Alhagi maurorum

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Description

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID643fdebea1468987804978
Scientific name	Alhagi maurorum
Authority	Medik.
First published in	Vorles. Churpfälz. Phys.-Ökon. Ges.2: 398 (1787)

Description Top

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Alhagi maurorum, also known as camelthorn or mannaplant, is a legume shrub native to the Mediterranean region and Russia. It has been introduced to other parts of the world, including Australia and the western United States. The plant has a massive rhizome system and can grow up to four feet in height. It has small pink flowers and brown legume pods with mottled brown beans. In its native range, it has been used in folk medicine for various ailments and is mentioned in the Qur'an as a source of sweet manna. However, it is considered a noxious weed outside of its native range and can be harmful to forage and grazing land.

Synonyms Top

Scientific name	Authority	First published in
Alhagi camelorum	DC.
Hedysarum alhagi	L.	Sp. Pl.: 745 (1753)
Alhagi camelorum var. spinis-elongatis	Boiss.
Alhagi maurorum subsp. maurorum	Medik.

Common names Top

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Language	Common/alternative name
English	persian manna
English	camelthorn
Spanish	alhagi pseudalhagi
Arabic	عاقول مغربي
Azerbaijani	alhagi camelorum
Azerbaijani	alhagi pseudalhagi
Azerbaijani	hedysarum alhagi
Azerbaijani	hedysarum pseudalhagi
Azerbaijani	adi dəvətikanı
azb	عادی دوتیکانی
Bulgarian	камилски бодил
Czech	manovec mouřenínský
Persian	خار انگبین
Finnish	kamelinkuropalko
Hebrew	הגה מצויה
Hebrew	הגה מצוי
Italian	alhagi pseudalhagi
Kazakh	Кәдімгі жантақ
Korean	자밀
Malayalam	ഒട്ടകമുള്ള്
nv	chʼil hoshí
Punjab	جوانسہ
Russian	Верблюжья колючка мавров
sd	ڪانڊيرو
Vietnamese	alhagi pseudalhagi
Chinese	骆驼刺
Chinese	駱駝刺

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name	Authority	First published in
Alhagi maurorum var. maurorum		Unknown
Alhagi maurorum var. turcorum	(Boiss.) Meilke	Fl. Cyprus1: 806 (1977)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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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
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - Xinjiang
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Tadzhikistan
  - Turkmenistan
  - Uzbekistan
- Siberia
  - Altay
- Western Asia
  - Afghanistan
  - Cyprus
  - Iran
  - Lebanon-Syria
  - Palestine

Asia-tropical click to expand
- Indian Subcontinent
  - India
  - Pakistan
  - West Himalaya

Australasia click to expand
- Australia
  - New South Wales
  - South Australia
  - Victoria
  - Western Australia

Europe click to expand
- Eastern Europe
  - East European Russia
  - South European Russia
- Middle Europe
  - Czechoslovakia

Northern America click to expand
- Northwestern U.S.A.
  - Colorado
- South-central U.S.A.
  - New Mexico
  - Texas
- Southwestern U.S.A.
  - California
  - Utah

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000212422
UNII	6MR1V69093
USDA Plants	ALMA12
Tropicos	13046533
INPN	967569
KEW	urn:lsid:ipni.org:names:473473-1
The Plant List	ild-7497
Open Tree Of Life	809997
Observations.org	387220
NCBI Taxonomy	47037
Nature Serve	2.159674
IPNI	473473-1
iNaturalist	75323
GBIF	2945092
Freebase	/m/03d84qf
EPPO	ALHPS
EOL	703028
Elurikkus	338900
Calflora (Californian flora)	11317
USDA GRIN	2198
Wikipedia	Alhagi_maurorum
CMAUP	NPO22283

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

The sustainable use of diverse plants accustomed by different ethnic groups in Sibi District, Balochistan, Pakistan

Maria B, Saeed S, Ahmed A, Ahmed M, Rehman A

PLoS One

21-Feb-2024

PMCID:	PMC10880983
doi:	10.1371/journal.pone.0294989
PMID:	38381718

Management of Rumex dentatus L. in Vicia faba L. cultivations via Ononis vaginalis Vahl. As a potential bioherbicide

Elghobashy RM, Rashed SA, Fakhry AM, Mostafa RM, Essawy HS, El-Darier SM

Heliyon

18-Feb-2024

PMCID:	PMC10884923
doi:	10.1016/j.heliyon.2024.e26381
PMID:	38404847

Phytotoxicity effect of a highly toxic isolate of Alternaria alternata metabolites from Iran

Sedighi A, Mohammadi A

Toxicon X

15-Feb-2024

PMCID:	PMC10878783
doi:	10.1016/j.toxcx.2024.100186
PMID:	38380155

A multidisciplinary approach to the antioxidant and hepatoprotective activities of Arbutus pavarii Pampan fruit; in vitro and in Vivo biological evaluations, and in silico investigations

Elshibani FA, Alamami AD, Mohammed HA, Rasheed RA, El Sabban RM, Yehia MA, Abdel Mageed SS, Majrashi TA, Elkaeed EB, El Hassab MA, Eldehna WM, El-Ashrey MK

J Enzyme Inhib Med Chem

28-Dec-2023

PMCID:	PMC10763860
doi:	10.1080/14756366.2023.2293639
PMID:	38153110

Characterization and Determination of the Antibacterial Activity of Baccharis dracunculifolia Essential-Oil Nanoemulsions

Monteiro ED, da Silva FS, Gomes KO, do Prado BA, dos Santos RD, Gomes da Camara CA, de Moraes MM, da Silva IC, de Macêdo VT, Gelfuso GM, de Sá Barreto LC, Orsi DC

Antibiotics (Basel)

29-Nov-2023

PMCID:	PMC10740613
doi:	10.3390/antibiotics12121677
PMID:	38136711

The Main Medicinal Plants in Arid Regions of Uzbekistan and Their Traditional Use in Folk Medicine

Abduraimov OS, Li W, Shomurodov HF, Feng Y

Plants (Basel)

15-Aug-2023

PMCID:	PMC10458710
doi:	10.3390/plants12162950
PMID:	37631161

Comparison of the Effect of Hydroalcholic Extract of Alhagi maurorum and Hydrochlorothiazide on Excretion of 4–10 mm Kidney and Ureteral Stones in Adults: A Randomized Prospective Study

Mehrabi S, Beigi P, Salehpour Z

Adv Pharmacol Pharm Sci

14-Aug-2023

PMCID:	PMC10442181
doi:	10.1155/2023/6624981
PMID:	37609006

Analysis of antibacterial and cytotoxic potential of medicinal plants from Cholistan desert, Pakistan

Ejaz S, Nasim FU, Abdullah I, Rashid S, Ashraf M

Saudi J Biol Sci

28-Jul-2023

PMCID:	PMC10424204
doi:	10.1016/j.sjbs.2023.103750
PMID:	37583872

Prevalence, motivation, and associated factors of medicinal herbs consumption in pregnant women from Eastern Mediterranean Regional Office: a systematic review

Bouqoufi A, Lahlou L, Ait El Hadj F, Abdessadek M, Obtel M, Khabbal Y

Pharm Biol

14-Jul-2023

PMCID:	PMC10351469
doi:	10.1080/13880209.2023.2229388
PMID:	37452524

Plants, Cells, Algae, and Cyanobacteria In Vitro and Cryobank Collections at the Institute of Plant Physiology, Russian Academy of Sciences—A Platform for Research and Production Center

Yuorieva N, Sinetova M, Messineva E, Kulichenko I, Fomenkov A, Vysotskaya O, Osipova E, Baikalova A, Prudnikova O, Titova M, Nosov AV, Popova E

Biology (Basel)

09-Jun-2023

PMCID:	PMC10295647
doi:	10.3390/biology12060838
PMID:	37372123

Potential use of saline resources for biofuel production using halophytes and marine algae: prospects and pitfalls

Abideen Z, Ansari R, Hasnain M, Flowers TJ, Koyro HW, El-Keblawy A, Abouleish M, Khan MA

Front Plant Sci

02-Jun-2023

PMCID:	PMC10272829
doi:	10.3389/fpls.2023.1026063
PMID:	37332715

Fascioliasis associated with chronic cholecystitis in a woman from Sistan and Baluchestan province, a non-endemic region in Southeastern Iran

Shafiee M, Nasibi S, Lashkarizadeh MR, Fasihi Harandi M

BMC Infect Dis

19-May-2023

PMCID:	PMC10199601
doi:	10.1186/s12879-023-08310-z
PMID:	37208607

Combined treatment with Alhagi maurorum and docetaxel inhibits breast cancer progression via targeting HIF-1α/VEGF mediated tumor angiogenesis in vivo

Bahamin N, Rafieian-Kopaei M, Ahmadian S, Karimi I, Doustimotlagh AH, Mobini G, Bijad E, Shafiezadeh M

Heliyon

15-May-2023

PMCID:	PMC10205524
doi:	10.1016/j.heliyon.2023.e16292
PMID:	37234651

Halophytes as new model plant species for salt tolerance strategies

Mann A, Lata C, Kumar N, Kumar A, Kumar A, Sheoran P

Front Plant Sci

11-May-2023

PMCID:	PMC10211249
doi:	10.3389/fpls.2023.1137211
PMID:	37251767

Can Alhaji maurorum as a halophyte plant be ensiled with molasses and Saccharomyces cerevisiae well?

Kazemi M, Valizadeh R

AMB Express

04-Mar-2023

PMCID:	PMC9985526
doi:	10.1186/s13568-023-01529-8
PMID:	36871064

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Alkaloids and derivatives / Cytochalasans
(3S)-3beta-Benzyl-4alpha-methyl-5-(hydroxymethyl)-7alpha,7abeta-[(1E,4S,6R,7E,9R)-4,6-dimethyl-5-oxo-6-hydroxy-9-acetoxy-1,7-nonadiene-1,9-diyl]-2,3,3abeta,4,7,7a-hexahydro-1H-isoindole-1-one	102258993	Click to see CC1CC=CC2C=C(C(C3C2(C(C=CC(C1=O)(C)O)OC(=O)C)C(=O)NC3CC4=CC=CC=C4)C)CO	507.60	unknown	via CMAUP database
cytochalasin D	5458428	Click to see CC1CC=CC2C(C(=C)C(C3C2(C(C=CC(C1=O)(C)O)OC(=O)C)C(=O)NC3CC4=CC=CC=C4)C)O	507.60	unknown	via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
Berberine	2353	Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC	336.40	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
(3R)-3-Methyl-5,8-dihydroxy-7-chloro-3,4-dihydro-1H-2-benzopyran-1-one	102258989	Click to see CC1CC2=C(C(=C(C=C2O)Cl)O)C(=O)O1	228.63	unknown	via CMAUP database
3,4-Dihydroxybenzoic acid	72	Click to see C1=CC(=C(C=C1C(=O)O)O)O	154.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
4-Hydroxy-3,5-dimethoxybenzoate	54694262	Click to see COC1=CC(=CC(=C1[O-])OC)C(=O)O	197.16	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Phthalate esters / m-Phthalate esters
(3R)-1-Oxo-3-methyl-8-hydroxy-3,4-dihydro-1H-2-benzopyran-5-carboxylic acid	25769005	Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)C(=O)O	222.19	unknown	via CMAUP database
(3S)-8-Hydroxy-3-methyl-1-oxoisochromane-5-carboxylic acid	486250	Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)C(=O)O	222.19	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
Hordenine	68313	Click to see CN(C)CCC1=CC=C(C=C1)O	165.23	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4743116/ https://doi.org/10.1055/S-0028-1099394
N-Methylmescaline	138365	Click to see CNCCC1=CC(=C(C(=C1)OC)OC)OC	225.28	unknown	https://doi.org/10.1055/S-0028-1099394 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4743116/
N-Methylphenethylamine	11503	Click to see CNCCC1=CC=CC=C1	135.21	unknown	https://doi.org/10.1055/S-0028-1099394 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4743116/
N-Methyltyramine	9727	Click to see CNCCC1=CC=C(C=C1)O	151.21	unknown	https://doi.org/10.1055/S-0028-1099394
Phenethylamine	1001	Click to see C1=CC=C(C=C1)CCN	121.18	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4743116/ https://doi.org/10.1055/S-0028-1099394
> Benzenoids / Naphthalenes
Tuberclariol A	44555346	Click to see CC1CC=CC2=C1C(=C(C=C2)C(CO)(CO)O)C	248.32	unknown	via CMAUP database
> Benzenoids / Tetralins
(3R)-3,6,8-Trihydroxy-7-chlorotetralin-1-one	102258990	Click to see C1C(CC(=O)C2=C(C(=C(C=C21)O)Cl)O)O	228.63	unknown	via CMAUP database
Isosclerone	13369486	Click to see C1CC(=O)C2=C(C1O)C=CC=C2O	178.18	unknown	via CMAUP database
Tuberclariol B	44255026	Click to see CC1CC(C(C2=C1C(=C(C=C2)C(=C)CO)C)O)O	248.32	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans
9,9'-O-Isopropyllidene-isolariciresinol	91885030	Click to see CC1(OCC2CC3=CC(=C(C=C3C(C2CO1)C4=CC(=C(C=C4)O)OC)O)OC)C	400.50	unknown	via CMAUP database
Isotaxiresinol 9,9'-acetonide	102004573	Click to see CC1(OCC2CC3=CC(=C(C=C3C(C2CO1)C4=CC(=C(C=C4)O)O)O)OC)C	386.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
4-[(3S,3aR,6R,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]benzene-1,2-diol	101568249	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)O)O	344.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
Taxumairin	101936591	Click to see CCOCC1C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)O)OC)CO	404.50	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(7R)-7-Hydroxylariciresinol	10022393	Click to see COC1=C(C=CC(=C1)C2C(C(CO2)C(C3=CC(=C(C=C3)O)OC)O)CO)O	376.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(3S)-3beta-Hydroxy-3-(3-methoxy-4-hydroxybenzyl)-4beta-[(alphaR)-alpha,4-dihydroxy-3-methoxybenzyl]tetrahydrofuran-2-one	101369318	Click to see COC1=C(C=CC(=C1)CC2(C(COC2=O)C(C3=CC(=C(C=C3)O)OC)O)O)O	390.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
13alpha-Ethenyl-13-methyl-19-hydroxy-podocarpa-8(14)-ene-7-one	100952776	Click to see CC1(CCC2C(=C1)C(=O)CC3C2(CCCC3(C)CO)C)C=C	302.50	unknown	via CMAUP database
Hinokiol	12310492	Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CCC(C3(C)C)O)C)O	302.50	unknown	via CMAUP database
Margocilin	101529198	Click to see CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCC(C3(C)C)O)C)O	316.40	unknown	via CMAUP database
Sandaracopimaric acid	221580	Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C	302.50	unknown	via CMAUP database
Sugiol	94162	Click to see CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O	300.40	unknown	via CMAUP database
Taxamairin A	130631	Click to see CC(C)C1=C(C(=C2C=C3C=CC(=O)C(C3=CC(=O)C2=C1)(C)C)O)OC	338.40	unknown	via CMAUP database
Taxamairin B	130632	Click to see CC(C)C1=C(C(=C2C=C3C=CC(=O)C(C3=CC(=O)C2=C1)(C)C)OC)OC	352.40	unknown	via CMAUP database
Taxamairin H	100952784	Click to see CC(C)C1=C(C(=C2C(=C1)C=CC3=C(C2=O)C=CC(=O)C3(C)C)O)OC	338.40	unknown	via CMAUP database
Taxusabietane A	76330776	Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCC(=O)C3(C)C)C)O)OC	344.40	unknown	via CMAUP database
Taxusabietane B	100952777	Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)C3C4(C2(C=CC(=O)C4(C)C)C=O)O3)OC)OC	384.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Taxanes and derivatives
(1S)-2alpha,5alpha,9alpha,10beta,13alpha-Pentaacetoxy-4,20-epoxytax-11-ene-1,7beta-diol	5316776	Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)O)C)OC(=O)C)OC(=O)C	610.60	unknown	via CMAUP database
(1S)-5beta,20-Epoxy-1,11-cyclo-11,15-secotaxa-11-ene-2alpha,4,7beta,9alpha,10beta,13alpha,15-heptol 2,4,7,10-tetraacetate	10918805	Click to see CC1=C2C(C(C3(C(CC4C(C3C(C2(CC1O)C(C)(C)O)OC(=O)C)(CO4)OC(=O)C)OC(=O)C)C)O)OC(=O)C	568.60	unknown	via CMAUP database
[(1'R,2S,2'R,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',7',9',10',13'-pentaacetyloxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-5'-yl] (3R)-3-(dimethylamino)-3-phenylpropanoate	5319245	Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)CC1OC(=O)C)OC(=O)C)CO4)OC(=O)CC(C5=CC=CC=C5)N(C)C)OC(=O)C)C)OC(=O)C)OC(=O)C	769.90	unknown	via CMAUP database
[(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-1',2',9',10',13'-pentaacetyloxy-5'-hydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-7'-yl] acetate	5319668	Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)OC(=O)C)OC(=O)C)CO4)O)OC(=O)C)C)OC(=O)C)OC(=O)C	652.70	unknown	via CMAUP database
[(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',5',9',10'-tetraacetyloxy-1',13'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-7'-yl] acetate	5321730	Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1O)O)OC(=O)C)CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)OC(=O)C	610.60	unknown	via CMAUP database
[(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',5',9',13'-tetraacetyloxy-1',10'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-7'-yl] acetate	5321728	Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)O	610.60	unknown	via CMAUP database
[(1E,3S,4R,6S,9R,11S,12S,14S)-12-acetyloxy-3,9,14-trihydroxy-7,11,16,16-tetramethyl-10-oxo-6-tricyclo[9.3.1.14,8]hexadeca-1,7-dienyl] acetate	24862000	Click to see CC1=C2C(C(=O)C3(CC(=CC(C(C2(C)C)CC1OC(=O)C)O)C(CC3OC(=O)C)O)C)O	450.50	unknown	via CMAUP database
[(1E,3S,4R,6S,9R,11S,12S,14S)-3,12,14-triacetyloxy-9-hydroxy-7,11,16,16-tetramethyl-10-oxo-6-tricyclo[9.3.1.14,8]hexadeca-1,7-dienyl] acetate	101006401	Click to see CC1=C2C(C(=O)C3(CC(=CC(C(C2(C)C)CC1OC(=O)C)OC(=O)C)C(CC3OC(=O)C)OC(=O)C)C)O	534.60	unknown	via CMAUP database
1-Acetoxy-5-deacetylbaccatin I	102004901	Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)OC(=O)C)OC(=O)C)CO4)O)OC(=O)C)C)OC(=O)C)OC(=O)C	652.70	unknown	via CMAUP database
1-Hydroxybaccatin I; 1beta-Hydroxybaccatin I	5318150	Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)OC(=O)C	652.70	unknown	via CMAUP database
13-O-Deacetyltaxumairol Z	10864961	Click to see CC1=C2C(C(C3(C(CC4C(C3C(C2(CC1O)C(C)(C)O)OC(=O)C5=CC=CC=C5)(CO4)OC(=O)C)O)COC(=O)C)O)O	604.60	unknown	via CMAUP database
1beta-Hydroxy-7-deacetylbaccatin I	21159039	Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)O)C)OC(=O)C)OC(=O)C	610.60	unknown	via CMAUP database
1beta-Hydroxy-9-deacetylbaccatin I	21159040	Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)OC(=O)C)C)O)OC(=O)C	610.60	unknown	via CMAUP database
2alpha,7beta,9,10beta-Tetraacetoxy-3,8-secotaxa-3,8,11-triene-5alpha,13alpha,20-triol	6325022	Click to see CC1=C2C(C(=C(C(CC(C(=CC(C(C2(C)C)CC1O)OC(=O)C)CO)O)OC(=O)C)C)OC(=O)C)OC(=O)C	552.60	unknown	via CMAUP database
2alpha,9,10beta,13alpha-Tetraacetoxy-3,8-secotaxa-3,8,11-triene-5alpha,7beta,20-triol	6325023	Click to see CC1=C(C(C2=C(C(CC(C2(C)C)C(C=C(C(CC1O)O)CO)OC(=O)C)OC(=O)C)C)OC(=O)C)OC(=O)C	552.60	unknown	via CMAUP database
4,20-Epoxy-2alpha,5alpha,10beta,13alpha-tetraacetoxy-1,7beta,9alpha-trihydroxytaxa-11-ene	5321726	Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)O)C)O)OC(=O)C	568.60	unknown	via CMAUP database
9alpha,10beta-Diacetoxy-4,20-epoxytaxa-11-ene-2alpha,5alpha,14beta-triol	11247972	Click to see CC1=C2C(C(C3(CCC(C4(C3C(C(C2(C)C)C(C1)O)O)CO4)O)C)OC(=O)C)OC(=O)C	452.50	unknown	via CMAUP database
Taxin B	5321699	Click to see CC1=C2C(C(=O)C3(CC(=CC(C(C2(C)C)CC1OC(=O)C)OC(=O)C)C(CC3OC(=O)C)O)C)OC(=O)C	534.60	unknown	via CMAUP database
Taxumain A	5321723	Click to see CC1=C2C(C(C3(C(CC(C(C3C(C2(CC1O)C(C)(C)O)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C)C)OC(=O)C)O	612.70	unknown	via CMAUP database
Taxumain B	5321724	Click to see CC1=C2C(C(C3(C(CC(C(C3C(C2(CC1OC(=O)C)C(C)(C)O)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C)C)OC(=O)C)O	654.70	unknown	via CMAUP database
Taxumairol B	10053709	Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)O)C)O)OC(=O)C	568.60	unknown	via CMAUP database
Taxumairol C	102066555	Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)O)C)O)O	526.60	unknown	via CMAUP database
Taxumairol D	102065502	Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)O	610.60	unknown	via CMAUP database
taxumairol F	10651372	Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1O)O)OC(=O)C)CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)OC(=O)C	610.60	unknown	via CMAUP database
Taxumairol K	10769688	Click to see CC1=C2C(C(C3(C(CC4C(C3C(C2(CC1O)C(C)(C)O)OC(=O)C)(CO4)OC(=O)C)O)C)OC(=O)C5=CC=CC=C5)O	588.60	unknown	via CMAUP database
Taxumairol U	11124920	Click to see CC1=C2C(C(C3(C(CC(C(C3C(C2(CC1OC(=O)C)C(C)(C)O)O)COC(=O)C)OC(=O)C)OC(=O)C)C)OC(=O)C)O	612.70	unknown	via CMAUP database
Taxumairol V	10875480	Click to see CC1=C2C(C(C3(C(CC(C(C3C(C2(CC1O)C(C)(C)O)O)COC(=O)C)OC(=O)C)OC(=O)C)C)OC(=O)C)O	570.60	unknown	via CMAUP database
Taxumairol Z	10886794	Click to see CC1=C2C(C(C3(C(CC4C(C3C(C2(CC1OC(=O)C)C(C)(C)O)OC(=O)C5=CC=CC=C5)(CO4)OC(=O)C)O)COC(=O)C)O)O	646.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin K compounds
Phytonadione	5284607	Click to see CC1=C(C(=O)C2=CC=CC=C2C1=O)CC=C(C)CCCC(C)CCCC(C)CCCC(C)C	450.70	unknown	https://doi.org/10.1007/S10600-016-1871-5
Vitamin K	5280483	Click to see CC1=C(C(=O)C2=CC=CC=C2C1=O)CC=C(C)CCCC(C)CCCC(C)CCCC(C)C	450.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-4,7,8-triacetyloxy-12,13-dihydroxy-5,9-dimethyl-2-prop-1-en-2-yl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-10-yl] acetate	10918656	Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C2(CC1OC(=O)C)C(=C)C)OC4)O)O)OC(=O)C)C)OC(=O)C)OC(=O)C	550.60	unknown	via CMAUP database
[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-7,8-diacetyloxy-4,12,13-trihydroxy-5,9-dimethyl-2-prop-1-en-2-yl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-10-yl] acetate	10907330	Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C2(CC1O)C(=C)C)OC4)O)O)OC(=O)C)C)OC(=O)C)OC(=O)C	508.60	unknown	via CMAUP database
2-[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-7,8,10-triacetyloxy-4,12,13-trihydroxy-5,9-dimethyl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-2-yl]propan-2-yl benzoate	11814223	Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C2(CC1O)C(C)(C)OC(=O)C5=CC=CC=C5)OC4)O)O)OC(=O)C)C)OC(=O)C)OC(=O)C	630.70	unknown	via CMAUP database
Sporogen-AO 1	177175	Click to see CC1C(CCC2=CC(=O)C3(C(C12C)O3)C(=C)C)O	248.32	unknown	via CMAUP database
Taxumairol X	11733602	Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C2(CC1O)C(C)(C)O)OC4)O)O)OC(=O)C)C)OC(=O)C)O	484.50	unknown	via CMAUP database
Taxumairol Y	11005902	Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C2(CC1OC(=O)C)C(C)(C)O)OC4)O)O)OC(=O)C)C)OC(=O)C)O	526.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
Taxusabietane D	100952779	Click to see CC(C)C1=C(C(=C2C(=C1)C(CC3C2(CCC(=O)C3(C)C)COC(=O)C)OC(=O)C)O)OC4C(C(C(C(O4)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C	762.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,9S,10S)-3,4-dimethoxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6,13-tetraene-8,12,15-trione	100952778	Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)C3C4C2(C=CC(=O)C4(C)C)C(=O)O3)OC)OC	384.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
alpha-Carotene	6419725	Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CCCC2(C)C)C)C)C	536.90	unknown	https://doi.org/10.1007/S10600-016-1871-5
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1007/S10600-016-1871-5
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
Hovenine A	5318090	Click to see CCC(C)C(C(=O)NC1C(OC2=CC=C(C=C2)C=CNC(=O)C(NC1=O)CC(C)C)C(C)C)NC	486.60	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
2-[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-4,7,8,10,13-pentaacetyloxy-12-hydroxy-5,9-dimethyl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-2-yl]propan-2-yl benzoate	11072583	Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C2(CC1OC(=O)C)C(C)(C)OC(=O)C5=CC=CC=C5)OC4)OC(=O)C)O)OC(=O)C)C)OC(=O)C)OC(=O)C	714.80	unknown	via CMAUP database
Taxacin	15226199	Click to see CC(=O)OC1CC(C(=C)C2C1(C(C(C3(C4(COC3(C(=O)CC4C2OC(=O)C)C)C)O)OC(=O)C)OC(=O)C)COC(=O)C5=CC=CC=C5)OC(=O)C=CC6=CC=CC=C6	816.80	unknown	via CMAUP database
Taxumairol R	21593833	Click to see CC(=O)OC1CC(C2(C(C1=C)C(C3CC(=O)C4(C(C3(CO4)C)(C(C2OC(=O)C)OC(=O)C)O)C)OC(=O)C)COC(=O)C5=CC=CC=C5)OC(=O)C	728.70	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
Taxumairone A	10027779	Click to see CC1=C2C(C(=O)C3(CC(=CC(C(C2(C)C)CC1OC(=O)C)OC(=O)C)C(=O)C=C3)C)OC(=O)C	472.50	unknown	via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Aralkylamines
1-Phenylethylamine	7408	Click to see CC(C1=CC=CC=C1)N	121.18	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4743116/
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Flavaspidic acid	8237	Click to see CCCC(=O)C1=C(C(=C(C(=C1O)CC2=C(C(C(=O)C(=C2O)C(=O)CCC)(C)C)O)O)C)O	446.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
(3R)-1-Oxo-3-methyl-8-hydroxy-3,4-dihydro-1H-2-benzopyran-5-carbaldehyde	44577733	Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)C=O	206.19	unknown	via CMAUP database
3-Methyl-6-methoxy-8-hydroxy-3,4-dihydroisocoumarin	93040	Click to see CC1CC2=C(C(=CC(=C2)OC)O)C(=O)O1	208.21	unknown	via CMAUP database
Cis-7-chloro-4-hydroxymellein	102258988	Click to see CC1C(C2=C(C(=C(C=C2)Cl)O)C(=O)O1)O	228.63	unknown	via CMAUP database
trans-4-Hydroxymellein	10262028	Click to see CC1C(C2=C(C(=CC=C2)O)C(=O)O1)O	194.18	unknown	via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Thiamines
3-(4-Amino-2-methyl-pyrimidin-5-ylmethyl)-5-(2-hydroxy-ethyl)-4-methyl-thiazol-3-ium	1130	Click to see CC1=C(SC=[N+]1CC2=CN=C(N=C2N)C)CCO	265.36	unknown	https://doi.org/10.1007/S10600-016-1871-5
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(5R)-5-hydroxy-4-methoxy-5-prop-1-en-2-ylfuran-2-one	40468114	Click to see CC(=C)C1(C(=CC(=O)O1)OC)O	170.16	unknown	via CMAUP database
Ascorbic Acid	54670067	Click to see C(C(C1C(=C(C(=O)O1)O)O)O)O	176.12	unknown	https://doi.org/10.1007/S10600-016-1871-5
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(5S)-1,7-dioxaspiro[4.4]non-2-ene-4,8-dione	639435	Click to see C1C(=O)OCC12C(=O)C=CO2	154.12	unknown	via CMAUP database
Sphaeropsidin A	51361447	Click to see CC1(CCCC23C1C(C(=O)C4=CC(CCC42O)(C)C=C)(OC3=O)O)C	346.40	unknown	via CMAUP database
Sphaeropsidin B	57396736	Click to see CC1(CCCC23C1C(C(C4=CC(CCC42O)(C)C=C)O)(OC3=O)O)C	348.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Oxocins
(4S,6S,7Z,9S,10S)-4,6,9-Trihydroxy-10-nonyl-1-oxa-7-cyclodecene-2-one	44632077	Click to see CCCCCCCCCC1C(C=CC(CC(CC(=O)O1)O)O)O	328.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Xylaric acid	3084064	Click to see C1=COC=C(C1=O)CC(=O)O	154.12	unknown	via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines
(S)-6,7-Dimethoxy-1-methyl-1,2,3,4-tetrahydroisoquinoline	164752	Click to see CC1C2=CC(=C(C=C2CCN1)OC)OC	207.27	unknown	https://doi.org/10.1055/S-0028-1099394 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4743116/
6,7-Dimethoxy-1-methyl-1,2,3,4-tetrahydroisoquinoline	10302	Click to see CC1C2=CC(=C(C=C2CCN1)OC)OC	207.27	unknown	https://doi.org/10.1055/S-0028-1099394 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4743116/
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
[(2R,3S,4S,5R,6S)-6-[[(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-4-[(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-4-[(2R,3R)-3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-8-yl]-3,4-dihydro-2H-chromen-8-yl]-3,5-dihydroxy-3,4-dihydro-2H-chromen-7-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate	163189773	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)OC7C(C(C(C(O7)COC(=O)C8=CC(=C(C(=C8)O)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C(=C1)O)O)O)O	1197.00	unknown	https://doi.org/10.1007/S10600-010-9615-4
[6-[[2-(3,4-dihydroxyphenyl)-4-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-4-[3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-8-yl]-3,4-dihydro-2H-chromen-8-yl]-3,5-dihydroxy-3,4-dihydro-2H-chromen-7-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate	162844282	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)OC7C(C(C(C(O7)COC(=O)C8=CC(=C(C(=C8)O)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C(=C1)O)O)O)O	1197.00	unknown	https://doi.org/10.1007/S10600-010-9615-4
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol	9064	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/10.1007/BF00575060
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
(2S,3R,4S)-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,4,5,7-tetrol	154496890	Click to see C1=C(C=C(C(=C1O)O)O)C2C(C(C3=C(C=C(C=C3O2)O)O)O)O	322.27	unknown	https://doi.org/10.1007/BF00575060
Epigallocatechin	72277	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O	306.27	unknown	https://doi.org/10.1007/BF00575060
Leucodelphinidin	44563331	Click to see C1=C(C=C(C(=C1O)O)O)C2C(C(C3=C(C=C(C=C3O2)O)O)O)O	322.27	unknown	https://doi.org/10.1007/BF00575060
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavan-4-ols
4-Flavanol	253959	Click to see C1C(C2=CC=CC=C2OC1C3=CC=CC=C3)O	226.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin	5281654	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	316.26	unknown	https://doi.org/10.1007/BF00571238 https://doi.org/10.1007/S10600-009-9287-0
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	https://doi.org/10.1007/BF00571238 https://doi.org/10.1007/S10600-009-9287-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2R)-7-hydroxy-5-methoxy-2-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydrochromen-4-one	163085773	Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1016/S0031-9422(99)00010-2
(2S)-7-hydroxy-5-methoxy-2-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydrochromen-4-one	100982375	Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1016/S0031-9422(99)00010-2
7-Hydroxy-5-methoxy-2-[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydrochromen-4-one	74819417	Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1016/S0031-9422(99)00010-2
Alhagitin	42608057	Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1016/S0031-9422(99)00010-2
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Avicularin	5490064	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O	434.30	unknown	https://doi.org/10.1007/BF00571238
Distichin	139031084	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(CO4)O)O)O)O	448.40	unknown	https://doi.org/10.1007/BF00571238
Isorhamnetin 3-robinobioside	6223069	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O	624.50	unknown	https://doi.org/10.1007/S10600-009-9287-0
Narcissin	5481663	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O	624.50	unknown	https://doi.org/10.1007/S10600-009-9287-0
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/10.1007/BF00571238
Rutin	5280805	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1007/S10600-009-9287-0
Vitamin P	5293655	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1007/S10600-009-9287-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-2,3-dihydrochromen-4-one	100982376	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)OC6C(C(C(C(O6)CO)O)O)O)O)O)O)O)O	772.70	unknown	https://doi.org/10.1016/S0031-9422(99)00010-2
(2S)-7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-2,3-dihydrochromen-4-one	163078158	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)OC6C(C(C(C(O6)CO)O)O)O)O)O)O)O)O	772.70	unknown	https://doi.org/10.1016/S0031-9422(99)00010-2
7-[4,5-Dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxy-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-2,3-dihydrochromen-4-one	74819397	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)OC6C(C(C(C(O6)CO)O)O)O)O)O)O)O)O	772.70	unknown	https://doi.org/10.1016/S0031-9422(99)00010-2
Alhagidin	42607984	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)OC6C(C(C(C(O6)CO)O)O)O)O)O)O)O)O	772.70	unknown	https://doi.org/10.1016/S0031-9422(99)00010-2

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Alhagi maurorum

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