Scientific name	Authority	First published in
Ixora versicolor	Hassk.	Tijdschr. Ned.-Indië 10: 135 (1843)
Helicteres chrysocalyx	Miq. ex Mast.	Fl. Brit. India 1: 365 (1874)
Helicteres grewiifolia	DC.	Prodr. 1: 477 (1824)
Helicteres macrophylla	Wight	Prodr. Fl. Ind. Orient. : 60 (1834)
Isora corylifolia	Schott & Endl.	Melet. Bot. : 31 (1832)
Helicteres roxburghii	G.Don	Gen. Hist. 1: 506 (1831)
Helicteres ovata var. isora-murri	Lam.	Encycl. 3: 88 1789
Helicteres ovata var. fructus-regis	Lam.	Encycl. 3: 88 1789
Helicteres grewiaefolia	DC.	Prodr. 1: 476 1824
Helicteres baruensis var. ovata	DC.	Prodr. 1: 476 (1824)
Isora grewiaefolia	(DC.) Schott & Endl.	Mélanges Bot. 31 1832
Helicteres isora var. microphylla	Hassk.	Flor. (B.Z.) 514 1856
Helicteres isora var. glabrescens	Mast.	Fl. Brit. India 1(2): 365 1874
Helicteres isora var. tomentosa	Mast.	Fl. Brit. India 1(2): 365 1874

Common names Top

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Filter by language:

Language	Common/alternative name
ace	puta taloe
Arabic	سوار الهند
Bengali	অন্তমরা
Persian	بهمنپیچ
Malayalam	east indian screw tree
Malayalam	ഇടമ്പിരി
Malayalam	ഇടമ്പിരി വലമ്പിരി
Malayalam	മരോട്
Malayalam	വലമ്പിരി
Malayalam	ഇടംപിരി വലംപിരി
Marathi	मुरडशेंग
Tamil	இடம்புரி
Telugu	ఆడశ్యామలి
Telugu	శ్యామలి
Thai	ปอบิด
Chinese	鞭龙
Chinese	扭蒴山芝麻
Chinese	纽蒴山芝麻
Chinese	火索麻

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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
  - Hainan

Asia-tropical click to expand
- Indian Subcontinent
  - Bangladesh
  - India
  - Nepal
  - Pakistan
  - Sri Lanka
- Indo-China
  - Andaman Islands
  - Cambodia
  - Laos
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Malaya
  - Maluku

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000718114
UNII	54Q9269RP5
Tropicos	30400016
KEW	urn:lsid:ipni.org:names:321222-2
The Plant List	kew-2843218
Open Tree Of Life	3942803
NCBI Taxonomy	1382013
IPNI	321222-2
iNaturalist	356161
GBIF	5546922
Freebase	/m/0ndjmr9
USDA GRIN	101973
Wikipedia	Helicteres_isora

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 mechanistic role of natural antimicrobials in preventing Staphylococcus aureus invasion of MAC-T cells using an in vitro mastitis model

Balta I, McCleery D, David SR, Pet E, Stef D, Iancu T, Pet I, Stef L, Corcionivoschi N

Ir Vet J

27-Feb-2024

PMCID:	PMC10898119
doi:	10.1186/s13620-024-00265-0
PMID:	38414081

Diosgenin alleviates D-galactose-induced oxidative stress in rats’ brain and liver targeting aging and apoptotic marker genes

El-Far AH, Elghaity MM, Mohamed SA, Noreldin AE, Elewa YH, Al Jaouni SK, Alsenosy AA

Front Mol Biosci

23-Feb-2024

PMCID:	PMC10922004
doi:	10.3389/fmolb.2024.1303379
PMID:	38463710

Screening herbal extracts as biostimulant to increase germination, plant growth and secondary metabolite production in wheatgrass

Yadav A, Singh S, Yadav V

Sci Rep

05-Jan-2024

PMCID:	PMC10770375
doi:	10.1038/s41598-023-50513-6
PMID:	38182633

Review green synthesis of silver nanoparticles by using plant extracts and their antimicrobial activity

Abada E, Mashraqi A, Modafer Y, Al Abboud MA, El-Shabasy A

Saudi J Biol Sci

26-Nov-2023

PMCID:	PMC10749906
doi:	10.1016/j.sjbs.2023.103877
PMID:	38148949

Recent Advances in the Application of Cucurbitacins as Anticancer Agents

Zieniuk B, Pawełkowicz M

Metabolites

14-Oct-2023

PMCID:	PMC10608718
doi:	10.3390/metabo13101081
PMID:	37887406

Characterization and Bioactivity of Piper chaudocanum L. Extract-Doped ZnO Nanoparticles Biosynthesized by Co-Precipitation Method

Truong TT, Khieu TT, Luu HN, Truong HB, Nguyen VK, Vuong TX, Tran TK

Materials (Basel)

03-Aug-2023

PMCID:	PMC10420328
doi:	10.3390/ma16155457
PMID:	37570161

Biogenic Fabrication of Silver Nanoparticles Using Calotropis procera Flower Extract with Enhanced Biomimetics Attributes

Nagime PV, Singh S, Shaikh NM, Gomare KS, Chitme H, Abdel-Wahab BA, Alqahtany YS, Khateeb MM, Habeeb MS, Bakir MB

Materials (Basel)

30-May-2023

PMCID:	PMC10254777
doi:	10.3390/ma16114058
PMID:	37297192

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

Antifungal activity of volatile and non-volatile metabolites of endophytes of Chloranthus elatior Sw.

Santra HK, Banerjee D

Front Plant Sci

17-May-2023

PMCID:	PMC10229785
doi:	10.3389/fpls.2023.1156323
PMID:	37265637

Phytochemicals: potential alternative strategy to fight Salmonella enterica serovar Typhimurium

Almuzaini AM

Front Vet Sci

16-May-2023

PMCID:	PMC10228746
doi:	10.3389/fvets.2023.1188752
PMID:	37261108

Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India?

Kumar BM

Agrofor Syst

07-Apr-2023

PMCID:	PMC10081327
doi:	10.1007/s10457-023-00821-7
PMID:	37193256

Methyl jasmonate and salicylic acid as powerful elicitors for enhancing the production of secondary metabolites in medicinal plants: an updated review

Jeyasri R, Muthuramalingam P, Karthick K, Shin H, Choi SH, Ramesh M

Plant Cell Tissue Organ Cult

20-Mar-2023

PMCID:	PMC10026785
doi:	10.1007/s11240-023-02485-8
PMID:	37197003

Recent developments in detection and therapeutic approaches for antibiotic-resistant bacterial infections

Moorthy K, Chang KC, Yang HH, Su WM, Chiang CK, Yuan Z

J Food Drug Anal

15-Mar-2023

PMCID:	PMC10208662
doi:	10.38212/2224-6614.3433
PMID:	37224551

Advances in the Biosynthesis and Molecular Evolution of Steroidal Saponins in Plants

Li Y, Yang H, Li Z, Li S, Li J

Int J Mol Sci

30-Jan-2023

PMCID:	PMC9917158
doi:	10.3390/ijms24032620
PMID:	36768941

Drought alleviation efficacy of a galactose rich polysaccharide isolated from endophytic Mucor sp. HELF2: A case study on rice plant

Santra HK, Banerjee D

Front Microbiol

26-Jan-2023

PMCID:	PMC9910089
doi:	10.3389/fmicb.2022.1064055
PMID:	36777025

Phytochemical Profile Top

Add a new one!

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

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Benzene and substituted derivatives / Cyclohexylphenols
[(2S)-3-(3,4-dihydroxyphenyl)-1-methoxy-1-oxopropan-2-yl] (1S,2R,3S,4S,7R,8S)-3-(3,4-dihydroxyphenyl)-6-[(E)-3-[(2S)-3-(3,4-dihydroxyphenyl)-1-methoxy-1-oxopropan-2-yl]oxy-3-oxoprop-1-enyl]-7,8-dihydroxybicyclo[2.2.2]oct-5-ene-2-carboxylate	163190017	Click to see COC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC3C(C(C2C(C3O)O)C(=O)OC(CC4=CC(=C(C=C4)O)O)C(=O)OC)C5=CC(=C(C=C5)O)O	750.70	unknown	https://doi.org/10.1002/(SICI)1522-2675(19990310)82:3<408::AID-HLCA408>3.0.CO;2-H
[3-(3,4-Dihydroxyphenyl)-1-methoxy-1-oxopropan-2-yl] 3-(3,4-dihydroxyphenyl)-6-[3-[3-(3,4-dihydroxyphenyl)-1-methoxy-1-oxopropan-2-yl]oxy-3-oxoprop-1-enyl]-7,8-dihydroxybicyclo[2.2.2]oct-5-ene-2-carboxylate	162937011	Click to see COC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC3C(C(C2C(C3O)O)C(=O)OC(CC4=CC(=C(C=C4)O)O)C(=O)OC)C5=CC(=C(C=C5)O)O	750.70	unknown	https://doi.org/10.1002/(SICI)1522-2675(19990310)82:3<408::AID-HLCA408>3.0.CO;2-H
methyl (1S,2R,3S,4S,7S)-3-(3,4-dihydroxyphenyl)-6-[(E)-3-[(2S)-3-(3,4-dihydroxyphenyl)-1-methoxy-1-oxopropan-2-yl]oxy-3-oxoprop-1-enyl]-7-hydroxy-8-oxobicyclo[2.2.2]oct-5-ene-2-carboxylate	163194739	Click to see COC(=O)C1C(C2C=C(C1C(C2=O)O)C=CC(=O)OC(CC3=CC(=C(C=C3)O)O)C(=O)OC)C4=CC(=C(C=C4)O)O	568.50	unknown	https://doi.org/10.1002/(SICI)1522-2675(19990310)82:3<408::AID-HLCA408>3.0.CO;2-H
Methyl 3-(3,4-dihydroxyphenyl)-6-[3-[3-(3,4-dihydroxyphenyl)-1-methoxy-1-oxopropan-2-yl]oxy-3-oxoprop-1-enyl]-7-hydroxy-8-oxobicyclo[2.2.2]oct-5-ene-2-carboxylate	85110920	Click to see COC(=O)C1C(C2C=C(C1C(C2=O)O)C=CC(=O)OC(CC3=CC(=C(C=C3)O)O)C(=O)OC)C4=CC(=C(C=C4)O)O	568.50	unknown	https://doi.org/10.1002/(SICI)1522-2675(19990310)82:3<408::AID-HLCA408>3.0.CO;2-H
> Benzenoids / Fluorenes
[3-(3,4-dihydroxyphenyl)-1-methoxy-1-oxopropan-2-yl] 11-[(E)-3-[3-(3,4-dihydroxyphenyl)-1-methoxy-1-oxopropan-2-yl]oxy-3-oxoprop-1-enyl]-1,4,5-trihydroxy-14-oxotetracyclo[8.3.1.02,7.08,13]tetradeca-2,4,6,11-tetraene-9-carboxylate	100935400	Click to see COC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC3C4C(C2C(=O)C3(C5=CC(=C(C=C45)O)O)O)C(=O)OC(CC6=CC(=C(C=C6)O)O)C(=O)OC	746.70	unknown	https://doi.org/10.1002/(SICI)1522-2675(19990310)82:3<408::AID-HLCA408>3.0.CO;2-H
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
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/10.26510/2394-0859.PBE.2017.07
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/10.26510/2394-0859.PBE.2017.07
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cucurbitacins
Isocucurbitacin B	5352014	Click to see CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3CC(=O)C(C4(C)C)O)C)C)C)O)O	558.70	unknown	https://doi.org/10.1021/NP50039A033
> 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/10.26510/2394-0859.PBE.2017.07
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://doi.org/10.26510/2394-0859.PBE.2017.07
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S)-3-(3,4-dihydroxyphenyl)-2-[(E)-3-[3-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoyl]oxypropanoic acid	10815866	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O	522.50	unknown	https://doi.org/10.1248/CPB.47.1444
(2S)-3-(4-hydroxyphenyl)-2-[(E)-3-[3-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoyl]oxypropanoic acid	10720349	Click to see C1=CC(=CC=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O	506.50	unknown	https://doi.org/10.1248/CPB.47.1444
(2S)-3-[3-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2-[(E)-3-[3-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoyl]oxypropanoic acid	10508776	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O	684.60	unknown	https://doi.org/10.1248/CPB.47.1444
3-(3,4-Dihydroxyphenyl)-2-[3-[3-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoyloxy]propanoic acid	75614557	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O	522.50	unknown	https://doi.org/10.1248/CPB.47.1444
3-(4-Hydroxyphenyl)-2-[3-[3-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoyloxy]propanoic acid	85244613	Click to see C1=CC(=CC=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O	506.50	unknown	https://doi.org/10.1248/CPB.47.1444
3-[3-Hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2-[3-[3-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoyloxy]propanoic acid	85098391	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O	684.60	unknown	https://doi.org/10.1248/CPB.47.1444
> 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/10.1248/CPB.47.1444
3-(3,4-dihydroxyphenyl)-2-[(2E)-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/10.1248/CPB.47.1444
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
methyl (2S,3S,4R,5R,6S)-6-[5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxochromen-8-yl]-3,4,5-trihydroxyoxane-2-carboxylate	162933403	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)C(=O)OC)O)O)O)O	490.40	unknown	https://doi.org/10.1002/(SICI)1522-2675(19990310)82:3<408::AID-HLCA408>3.0.CO;2-H
methyl (2S,3S,4R,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-8-yl]-3,4,5-trihydroxyoxane-2-carboxylate	162849047	Click to see COC(=O)C1C(C(C(C(O1)C2=C(C=C(C3=C2OC(=CC3=O)C4=CC=C(C=C4)O)O)O)O)O)O	460.40	unknown	https://doi.org/10.1002/(SICI)1522-2675(19990310)82:3<408::AID-HLCA408>3.0.CO;2-H
Methyl 6-[5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxochromen-8-yl]-3,4,5-trihydroxyoxane-2-carboxylate	162933402	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)C(=O)OC)O)O)O)O	490.40	unknown	https://doi.org/10.1002/(SICI)1522-2675(19990310)82:3<408::AID-HLCA408>3.0.CO;2-H
Methyl 6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-8-yl]-3,4,5-trihydroxyoxane-2-carboxylate	162849046	Click to see COC(=O)C1C(C(C(C(O1)C2=C(C=C(C3=C2OC(=CC3=O)C4=CC=C(C=C4)O)O)O)O)O)O	460.40	unknown	https://doi.org/10.1002/(SICI)1522-2675(19990310)82:3<408::AID-HLCA408>3.0.CO;2-H
> 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-4-hydroxy-3,5-disulfooxyoxane-2-carboxylic acid	5318665	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)OS(=O)(=O)O)O)OS(=O)(=O)O)O	622.50	unknown	https://doi.org/10.1016/S0031-9422(01)00005-X
(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/10.1016/S0031-9422(01)00005-X
(2S,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-methoxyphenyl)-4-oxochromen-8-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid	11968644	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)O	476.40	unknown	https://doi.org/10.1016/S0031-9422(01)00005-X
(2S,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-methoxyphenyl)-4-oxochromen-8-yl]oxy-4-hydroxy-3,5-disulfooxyoxane-2-carboxylic acid	5318670	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)OS(=O)(=O)O)O)OS(=O)(=O)O	636.50	unknown	https://doi.org/10.1016/S0031-9422(01)00005-X
6-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-8-yl]oxy-4-hydroxy-3,5-disulfooxyoxane-2-carboxylic acid	73981634	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)OS(=O)(=O)O)O)OS(=O)(=O)O)O	622.50	unknown	https://doi.org/10.1016/S0031-9422(01)00005-X
6-[5,7-Dihydroxy-2-(4-methoxyphenyl)-4-oxochromen-8-yl]oxy-3,4-dihydroxy-5-sulfooxyoxane-2-carboxylic acid	73981639	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/10.1016/S0031-9422(01)00005-X
6-[5,7-Dihydroxy-2-(4-methoxyphenyl)-4-oxochromen-8-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid	73981635	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)O	476.40	unknown	https://doi.org/10.1016/S0031-9422(01)00005-X
6-[5,7-Dihydroxy-2-(4-methoxyphenyl)-4-oxochromen-8-yl]oxy-4-hydroxy-3,5-disulfooxyoxane-2-carboxylic acid	73981637	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)OS(=O)(=O)O)O)OS(=O)(=O)O	636.50	unknown	https://doi.org/10.1016/S0031-9422(01)00005-X
butyl (2R,3R,4R,5S,6R)-6-[5,7-dihydroxy-2-(4-methoxyphenyl)-4-oxochromen-8-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylate	163051662	Click to see CCCCOC(=O)C1C(C(C(C(O1)OC2=C(C=C(C3=C2OC(=CC3=O)C4=CC=C(C=C4)OC)O)O)O)O)O	532.50	unknown	https://doi.org/10.1016/S0031-9422(01)00005-X
butyl (2S,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-methoxyphenyl)-4-oxochromen-8-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylate	5323572	Click to see CCCCOC(=O)C1C(C(C(C(O1)OC2=C(C=C(C3=C2OC(=CC3=O)C4=CC=C(C=C4)OC)O)O)O)O)O	532.50	unknown	https://doi.org/10.1016/S0031-9422(01)00005-X
butyl (3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-methoxyphenyl)-4-oxochromen-8-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylate	163185457	Click to see CCCCOC(=O)C1C(C(C(C(O1)OC2=C(C=C(C3=C2OC(=CC3=O)C4=CC=C(C=C4)OC)O)O)O)O)O	532.50	unknown	https://doi.org/10.1016/S0031-9422(01)00005-X
Butyl 6-[5,7-dihydroxy-2-(4-methoxyphenyl)-4-oxochromen-8-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylate	20980953	Click to see CCCCOC(=O)C1C(C(C(C(O1)OC2=C(C=C(C3=C2OC(=CC3=O)C4=CC=C(C=C4)OC)O)O)O)O)O	532.50	unknown	https://doi.org/10.1016/S0031-9422(01)00005-X
Hibifolin	5490334	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O	494.40	unknown	https://doi.org/10.1021/NP50122A013
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Trifolin	5282149	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/10.1021/NP50122A013
> 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/10.1021/NP50122A013

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Helicteres isora

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