Scientific name	Authority	First published in
Helicteres parviflora	Ridl.	J. Straits Branch Roy. Asiat. Soc. 59: 77 (1911)
Helicteres virgata	Wall. ex G.Don	Gen. Hist. 1: 508 (1831)
Helicteres salicifolia	C.Presl	Reliq. Haenk. 2: 139 (1835)
Oudemansia virgata	(Wall. ex G.Don) Hassk.	Retzia 1: 134 (1855)
Oudemansia javensis var. angustifolia	(L.) Hassk.	Retzia 1: 134 1855
Helicteres angustifolia var. virgata	Kuntze	Revis. Gen. Pl. 1: 79 1891
Helicteres angustifolia var. acuminatissima	Kuntze	Revis. Gen. Pl. 1: 79 1891
Helicteres angustifolia var. gaudichaudii	Kuntze	Revis. Gen. Pl. 1: 79 1891
Helicteres angustifolia var. meyeniana	Kuntze	Revis. Gen. Pl. 1: 79 1891
Helicteres angustifolia var. naumanniana	Kuntze	Revis. Gen. Pl. 1: 79 1891
Helicteres angustifolia var. obtusa	(Wall. ex Kurz) Pierre	Fl. Forest. Cochinch. 13: t. 211, f. 14–25 t. 211, f. 14-25 1889

Common names Top

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Filter by language:

Language	Common/alternative name
Chinese	山油麻
Chinese	山芝麻
Chinese	坡油麻

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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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
- China
  - China South-central
  - China Southeast
  - Hainan
- Eastern Asia
  - Nansei-shoto
  - Taiwan

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

Pacific click to expand
- Northwestern Pacific
  - Caroline Islands

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000718077
Tropicos	30401866
KEW	urn:lsid:ipni.org:names:823419-1
The Plant List	kew-2843159
Open Tree Of Life	283046
NCBI Taxonomy	190244
IPNI	823419-1
iNaturalist	556220
GBIF	5547507
EPPO	HCTAN
EOL	2889498
USDA GRIN	423432
CMAUP	NPO7216

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

Structural Characterization of Polygonatum Cyrtonema Polysaccharide and Its Immunomodulatory Effects on Macrophages

Wen R, Luo L, Zhang R, Zhou X, Wang W, Gong L

Molecules

30-Apr-2024

PMCID:	PMC11085417
doi:	10.3390/molecules29092076
PMID:	38731567

Purification and Structural Characterization of Polysaccharides from Polygonum multiflorum Thunb. and Their Immunostimulatory Activity in RAW264.7 Cells

Gou Y, Gu D, Fan J, Yang J, Zan K, Liu J, Jin H, Wang Y, Wei F, Ma S

Foods

19-Mar-2024

PMCID:	PMC10969798
doi:	10.3390/foods13060932
PMID:	38540922

Correction: Zhang et al. Genotype–Environment Interaction and Horizontal and Vertical Distributions of Heartwood for Acacia melanoxylon R.Br. Genes 2023, 14, 1299

Zhang R, Zeng B, Chen T, Hu B

Genes (Basel)

09-Feb-2024

PMCID:	PMC10887675
doi:	10.3390/genes15020221
PMID:	38397249

Mulberry Leaf Polysaccharides Attenuate Oxidative Stress Injury in Peripheral Blood Leukocytes by Regulating Endoplasmic Reticulum Stress

Jiang W, Lin Y, Qian L, Lu S, Shen H, Ge X, Miao L

Antioxidants (Basel)

23-Jan-2024

PMCID:	PMC10886326
doi:	10.3390/antiox13020136
PMID:	38397734

Editorial: Oxidative stress link associated with mitochondrial bioenergetics: relevance in cell aging and age-related pathologies

Kalra RS, Kumar S, Tomar D

Front Cell Dev Biol

05-Sep-2023

PMCID:	PMC10509040
doi:	10.3389/fcell.2023.1273420
PMID:	37736499

Bioactivity-guided fractionation of Helicteres angustifolia L. extract and its molecular evidence for tumor suppression

Li K, Sun S, Xiao L, Zhang Z

Front Cell Dev Biol

22-Jun-2023

PMCID:	PMC10323433
doi:	10.3389/fcell.2023.1157172
PMID:	37427379

Genotype–Environment Interaction and Horizontal and Vertical Distributions of Heartwood for Acacia melanoxylon R.Br

Zhang R, Zeng B, Chen T, Hu B

Genes (Basel)

20-Jun-2023

PMCID:	PMC10298161
doi:	10.3390/genes14061299
PMID:	37372479

Application of Rosmarinic Acid with Its Derivatives in the Treatment of Microbial Pathogens

Kernou ON, Azzouz Z, Madani K, Rijo P

Molecules

22-May-2023

PMCID:	PMC10220798
doi:	10.3390/molecules28104243
PMID:	37241981

Antibacterial and Antifungal Terpenes from the Medicinal Angiosperms of Asia and the Pacific: Haystacks and Gold Needles

Wiart C, Kathirvalu G, Raju CS, Nissapatorn V, Rahmatullah M, Paul AK, Rajagopal M, Sathiya Seelan JS, Rusdi NA, Lanting S, Sulaiman M

Molecules

04-May-2023

PMCID:	PMC10180233
doi:	10.3390/molecules28093873
PMID:	37175283

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

Specialized metabolites from plants as a source of new multi-target antiviral drugs: a systematic review

Ponticelli M, Bellone ML, Parisi V, Iannuzzi A, Braca A, de Tommasi N, Russo D, Sileo A, Quaranta P, Freer G, Pistello M, Milella L

Phytochem Rev

12-Mar-2023

PMCID:	PMC10008214
doi:	10.1007/s11101-023-09855-2
PMID:	37359711

Multifunctional Roles of Betulinic Acid in Cancer Chemoprevention: Spotlight on JAK/STAT, VEGF, EGF/EGFR, TRAIL/TRAIL-R, AKT/mTOR and Non-Coding RNAs in the Inhibition of Carcinogenesis and Metastasis

Farooqi AA, Turgambayeva A, Tashenova G, Tulebayeva A, Bazarbayeva A, Kapanova G, Abzaliyeva S

Molecules

21-Dec-2022

PMCID:	PMC9822120
doi:	10.3390/molecules28010067
PMID:	36615262

Structure–immunomodulatory activity relationships of dietary polysaccharides

Chen R, Xu J, Wu W, Wen Y, Lu S, El-Seedi HR, Zhao C

Curr Res Food Sci

28-Aug-2022

PMCID:	PMC9445227
doi:	10.1016/j.crfs.2022.08.016
PMID:	36082139

Ethnobotany of medicinal plants used by the Yao people in Gongcheng County, Guangxi, China

Lu Z, Chen H, Lin C, Ou G, Li J, Xu W

J Ethnobiol Ethnomed

21-Jun-2022

PMCID:	PMC9210605
doi:	10.1186/s13002-022-00544-6
PMID:	35729593

A Comprehensive Review of Rosmarinic Acid: From Phytochemistry to Pharmacology and Its New Insight

Guan H, Luo W, Bao B, Cao Y, Cheng F, Yu S, Fan Q, Zhang L, Wu Q, Shan M

Molecules

20-May-2022

PMCID:	PMC9143754
doi:	10.3390/molecules27103292
PMID:	35630768

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 / Naphthalenes / Naphthoquinones
(4R)-4,8,12-trimethyl-2-oxatricyclo[7.3.1.05,13]trideca-1(12),5(13),6,8-tetraene-10,11-dione	139071911	Click to see CC1COC2=C(C(=O)C(=O)C3=C(C=CC1=C32)C)C	242.27	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005 https://doi.org/10.1016/0031-9422(90)80061-K
(4R)-6-methoxy-4,8,12-trimethyl-2-oxatricyclo[7.3.1.05,13]trideca-1(12),5,7,9(13)-tetraene-10,11-dione	162876729	Click to see CC1COC2=C(C(=O)C(=O)C3=C2C1=C(C=C3C)OC)C	272.29	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005 https://doi.org/10.1016/0031-9422(90)80061-K
(4S)-6-hydroxy-4,8,12-trimethyl-2-oxatricyclo[7.3.1.05,13]trideca-1(12),5,7,9(13)-tetraene-10,11-dione	73353443	Click to see CC1COC2=C(C(=O)C(=O)C3=C2C1=C(C=C3C)O)C	258.27	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005 https://doi.org/10.1016/0031-9422(90)80061-K
6-Methoxy-4,8,12-trimethyl-2-oxatricyclo[7.3.1.05,13]trideca-1(12),5,7,9(13)-tetraene-10,11-dione	14544217	Click to see CC1COC2=C(C(=O)C(=O)C3=C2C1=C(C=C3C)OC)C	272.29	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005 https://doi.org/10.1016/0031-9422(90)80061-K
Mansonone E	94303	Click to see CC1COC2=C(C(=O)C(=O)C3=C(C=CC1=C32)C)C	242.27	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005 https://doi.org/10.1016/0031-9422(90)80061-K
Mansonone F	94304	Click to see CC1=C2C3=C(C=C1)C(=COC3=C(C(=O)C2=O)C)C	240.25	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005 https://doi.org/10.1016/0031-9422(90)80061-K
Mansonone H	615515	Click to see CC1COC2=C(C(=O)C(=O)C3=C2C1=C(C=C3C)O)C	258.27	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005 https://doi.org/10.1016/S0031-9422(00)81461-2 https://doi.org/10.1016/0031-9422(90)80061-K
> Benzenoids / Phenols / Methoxyphenols
3-(4-Hydroxy-3-methoxyphenyl)-prop-2-enol	9983	Click to see COC1=C(C=CC(=C1)C=CCO)O	180.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Coniferyl Alcohol	1549095	Click to see COC1=C(C=CC(=C1)C=CCO)O	180.20	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Syringaresinol	11604108	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
(+/-)-Pinoresinol	234817	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O	358.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Pinoresinol	73399	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O	358.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Syringaresinol	100067	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Syringaresinol, (+)-	443023	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(-)-Lariciresinol	23815394	Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O	360.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Lariciresinol, (+)-	134203	Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)O	360.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Methyl 3-phenylpropionate	7643	Click to see COC(=O)CCC1=CC=CC=C1	164.20	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Heptadecanoic acid, 4-methyl-	5319673	Click to see CCCCCCCCCCCCCC(C)CCC(=O)O	284.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,2R,4As,8aS)-1-[(3S)-5-hydroxy-3-methylpentyl]-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol	11130717	Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CCO	310.50	unknown	via CMAUP database
(3S)-5-[(1S,4aS,8aR)-2,5,5,8a-tetramethyl-4-oxo-4a,6,7,8-tetrahydro-1H-naphthalen-1-yl]-3-methylpentanoic acid	93233226	Click to see CC1=CC(=O)C2C(CCCC2(C1CCC(C)CC(=O)O)C)(C)C	320.50	unknown	via CMAUP database
(4aalpha)-2-Hydroxy-2beta,5,5,8abeta-tetramethyldecalin-1beta-((R)-3-methylvaleric acid)	11868539	Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CC(=O)O	324.50	unknown	via CMAUP database
Labdanic Acid Methyl Ester	7057547	Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CC(=O)OC	338.50	unknown	via CMAUP database
Labdanolic acid	11186394	Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CC(=O)O	324.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
1,2-Naphthalenedione, 6-hydroxy-3,8-dimethyl-5-(1-methylethyl)-	608583	Click to see CC1=CC2=C(C(=CC(=C2C(C)C)O)C)C(=O)C1=O	244.28	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Ledol	92812	Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O	222.37	unknown	via CMAUP database
Viridiflorol	11996452	Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O	222.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aS,5aS,5bR,7aR,9S,11aR,11bR,13aR,13bR)-5a-(benzoyloxymethyl)-9-hydroxy-5b,8,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid	11692717	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)COC(=O)C6=CC=CC=C6)C)(C)C)O)C)C(=O)O	576.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
(1R,3aS,5aS,5bR,7aR,9S,11aS,11bR,13aR,13bS)-9-acetyloxy-5a-(benzoyloxymethyl)-5b,8,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid	163035404	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)COC(=O)C6=CC=CC=C6)C)(C)C)OC(=O)C)C)C(=O)O	618.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
(4aS,6aS,6aS,6bR,8aS,10S,12aR,14bR)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	51892422	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
[(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] acetate	479957	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)CO	484.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
[3a-(Hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] acetate	3129301	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)CO	484.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
3-Hydroxyolean-12-en-28-oic acid	619166	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
5a-(Benzoyloxymethyl)-9-hydroxy-5b,8,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid	73063852	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)COC(=O)C6=CC=CC=C6)C)(C)C)O)C)C(=O)O	576.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
9-[3-(3,4-Dihydroxyphenyl)prop-2-enoyloxy]-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid	74340583	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)O)C)C(=O)O	618.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005 https://doi.org/10.1002/CBDV.200890053
9-Acetyloxy-5a-(benzoyloxymethyl)-5b,8,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid	73201167	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)COC(=O)C6=CC=CC=C6)C)(C)C)OC(=O)C)C)C(=O)O	618.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid	2371	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/10.1016/J.PHYTOCHEM.2006.03.005
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/10.1016/J.PHYTOCHEM.2006.03.005
CID 21120946	21120946	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)COC(=O)C6=CC=CC=C6)C)(C)C)OC(=O)C)C)C(=O)OC	632.90	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Helicteric acid	15940296	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)COC(=O)C6=CC=CC=C6)C)(C)C)OC(=O)C)C)C(=O)O	618.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
methyl (1R,3aS,5aS,5bR,7aR,9S,11aR,11bR,13aR,13bR)-5a-(benzoyloxymethyl)-9-hydroxy-5b,8,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate	11685744	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)COC(=O)C6=CC=CC=C6)C)(C)C)O)C)C(=O)OC	590.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
methyl (1R,3aS,5aS,5bR,7aR,9S,11aR,11bR,13aR,13bR)-9-acetyloxy-5a-[(4-hydroxybenzoyl)oxymethyl]-5b,8,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate	102186522	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)COC(=O)C6=CC=C(C=C6)O)C)(C)C)OC(=O)C)C)C(=O)OC	648.90	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Methyl 10-acetyloxy-6a-(benzoyloxymethyl)-2,2,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	5319672	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)OC)COC(=O)C6=CC=CC=C6)C)C	632.90	unknown	via CMAUP database
Methyl 5a-(benzoyloxymethyl)-9-hydroxy-5b,8,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate	73061531	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)COC(=O)C6=CC=CC=C6)C)(C)C)O)C)C(=O)OC	590.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Methyl 9-acetyloxy-5a-(benzoyloxymethyl)-5b,8,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate	5319671	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)COC(=O)C6=CC=CC=C6)C)(C)C)OC(=O)C)C)C(=O)OC	632.90	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Methyl 9-acetyloxy-5a-[(4-hydroxybenzoyl)oxymethyl]-5b,8,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate	163069808	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)COC(=O)C6=CC=C(C=C6)O)C)(C)C)OC(=O)C)C)C(=O)OC	648.90	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Methyl helicterilate	128136	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)OC)COC(=O)C6=CC=CC=C6)C)C	632.90	unknown	via CMAUP database
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Pyracrenic acid	6439576	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)O)C)C(=O)O	618.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005 https://doi.org/10.1002/CBDV.200890053
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
(8S,9R,10S,13S,14S,16R,17R)-2,16-dihydroxy-4,4,10,13-tetramethyl-17-[(2R,5R)-2,5,6-trihydroxy-6-methyl-3-oxoheptan-2-yl]-7,8,9,12,14,15,16,17-octahydrocyclopenta[a]phenanthrene-3,11-dione	163020405	Click to see CC1(C2=CCC3C4CC(C(C4(CC(=O)C3C2(C=C(C1=O)O)C)C)C(C)(C(=O)CC(C(C)(C)O)O)O)O)C	518.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
2,16-Dihydroxy-4,4,10,13-tetramethyl-17-(2,5,6-trihydroxy-6-methyl-3-oxoheptan-2-yl)-7,8,9,12,14,15,16,17-octahydrocyclopenta[a]phenanthrene-3,11-dione	163020404	Click to see CC1(C2=CCC3C4CC(C(C4(CC(=O)C3C2(C=C(C1=O)O)C)C)C(C)(C(=O)CC(C(C)(C)O)O)O)O)C	518.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Tetrahydroxy bile acids, alcohols and derivatives
(2S,8S,9R,10S,13S,14S,16R,17R)-17-[(E,2R)-2,6-dihydroxy-6-methyl-3-oxohept-4-en-2-yl]-2,16-dihydroxy-4,4,10,13-tetramethyl-1,2,7,8,9,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,11-dione	163066852	Click to see CC1(C2=CCC3C4CC(C(C4(CC(=O)C3C2(CC(C1=O)O)C)C)C(C)(C(=O)C=CC(C)(C)O)O)O)C	502.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
17-(2,6-Dihydroxy-6-methyl-3-oxohept-4-en-2-yl)-2,16-dihydroxy-4,4,10,13-tetramethyl-1,2,7,8,9,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,11-dione	163066851	Click to see CC1(C2=CCC3C4CC(C(C4(CC(=O)C3C2(CC(C1=O)O)C)C)C(C)(C(=O)C=CC(C)(C)O)O)O)C	502.60	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cucurbitacins
(8S,9R,10R,13R,14S,16R,17R)-2,16-dihydroxy-4,4,9,13,14-pentamethyl-17-[(2R,5S)-2,5,6-trihydroxy-6-methyl-3-oxoheptan-2-yl]-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthrene-3,11-dione	57402770	Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2C=C(C1=O)O)C)C)C(C)(C(=O)CC(C(C)(C)O)O)O)O)C)C	532.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
[6-hydroxy-6-(16-hydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-2-sulfooxy-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-methyl-5-oxohept-3-en-2-yl] acetate	73241701	Click to see CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3CC(C(=O)C4(C)C)OS(=O)(=O)O)C)C)C)O)O	638.80	unknown	https://doi.org/10.1248/CPB.54.1605
cucurbitacin B 2-sulfate	16093748	Click to see CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3CC(C(=O)C4(C)C)OS(=O)(=O)O)C)C)C)O)O	638.80	unknown	https://doi.org/10.1248/CPB.54.1605
Cucurbitacin D	5281318	Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2CC(C1=O)O)C)C)C(C)(C(=O)C=CC(C)(C)O)O)O)C)C	516.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Cucurbitacin J	441819	Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2C=C(C1=O)O)C)C)C(C)(C(=O)CC(C(C)(C)O)O)O)O)C)C	532.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids
(2R,3R,7R,8S,9S,10R,13S,14S,17S)-17-[(1S)-1-hydroxy-2-methoxyethyl]-3-methoxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-2,7-diol	102186523	Click to see CC12CCC3C(C1CCC2C(COC)O)C(C=C4C3(CC(C(C4)OC)O)C)O	394.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
17-(1-hydroxy-2-methoxyethyl)-3-methoxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-2,7-diol	162855230	Click to see CC12CCC3C(C1CCC2C(COC)O)C(C=C4C3(CC(C(C4)OC)O)C)O	394.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
(2S,8S,9R,10R,13R,14S,16R,17R)-16-hydroxy-4,4,9,13,14-pentamethyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-[(2R,5R)-2,5,6-trihydroxy-6-methyl-3-oxoheptan-2-yl]-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-3,11-dione	163007626	Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2CC(C1=O)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)(C(=O)CC(C(C)(C)O)O)O)O)C)C	696.80	unknown	https://doi.org/10.1248/CPB.54.1605
[6-hydroxy-6-[16-hydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methyl-5-oxohept-3-en-2-yl] acetate	72968961	Click to see CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3CC(C(=O)C4(C)C)OC5C(C(C(C(O5)CO)O)O)O)C)C)C)O)O	720.80	unknown	https://doi.org/10.1248/CPB.54.1605
16-hydroxy-4,4,9,13,14-pentamethyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-17-(2,5,6-trihydroxy-6-methyl-3-oxoheptan-2-yl)-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-3,11-dione	73241702	Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2CC(C1=O)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)(C(=O)CC(C(C)(C)O)O)O)O)C)C	696.80	unknown	https://doi.org/10.1248/CPB.54.1605
17-(2,6-dihydroxy-6-methyl-3-oxohept-4-en-2-yl)-16-hydroxy-4,4,9,13,14-pentamethyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-3,11-dione	73804168	Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2CC(C1=O)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)(C(=O)C=CC(C)(C)O)O)O)C)C	678.80	unknown	https://doi.org/10.1248/CPB.54.1605
Arvenin I	6441104	Click to see CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3CC(C(=O)C4(C)C)OC5C(C(C(C(O5)CO)O)O)O)C)C)C)O)O	720.80	unknown	https://doi.org/10.1248/CPB.54.1605
arvenin III	21579640	Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2CC(C1=O)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)(C(=O)C=CC(C)(C)O)O)O)C)C	678.80	unknown	https://doi.org/10.1248/CPB.54.1605
> 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/J.PHYTOCHEM.2006.03.005
Beta-Sitosterol	222284	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/J.PHYTOCHEM.2006.03.005
> Organoheterocyclic compounds / Naphthofurans
(3aS,5aR,9aS,9bR)-3a,6,6,9a-tetramethyl-2,4,5,5a,7,8,9,9b-octahydro-1H-benzo[e][1]benzofuran	12838593	Click to see CC1(CCCC2(C1CCC3(C2CCO3)C)C)C	236.39	unknown	via CMAUP database
8,12-Epoxy-13,14,15,16-tetranorlabdane	11861328	Click to see CC1(CCCC2(C1CCC3(C2CCO3)C)C)C	236.39	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Dihydrodehydrodiconiferyl alcohol	384679	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCO	360.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
> Phenylpropanoids and polyketides / Cinnamaldehydes
3-(3,4-Dimethoxyphenyl)-2-propenal	107557	Click to see COC1=C(C=C(C=C1)C=CC=O)OC	192.21	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
3,4-Dimethoxy cinnamaldehyde	5375268	Click to see COC1=C(C=C(C=C1)C=CC=O)OC	192.21	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-rosmarinic acid	639655	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	360.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
3-(3,4-Dihydroxyphenyl)-2-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]propanoic acid	5099	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	360.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Rosmarinic acid	5281792	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	360.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
6,10,11-Trihydroxy-4,8,12-trimethyl-2-oxatricyclo[7.3.1.05,13]trideca-1(13),4,9,11-tetraen-3-one	75059643	Click to see CC1CC(C2=C(C(=O)OC3=C2C1=C(C(=C3C)O)O)C)O	276.28	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Vcbhabvpyyfxjs-xrgyyrrgsa-	44631546	Click to see CC1CC(C2=C(C(=O)OC3=C2C1=C(C(=C3C)O)O)C)O	276.28	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
> 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	via CMAUP database
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
Myricetin	5281672	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	318.23	unknown	via CMAUP database
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	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-8-O-glucuronides
(2S,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-8-yl]oxy-3,4-dihydroxy-5-sulfooxyoxane-2-carboxylic acid	163106804	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)OS(=O)(=O)O)O	542.40	unknown	https://doi.org/10.3987/COM-94-6710
(2S,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-methoxyphenyl)-4-oxochromen-8-yl]oxy-3,4-dihydroxy-5-sulfooxyoxane-2-carboxylic acid	5318672	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)OS(=O)(=O)O	556.50	unknown	https://doi.org/10.3987/COM-94-6710
methyl (2S,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-methoxyphenyl)-4-oxochromen-8-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylate	163193559	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)OC)O)O)O	490.40	unknown	https://doi.org/10.3987/COM-94-6710
Methyl 6-[5,7-dihydroxy-2-(4-methoxyphenyl)-4-oxochromen-8-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylate	162898551	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)OC)O)O)O	490.40	unknown	https://doi.org/10.3987/COM-94-6710
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	5315208	Click to see C1C(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	596.50	unknown	via CMAUP database
3-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one	42613954	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O	626.50	unknown	via CMAUP database
5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(6-O-I(2)-D-xylopyranosyl-I(2)-D-glucopyranosyl)oxy]-4H-1-benzopyran-4-one	102148697	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O	610.50	unknown	via CMAUP database
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5462193	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Astragalin	5282102	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Isoquercetin	5280804	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	via CMAUP database
Kaempferol-3-O-rutinoside	5318767	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	594.50	unknown	via CMAUP database
myricetin 3-O-beta-D-glucopyranoside	5318606	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O	480.40	unknown	via CMAUP database
Myricetin-3-O-rutinoside	21577860	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)O	626.50	unknown	via CMAUP database
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	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Isokaempferide	5280862	Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	300.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
[5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxochromen-8-yl] (2S,3S,4S,5R,6R)-3,4,5,6-tetrahydroxyoxane-2-carboxylate	163003716	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC(=O)C4C(C(C(C(O4)O)O)O)O)O	492.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
[5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxochromen-8-yl] 3,4,5,6-tetrahydroxyoxane-2-carboxylate	163003715	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC(=O)C4C(C(C(C(O4)O)O)O)O)O	492.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Acacetin	5280442	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	284.26	unknown	via CMAUP database
Ermanin	5352001	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC	314.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5,8-Dihydroxy-7,4'-dimethoxyflavone	15289454	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC)O	314.29	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.03.005
Genkwanin	5281617	Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O	284.26	unknown	via CMAUP database
Jaranol	5318869	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O	314.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-Phenylpropionic acid	107	Click to see C1=CC=C(C=C1)CCC(=O)O	150.17	unknown	via CMAUP database

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Helicteres angustifolia

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