Cratoxylum cochinchinense

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	UUID644013fc70a9b720810266
Scientific name	Cratoxylum cochinchinense
Authority	(Lour.) Blume
First published in	Ann. Mus. Bot. Lugduno-Batavi 2: 17 (1856)

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
Vismia cochinchinensis	(Lour.) Spreng.	Syst. Veg. 3: 350 (1826)
Ancistrolobus brevipes	Turcz.	Bull. Soc. Imp. Naturalistes Moscou 31(1): 383. 1858
Ancistrolobus ligustrinus	Spach	Ann. Sci. Nat., Bot. sér. 2, 5: 352. 1836
Cratoxylum biflorum	(Lam.) Turcz.	Bull. Soc. Imp. Naturalistes Moscou 36(I): 580 (1863)
Cratoxylum carneum	Kurz	J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 43: 84 (1874)
Cratoxylum chinense	(Hance) Merr.	Philipp. J. Sci., C 4: 292 (1909)
Cratoxylum hypoleuca	Elmer	Leafl. Philipp. Bot. 5: 1787 (1913)
Cratoxylum lanceolatum	Miq.	Fl. Ned. Ind., Eerste Bijv. : 500 (1861)
Cratoxylum ligustrinum	(Spach) Blume	Ann. Mus. Bot. Lugduno-Batavi 2: 16 (1856)
Cratoxylum myrtifolium	Blume	Ann. Mus. Bot. Lugduno-Batavi 2: 17 (1856)
Cratoxylum petiolatum	Blume	Ann. Mus. Bot. Lugduno-Batavi 2: 17 (1856)
Cratoxylum polyanthum	Korth.	Verh. Nat. Gesch. Ned. Bezitt., Bot. : t. 36 (1841)
Cratoxylum wightii	Blume	Ann. Mus. Bot. Lugduno-Batavi 2: 18 (1856)
Hypericum carneum	Wall.	Numer. List : n.º 4820 (1831)
Hypericum horridum	Wall.	Numer. List : n.º 4822 (1831)
Hypericum loureiroi	K.Koch	Hort. Dendrol. : 65 (1853)
Hypericum pulchellum	Willd.	Enum. Pl. Hort. Berol. , Suppl.: 53 (1814)
Cratoxylum polyanthum var. ligustrinum	Blume	Mus. Bot. 2: 16. 1856
Cratoxylum polyanthum var. ligustrinum	(Spach) Dyer
Elodes chinensis	Hance	London J. Bot. 7: 472 (1848)
Hypericum biflorum	Lam.	Encycl. 4: 170 (1797)
Stalagmites erosipetala	Miq.
Hypericum cochinchinense	Lour.	Fl. Cochinch. : 472 (1790)
Elodes pulchella	Hort.Chels. ex Loudon	Hort. Brit. [Loudon], ed. 2. 587. 1832 ; first additional supplement (cited in IK as 'Hort. Brit. Suppl. i.')

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	yellow cow wood
Thai	ติ้วเกลี้ยง
Vietnamese	thành ngạnh
Vietnamese	lành ngạnh
Vietnamese	lành ngạnh nam
Chinese	黄牛茶
Chinese	黄牛木
Chinese	蕉笼木
Chinese	黄芽木
Chinese	黃牛木

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!

No variety added yet.

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

Asia-tropical click to expand
- Indo-China
  - Andaman Islands
  - Cambodia
  - Laos
  - Myanmar
  - Nicobar Nicobar
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Malaya
  - Philippines
  - Sumatera

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000625754
Tropicos	7801610
KEW	urn:lsid:ipni.org:names:433054-1
The Plant List	kew-2742412
Open Tree Of Life	382590
NCBI Taxonomy	271749
IUCN Red List	33936
IPNI	433054-1
iNaturalist	183979
GBIF	3712064
Freebase	/m/02w0f3f
EOL	2889737
USDA GRIN	425300
Wikipedia	Cratoxylum_cochinchinense
CMAUP	NPO24928

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

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

Complete Chloroplast Genome of Hypericum perforatum and Dynamic Evolution in Hypericum (Hypericaceae)

Liu X, Bai Y, Wang Y, Chen Y, Dong W, Zhang Z

Int J Mol Sci

09-Nov-2023

PMCID:	PMC10671389
doi:	10.3390/ijms242216130
PMID:	38003320

Xanthones with Potential Anti-Inflammatory and Anti-HIV Effects from the Stems and Leaves of Cratoxylum cochinchinense

Zhang Y, Guo JM, Zhang MM, Wang R, Liang CH, Zhao YM, Deng YY, Liu YP, Fu YH

Molecules

14-Aug-2023

PMCID:	PMC10458312
doi:	10.3390/molecules28166050
PMID:	37630303

Investigation of bacterial neuraminidase inhibition of xanthones bearing geranyl and prenyl groups from Cratoxylum cochinchinense

Kim JY, Li ZP, Lee G, Kim JH, Shah AB, Lee YH, Park KH

Front Chem

09-Aug-2023

PMCID:	PMC10445491
doi:	10.3389/fchem.2023.1245071
PMID:	37621851

Antimicrobial, Cytotoxic, and α-Glucosidase Inhibitory Activities of Ethanol Extract and Chemical Constituents Isolated from Homotrigona apicalis Propolis—In Vitro and Molecular Docking Studies

Phuong DT, Van Phuong N, Le Tuan N, Cong NT, Hang NT, Thanh LN, Hue VT, Vuong NQ, Ha NT, Popova M, Trusheva B, Bankova V

Life (Basel)

03-Aug-2023

PMCID:	PMC10455239
doi:	10.3390/life13081682
PMID:	37629539

Ethnobotanical study on herbal tea drinks in Guangxi, China

Long T, Hu R, Cheng Z, Xu C, Hu Q, Liu Q, Gu R, Huang Y, Long C

J Ethnobiol Ethnomed

31-Mar-2023

PMCID:	PMC10064729
doi:	10.1186/s13002-023-00579-3
PMID:	37004116

Xanthones: Biosynthesis and Trafficking in Plants, Fungi and Lichens

Badiali C, Petruccelli V, Brasili E, Pasqua G

Plants (Basel)

04-Feb-2023

PMCID:	PMC9967055
doi:	10.3390/plants12040694
PMID:	36840041

The Role of Propolis as a Natural Product with Potential Gastric Cancer Treatment Properties: A Systematic Review

Rivera-Yañez N, Ruiz-Hurtado PA, Rivera-Yañez CR, Arciniega-Martínez IM, Yepez-Ortega M, Mendoza-Arroyo B, Rebollar-Ruíz XA, Méndez-Cruz AR, Reséndiz-Albor AA, Nieto-Yañez O

Foods

16-Jan-2023

PMCID:	PMC9858610
doi:	10.3390/foods12020415
PMID:	36673507

Chemical Profile and Antioxidant Capacity of Propolis from Tetragonula, Lepidotrigona, Lisotrigona and Homotrigona Stingless Bee Species in Vietnam

Popova M, Trusheva B, Chimshirova R, Antonova D, Gechovska K, Thanh LN, Lien NT, Phuong DT, Bankova V

Molecules

14-Nov-2022

PMCID:	PMC9696581
doi:	10.3390/molecules27227834
PMID:	36431935

Characterization of the plastid genome of Cratoxylum species (Hypericaceae) and new insights into phylogenetic relationships

Sudmoon R, Kaewdaungdee S, Tanee T, Siripiyasing P, Ameamsri U, Syazwan SA, Lee SY, Chaveerach A

Sci Rep

05-Nov-2022

PMCID:	PMC9637187
doi:	10.1038/s41598-022-23639-2
PMID:	36335203

From tumor mutational burden to characteristic targets analysis: Identifying the predictive biomarkers and natural product interventions in cancer management

Liu C, Yu Y, Wang G, Liu J, Liu R, Liu L, Yang X, Li H, Gao C, Lu Y, Zhuang J

Front Nutr

20-Sep-2022

PMCID:	PMC9530334
doi:	10.3389/fnut.2022.989989
PMID:	36204371

Cratoxylumxanthone C, a natural xanthone, inhibits lung cancer proliferation and metastasis by regulating STAT3 and FAK signal pathways

Li Y, Wang H, Liu W, Hou J, Xu J, Guo Y, Hu P

Front Pharmacol

09-Aug-2022

PMCID:	PMC9396379
doi:	10.3389/fphar.2022.920422
PMID:	36016565

The metabolic and molecular mechanisms of α-mangostin in cardiometabolic disorders (Review)

John OD, Mushunje AT, Surugau N, Mac Guad R

Int J Mol Med

27-Jul-2022

PMCID:	PMC9354700
doi:	10.3892/ijmm.2022.5176
PMID:	35904170

Protective Effects of Gamma-mangostin on Hydrogen Peroxideinduced Cytotoxicity in Human Retinal Pigment Epithelial Cells

HU PS, HSIA NY, CHIEN WC, MONG MC, HSIA TC, CHANG HM, WANG YC, CHANG WS, BAU DT, TSAI CW

In Vivo

03-Jul-2022

PMCID:	PMC9301439
doi:	10.21873/invivo.12879
PMID:	35738618

Multitarget Action of Xanthones from Garcinia mangostana against α-Amylase, α-Glucosidase and Pancreatic Lipase

Cardozo-Muñoz J, Cuca-Suárez LE, Prieto-Rodríguez JA, Lopez-Vallejo F, Patiño-Ladino OJ

Molecules

20-May-2022

PMCID:	PMC9144329
doi:	10.3390/molecules27103283
PMID:	35630761

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
> Alkaloids and derivatives / Aporphines
Norisocorydine	12313549	Click to see COC1=C(C2=C(CC3C4=C2C(=C(C=C4CCN3)OC)OC)C=C1)O	327.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254373/
> Benzenoids / Anthracenes
(3R)-3,8,9-trihydroxy-6-methoxy-3-methyl-7-(3-methylbut-2-enyl)-2,4-dihydroanthracen-1-one	92471155	Click to see CC(=CCC1=C(C2=C(C3=C(CC(CC3=O)(C)O)C=C2C=C1OC)O)O)C	356.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254373/
(3R)-7-[(2E)-3,7-dimethylocta-2,6-dienyl]-3,8,9-trihydroxy-6-methoxy-3-methyl-2,4-dihydroanthracen-1-one	163186968	Click to see CC(=CCCC(=CCC1=C(C2=C(C3=C(CC(CC3=O)(C)O)C=C2C=C1OC)O)O)C)C	424.50	unknown	https://doi.org/10.1139/V08-076 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254373/
(3S)-3,8,9-trihydroxy-6-methoxy-3-methyl-7-(3-methylbut-3-enyl)-2,4-dihydroanthracen-1-one	163025722	Click to see CC(=C)CCC1=C(C2=C(C3=C(CC(CC3=O)(C)O)C=C2C=C1OC)O)O	356.40	unknown	https://doi.org/10.1139/V08-076
3,8,9-Trihydroxy-6-methoxy-3-methyl-7-(3-methylbut-3-enyl)-2,4-dihydroanthracen-1-one	163025721	Click to see CC(=C)CCC1=C(C2=C(C3=C(CC(CC3=O)(C)O)C=C2C=C1OC)O)O	356.40	unknown	https://doi.org/10.1139/V08-076
7-(3,7-Dimethylocta-2,6-dienyl)-3,8,9-trihydroxy-6-methoxy-3-methyl-2,4-dihydroanthracen-1-one	162974574	Click to see CC(=CCCC(=CCC1=C(C2=C(C3=C(CC(CC3=O)(C)O)C=C2C=C1OC)O)O)C)C	424.50	unknown	https://doi.org/10.1139/V08-076 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254373/
> Benzenoids / Anthracenes / Anthraquinones
1,8-Dihydroxy-3-methoxy-6-methyl-2-(3-methylbut-2-enyl)anthracene-9,10-dione	11783130	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C(=C(C=C3C2=O)OC)CC=C(C)C)O	352.40	unknown	https://doi.org/10.1139/V08-076
3-(3,7-Dimethylocta-2,6-dienyloxy)-1,8-dihydroxy-6-methyl-9,10-anthraquinone	333635	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OCC=C(C)CCC=C(C)C	406.50	unknown	https://doi.org/10.1016/S0031-9422(98)00467-1
Geranyloxyemodin	5785070	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OCC=C(C)CCC=C(C)C	406.50	unknown	https://doi.org/10.1016/S0031-9422(98)00467-1
> Benzenoids / Benzene and substituted derivatives / Styrenes
(3R,4R)-4-ethenyl-3-[(Z)-3-hydroxy-3-phenylprop-2-enoyl]-4-methyloxolan-2-one	163187405	Click to see CC1(COC(=O)C1C(=O)C=C(C2=CC=CC=C2)O)C=C	272.29	unknown	https://doi.org/10.1016/0031-9422(94)00862-N
(3R,4S)-4-ethenyl-3-(3-hydroxy-3-phenylprop-2-enoyl)-4-methyloxolan-2-one	163003395	Click to see CC1(COC(=O)C1C(=O)C=C(C2=CC=CC=C2)O)C=C	272.29	unknown	https://doi.org/10.1021/NP900109Y
(3R,4S)-4-ethenyl-3-[(Z)-3-hydroxy-3-phenylprop-2-enoyl]-4-methyloxolan-2-one	163187402	Click to see CC1(COC(=O)C1C(=O)C=C(C2=CC=CC=C2)O)C=C	272.29	unknown	https://doi.org/10.1021/NP900109Y
(3S,4S)-4-ethenyl-3-hydroxy-3-(3-hydroxy-3-phenylprop-2-enoyl)-4-methyloxolan-2-one	162936458	Click to see CC1(COC(=O)C1(C(=O)C=C(C2=CC=CC=C2)O)O)C=C	288.29	unknown	https://doi.org/10.1021/NP900109Y
4-ethenyl-3-[(E)-3-hydroxy-3-phenylprop-2-enoyl]-4-methyloxolan-2-one	101919090	Click to see CC1(COC(=O)C1C(=O)C=C(C2=CC=CC=C2)O)C=C	272.29	unknown	https://doi.org/10.1021/NP900109Y https://doi.org/10.1016/0031-9422(94)00862-N
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
Hanultarin	25147697	Click to see COC1=C(C=CC(=C1)CC(CO)C(CC2=CC(=C(C=C2)O)OC)COC(=O)C=CC3=CC(=C(C=C3)O)OC)O	538.60	unknown	https://doi.org/10.1021/NP900109Y
> Lignans, neolignans and related compounds / Furanoid lignans
Episesamin	5204	Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6	354.40	unknown	https://doi.org/10.1021/NP1004483
Sesamin	72307	Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6	354.40	unknown	https://doi.org/10.1021/NP1004483
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
[2-(1,3-Benzodioxol-5-yl)-4-(1,3-benzodioxol-5-ylmethyl)oxolan-3-yl]methanol	14409639	Click to see C1C(C(C(O1)C2=CC3=C(C=C2)OCO3)CO)CC4=CC5=C(C=C4)OCO5	356.40	unknown	https://doi.org/10.1021/NP900109Y
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3R,4S,5S,6R)-2-[4-[(3S,3aR,6S,6aR)-6-[3-methoxy-4-[(2R,3R,4S,5S,6S)-3,4,5-trihydroxy-6-methoxyoxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	163008974	Click to see COC1C(C(C(C(O1)OC2=C(C=C(C=C2)C3C4COC(C4CO3)C5=CC(=C(C=C5)OC6C(C(C(C(O6)CO)O)O)O)OC)OC)O)O)O	682.70	unknown	https://doi.org/10.1016/J.TET.2009.01.083
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
(1R,6S,9S,10R,13R)-3-benzoyl-6-(2-hydroxypropan-2-yl)-9-methyl-1,13-bis(3-methylbut-2-enyl)-5-oxatricyclo[7.2.2.04,10]tridec-3-ene-2,11-dione	162971433	Click to see CC(=CCC1CC2(C(=O)C3C1(CCC(OC3=C(C2=O)C(=O)C4=CC=CC=C4)C(C)(C)O)C)CC=C(C)C)C	518.70	unknown	https://doi.org/10.1016/J.PHYTOL.2010.11.006 https://doi.org/10.1016/J.PHYTOL.2011.01.001
(1R)-1-[(2E)-3,7-dimethylocta-2,6-dienyl]-3,8-dihydroxy-1,5,5-tris(3-methylbut-2-enyl)xanthene-2,6,9-trione	163195591	Click to see CC(=CCCC(=CCC1(C2=C(C=C(C1=O)O)OC3=C(C2=O)C(=CC(=O)C3(CC=C(C)C)CC=C(C)C)O)CC=C(C)C)C)C	600.80	unknown	https://doi.org/10.3987/COM-09-S(S)28
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3103643/
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
(6R)-3,5-dihydroxy-4-[[(1S,2R,5R)-2-hydroxy-2-methyl-5-prop-1-en-2-ylcyclopentyl]methyl]-6-methyl-2-[(2S)-2-methylbutanoyl]-6-(3-methylbut-2-enyl)cyclohexa-2,4-dien-1-one	10411215	Click to see CCC(C)C(=O)C1=C(C(=C(C(C1=O)(C)CC=C(C)C)O)CC2C(CCC2(C)O)C(=C)C)O	444.60	unknown	https://doi.org/10.1246/CL.1987.1337
3,5-Dihydroxy-4-[(2-hydroxy-2-methyl-5-prop-1-en-2-ylcyclopentyl)methyl]-6-methyl-2-(2-methylbutanoyl)-6-(3-methylbut-2-enyl)cyclohexa-2,4-dien-1-one	44272986	Click to see CCC(C)C(=O)C1=C(C(=C(C(C1=O)(C)CC=C(C)C)O)CC2C(CCC2(C)O)C(=C)C)O	444.60	unknown	https://doi.org/10.1021/OL2021548 https://doi.org/10.1246/CL.1987.1337
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocotrienols
(2R)-5-[[(2S)-2,8-dimethyl-2-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trienyl]-3,4-dihydrochromen-6-yl]oxy]-2,8-dimethyl-2-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trienyl]-3,4-dihydrochromen-6-ol	162874014	Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)OC3=C(C=C(C4=C3CCC(O4)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)C)O	791.20	unknown	https://doi.org/10.1016/S0031-9422(00)95100-8
(2S)-2,8-dimethyl-2-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trienyl]chroman-6-ol	13988400	Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)O	396.60	unknown	https://doi.org/10.1016/S0031-9422(00)95100-8
(2S)-5-[(2S)-6-hydroxy-2,7,8-trimethyl-2-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trienyl]-3,4-dihydrochromen-5-yl]-2,7,8-trimethyl-2-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trienyl]-3,4-dihydrochromen-6-ol	101661996	Click to see CC1=C(C2=C(CCC(O2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)C(=C1O)C3=C(C(=C(C4=C3CCC(O4)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)C)C)O)C	819.20	unknown	https://doi.org/10.1016/S0031-9422(00)95100-8
(c)(1/2)-Tocotrienol pound>>Tocotrienol, delta	53394607	Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)O	396.60	unknown	https://doi.org/10.1016/S0031-9422(00)95100-8 https://doi.org/10.1016/J.PHYTOL.2010.11.006
5-[[2,8-Dimethyl-2-(4,8,12-trimethyltrideca-3,7,11-trienyl)-3,4-dihydrochromen-6-yl]oxy]-2,8-dimethyl-2-(4,8,12-trimethyltrideca-3,7,11-trienyl)-3,4-dihydrochromen-6-ol	162874012	Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)OC3=C(C=C(C4=C3CCC(O4)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)C)O	791.20	unknown	https://doi.org/10.1016/S0031-9422(00)95100-8
5-[6-Hydroxy-2,7,8-trimethyl-2-(4,8,12-trimethyltrideca-3,7,11-trienyl)-3,4-dihydrochromen-5-yl]-2,7,8-trimethyl-2-(4,8,12-trimethyltrideca-3,7,11-trienyl)-3,4-dihydrochromen-6-ol	162950926	Click to see CC1=C(C2=C(CCC(O2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)C(=C1O)C3=C(C(=C(C4=C3CCC(O4)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)C)C)O)C	819.20	unknown	https://doi.org/10.1016/S0031-9422(00)95100-8
delta-Tocotrienol	5282350	Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)CCC=C(C)C)O	396.60	unknown	https://doi.org/10.1016/S0031-9422(00)95100-8 https://doi.org/10.1016/J.PHYTOL.2010.11.006
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2S,5S,8R,9R)-4,4,8-trimethyltricyclo[6.3.1.01,5]dodecane-2,9-diol	162902598	Click to see CC1(CC(C23C1CCC(C2)(C(CC3)O)C)O)C	238.37	unknown	https://doi.org/10.1021/NP900109Y
alpha-Multijugenol	70566040	Click to see CC1=CCC2C(CC2(C)C)C(=C)CCC1O	220.35	unknown	https://doi.org/10.1021/NP900109Y
beta-CARYOPHYLLENE OXIDE	1742210	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1021/NP900109Y
Bicyclo(7.2.0)undec-3-en-5-ol, 4,11,11-trimethyl-8-methylene-, (1R,3E,5R,9S)-	6450454	Click to see CC1=CCC2C(CC2(C)C)C(=C)CCC1O	220.35	unknown	https://doi.org/10.1021/NP900109Y
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1021/NP900109Y
Caryophyllene epoxide	14350	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1021/NP900109Y
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1R,3R,4R,10S,11S,13S)-1-hydroxy-13-methyl-3,10-bis(prop-1-en-2-yl)-5,14-dioxatricyclo[9.2.1.14,7]pentadec-7(15)-ene-2,6,12-trione	11588543	Click to see CC1C(=O)C2C(CCC3=CC(C(C(=O)C1(O2)O)C(=C)C)OC3=O)C(=C)C	360.40	unknown	via CMAUP database
4'-Ethenyl-4',11-dimethyl-8-(6-methylhept-5-en-2-yl)-2-phenylspiro[3-oxatricyclo[5.4.0.02,6]undec-10-ene-4,3'-oxolane]-2',5-dione	72980936	Click to see CC1=CCC(C2C1C3(C2C(=O)C4(O3)C(=O)OCC4(C)C=C)C5=CC=CC=C5)C(C)CCC=C(C)C	474.60	unknown	https://doi.org/10.1021/NP900109Y
Biyouyanagin A	70697727	Click to see CC1=CCC(C2C1C3(C2C(=O)C4(O3)C(=O)OCC4(C)C=C)C5=CC=CC=C5)C(C)CCC=C(C)C	474.60	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2562601/
Kallosin A	10980852	Click to see CC(=C)C1CCC2=CC(C(C3=CC(C1O)(C(=O)O3)C)C(=C)C)OC2=O	344.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(4S,5S,7E,10R,11R)-5,8-dihydroxy-7-methyl-4,10-bis(prop-1-en-2-yl)-12-oxabicyclo[9.2.1]tetradeca-1(14),7-diene-6,9,13-trione	12000325	Click to see CC1=C(C(=O)C(C2C=C(CCC(C(C1=O)O)C(=C)C)C(=O)O2)C(=C)C)O	360.40	unknown	via CMAUP database
Kallolide D	11566668	Click to see CC1=C2C(C(CCC3=CC(C(C(C1=O)(O2)O)C(=C)C)OC3=O)C(=C)C)O	360.40	unknown	via CMAUP database
Kallolide H	11560083	Click to see CC1=CC(=O)C(C2C=C(CCC(C(C1=O)OC(=O)C)C(=C)C)C(=O)O2)C(=C)C	386.40	unknown	via CMAUP database
Kollolide C acetate	11704081	Click to see CC1=C(C(=O)C(C2C=C(CCC(C(C1=O)OC(=O)C)C(=C)C)C(=O)O2)C(=C)C)O	402.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2S,4aR,5S,8aR)-1,1,4a-trimethyl-6-methylidene-5-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trienyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalen-2-ol	162922498	Click to see CC(=CCCC(=CCCC(=CCCC1C(=C)CCC2C1(CCC(C2(C)C)O)C)C)C)C	426.70	unknown	https://doi.org/10.1016/J.PHYTOL.2010.11.006
(2S,4aR,5S,8aR)-1,1,4a,6-tetramethyl-5-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trienyl]-2,3,4,5,8,8a-hexahydronaphthalen-2-ol	162882007	Click to see CC1=CCC2C(C(CCC2(C1CCC=C(C)CCC=C(C)CCC=C(C)C)C)O)(C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(98)00467-1
(2S,4aR,5S,8aS)-1,1,4a-trimethyl-6-methylidene-5-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trienyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalen-2-ol	163191186	Click to see CC(=CCCC(=CCCC(=CCCC1C(=C)CCC2C1(CCC(C2(C)C)O)C)C)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(00)95100-8
(2S,4aS,5S,8aR)-1,1,4a,6-tetramethyl-5-[(3E,7E)-4,8,12-trimethyltrideca-3,7,11-trienyl]-2,3,4,5,8,8a-hexahydronaphthalen-2-ol	162882006	Click to see CC1=CCC2C(C(CCC2(C1CCC=C(C)CCC=C(C)CCC=C(C)C)C)O)(C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(98)00467-1
1,1,4a-trimethyl-6-methylidene-5-(4,8,12-trimethyltrideca-3,7,11-trienyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalen-2-ol	162922497	Click to see CC(=CCCC(=CCCC(=CCCC1C(=C)CCC2C1(CCC(C2(C)C)O)C)C)C)C	426.70	unknown	https://doi.org/10.1016/J.PHYTOL.2010.11.006 https://doi.org/10.1016/S0031-9422(00)95100-8
1,1,4a,6-Tetramethyl-5-(4,8,12-trimethyltrideca-3,7,11-trienyl)-2,3,4,5,8,8a-hexahydronaphthalen-2-ol	78385420	Click to see CC1=CCC2C(C(CCC2(C1CCC=C(C)CCC=C(C)CCC=C(C)C)C)O)(C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(98)00467-1
Betulinic Acid	64971	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	456.70	unknown	https://doi.org/10.1021/NP1004483
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/S0031-9422(00)95100-8
Lup-20(29)-en-3-ol, (3beta)-	521518	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(98)00467-1
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(98)00467-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3103643/
Glucoclionasterol	12309067	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3103643/
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3103643/
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
Trimethyl citrate	74112	Click to see COC(=O)CC(CC(=O)OC)(C(=O)OC)O	234.20	unknown	https://doi.org/10.1016/J.PHYTOL.2010.11.006 https://doi.org/10.1016/J.PHYTOL.2011.01.001
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Acyloins
Methyl 1',3,7-trihydroxy-3,4',7-trimethyl-4'-(3-methylbut-2-enyl)-3',5'-dioxospiro[1,2,3a,4,6,7a-hexahydroindene-5,2'-cyclopentane]-1'-carboxylate	74976237	Click to see CC(=CCC1(C(=O)C2(CC3C(CCC3(C)O)C(C2)(C)O)C(C1=O)(C(=O)OC)O)C)C	422.50	unknown	https://doi.org/10.1021/NP900109Y
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(3R,4S)-4-ethenyl-3-[(1R)-1-hydroxy-3-oxo-3-phenylpropyl]-4-methyloxolan-2-one	44255234	Click to see CC1(COC(=O)C1C(CC(=O)C2=CC=CC=C2)O)C=C	274.31	unknown	https://doi.org/10.1021/NP900109Y
4-Ethenyl-3-(1-hydroxy-3-oxo-3-phenylpropyl)-4-methyloxolan-2-one	74976283	Click to see CC1(COC(=O)C1C(CC(=O)C2=CC=CC=C2)O)C=C	274.31	unknown	https://doi.org/10.1021/NP900109Y
Aspidinol D	50908690	Click to see CCC(C)C(=O)C1=C(C(=C(C=C1O)OC)C)O	238.28	unknown	https://doi.org/10.1021/NP1004483
> Organoheterocyclic compounds / Benzodioxanes / Phenylbenzodioxanes / Phenylbenzo-1,4-dioxanes
(2R,3R)-5-hydroxy-3-(4-hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)-2,3-dihydro-[1,4]dioxino[2,3-c]xanthen-7-one	44513407	Click to see COC1=C(C=CC(=C1)C2C(OC3=C4C(=CC(=C3O2)O)C(=O)C5=CC=CC=C5O4)CO)O	422.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.08.015
(2R,3R)-8,10-dihydroxy-3-(4-hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)-2,3-dihydro-[1,4]dioxino[2,3-c]xanthen-7-one	162874404	Click to see COC1=C(C=CC(=C1)C2C(OC3=C(O2)C=CC4=C3OC5=CC(=CC(=C5C4=O)O)O)CO)O	438.40	unknown	https://doi.org/10.1016/0031-9422(94)00526-Y
(2S,3R)-8,10-dihydroxy-3-(4-hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)-2,3-dihydro-[1,4]dioxino[2,3-c]xanthen-7-one	101918998	Click to see COC1=C(C=CC(=C1)C2C(OC3=C(O2)C=CC4=C3OC5=CC(=CC(=C5C4=O)O)O)CO)O	438.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.08.015 https://doi.org/10.1016/0031-9422(94)00526-Y
2-Ethyl-8,10-dihydroxy-3-(4-hydroxy-3-methoxyphenyl)-2,3-dihydro-[1,4]dioxino[2,3-c]xanthen-7-one	162925233	Click to see CCC1C(OC2=C(O1)C3=C(C=C2)C(=O)C4=C(C=C(C=C4O3)O)O)C5=CC(=C(C=C5)O)OC	436.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.08.015
5-Hydroxy-3-(4-hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)-2,3-dihydro-[1,4]dioxino[2,3-c]xanthen-7-one	75038344	Click to see COC1=C(C=CC(=C1)C2C(OC3=C4C(=CC(=C3O2)O)C(=O)C5=CC=CC=C5O4)CO)O	422.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.08.015
8,10-Dihydroxy-3-(4-hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)-2,3-dihydro-[1,4]dioxino[2,3-c]xanthen-7-one	162874403	Click to see COC1=C(C=CC(=C1)C2C(OC3=C(O2)C=CC4=C3OC5=CC(=CC(=C5C4=O)O)O)CO)O	438.40	unknown	https://doi.org/10.1016/0031-9422(94)00526-Y
8,10-Dihydroxy-3-(4-hydroxy-3,5-dimethoxy-phenyl)-2-(hydroxymethyl)-2,3-dihydro-[1,4]dioxino[2,3-c]xanthen-7-one	14427464	Click to see COC1=CC(=CC(=C1O)OC)C2C(OC3=C(O2)C=CC4=C3OC5=CC(=CC(=C5C4=O)O)O)CO	468.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.08.015
> Organoheterocyclic compounds / Benzodioxoles
1,3-benzodioxol-5-yl-[(3S,5R)-5-(1,3-benzodioxol-5-yl)oxolan-3-yl]methanone	71552491	Click to see C1C(COC1C2=CC3=C(C=C2)OCO3)C(=O)C4=CC5=C(C=C4)OCO5	340.30	unknown	https://doi.org/10.1021/NP1004483
1,3-Benzodioxol-5-yl-[5-(1,3-benzodioxol-5-yl)oxolan-3-yl]methanone	75576334	Click to see C1C(COC1C2=CC3=C(C=C2)OCO3)C(=O)C4=CC5=C(C=C4)OCO5	340.30	unknown	https://doi.org/10.1021/NP1004483
hyperione A, (rel)-	50899859	Click to see C1C(COC1C2=CC3=C(C=C2)OCO3)C(=O)C4=CC5=C(C=C4)OCO5	340.30	unknown	https://doi.org/10.1021/NP1004483
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(1R,2R,13S,15S)-6,8-dihydroxy-13-methoxy-17,17-dimethyl-15-(3-methylbut-2-enyl)-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraene-10,14-dione	163027805	Click to see CC(=CCC12C(=O)C3(CC(C14C(=C3)C(=O)C5=C(C=C(C=C5O4)O)O)C(O2)(C)C)OC)C	426.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.10.008
(1S,2S,13R,15R)-6,8-dihydroxy-13-methoxy-17,17-dimethyl-15-(3-methylbut-2-enyl)-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraene-10,14-dione	163027804	Click to see CC(=CCC12C(=O)C3(CC(C14C(=C3)C(=O)C5=C(C=C(C=C5O4)O)O)C(O2)(C)C)OC)C	426.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.10.008
(1S,2S,13R,15S)-8-hydroxy-13-methoxy-17,17-dimethyl-15-(3-methylbut-2-enyl)-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraene-10,14-dione	162980614	Click to see CC(=CCC12C(=O)C3(CC(C14C(=C3)C(=O)C5=C(C=CC=C5O4)O)C(O2)(C)C)OC)C	410.50	unknown	https://doi.org/10.1248/CPB.54.745
(1S,2S,13R)-8-hydroxy-13-methoxy-17,17-dimethyl-15-(3-methylbut-2-enyl)-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraene-10,14-dione	163190407	Click to see CC(=CCC12C(=O)C3(CC(C14C(=C3)C(=O)C5=C(C=CC=C5O4)O)C(O2)(C)C)OC)C	410.50	unknown	https://doi.org/10.1248/CPB.54.745
[7-(3,7-Dimethylocta-2,6-dienoxy)-3-hydroxy-9-oxoxanthen-1-yl] acetate	74817712	Click to see CC(=CCCC(=CCOC1=CC2=C(C=C1)OC3=C(C2=O)C(=CC(=C3)O)OC(=O)C)C)C	422.50	unknown	https://doi.org/10.1016/J.TET.2009.01.083
[7-[(2E)-3,7-dimethylocta-2,6-dienoxy]-3-hydroxy-9-oxoxanthen-1-yl] acetate	42604440	Click to see CC(=CCCC(=CCOC1=CC2=C(C=C1)OC3=C(C2=O)C(=CC(=C3)O)OC(=O)C)C)C	422.50	unknown	https://doi.org/10.1016/J.TET.2009.01.083
1-Hydroxy-5,6-dimethoxyxanthone	90906816	Click to see COC1=C(C2=C(C=C1)C(=O)C3=C(C=CC=C3O2)O)OC	272.25	unknown	https://doi.org/10.1016/J.PHYTOL.2010.11.006
1,3-Dihydroxy-2,4-dimethoxy-9h-xanthen-9-one	90852378	Click to see COC1=C(C(=C2C(=C1O)C(=O)C3=CC=CC=C3O2)OC)O	288.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.043
1,3-Dihydroxy-7-(6-hydroxy-3,7-dimethylocta-2,7-dienoxy)xanthen-9-one	162950744	Click to see CC(=C)C(CCC(=CCOC1=CC2=C(C=C1)OC3=CC(=CC(=C3C2=O)O)O)C)O	396.40	unknown	https://doi.org/10.1139/V08-076
1,3-Dihydroxy-7-(7-hydroxy-3,7-dimethylocta-2,5-dienoxy)xanthen-9-one	162846414	Click to see CC(=CCOC1=CC2=C(C=C1)OC3=CC(=CC(=C3C2=O)O)O)CC=CC(C)(C)O	396.40	unknown	https://doi.org/10.1139/V08-076
1,3-dihydroxy-7-[(2E,5E)-7-hydroxy-3,7-dimethylocta-2,5-dienoxy]xanthen-9-one	102519728	Click to see CC(=CCOC1=CC2=C(C=C1)OC3=CC(=CC(=C3C2=O)O)O)CC=CC(C)(C)O	396.40	unknown	https://doi.org/10.1139/V08-076
1,3-dihydroxy-7-[(2E,6R)-6-hydroxy-3,7-dimethylocta-2,7-dienoxy]xanthen-9-one	163193210	Click to see CC(=C)C(CCC(=CCOC1=CC2=C(C=C1)OC3=CC(=CC(=C3C2=O)O)O)C)O	396.40	unknown	https://doi.org/10.1139/V08-076
1,3,5-Trihydroxy-6-methoxyxanthone	5479775	Click to see COC1=C(C2=C(C=C1)C(=O)C3=C(C=C(C=C3O2)O)O)O	274.22	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.043
1,3,5-Trihydroxy-6,7-dimethoxy-9h-xanthen-9-one	85922478	Click to see COC1=C(C(=C2C(=C1)C(=O)C3=C(C=C(C=C3O2)O)O)O)OC	304.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.043
1,3,5,6-Tetrahydroxyxanthone	5479774	Click to see C1=CC(=C(C2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)O	260.20	unknown	https://doi.org/10.1016/0031-9422(94)00526-Y
1,3,7-Trihydroxy-5-methoxy-9h-xanthen-9-one	91300928	Click to see COC1=CC(=CC2=C1OC3=CC(=CC(=C3C2=O)O)O)O	274.22	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.043
1,5,6-Trihydroxy-3-methoxy-9H-xanthen-9-one	86219227	Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)C=CC(=C3O)O)O	274.22	unknown	https://doi.org/10.1248/CPB.55.19
1,6-Dihydroxy-7,8-dimethoxyxanthone	14630572	Click to see COC1=C(C2=C(C=C1O)OC3=CC=CC(=C3C2=O)O)OC	288.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.043
1,7-Dihydroxy-3-(6-hydroxy-3,7-dimethylocta-2,7-dienoxy)xanthen-9-one	162909466	Click to see CC(=C)C(CCC(=CCOC1=CC(=C2C(=C1)OC3=C(C2=O)C=C(C=C3)O)O)C)O	396.40	unknown	https://doi.org/10.1139/V08-076
1,7-dihydroxy-3-[(2E,6R)-6-hydroxy-3,7-dimethylocta-2,7-dienoxy]xanthen-9-one	163189358	Click to see CC(=C)C(CCC(=CCOC1=CC(=C2C(=C1)OC3=C(C2=O)C=C(C=C3)O)O)C)O	396.40	unknown	https://doi.org/10.1139/V08-076
1,7-Dihydroxy-4-methoxyxanthone	5465785	Click to see COC1=C2C(=C(C=C1)O)C(=O)C3=C(O2)C=CC(=C3)O	258.23	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3103643/
2-Hydroxy-1-methoxy-xanthen-9-one	10399460	Click to see COC1=C(C=CC2=C1C(=O)C3=CC=CC=C3O2)O	242.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.08.015 https://doi.org/10.1016/J.PHYTOCHEM.2006.05.043
2,5-Dihydroxy-1-methoxyxanthone	10848779	Click to see COC1=C(C=CC2=C1C(=O)C3=C(O2)C(=CC=C3)O)O	258.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.043
2,5-Dihydroxyxanthone	182216	Click to see C1=CC2=C(C(=C1)O)OC3=C(C2=O)C=C(C=C3)O	228.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.043
3-(3,7-Dimethyl-6-oxoocta-2,7-dienoxy)-1,7-dihydroxyxanthen-9-one	163034482	Click to see CC(=C)C(=O)CCC(=CCOC1=CC(=C2C(=C1)OC3=C(C2=O)C=C(C=C3)O)O)C	394.40	unknown	https://doi.org/10.3987/COM-08-11628
3-(3,7-Dimethylocta-2,6-dienoxy)-1,7-dihydroxyxanthen-9-one	77916031	Click to see CC(=CCCC(=CCOC1=CC(=C2C(=C1)OC3=C(C2=O)C=C(C=C3)O)O)C)C	380.40	unknown	https://doi.org/10.1016/J.TET.2009.01.083 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254373/ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3103643/
3-[(2E)-3,7-dimethyl-6-oxoocta-2,7-dienoxy]-1,7-dihydroxyxanthen-9-one	102288097	Click to see CC(=C)C(=O)CCC(=CCOC1=CC(=C2C(=C1)OC3=C(C2=O)C=C(C=C3)O)O)C	394.40	unknown	https://doi.org/10.3987/COM-08-11628
3,4-Dihydroxy-2-methoxyxanthone	10038117	Click to see COC1=C(C(=C2C(=C1)C(=O)C3=CC=CC=C3O2)O)O	258.23	unknown	https://doi.org/10.1248/CPB.55.19
3,5-Dihydroxy-1,2-dimethoxy-9h-xanthen-9-one	154926285	Click to see COC1=C(C2=C(C=C1O)OC3=C(C2=O)C=CC=C3O)OC	288.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.043
3,5,6-Trihydroxy-1-methoxy-9h-xanthen-9-one	11277329	Click to see COC1=CC(=CC2=C1C(=O)C3=C(O2)C(=C(C=C3)O)O)O	274.22	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.08.015
3,6-Dihydroxy-1,2-dimethoxyxanthone	16105269	Click to see COC1=C(C2=C(C=C1O)OC3=C(C2=O)C=CC(=C3)O)OC	288.25	unknown	https://doi.org/10.1248/CPB.55.19
4-Hydroxy-2,3-dimethoxyxanthone	378690	Click to see COC1=C(C(=C2C(=C1)C(=O)C3=CC=CC=C3O2)O)OC	272.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.08.015
4,6-Dihydroxy-2,3-dimethoxyxanthone	16105267	Click to see COC1=C(C(=C2C(=C1)C(=O)C3=C(O2)C=C(C=C3)O)O)OC	288.25	unknown	https://doi.org/10.1248/CPB.55.19
4,7-Dihydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydro-5h-furo[3,2-b]xanthen-5-one	44632003	Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C=CC(=C4)O)O	328.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.043
6,8-Dihydroxy-17,17-dimethyl-15-(3-methylbut-2-enyl)-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraene-10,14-dione	74027120	Click to see CC(=CCC12C(=O)C3CC(C14C(=C3)C(=O)C5=C(C=C(C=C5O4)O)O)C(O2)(C)C)C	396.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.10.008
7-(3,7-Dimethyl-6-oxoocta-2,7-dienoxy)-1,3-dihydroxyxanthen-9-one	163035805	Click to see CC(=C)C(=O)CCC(=CCOC1=CC2=C(C=C1)OC3=CC(=CC(=C3C2=O)O)O)C	394.40	unknown	https://doi.org/10.3987/COM-08-11628
7-(3,7-Dimethylocta-2,6-dienoxy)-1,3-dihydroxyxanthen-9-one	78384970	Click to see CC(=CCCC(=CCOC1=CC2=C(C=C1)OC3=CC(=CC(=C3C2=O)O)O)C)C	380.40	unknown	https://doi.org/10.1016/J.TET.2009.01.083 https://doi.org/10.1016/S0031-9422(98)00467-1 https://doi.org/10.1139/V08-076 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254373/
7-[(2E)-3,7-dimethyl-6-oxoocta-2,7-dienoxy]-1,3-dihydroxyxanthen-9-one	102288096	Click to see CC(=C)C(=O)CCC(=CCOC1=CC2=C(C=C1)OC3=CC(=CC(=C3C2=O)O)O)C	394.40	unknown	https://doi.org/10.3987/COM-08-11628
7-[(2E)-3,7-dimethylocta-2,6-dienoxy]-1,3-dihydroxyxanthen-9-one	5317563	Click to see CC(=CCCC(=CCOC1=CC2=C(C=C1)OC3=CC(=CC(=C3C2=O)O)O)C)C	380.40	unknown	https://doi.org/10.1016/J.TET.2009.01.083 https://doi.org/10.1016/S0031-9422(98)00467-1 https://doi.org/10.1139/V08-076 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254373/
8-Hydroxy-1,2,3-trimethoxyxanthen-9-one	14756203	Click to see COC1=C(C(=C2C(=C1)OC3=CC=CC(=C3C2=O)O)OC)OC	302.28	unknown	https://doi.org/10.1016/J.PHYTOL.2010.11.006
8-Hydroxy-13-methoxy-17,17-dimethyl-15-(3-methylbut-2-enyl)-3,16-dioxapentacyclo[11.4.1.02,11.02,15.04,9]octadeca-4,6,8,11-tetraene-10,14-dione	73019072	Click to see CC(=CCC12C(=O)C3(CC(C14C(=C3)C(=O)C5=C(C=CC=C5O4)O)C(O2)(C)C)OC)C	410.50	unknown	https://doi.org/10.1016/J.TET.2009.01.083 https://doi.org/10.1016/J.PHYTOCHEM.2005.10.008 https://doi.org/10.1248/CPB.54.745
9H-Xanthen-9-one, 2-hydroxy-5-methoxy-	156048	Click to see COC1=CC=CC2=C1OC3=C(C2=O)C=C(C=C3)O	242.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.08.015
9H-Xanthen-9-one, 3-hydroxy-2,4-dimethoxy-	12214333	Click to see COC1=C(C(=C2C(=C1)C(=O)C3=CC=CC=C3O2)OC)O	272.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.043
9H-Xanthen-9-one, 3,5-dihydroxy-1-methoxy-	5479771	Click to see COC1=CC(=CC2=C1C(=O)C3=C(O2)C(=CC=C3)O)O	258.23	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2009.08.015
Buchanaxanthone	5481840	Click to see COC1=C(C=CC2=C1OC3=CC=CC(=C3C2=O)O)O	258.23	unknown	https://doi.org/10.1016/J.PHYTOL.2010.11.006
Cochinchinone C	70697833	Click to see CC(=CCC12C(=O)C3(CC(C14C(=C3)C(=O)C5=C(C=CC=C5O4)O)C(O2)(C)C)OC)C	410.50	unknown	https://doi.org/10.1016/J.TET.2009.01.083 https://doi.org/10.1016/J.PHYTOCHEM.2005.10.008 https://doi.org/10.1248/CPB.54.745
Cochinchinone D	73026577	Click to see CC(=CCC12C(=O)C3(CC(C14C(=C3)C(=O)C5=C(C=C(C=C5O4)O)O)C(O2)(C)C)OC)C	426.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.10.008
Cochinchinone G	70697909	Click to see CC(=CCCC(=CCOC1=CC(=C2C(=C1)OC3=C(C2=O)C=C(C=C3)O)O)C)C	380.40	unknown	https://doi.org/10.1016/J.TET.2009.01.083 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254373/ https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3103643/
Cochinchinoxanthone	53355017	Click to see CC(=CCC12C(=O)C3CC(C14C(=C3)C(=O)C5=C(C=C(C=C5O4)O)O)C(O2)(C)C)C	396.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.10.008 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3103643/
Euxanthone	5281631	Click to see C1=CC(=C2C(=C1)OC3=C(C2=O)C=C(C=C3)O)O	228.20	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3103643/
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/10.1139/V08-076
Mangiferin	5281647	Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O	422.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 2-prenylated xanthones
(3R)-6,9-dihydroxy-3-methyl-5-(3-methylbut-2-enyl)-3-(4-methylpent-3-enyl)pyrano[2,3-c]xanthen-7-one	163065026	Click to see CC(=CCCC1(C=CC2=C3C(=C(C(=C2O1)CC=C(C)C)O)C(=O)C4=C(O3)C=CC(=C4)O)C)C	446.50	unknown	https://doi.org/10.1016/J.TET.2009.01.083
1,3-Dihydroxy-5,6-dimethoxy-7-(3-methylbut-2-enyl)xanthen-9-one	162898974	Click to see CC(=CCC1=CC2=C(C(=C1OC)OC)OC3=CC(=CC(=C3C2=O)O)O)C	356.40	unknown	https://doi.org/10.1016/J.PHYTOL.2010.11.006 https://doi.org/10.1016/J.PHYTOL.2011.01.001
1,3,5-Trihydroxy-6-methoxy-7-(3-methylbut-2-enyl)xanthen-9-one	162866654	Click to see CC(=CCC1=CC2=C(C(=C1OC)O)OC3=CC(=CC(=C3C2=O)O)O)C	342.30	unknown	https://doi.org/10.1016/J.PHYTOL.2010.11.006 https://doi.org/10.1016/J.PHYTOL.2011.01.001
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.PHYTOCHEM.2006.05.043
5,11-Dihydroxy-9-methoxy-3,3-dimethyl-10-(3-methylbut-2-enyl)-1,2-dihydropyrano[3,2-a]xanthen-12-one	118735083	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C=C(C4=C3CCC(O4)(C)C)O)OC)C	410.50	unknown	https://doi.org/10.1016/J.PHYTOL.2010.11.006
6,9-Dihydroxy-3-methyl-5-(3-methylbut-2-enyl)-3-(4-methylpent-3-enyl)pyrano[2,3-c]xanthen-7-one	42604307	Click to see CC(=CCCC1(C=CC2=C3C(=C(C(=C2O1)CC=C(C)C)O)C(=O)C4=C(O3)C=CC(=C4)O)C)C	446.50	unknown	https://doi.org/10.1016/J.TET.2009.01.083
Cowaxanthone D	11704200	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C=C(C4=C3C=CC(O4)(C)C)O)OC)C	408.40	unknown	https://doi.org/10.1016/J.TET.2009.01.083
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/J.PHYTOCHEM.2005.10.008
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
(3S)-6-(3,7-dimethylocta-2,6-dienyl)-3,5,10-trihydroxy-2,2-dimethyl-3,4-dihydropyrano[2,3-a]xanthen-12-one	162987263	Click to see CC(=CCCC(=CCC1=C2C(=C3C(=C1O)CC(C(O3)(C)C)O)C(=O)C4=C(O2)C=CC(=C4)O)C)C	464.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3103643/
1,3,7-trihydroxy-2-[(2R)-2-hydroxy-3-methylbut-3-enyl]-4-(3-methylbut-2-enyl)xanthen-9-one	163029641	Click to see CC(=CCC1=C(C(=C(C2=C1OC3=C(C2=O)C=C(C=C3)O)O)CC(C(=C)C)O)O)C	396.40	unknown	https://doi.org/10.1016/J.PHYTOL.2010.11.006
1,3,7-Trihydroxy-2,4-diisoprenylxanthone	10643491	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	https://doi.org/10.1016/J.TET.2009.01.083 https://doi.org/10.1016/S0031-9422(98)00467-1 https://doi.org/10.1016/J.PHYTOCHEM.2005.10.008 https://doi.org/10.1248/CPB.54.745 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3103643/
12-(3,7-Dimethylocta-2,6-dienyl)-5,8-dihydroxy-2,2-dimethylpyrano[3,2-b]xanthen-6-one	74817579	Click to see CC(=CCCC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C=C(C=C4)O)O)C=CC(O2)(C)C)C)C	446.50	unknown	https://doi.org/10.1016/J.TET.2009.01.083
12-[(2E)-3,7-dimethylocta-2,6-dienyl]-5,8-dihydroxy-2,2-dimethylpyrano[3,2-b]xanthen-6-one	42604190	Click to see CC(=CCCC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C=C(C=C4)O)O)C=CC(O2)(C)C)C)C	446.50	unknown	https://doi.org/10.1016/J.TET.2009.01.083
2-(3,7-Dimethylocta-2,6-dienyl)-1,3,7-trihydroxy-4-(3-methylbut-2-enyl)xanthen-9-one	85503167	Click to see CC(=CCCC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=C(O2)C=CC(=C3)O)CC=C(C)C)O)C)C	448.50	unknown	https://doi.org/10.3987/COM-08-11628 https://doi.org/10.1016/S0031-9422(98)00467-1 https://doi.org/10.1016/S0031-9422(00)95100-8
2-[(2E)-3,7-dimethylocta-2,6-dienyl]-1,3,7-trihydroxy-4-(3-methylbut-2-enyl)xanthen-9-one	38361556	Click to see CC(=CCCC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=C(O2)C=CC(=C3)O)CC=C(C)C)O)C)C	448.50	unknown	https://doi.org/10.3987/COM-08-11628 https://doi.org/10.1016/S0031-9422(98)00467-1 https://doi.org/10.1016/S0031-9422(00)95100-8
4-(3,7-Dimethylocta-2,6-dienyl)-1,3,6,7-tetrahydroxy-2-(3-methylbut-2-enyl)xanthen-9-one	75297119	Click to see CC(=CCCC(=CCC1=C2C(=C(C(=C1O)CC=C(C)C)O)C(=O)C3=CC(=C(C=C3O2)O)O)C)C	464.50	unknown	https://doi.org/10.3987/COM-08-11628
4-(3,7-Dimethylocta-2,6-dienyl)-1,3,7-trihydroxy-2-(3-methylbut-2-enyl)xanthen-9-one	73036428	Click to see CC(=CCCC(=CCC1=C2C(=C(C(=C1O)CC=C(C)C)O)C(=O)C3=C(O2)C=CC(=C3)O)C)C	448.50	unknown	https://doi.org/10.1016/J.TET.2009.01.083 https://doi.org/10.3987/COM-08-11628 https://doi.org/10.1016/J.PHYTOCHEM.2005.10.008 https://doi.org/10.1016/J.PHYTOL.2010.11.006 https://doi.org/10.1248/CPB.54.745 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3103643/
4-(3,7-Dimethylocta-2,6-dienyl)-1,3,7-trihydroxyxanthen-9-one	73812991	Click to see CC(=CCCC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=C(O2)C=CC(=C3)O)C)C	380.40	unknown	https://doi.org/10.1139/V08-076 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254373/
4-[(2E)-3,7-dimethylocta-2,6-dienyl]-1,3,7-trihydroxyxanthen-9-one	21626041	Click to see CC(=CCCC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=C(O2)C=CC(=C3)O)C)C	380.40	unknown	https://doi.org/10.1139/V08-076 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254373/
5-(3,7-Dimethylocta-2,6-dienyl)-1,3,6,7-tetrahydroxy-2-(3-methylbut-2-enyl)xanthen-9-one	73031704	Click to see CC(=CCCC(=CCC1=C2C(=CC(=C1O)O)C(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)C)C	464.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.10.008
5,8-Dihydroxy-2,2-dimethyl-12-(3,7,7-trimethyloct-2-enyl)pyrano[3,2-b]xanthen-6-one	162938531	Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C=C(C=C4)O)O)C=CC(O2)(C)C)CCCC(C)(C)C	462.60	unknown	https://doi.org/10.1016/J.TET.2009.01.083
Cochinchinone A	11633740	Click to see CC(=CCCC(=CCC1=C2C(=C(C(=C1O)CC=C(C)C)O)C(=O)C3=C(O2)C=CC(=C3)O)C)C	448.50	unknown	https://doi.org/10.1016/J.TET.2009.01.083 https://doi.org/10.3987/COM-08-11628 https://doi.org/10.1016/J.PHYTOCHEM.2005.10.008 https://doi.org/10.1016/J.PHYTOL.2010.11.006 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3103643/ https://doi.org/10.1248/CPB.54.745
Cochinchinone B	11619632	Click to see CC(=CCCC(=CCC1=C2C(=CC(=C1O)O)C(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)C)C	464.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.10.008
Cochinensoxanthone	53355018	Click to see CC(=CCCC(=CCC1=C2C(=C3C(=C1O)CC(C(O3)(C)C)O)C(=O)C4=C(O2)C=CC(=C4)O)C)C	464.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3103643/
Pruniflorone Q	49799114	Click to see CC(=CCCC(=CCC1=C2C(=C(C(=C1O)CC=C(C)C)O)C(=O)C3=CC(=C(C=C3O2)O)O)C)C	464.50	unknown	https://doi.org/10.3987/COM-08-11628
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/10.1016/S0031-9422(00)95100-8
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 8-prenylated xanthones
(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/10.1016/0031-9422(94)00526-Y
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	https://doi.org/10.1016/J.PHYTOCHEM.2005.10.008
1,6,7-Trihydroxy-3-methoxy-2,8-bis(3-methylbut-2-enyl)xanthen-9-one	11589626	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C=C(C(=C3CC=C(C)C)O)O)OC)C	410.50	unknown	https://doi.org/10.3987/COM-08-11628
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/10.1016/0031-9422(94)00526-Y
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://doi.org/10.1016/0031-9422(94)00526-Y
4,8-Dihydroxy-2,3-dimethoxy-1-(3-methylbut-2-enyl)-9H-xanthen-9-one	139073736	Click to see CC(=CCC1=C2C(=C(C(=C1OC)OC)O)OC3=CC=CC(=C3C2=O)O)C	356.40	unknown	https://doi.org/10.1016/J.TET.2009.01.083
5-O-methylcelebixanthone	11537710	Click to see CC(=CCC1=C2C(=C(C(=C1OC)O)OC)OC3=CC=CC(=C3C2=O)O)C	356.40	unknown	https://doi.org/10.1248/CPB.54.745
8-(3,7-Dimethylocta-2,6-dienyl)-1,3,7-trihydroxy-2-(3-methylbut-2-enyl)xanthen-9-one	75307340	Click to see CC(=CCCC(=CCC1=C(C=CC2=C1C(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)O)C)C	448.50	unknown	https://doi.org/10.3987/COM-08-11628
8-[(2E)-3,7-dimethylocta-2,6-dienyl]-1,3,7-trihydroxy-2-(3-methylbut-2-enyl)xanthen-9-one	49857751	Click to see CC(=CCCC(=CCC1=C(C=CC2=C1C(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)O)C)C	448.50	unknown	https://doi.org/10.3987/COM-08-11628
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/10.3987/COM-08-11628 https://doi.org/10.1016/S0031-9422(00)95100-8 https://doi.org/10.1248/CPB.54.745 https://doi.org/10.1016/J.PHYTOL.2010.11.006 https://doi.org/10.1016/J.TET.2009.01.083 https://doi.org/10.1016/J.PHYTOCHEM.2005.10.008 https://doi.org/10.1016/S0031-9422(98)00467-1
Celebixanthone	70680260	Click to see CC(=CCC1=C2C(=C(C(=C1OC)O)O)OC3=CC=CC(=C3C2=O)O)C	342.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2005.10.008 https://doi.org/10.1248/CPB.54.745
Cratoxylone	102004659	Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(O2)C=C(C(=C3O)CCC(C)(C)O)O)O)OC)C	428.50	unknown	https://doi.org/10.1016/S0031-9422(00)95100-8
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://doi.org/10.1016/0031-9422(94)00526-Y
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://www.ncbi.nlm.nih.gov/pmc/articles/PMC3103643/
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.PHYTOCHEM.2005.10.008 https://doi.org/10.1016/S0031-9422(00)95100-8
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/10.1016/S0031-9422(98)00467-1 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3103643/ https://doi.org/10.1248/CPB.54.745 https://doi.org/10.3987/COM-08-11628 https://doi.org/10.1016/J.TET.2009.01.083 https://doi.org/10.1016/S0031-9422(00)95100-8 https://doi.org/10.1016/J.PHYTOCHEM.2005.10.008
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
(2S)-5,9,10-trihydroxy-2-methyl-12-(2-methylbut-3-en-2-yl)-2-(4-methylpent-3-enyl)pyrano[3,2-b]xanthen-6-one	162985484	Click to see CC(=CCCC1(C=CC2=C(C3=C(C(=C2O1)C(C)(C)C=C)OC4=C(C3=O)C=CC(=C4O)O)O)C)C	462.50	unknown	https://doi.org/10.1016/J.TET.2009.01.083
5,8,10-Trihydroxy-2,2-dimethylpyrano[2,3-b]xanthen-11-one	162940121	Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)OC4=CC(=CC(=C4C3=O)O)O)C	326.30	unknown	https://doi.org/10.1016/J.PHYTOL.2010.11.006 https://doi.org/10.1016/J.PHYTOL.2011.01.001
5,9,10-Trihydroxy-2-methyl-12-(2-methylbut-3-en-2-yl)-2-(4-methylpent-3-enyl)pyrano[3,2-b]xanthen-6-one	101403356	Click to see CC(=CCCC1(C=CC2=C(C3=C(C(=C2O1)C(C)(C)C=C)OC4=C(C3=O)C=CC(=C4O)O)O)C)C	462.50	unknown	https://doi.org/10.1016/J.TET.2009.01.083
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	https://doi.org/10.1016/J.TET.2009.01.083 https://doi.org/10.1016/J.PHYTOCHEM.2005.10.008
toxyloxanthone B	14886044	Click to see CC1(C=CC2=C(O1)C(=CC3=C2C(=O)C4=C(C=C(C=C4O3)O)O)O)C	326.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.043
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(+)-Kallolide B	15760798	Click to see CC1=C2CC(CCC3=CC(C(C(=C1)O2)C(=C)C)OC3=O)C(=C)C	312.40	unknown	via CMAUP database
2-O-Ethylkallolide A	10665972	Click to see CCOC1C(CCC2=CC(C(C3=CC(=C1O3)C)C(=C)C)OC2=O)C(=C)C	356.50	unknown	via CMAUP database
kallolide A	394352	Click to see CC1=C2C(C(CCC3=CC(C(C(=C1)O2)C(=C)C)OC3=O)C(=C)C)O	328.40	unknown	via CMAUP database
Kallolide A acetate	10090556	Click to see CC1=C2C(C(CCC3=CC(C(C(=C1)O2)C(=C)C)OC3=O)C(=C)C)OC(=O)C	370.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(5R,9S)-9-ethenyl-9-methyl-2-propan-2-yl-1,7-dioxaspiro[4.4]non-2-ene-4,6-dione	10857441	Click to see CC(C)C1=CC(=O)C2(O1)C(=O)OCC2(C)C=C	236.26	unknown	https://doi.org/10.1016/0031-9422(94)00862-N
(5S,9S)-2-[(2S)-butan-2-yl]-9-ethenyl-9-methyl-1,7-dioxaspiro[4.4]non-2-ene-4,6-dione	10848289	Click to see CCC(C)C1=CC(=O)C2(O1)C(=O)OCC2(C)C=C	250.29	unknown	https://doi.org/10.1021/NP900109Y https://doi.org/10.1016/0031-9422(94)00862-N
2-Butan-2-yl-9-ethenyl-9-methyl-1,7-dioxaspiro[4.4]non-2-ene-4,6-dione	14334127	Click to see CCC(C)C1=CC(=O)C2(O1)C(=O)OCC2(C)C=C	250.29	unknown	https://doi.org/10.1039/A704159D https://doi.org/10.1016/0031-9422(94)00862-N https://doi.org/10.1246/CL.1989.683
9-Ethenyl-9-methyl-2-phenyl-1,7-dioxaspiro[4.4]non-2-ene-4,6-dione	72756217	Click to see CC1(COC(=O)C12C(=O)C=C(O2)C3=CC=CC=C3)C=C	270.28	unknown	https://doi.org/10.1016/0031-9422(94)00862-N
Hyperolactone C	11219432	Click to see CC1(COC(=O)C12C(=O)C=C(O2)C3=CC=CC=C3)C=C	270.28	unknown	https://doi.org/10.1021/NP900109Y https://doi.org/10.1016/0031-9422(94)00862-N
> Organoheterocyclic compounds / Naphthopyrans
(9R)-9,12-dihydroxy-5-methoxy-2,2,9-trimethyl-8,10-dihydronaphtho[6,7-h]chromen-11-one	154497676	Click to see CC1(C=CC2=C(O1)C3=C(C4=C(CC(CC4=O)(C)O)C=C3C=C2OC)O)C	354.40	unknown	https://doi.org/10.1139/V08-076 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254373/
Vismione B	10247551	Click to see CC1(C=CC2=C(O1)C3=C(C4=C(CC(CC4=O)(C)O)C=C3C=C2OC)O)C	354.40	unknown	https://doi.org/10.1139/V08-076 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6254373/
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
methyl 5-[[(1R,4aR,5R,6S,8aS)-6-hydroxy-5-(3-hydroxy-3-methylbutyl)-5,8a-dimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methyl]-6-methoxy-2-methyl-4-oxopyran-3-carboxylate	162886714	Click to see CC1=C(C(=O)C(=C(O1)OC)CC2C(=C)CCC3C2(CCC(C3(C)CCC(C)(C)O)O)C)C(=O)OC	490.60	unknown	https://doi.org/10.1016/J.PHYTOL.2010.11.006 https://doi.org/10.1016/J.PHYTOL.2011.01.001
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
(3S,4S)-4-ethenyl-3-hydroxy-3-[(Z)-3-hydroxy-3-phenylprop-2-enoyl]-4-methyloxolan-2-one	53304447	Click to see CC1(COC(=O)C1(C(=O)C=C(C2=CC=CC=C2)O)O)C=C	288.29	unknown	https://doi.org/10.1021/NP900109Y
4-hydroxyhyperolactone D	46883483	Click to see CC1(COC(=O)C1(C(=O)C=C(C2=CC=CC=C2)O)O)C=C	288.29	unknown	https://doi.org/10.1021/NP900109Y
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans
1-[2,9a-Bis(1,3-benzodioxol-5-yl)-7-hydroxy-5-methoxy-6-methyl-2,3,3a,4-tetrahydrofuro[2,3-b]chromen-8-yl]-3-methylbutan-1-one	75576371	Click to see CC1=C(C(=C2C(=C1OC)CC3CC(OC3(O2)C4=CC5=C(C=C4)OCO5)C6=CC7=C(C=C6)OCO7)C(=O)CC(C)C)O	560.60	unknown	https://doi.org/10.1021/NP1004483
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Quercitrin	5280459	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.05.043
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
(2R)-1-[(2S,3aS,9aR)-2,9a-bis(1,3-benzodioxol-5-yl)-7-hydroxy-5-methoxy-6-methyl-2,3,3a,4-tetrahydrofuro[2,3-b]chromen-8-yl]-2-methylbutan-1-one	163193369	Click to see CCC(C)C(=O)C1=C2C(=C(C(=C1O)C)OC)CC3CC(OC3(O2)C4=CC5=C(C=C4)OCO5)C6=CC7=C(C=C6)OCO7	560.60	unknown	https://doi.org/10.1021/NP1004483

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.

Cratoxylum cochinchinense

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