.30	unknown	https://doi.org/10.1016/0031-9422(95)00042-6 https://doi.org/10.1016/J.FITOTE.2010.02.002 https://doi.org/10.1021/NP0303254 https://doi.org/10.1016/0031-9422(81)85250-8 https://doi.org/10.1016/J.BMCL.2010.08.061 https://doi.org/10.1016/J.BMC.2010.07.033 https://doi.org/10.1021/NP000583Q
1,5,8-Trihydroxy-3-methoxy-2-(3-methylbut-2-en-1-yl)-9H-xanthen-9-one	14162674	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(C=CC(=C3O2)O)O)OC)C	342.30	unknown	https://doi.org/10.1002/HLCA.201100157 https://doi.org/10.1016/0031-9422(88)80804-5
1,6-Dihydroxy-3-methoxy-2-prenylxanthone	14162675	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C=C(C=C3)O)OC)C	326.30	unknown	https://doi.org/10.1016/0031-9422(88)80804-5
1,6-Dihydroxy-3,7-dimethoxy-2-(3-methyl-2-butenyl)-8-(3-hydroxy-3-methyl-1E-butenyl)-xanthone	5319262	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C=C(C(=C3C=CC(C)(C)O)OC)O)OC)C	440.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887388/ https://doi.org/10.1016/S0031-9422(02)00142-5 https://doi.org/10.1016/J.PHYTOCHEM.2007.09.023 https://doi.org/10.1248/CPB.51.857
1,6-Dihydroxy-8-(3-hydroxy-3-methylbut-1-enyl)-3,7-dimethoxy-2-(3-methylbut-2-enyl)xanthen-9-one	78385239	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C=C(C(=C3C=CC(C)(C)O)OC)O)OC)C	440.50	unknown	https://doi.org/10.1016/S0031-9422(02)00142-5
1,7-Dihydroxy-3-methoxy-2-prenylxanthone	509269	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C=CC(=C3)O)OC)C	326.30	unknown	https://doi.org/10.1016/0031-9422(95)00042-6 https://doi.org/10.1016/J.FITOTE.2010.02.002 https://doi.org/10.1021/NP000583Q https://doi.org/10.1248/CPB.51.857 https://doi.org/10.1016/S0031-9422(96)00410-4
1,8,10-Trihydroxy-2-(1-hydroxy-1-methylethyl)-9-(3-methyl-2-butenyl)-1,2-dihydro-11H-furo[3,2-a]xanthene-11-one	24829255	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C4=C(C=C3)OC(C4O)C(C)(C)O)O)C	412.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.023
2-(3,7-Dimethylocta-2,6-dienyl)-1,3,5-trihydroxyxanthen-9-one	5495932	Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C=CC=C3O)O)C)C	380.40	unknown	https://doi.org/10.1016/0031-9422(95)00042-6 https://doi.org/10.1021/JF052649Z
2-(3,7-Dimethylocta-2,6-dienyl)-1,3,5,8-tetrahydroxyxanthen-9-one	72988981	Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC3=C(C=CC(=C3C2=O)O)O)O)C)C	396.40	unknown	https://doi.org/10.1021/JF052649Z https://doi.org/10.1002/HLCA.201100157 https://doi.org/10.1016/J.BMC.2010.07.033
Cowagarcinone B	5316764	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=CC(=C(C=C3O2)O)OC)OC)C	356.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.06.025 https://doi.org/10.1016/J.PHYTOCHEM.2005.02.025
Garcimangosone C	10916629	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C4=C(C=C3O)OC(C(C4)O)(C)C)O)C	412.40	unknown	https://doi.org/10.1021/NP000583Q
garcinone B	5495928	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C4=C(C(=C3)O)OC(C=C4)(C)C)O)C	394.40	unknown	https://doi.org/10.1016/S0031-9422(82)85052-8 https://doi.org/10.1248/CPB.51.857 https://doi.org/10.1021/NP000583Q https://doi.org/10.1248/CPB.54.301 https://doi.org/10.1248/CPB.41.958 https://doi.org/10.1016/0031-9422(81)85250-8 https://doi.org/10.1021/NP010566G https://doi.org/10.1016/J.FITOTE.2010.02.002
Mangostenone D	11696901	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C4=C(C(=C3)O)OC(CC4)(C)C)O)C	396.40	unknown	https://doi.org/10.1248/CPB.54.301 https://doi.org/10.1002/HLCA.201100157
Mangostenone G	49866103	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C4=C(C(=C3)O)OC(C4)C(=C)C)O)C	394.40	unknown	https://doi.org/10.1016/J.BMC.2010.07.033
Mangostinone	6478778	Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C=CC=C3O)O)C)C	380.40	unknown	https://doi.org/10.1016/0031-9422(95)00042-6 https://doi.org/10.1021/NP010566G https://doi.org/10.1021/NP020546U https://doi.org/10.1021/JF052649Z https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2572570/ https://doi.org/10.1248/CPB.51.857 https://doi.org/10.1016/J.PHYTOCHEM.2005.02.025 https://doi.org/10.1248/CPB.54.301
smeathxanthone A	11509473	Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC3=C(C=CC(=C3C2=O)O)O)O)C)C	396.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2572570/ https://doi.org/10.1002/HLCA.201100157 https://doi.org/10.1021/JF052649Z https://doi.org/10.1016/J.BMC.2010.07.033
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
(2S)-4,7-dihydroxy-2-(2-hydroxypropan-2-yl)-11-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-b]xanthen-5-one	163007755	Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C=C(C=C4)O)O)CC(O2)C(C)(C)O)C	396.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.04.032
(2S)-4,9-dihydroxy-2-(2-hydroxypropan-2-yl)-11-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-b]xanthen-5-one	162987335	Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C=CC=C4O)O)CC(O2)C(C)(C)O)C	396.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.04.032
1,3,8-trihydroxy-4-(3-hydroxy-3-methylbutanoyl)-2-(3-methylbut-2-enyl)xanthen-9-one	102234394	Click to see CC(=CCC1=C(C2=C(C(=C1O)C(=O)CC(C)(C)O)OC3=CC=CC(=C3C2=O)O)O)C	412.40	unknown	via CMAUP database
1,5,8-Trihydroxy-3-methoxy-2,4-bis(3-methylbut-2-enyl)xanthen-9-one	11711264	Click to see CC(=CCC1=C(C2=C(C(=C1OC)CC=C(C)C)OC3=C(C=CC(=C3C2=O)O)O)O)C	410.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2572570/ https://doi.org/10.1021/JF052649Z
10,16-Dihydroxy-6,6,19,19-tetramethyl-15-(3-methylbut-2-enyl)-5,13,18-trioxapentacyclo[12.8.0.03,12.04,9.017,22]docosa-1(22),3(12),4(9),7,10,14,16,20-octaen-2-one	71437595	Click to see CC(=CCC1=C2C(=C3C=CC(OC3=C1O)(C)C)C(=O)C4=C(O2)C=C(C5=C4OC(C=C5)(C)C)O)C	460.50	unknown	https://doi.org/10.1021/NP000583Q
5,9,11-Trihydroxy-3,3-dimethyl-6,10-bis(3-methylbut-2-enyl)-1,2-dihydropyrano[3,2-a]xanthen-12-one	163091100	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C(=C4C(=C3C2=O)CCC(O4)(C)C)O)CC=C(C)C)O)C	464.50	unknown	https://doi.org/10.1002/HLCA.201100157
8-Desoxygartanin	392450	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=C(O2)C(=CC=C3)O)CC=C(C)C)O)C	380.40	unknown	via CMAUP database
Caloxanthone A	10046140	Click to see CC(=CCC1=C2C(=CC(=C1O)O)C(=O)C3=C(C4=C(C=C3O2)OC(C=C4)(C)C)O)C	394.40	unknown	via CMAUP database
CudraxanthoneG	42645953	Click to see CC(=CCC1=C(C2=C(C(=C1OC)CC=C(C)C)OC3=C(C2=O)C=CC=C3O)O)C	394.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2572570/ https://doi.org/10.1021/JF052649Z
Garcinone A	70689919	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=C(O2)C=C(C=C3)O)CC=C(C)C)O)C	380.40	unknown	https://doi.org/10.1016/0031-9422(81)85250-8 https://doi.org/10.1016/S0031-9422(82)85052-8
Gartanin	5281633	Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=C(C=CC(=C3O2)O)O)CC=C(C)C)O)C	396.40	unknown	https://doi.org/10.1021/NP50051A021 https://doi.org/10.1111/J.2042-7158.1996.TB03988.X https://doi.org/10.1016/S0040-4020(01)98253-5 https://doi.org/10.1016/0031-9422(88)80804-5 https://doi.org/10.1016/0031-9422(95)00042-6 https://doi.org/10.1055/S-2002-35668 https://doi.org/10.1080/10286020801948490 https://doi.org/10.1021/NP000583Q https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887388/ https://doi.org/10.1248/CPB.54.301 https://doi.org/10.1248/CPB.41.958 https://doi.org/10.1016/S0031-9422(96)00410-4 https://doi.org/10.1016/J.BMC.2010.07.033 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9213587/ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2572570/ https://doi.org/10.1021/JF052649Z https://doi.org/10.1016/J.FITOTE.2010.02.002
Mangostenone B	21672078	Click to see CC(=CCC1=C2C(=C3CCC(OC3=C1O)(C)C)C(=O)C4=C(C5=C(C=C4O2)OC(C=C5)(C)C)O)C	462.50	unknown	https://doi.org/10.1021/NP010566G https://doi.org/10.1248/CPB.51.857
Mangoxanthone	101763994	Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C=C(C=C4)O)O)CC(O2)C(C)(C)O)C	396.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.04.032
Tovophyllin A	42645954	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C(=C4C(=C3C2=O)C=CC(O4)(C)C)O)CC=C(C)C)O)C	462.50	unknown	https://doi.org/10.1021/JF052649Z https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2572570/ https://doi.org/10.1021/NP000583Q https://doi.org/10.1055/S-2002-35668
Tovophyllin B	509268	Click to see CC(=CCC1=C2C(=C3C=CC(OC3=C1O)(C)C)C(=O)C4=C(C5=C(C=C4O2)OC(C=C5)(C)C)O)C	460.50	unknown	https://doi.org/10.1021/NP000583Q https://doi.org/10.1021/NP010566G https://doi.org/10.1016/J.PHYTOCHEM.2005.10.016 https://doi.org/10.1248/CPB.51.857
Trapezifolixanthone	188341	Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C=CC=C4O)O)C=CC(O2)(C)C)C	378.40	unknown	https://doi.org/10.1021/NP010566G https://doi.org/10.1016/J.FITOTE.2010.02.002 https://doi.org/10.1248/CPB.51.857
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 8-prenylated xanthones
(2R)-4-hydroxy-2-(2-hydroxypropan-2-yl)-7,8-dimethoxy-6-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-b]xanthen-5-one	163048406	Click to see CC(=CCC1=C2C(=CC(=C1OC)OC)OC3=CC4=C(CC(O4)C(C)(C)O)C(=C3C2=O)O)C	440.50	unknown	https://doi.org/10.1016/S0031-9422(02)00142-5
(2S,3R)-4,8-dihydroxy-2-(2-hydroxypropan-2-yl)-7-methoxy-6-(3-methylbut-2-enyl)-3-[1,3,6-trihydroxy-7-methoxy-2,8-bis(3-methylbut-2-enyl)-9-oxoxanthen-4-yl]-2,3-dihydrofuro[3,2-b]xanthen-5-one	163060590	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C4C5=C(C(=C(C6=C5OC7=C(C6=O)C(=C(C(=C7)O)OC)CC=C(C)C)O)CC=C(C)C)O)C(C)(C)O)O)O)OC)C	834.90	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887388/
(2S)-4,7-dihydroxy-2-(2-hydroxypropan-2-yl)-6-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-b]xanthen-5-one	154496056	Click to see CC(=CCC1=C(C=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C4)C(C)(C)O)O)O)C	396.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.023
(2S)-4,8-dihydroxy-2-(2-hydroxypropan-2-yl)-7-methoxy-6-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-b]xanthen-5-one	162957066	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C4)C(C)(C)O)O)O)OC)C	426.50	unknown	https://doi.org/10.1248/CPB.54.301
(2S)-4,8-dihydroxy-7-methoxy-6-(3-methylbut-2-enyl)-2-prop-1-en-2-yl-2,3-dihydrofuro[3,2-b]xanthen-5-one	163087336	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C4)C(=C)C)O)O)OC)C	408.40	unknown	https://doi.org/10.1016/J.BMC.2010.07.033
(3R)-3,9-dihydroxy-5,10-dimethoxy-2,2-dimethyl-11-(3-methylbut-2-enyl)-3,4-dihydropyrano[2,3-a]xanthen-12-one	163082788	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C4C(=C(C=C3O2)OC)CC(C(O4)(C)C)O)O)OC)C	440.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887388/
(3S)-3,5,9-trihydroxy-10-methoxy-2,2-dimethyl-11-(3-methylbut-2-enyl)-3,4-dihydropyrano[2,3-a]xanthen-12-one	162842817	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(O2)C=C(C4=C3OC(C(C4)O)(C)C)O)O)OC)C	426.50	unknown	https://doi.org/10.1248/CPB.54.301 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887388/ https://doi.org/10.1002/HLCA.201100157
(3S)-3,5,9-trihydroxy-8-methoxy-2,2-dimethyl-7-(3-methylbut-2-enyl)-3,4-dihydropyrano[3,2-b]xanthen-6-one	92448128	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C(C4)O)(C)C)O)O)OC)C	426.50	unknown	https://doi.org/10.1248/CPB.54.301 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887388/ https://doi.org/10.1016/J.BMC.2010.07.033 https://doi.org/10.1021/NP000583Q https://doi.org/10.1016/S0031-9422(96)00410-4
1-(3,3-Dimethylbutyl)-3,6,8-trihydroxy-2-methoxy-7-(3-methylbut-2-enyl)xanthen-9-one	89172625	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)OC)CCC(C)(C)C)O)C	426.50	unknown	via CMAUP database
1-[(2S)-2,3-dihydroxy-3-methylbutyl]-3,6,8-trihydroxy-2-methoxy-7-(3-methylbut-2-enyl)xanthen-9-one	163010748	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)OC)CC(C(C)(C)O)O)O)C	444.50	unknown	https://doi.org/10.1248/CPB.54.301
1-hydroxy-2-[(2R)-2-hydroxy-3-methylbut-3-enyl]-3,6,7-trimethoxy-8-(3-methylbut-2-enyl)xanthen-9-one	162956670	Click to see CC(=CCC1=C2C(=CC(=C1OC)OC)OC3=CC(=C(C(=C3C2=O)O)CC(C(=C)C)O)OC)C	454.50	unknown	https://doi.org/10.1016/S0031-9422(02)00142-5
1-Hydroxy-3,6,7-trimethoxy-2-(2-hydroxy-3-methyl-3-butenyl)-8-(3-methyl-2-butenyl)-xanthone	101193828	Click to see CC(=CCC1=C2C(=CC(=C1OC)OC)OC3=CC(=C(C(=C3C2=O)O)CC(C(=C)C)O)OC)C	454.50	unknown	https://doi.org/10.1016/S0031-9422(02)00142-5
1-Hydroxy-3,6,7-trimethoxy-2-(3-methyl-2-butenyl)-8-(2-hydroxy-3-methyl-3-butenyl)-xanthone	20978310	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(C(=C(C=C3O2)OC)OC)CC(C(=C)C)O)OC)C	454.50	unknown	https://doi.org/10.1016/S0031-9422(02)00142-5
1-hydroxy-8-[(2R)-2-hydroxy-3-methylbut-3-enyl]-3,6,7-trimethoxy-2-(3-methylbut-2-enyl)xanthen-9-one	163021718	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(C(=C(C=C3O2)OC)OC)CC(C(=C)C)O)OC)C	454.50	unknown	https://doi.org/10.1016/S0031-9422(02)00142-5
1-Isomangostin	5281641	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(O2)C=C(C4=C3OC(CC4)(C)C)O)O)OC)C	410.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2572570/ https://doi.org/10.1021/JF052649Z https://doi.org/10.1021/NP000583Q https://doi.org/10.1021/NP50051A021
1,3-dihydroxy-2-[(2R)-2-hydroxy-3-methylbut-3-enyl]-6,7-dimethoxy-8-(3-methylbut-2-enyl)xanthen-9-one	162924938	Click to see CC(=CCC1=C2C(=CC(=C1OC)OC)OC3=C(C2=O)C(=C(C(=C3)O)CC(C(=C)C)O)O)C	440.50	unknown	https://doi.org/10.1016/S0031-9422(02)00142-5
1,3-Dihydroxy-6,7-dimethoxy-2-(2-hydroxy-3-methyl-3-butenyl)-8-(3-methyl-2-butenyl)-xanthone	101193829	Click to see CC(=CCC1=C2C(=CC(=C1OC)OC)OC3=C(C2=O)C(=C(C(=C3)O)CC(C(=C)C)O)O)C	440.50	unknown	https://doi.org/10.1016/S0031-9422(02)00142-5
1,3,6-trihydroxy-2-[(2R)-2-hydroxy-3-methylbut-3-enyl]-7-methoxy-8-(3-methylbut-2-enyl)xanthen-9-one	156908054	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(O2)C=C(C(=C3O)CC(C(=C)C)O)O)O)OC)C	426.50	unknown	https://doi.org/10.1021/NP010566G
1,3,6-trihydroxy-2-[(2S)-2-hydroxy-3-methylbut-3-enyl]-7-methoxy-8-(3-methylbut-2-enyl)xanthen-9-one	154496974	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(O2)C=C(C(=C3O)CC(C(=C)C)O)O)O)OC)C	426.50	unknown	https://doi.org/10.1021/NP010566G
1,3,6,7-Tetrahydroxy-8-prenylxanthone	15307924	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)O)C	328.30	unknown	https://doi.org/10.1021/NP000583Q
1,3,7-Trihydroxy-2-(3-methyl-2-butenyl)-8-(3-methyl-3-hydroxybutyl)-9H-xanthene-9-one	102234393	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C=C3)O)CCC(C)(C)O)O)C	398.40	unknown	via CMAUP database
1,6-dihydroxy-2-[(2R)-2-hydroxy-3-methylbut-3-enyl]-3,7-dimethoxy-8-(3-methylbut-2-enyl)xanthen-9-one	162962935	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C(=C(C=C3O2)OC)CC(C(=C)C)O)O)O)OC)C	440.50	unknown	https://doi.org/10.1016/S0031-9422(02)00142-5
1,6-dihydroxy-2-[(2S)-2-hydroxy-3-methylbut-3-enyl]-3,7-dimethoxy-8-(3-methylbut-2-enyl)xanthen-9-one	162962936	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C(=C(C=C3O2)OC)CC(C(=C)C)O)O)O)OC)C	440.50	unknown	https://doi.org/10.1016/S0031-9422(02)00142-5
1,6-Dihydroxy-3,7-dimethoxy-2-(2-hydroxy-3-methyl-3-butenyl)-8-(3-methyl-2-butenyl)-xanthone	101193827	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C(=C(C=C3O2)OC)CC(C(=C)C)O)O)O)OC)C	440.50	unknown	https://doi.org/10.1016/S0031-9422(02)00142-5
1,6-Dihydroxy-3,7-dimethoxy-2-(3-methyl-2-butenyl)-8-(2-hydroxy-3-methyl-3-butenyl)-xanthone	101193826	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C=C(C(=C3CC(C(=C)C)O)OC)O)OC)C	440.50	unknown	https://doi.org/10.1016/S0031-9422(02)00142-5
1,6-Dihydroxy-3,7-dimethoxy-2-(3-methyl-2-butenyl)-8-(2-oxo-3-methyl-3-butenyl)-xanthone	129847853	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C=C(C(=C3CC(=O)C(=C)C)OC)O)OC)C	438.50	unknown	https://doi.org/10.1016/S0031-9422(02)00142-5
1,6-dihydroxy-8-[(2R)-2-hydroxy-3-methylbut-3-enyl]-3,7-dimethoxy-2-(3-methylbut-2-enyl)xanthen-9-one	162871148	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C=C(C(=C3CC(C(=C)C)O)OC)O)OC)C	440.50	unknown	https://doi.org/10.1016/S0031-9422(02)00142-5
11-Hydroxy-1-isomangostin	46880203	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(O2)C=C(C4=C3OC(C(C4)O)(C)C)O)O)OC)C	426.50	unknown	https://doi.org/10.1248/CPB.54.301 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887388/ https://doi.org/10.1002/HLCA.201100157
11-hydroxy-3-O-methyl-1-isomangostin	46880202	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C4C(=C(C=C3O2)OC)CC(C(O4)(C)C)O)O)OC)C	440.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887388/
11alpha-Mangostanin	46880204	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C4)C(C)(C)O)O)O)OC)C	426.50	unknown	https://doi.org/10.1248/CPB.54.301 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887388/ https://doi.org/10.1016/S0031-9422(02)00142-5 https://doi.org/10.1016/J.PHYTOCHEM.2007.09.023 https://doi.org/10.1248/CPB.51.857
3-Isomangostin	13873655	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(CC4)(C)C)O)O)OC)C	410.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887388/ https://doi.org/10.1021/NP000583Q https://doi.org/10.1021/NP50051A021
3,4,8-Trihydroxy-2-(2-hydroxypropan-2-yl)-7-methoxy-6-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-b]xanthen-5-one	73002369	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C4O)C(C)(C)O)O)O)OC)C	442.50	unknown	https://doi.org/10.1248/CPB.54.301
3,5,9-Trihydroxy-8-methoxy-2,2-dimethyl-7-(3-methylbut-2-enyl)pyrano[3,2-b]xanthen-6-one	68229267	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C(=C4)O)(C)C)O)O)OC)C	424.40	unknown	via CMAUP database
3,6-Dimethylmangostin	231412	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(C(=C(C=C3O2)OC)OC)CC=C(C)C)OC)C	438.50	unknown	via CMAUP database
4-Hydroxy-2-(2-hydroxypropan-2-yl)-7,8-dimethoxy-6-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-b]xanthen-5-one	163048405	Click to see CC(=CCC1=C2C(=CC(=C1OC)OC)OC3=CC4=C(CC(O4)C(C)(C)O)C(=C3C2=O)O)C	440.50	unknown	https://doi.org/10.1016/S0031-9422(02)00142-5
4-Hydroxy-6-(3-methyl-2-butenyl-)-7,8-dimethoxy-5H-furo[3,2-b]xanthene-5-one	101193830	Click to see CC(=CCC1=C2C(=CC(=C1OC)OC)OC3=C(C2=O)C(=C4C=COC4=C3)O)C	380.40	unknown	https://doi.org/10.1016/S0031-9422(02)00142-5
4,7-Dihydroxy-2-(2-hydroxypropan-2-yl)-6-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-b]xanthen-5-one	24829256	Click to see CC(=CCC1=C(C=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C4)C(C)(C)O)O)O)C	396.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.023
4,8-Dihydroxy-2-(1-hydroxy-1-methyl-ethyl)-7-methoxy-6-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-b]xanthen-5-one	5495930	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C4)C(C)(C)O)O)O)OC)C	426.50	unknown	https://doi.org/10.1248/CPB.54.301 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887388/ https://doi.org/10.1016/J.PHYTOCHEM.2007.09.023 https://doi.org/10.1016/S0031-9422(02)00142-5 https://doi.org/10.1248/CPB.51.857
4,8-Dihydroxy-2-(2-hydroxypropan-2-yl)-7-methoxy-6-(3-methylbut-2-enyl)-3-[1,3,6-trihydroxy-7-methoxy-2,8-bis(3-methylbut-2-enyl)-9-oxoxanthen-4-yl]-2,3-dihydrofuro[3,2-b]xanthen-5-one	75223645	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C4C5=C(C(=C(C6=C5OC7=C(C6=O)C(=C(C(=C7)O)OC)CC=C(C)C)O)CC=C(C)C)O)C(C)(C)O)O)O)OC)C	834.90	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887388/
4,8-Dihydroxy-7-methoxy-6-(3-methylbut-2-enyl)furo[3,2-b]xanthen-5-one	162846027	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(O2)C=C4C(=C3O)C=CO4)O)OC)C	366.40	unknown	https://doi.org/10.1016/J.FITOTE.2010.02.002
5-Hydroxy-8,9-dimethoxy-2,2-dimethyl-7-(3-methylbut-2-enyl)pyrano[3,2-b]xanthen-6-one	102187620	Click to see CC(=CCC1=C2C(=CC(=C1OC)OC)OC3=CC4=C(C=CC(O4)(C)C)C(=C3C2=O)O)C	422.50	unknown	https://doi.org/10.1016/S0031-9422(02)00142-5
6-Deoxy-gamma-mangostin	13873657	Click to see CC(=CCC1=C(C=CC2=C1C(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)O)C	380.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2007.09.023 https://doi.org/10.1248/CPB.41.958
7-Methoxy-2-(3-methyl-2-butenyl)-8-(3-methyl-2-oxo-3-butenyl)-1,3,6-trihydroxyxanthone	69074110	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)OC)CC(=O)C(=C)C)O)C	424.40	unknown	https://doi.org/10.1021/JF052649Z
9-Hydroxycalabaxanthone	5495929	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C=C4)(C)C)O)O)OC)C	408.40	unknown	via CMAUP database
9-Hydroxycalabaxanthone hydrate	56840489	Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C=C(C(=C4CCC(C)(C)O)OC)O)C	426.50	unknown	https://doi.org/10.1002/HLCA.201100157
beta-Mangostin	5495925	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C=C(C(=C3CC=C(C)C)OC)O)OC)C	424.50	unknown	https://doi.org/10.1021/NP50051A021 https://doi.org/10.1111/J.2042-7158.1996.TB03988.X https://doi.org/10.1016/S0031-9422(02)00142-5 https://doi.org/10.1016/0031-9422(95)00042-6 https://doi.org/10.1016/J.PHYMED.2003.09.012 https://doi.org/10.1002/JLAC.19304820119 https://doi.org/10.1248/CPB.51.857 https://doi.org/10.1021/NP020546U https://doi.org/10.1021/NP000583Q https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887388/ https://doi.org/10.1248/CPB.54.301 https://doi.org/10.1248/CPB.41.958 https://doi.org/10.1016/J.BMCL.2010.08.061 https://doi.org/10.1016/J.BMC.2010.07.033 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9213587/ https://doi.org/10.1021/NP010566G
Calabaxanthone	341188	Click to see CC(=CCC1=C(C=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C=C4)(C)C)O)OC)C	392.40	unknown	https://doi.org/10.1021/NP50051A021
Cratoxyxanthone	46879489	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C4C5=C(C(=C(C6=C5OC7=C(C6=O)C(=C(C(=C7)O)OC)CC=C(C)C)O)CC=C(C)C)O)C(C)(C)O)O)O)OC)C	834.90	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887388/
Demethylcalabaxanthone	509270	Click to see CC(=CCC1=C(C=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C=C4)(C)C)O)O)C	378.40	unknown	https://doi.org/10.1248/CPB.54.301 https://doi.org/10.1021/NP50051A021 https://doi.org/10.1248/CPB.51.857
di-O-acetylmangostin	44566652	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(C(=C(C=C3O2)OC(=O)C)OC)CC=C(C)C)OC(=O)C)C	494.50	unknown	via CMAUP database
Dulxanthone D	10405091	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)OC)C	342.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.04.032
gamma-Mangostin	5464078	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)O)CC=C(C)C)O)C	396.40	unknown	https://doi.org/10.1055/S-2006-957916 https://doi.org/10.1254/FPJ.110.SUPPLEMENT_153 https://doi.org/10.1055/S-2006-957943 https://doi.org/10.1021/NP50051A021 https://doi.org/10.1016/S0031-9422(82)85052-8 https://doi.org/10.1111/J.2042-7158.1996.TB03988.X https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3734031/ https://doi.org/10.1248/YAKUSHI1947.114.2_129 https://doi.org/10.1016/0031-9422(95)00042-6 https://doi.org/10.1055/S-2002-35668 https://doi.org/10.1016/J.PBB.2009.12.021 https://doi.org/10.1248/CPB.51.857 https://doi.org/10.1021/NP020546U https://doi.org/10.1021/NP000583Q https://doi.org/10.1016/J.FCT.2007.09.096 https://doi.org/10.1248/CPB.54.301 https://doi.org/10.1248/CPB.41.958 https://doi.org/10.1016/S0031-9422(96)00410-4 https://doi.org/10.1016/J.BMCL.2010.08.061 https://doi.org/10.1016/J.BMC.2010.07.033 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9213587/ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2572570/ https://doi.org/10.1021/JF052649Z https://doi.org/10.1016/J.FITOTE.2010.02.002
Garcimangosone A	10874207	Click to see CC(=CCC1=C2C(=C(C3=C1C(=O)C4=C(C5=C(C=C4O3)OC(C=C5)(C)C)O)O)C=CC(O2)(C)C)C	460.50	unknown	https://doi.org/10.1021/NP000583Q
Garcinone C	44159808	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)O)CCC(C)(C)O)O)C	414.40	unknown	https://doi.org/10.1248/CPB.54.301 https://doi.org/10.1016/J.FITOTE.2010.02.002 https://doi.org/10.1016/0031-9422(81)85250-8 https://doi.org/10.1016/S0031-9422(82)85052-8
Garcinone D	5495926	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)OC)CCC(C)(C)O)O)C	428.50	unknown	https://doi.org/10.1016/J.FITOTE.2010.02.002 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887388/ https://doi.org/10.1016/J.BMC.2010.07.033 https://doi.org/10.1021/JF052649Z https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2572570/ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9213587/ https://doi.org/10.1248/CPB.51.857 https://doi.org/10.1021/NP000583Q https://doi.org/10.1016/0031-9422(81)85250-8 https://doi.org/10.1248/CPB.54.301
Garcinone E	10298511	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C(=C(C(=C3C2=O)CC=C(C)C)O)O)CC=C(C)C)O)C	464.50	unknown	https://doi.org/10.1016/0031-9422(95)00042-6 https://doi.org/10.1016/J.BMCL.2010.08.061 https://doi.org/10.1021/NP020546U https://doi.org/10.1002/HLCA.201100157 https://doi.org/10.1248/CPB.41.958 https://doi.org/10.1021/JF052649Z https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2572570/ https://doi.org/10.1016/S0031-9422(96)00410-4 https://doi.org/10.1021/NP000583Q https://doi.org/10.1111/J.2042-7158.1996.TB03988.X https://doi.org/10.1248/CPB.54.301
Mangostanol	10048103	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C(C4)O)(C)C)O)O)OC)C	426.50	unknown	https://doi.org/10.1248/CPB.54.301 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887388/ https://doi.org/10.1016/J.BMC.2010.07.033 https://doi.org/10.1021/NP000583Q https://doi.org/10.1021/NP010566G https://doi.org/10.1016/S0031-9422(96)00410-4 https://doi.org/10.1248/CPB.51.857
Mangostenol	5495927	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(O2)C=C(C(=C3O)CC(C(=C)C)O)O)O)OC)C	426.50	unknown	https://doi.org/10.1021/NP010566G https://doi.org/10.1248/CPB.51.857
Mangostenone A	509267	Click to see CC(=CCC1=C2C(=C3C=CC(OC3=C1O)(C)C)OC4=CC5=C(C=CC(O5)(C)C)C(=C4C2=O)O)C	460.50	unknown	https://doi.org/10.1021/NP010566G https://doi.org/10.1248/CPB.51.857
Mangostenone C	11546716	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C4O)C(C)(C)O)O)O)OC)C	442.50	unknown	https://doi.org/10.1248/CPB.54.301
Mangostenone E	11495983	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)OC)CC(C(C)(C)O)O)O)C	444.50	unknown	https://doi.org/10.1248/CPB.54.301
Mangostenone F	49866102	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C4)C(=C)C)O)O)OC)C	408.40	unknown	https://doi.org/10.1016/J.BMC.2010.07.033
Mangostin	5281650	Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C(=C(C(=C3)O)OC)CC=C(C)C)O)C	410.50	unknown	https://doi.org/10.1021/NP010566G https://doi.org/10.1248/CPB.54.301 https://doi.org/10.1016/S0031-9422(96)00410-4 https://doi.org/10.1039/C39880000619 https://doi.org/10.1248/CPB.41.958 https://doi.org/10.1021/NP000583Q https://doi.org/10.1016/J.FITOTE.2007.02.019 https://doi.org/10.1016/J.BMC.2007.04.071 https://doi.org/10.1016/S0031-9422(82)85052-8 https://doi.org/10.1016/J.BMCL.2010.08.061 https://doi.org/10.1016/J.FCT.2007.09.096 https://doi.org/10.1016/0031-9422(88)80242-5 https://doi.org/10.1248/YAKUSHI1947.114.2_129 https://doi.org/10.1055/S-2006-957916 https://doi.org/10.1016/J.PHYMED.2003.09.012 https://doi.org/10.1055/S-2006-957943 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2572570/ https://doi.org/10.1248/CPB.51.857 https://doi.org/10.1021/JF052649Z https://doi.org/10.1016/J.PHYTOCHEM.2007.09.023 https://doi.org/10.1254/FPJ.110.SUPPLEMENT_153 https://doi.org/10.1016/J.PBB.2009.12.021 https://doi.org/10.1021/NP50051A021 https://doi.org/10.1016/J.FITOTE.2010.02.002 https://doi.org/10.1021/NP020546U https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9213587/ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887388/ https://doi.org/10.1016/0031-9422(95)00042-6 https://doi.org/10.1016/J.BMC.2010.07.033 https://doi.org/10.1111/J.2042-7158.1996.TB03988.X https://doi.org/10.1021/NP50004A002 https://doi.org/10.1039/P19900002671 https://doi.org/10.1055/S-2002-35668
Rubraxanthone	9953366	Click to see CC(=CCCC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)OC)C)C	410.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
5,13-Dihydroxy-3,3,10,10-tetramethyl-2,3-dihydro-10H-dipyrano[3,2-a:2',3'-i]xanthene-14(1H)-one	56840488	Click to see CC1(CCC2=C(O1)C(=CC3=C2C(=O)C4=C(C5=C(C=C4O3)OC(C=C5)(C)C)O)O)C	394.40	unknown	https://doi.org/10.1002/HLCA.201100157
BR-xanthone A	13964005	Click to see CC1(CCC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C=C(C5=C4CCC(O5)(C)C)O)C	396.40	unknown	https://doi.org/10.1016/0031-9422(88)80242-5 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9213587/
Brasilixanthone B	5324261	Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C=C(C5=C4C=CC(O5)(C)C)O)C	392.40	unknown	via CMAUP database
Garcimangosone B	11143989	Click to see CC1(CCC2=C3C(=CC(=C2O1)OC)OC4=CC5=C(C=CC(O5)(C)C)C(=C4C3=O)O)C	408.40	unknown	https://doi.org/10.1021/JF052649Z https://doi.org/10.1021/NP000583Q
Macluraxanthone	5281646	Click to see CC1(C=CC2=C(C3=C(C(=C2O1)C(C)(C)C=C)OC4=C(C3=O)C=CC(=C4O)O)O)C	394.40	unknown	via CMAUP database
O-Demethylforbexanthone	45269778	Click to see CC1(C=CC2=CC3=C(C(=C2O1)O)OC4=CC(=CC(=C4C3=O)O)O)C	326.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.04.032
Thwaitesixanthone	392169	Click to see CC1(C=CC2=C(O1)C=CC3=C2C(=O)C4=C(C5=C(C=C4O3)OC(C=C5)(C)C)O)C	376.40	unknown	https://doi.org/10.1248/CPB.54.301
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
(3R)-8-Hydroxy-3-methyl-3,4-dihydro-1H-2-benzopyran-1-one	114679	Click to see CC1CC2=C(C(=CC=C2)O)C(=O)O1	178.18	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
3-Methyl-4,8-dihydroxy-3,4-dihydroisocoumarin	169539	Click to see CC1C(C2=C(C(=CC=C2)O)C(=O)O1)O	194.18	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
cis-4-Hydroxymellein	10420140	Click to see CC1C(C2=C(C(=CC=C2)O)C(=O)O1)O	194.18	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
Mellein	28516	Click to see CC1CC2=C(C(=CC=C2)O)C(=O)O1	178.18	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
trans-4-Hydroxymellein	10262028	Click to see CC1C(C2=C(C(=CC=C2)O)C(=O)O1)O	194.18	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
> Organoheterocyclic compounds / Dioxanes / 1,3-dioxanes
3,4,12-Trimethyl-10,13-dioxatetracyclo[7.3.1.01,9.03,7]trideca-5,7-diene	75079840	Click to see CC1COC23C1(O2)CC4(C(C=CC4=C3)C)C	218.29	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
Botryosphaerihydrofuran	44605288	Click to see CC1COC23C1(O2)CC4(C(C=CC4=C3)C)C	218.29	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
> Organoheterocyclic compounds / Heteroaromatic compounds
2-Furylacetone	228583	Click to see CC(=O)CC1=CC=CO1	124.14	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
> Organoheterocyclic compounds / Isoindoles and derivatives / Isoindolines / Isoindolones
Stachybotrin C	10368882	Click to see CC(=CCCC(=CCCC1(C(CC2=C(C=C3C(=C2O1)CN(C3=O)CCC4=CC=C(C=C4)O)O)O)C)C)C	505.60	unknown	https://doi.org/10.1016/S0040-4020(01)98253-5 https://doi.org/10.1055/S-2002-35668 https://doi.org/10.1021/NP000583Q https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887388/ https://doi.org/10.1248/CPB.54.301 https://doi.org/10.1248/CPB.41.958 https://doi.org/10.1016/S0031-9422(96)00410-4 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9213587/ https://doi.org/10.1016/J.BMC.2010.07.033 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2572570/ https://doi.org/10.1021/JF052649Z https://doi.org/10.1016/J.FITOTE.2010.02.002
> Organoheterocyclic compounds / Lactones / Delta valerolactones
4-Hydroxy-6-propyloxan-2-one	13617298	Click to see CCCC1CC(CC(=O)O1)O	158.19	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
Tetrahydro-4-hydroxy-6-propylpyran-2-one	130907047	Click to see CCCC1CC(CC(=O)O1)O	158.19	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3S,4R,5R)-4-(Hydroxymethyl)-3,5-dimethyltetrahydrofuran-2-one	102125217	Click to see CC1C(C(OC1=O)C)CO	144.17	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
(3S,4S)-4-acetyl-3-methyloxolan-2-one	118708002	Click to see CC1C(COC1=O)C(=O)C	142.15	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
4-[(4-Acetyl-3-methyloxolan-2-yl)oxymethyl]-3,5-dimethyloxolan-2-one	75079746	Click to see CC1C(COC1OCC2C(C(=O)OC2C)C)C(=O)C	270.32	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
4-[[4-(Hydroxymethyl)-3,5-dimethyloxolan-2-yl]oxymethyl]-3,5-dimethyloxolan-2-one	162956264	Click to see CC1C(C(OC1OCC2C(C(=O)OC2C)C)C)CO	272.34	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
4-Acetyl-3-methyloxolan-2-one	25003520	Click to see CC1C(COC1=O)C(=O)C	142.15	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
4-Hydroxymethyl-3,5-dimethyldihydro-2-furanone	85727361	Click to see CC1C(C(OC1=O)C)CO	144.17	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
Botryosphaerilactone A	102161309	Click to see CC1C(C(OC1OCC2C(C(=O)OC2C)C)C)CO	272.34	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
Botryosphaerilactone B	44605080	Click to see CC1C(COC1OCC2C(C(=O)OC2C)C)C(=O)C	270.32	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
Botryosphaerilactone C	102161308	Click to see CC1C(C(OC1OCC2C(C(=O)OC2C)C)C)CO	272.34	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
> Organoheterocyclic compounds / Naphthofurans
[(1S,3R,8S,9S,10R,11S,13R)-11-acetyloxy-3-hydroxy-6,9,10-trimethyl-5-oxo-4,14-dioxatetracyclo[7.5.0.01,13.03,7]tetradec-6-en-8-yl] (Z)-2-methylbut-2-enoate	162993668	Click to see CC=C(C)C(=O)OC1C2=C(C(=O)OC2(CC34C1(C(C(CC3O4)OC(=O)C)C)C)O)C	420.50	unknown	https://doi.org/10.1016/S0031-9422(00)82235-9 https://doi.org/10.1016/J.BMCL.2010.08.061 https://doi.org/10.1016/J.FITOTE.2010.02.002 https://doi.org/10.1016/J.PHYTOCHEM.2007.09.023 https://doi.org/10.1016/S0031-9422(02)00142-5 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2887388/ https://doi.org/10.1016/J.BMC.2010.07.033 https://doi.org/10.1016/S0031-9422(96)00410-4 https://doi.org/10.1021/NP000583Q https://doi.org/10.1248/CPB.51.857 https://doi.org/10.1016/0031-9422(81)85250-8 https://doi.org/10.1248/CPB.54.301
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
6-Propyl-5,6-dihydro-2H-pyran-2-one	13949543	Click to see CCCC1CC=CC(=O)O1	140.18	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
Lasiolactone	89352705	Click to see CCCC1CC=CC(=O)O1	140.18	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
> Organoheterocyclic compounds / Pyridines and derivatives
Pyridine	1049	Click to see C1=CC=NC=C1	79.10	unknown	https://doi.org/10.1016/0031-9422(82)80025-3
> Organoheterocyclic compounds / Pyrrolidines / Pyrrolidones / Maleimides
3-Ethyl-4-methyl-1H-pyrrole-2,5-dione	29995	Click to see CCC1=C(C(=O)NC1=O)C	139.15	unknown	https://doi.org/10.1016/0031-9422(96)00276-2
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Egonol	485186	Click to see COC1=CC(=CC2=C1OC(=C2)C3=CC4=C(C=C3)OCO4)CCCO	326.30	unknown	https://doi.org/10.1016/J.BMCL.2010.08.061 https://doi.org/10.1248/CPB.41.958
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,2'R,3R,3'R)-2,2'-Bis(3,4-dihydroxyphenyl)-3,3',4,4'-tetrahydro-2H,2'H-4,8'-bichromene-3,3',5,5',7,7'-hexol	5320711	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1021/NP000583Q https://doi.org/10.1248/YAKUSHI1947.114.2_129
(2R,3R)-2-(3,4-dihydroxyphenyl)-6-[(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol	11649946	Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	via CMAUP database
5-Hydroxy-8-[5-hydroxy-7-methoxy-2-(4-methoxyphenyl)-4-oxochromen-8-yl]-7-methoxy-2-(4-methoxyphenyl)chromen-4-one	11103936	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)OC)O)OC	594.60	unknown	via CMAUP database
Endotelon	130556	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1021/NP000583Q
ent-Epicatechin-(4alpha->6)-ent-epicatechin	13990892	Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1021/NP000583Q
epigallocatechin-(4beta->8,2beta->O-7)-epicatechin	637122	Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C(=C6)O)O)O)O)O)C7=CC(=C(C=C7)O)O)O	592.50	unknown	via CMAUP database
Manniflavanone	198549	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)C4=C5C(=C(C=C4O)O)C(=O)C(C(O5)C6=CC(=C(C=C6)O)O)O)O)O	590.50	unknown	via CMAUP database
Pavetannin A2	10415767	Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O	576.50	unknown	via CMAUP database
Proanthocyanidin A1	9872976	Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O	576.50	unknown	https://doi.org/10.1021/NP000583Q
Procyanidin A1	5089889	Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O	576.50	unknown	https://doi.org/10.1021/NP000583Q
Procyanidin A2	124025	Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O	576.50	unknown	https://doi.org/10.1021/NP000583Q
Procyanidin B2, (+)-	122738	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1021/NP000583Q https://doi.org/10.1248/YAKUSHI1947.114.2_129
Procyanidin B5	124017	Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	https://doi.org/10.1021/NP000583Q
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol	1203	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	https://doi.org/10.1021/NP000583Q https://doi.org/10.1016/J.BMCL.2010.08.061
Cianidanol	9064	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
Epicatechin	72276	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	https://doi.org/10.1021/NP000583Q https://doi.org/10.1248/YAKUSHI1947.114.2_129 https://doi.org/10.1021/NP010566G https://doi.org/10.1016/J.BMCL.2010.08.061 https://doi.org/10.1016/S0031-9422(96)00410-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3-dihydrochromen-4-one	46173911	Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	450.40	unknown	via CMAUP database
(2R,3S)-2-(3,5-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3-dihydrochromen-4-one	6325418	Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=CC(=C4)O)O)O)O)O	450.40	unknown	https://doi.org/10.1016/J.BMCL.2010.08.061
2-(3,5-Dihydroxyphenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-2,3-dihydrochromen-4-one	75163656	Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=CC(=C4)O)O)O)O)O	450.40	unknown	https://doi.org/10.1016/J.BMCL.2010.08.061
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-3-[(2S,3S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	44258782	Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C(=CC(=C3C2=O)O)O)CC=C(C)C)C4=CC=C(C=C4)O)O)O)O	500.50	unknown	via CMAUP database
Astilbin	119258	Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	450.40	unknown	https://doi.org/10.1021/NP000583Q
Isoastilbin	316844	Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	450.40	unknown	https://doi.org/10.1021/NP000583Q
> Phenylpropanoids and polyketides / Macrolides and analogues
(4S,8R)-8,14-dihydroxy-16-methoxy-4-methyl-3-oxabicyclo[10.4.0]hexadeca-1(12),13,15-trien-2-one	134142479	Click to see CC1CCCC(CCCC2=C(C(=CC(=C2)O)OC)C(=O)O1)O	308.40	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
2-Hydroxy-4-methoxy-7-methyl-7,8,9,10,11,12,13,14-octahydro-6-oxabenzocyclododecen-5-one	602765	Click to see CC1CCCCCCCC2=C(C(=CC(=C2)O)OC)C(=O)O1	292.40	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
5R-Htdroxylasiodiplodin	10638525	Click to see CC1CC(CCCCCC2=C(C(=CC(=C2)O)OC)C(=O)O1)O	308.40	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
5S-Hydoroxylasiodiplodin	10733600	Click to see CC1CC(CCCCCC2=C(C(=CC(=C2)O)OC)C(=O)O1)O	308.40	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
8,14-Dihydroxy-16-methoxy-4-methyl-3-oxabicyclo[10.4.0]hexadeca-1(12),13,15-trien-2-one	75079841	Click to see CC1CCCC(CCCC2=C(C(=CC(=C2)O)OC)C(=O)O1)O	308.40	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007
Lasiodiplodin	14562696	Click to see CC1CCCCCCCC2=C(C(=CC(=C2)O)OC)C(=O)O1	292.40	unknown	https://doi.org/10.1016/J.PHYTOL.2012.11.007

Biological Material Top

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Garcinia mangostana

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top