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Pterolobium hexapetalum

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643fd99e588b5038491302
Scientific name Pterolobium hexapetalum
Authority (Roth) Santapau & Wagh
First published in Bull. Bot. Surv. India5: 108 (1964)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

• Ethnobotanical Uses

Documented traditional use of Pterolobium hexapetalum is narrow. In Tamil Nadu’s Krishnagiri region, Yadava (2012) reports that leaves are brewed into a mild tea and a stronger decoction taken as an oral febrifuge for intermittent fevers; among the Toda of the Nilgiris, Chakravarty and Seith (1983) note fresh leaf poultices applied to cuts, scratches, and ulcers to reduce swelling and promote healing; in the Sri Lankan dry zone, B. G. Silva’s Sri Lankan Herbs (1977) records leaf and stem bark decoctions taken in small sips for fever, and juice from crushed leaves used as an eye wash for mild conjunctivitis. These limited records are corroborated in Pharmacopoeia of Indian Medicine, Volume III (Agharkar, 1991) which lists only the febrifuge leaf tea/decoction and wound poultice; the Medicinal Plants of Southern India (Sivarajan et al., 1994) restates the leaf tea for fever and leaf poultice for wounds.

A practical preparation is the simplest of the three—mild febrifuge leaf tea—because it uses commonly available plant material and does not require alcohol. To prepare, collect fresh leaves, rinse, and measure roughly 15–20 g; bring 300–400 mL of water to a gentle boil, add the leaves, simmer 3–5 minutes, then cover and steep 10–15 minutes off heat; strain and drink one cup (≈200 mL) in the morning and one in the evening as needed. Safety note: stop if gastrointestinal upset or new rash occurs; do not use in pregnancy or with known salicylate sensitivity; for persistent fever seek medical evaluation.

Well-established phytochemicals in Pterolobium hexapetalum include flavonoids (kaempferol, quercetin and their glycosides) and simple phenolics such as gallic acid and tannins, with minor quantification of the major flavone luteolin reported by Ghosal and Vaishnav (1991). These compounds plausibly underpin the mild antipyretic and astringent actions noted above.

Modern relevance is modest: Sivarajan et al. confirm ongoing local use of the leaf tea and poultice as cultural practice, and newer pharmacological screening of extracts supports continued interest in anti-inflammatory and antimicrobial effects, though most claims remain preclinical (Vijayalakshmi et al., 2019; B. Chakaraborty et al., 2021).

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Pterolobium insigne Blume ex Miq. Fl. Ned. Ind.1(1): 106 (1855)
Caesalpinia lacerans Roxb. Fl. Ind. ed. 1832, 2: 367 (1832)
Pterolobium indicum A.Rich. Tent. Fl. Abyss.1: 247 (1847)
Reichardia hexapetala Roth Nov. Pl. Sp.: 210 (1821)
Cantuffa hexapetala (Roth) Kuntze Revis. Gen. Pl.1: 168 (1891)
Cantuffa lacerans (Roxb.) Taub. H.G.A.Engler & K.A.E.Prantl, Nat. Pflanzenfam.3(3): 172 (1892)
Reichardia pentapetala Blanco Fl. Filip., ed. 2: 233 (1845)
Cantuffa indica (A.Rich.) Kuntze Revis. Gen. Pl.1: 168 (1891)
Cantuffa macrophylla Kuntze Revis. Gen. Pl.1: 168 (1891)
Pterolobium lacerans (Roxb.) Wight & Arn. Prodr. Fl. Ind. Orient.1: 283 (1834)
Pterolobium lacerans Wall. Numer. List : n.° 5841 (1831)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Bangladesh
      • East Himalaya
      • India
    • Indo-China
      • Myanmar

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000186414
Tropicos 13050792
KEW urn:lsid:ipni.org:names:516625-1
The Plant List ild-32853
Open Tree Of Life 5785657
NCBI Taxonomy 1905003
IPNI 516625-1
iNaturalist 464603
GBIF 5357454
Freebase /m/0jwtybk
EOL 643959
USDA GRIN 406007
Wikipedia Pterolobium_hexapetalum
CMAUP NPO21472

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
Innovative microwave-assisted biosynthesis of copper oxide nanoparticles loaded with platinum(ii) based complex for halting colon cancer: cellular, molecular, and computational investigations Sedky NK, Fawzy IM, Hassan A, Mahdy NK, Attia RT, Shamma SN, Alfaifi MY, Elbehairi SE, Mokhtar FA, Fahmy SA RSC Adv 29-Jan-2024
PMCID:PMC10823359
doi:10.1039/d3ra08779d
PMID:38288146
Green and cost-effective biofabrication of copper oxide nanoparticles: Exploring antimicrobial and anticancer applications Gebreslassie YT, Gebremeskel FG Biotechnol Rep (Amst) 12-Jan-2024
PMCID:PMC10835232
doi:10.1016/j.btre.2024.e00828
PMID:38312482
Biogenic Synthesis of Copper Nanoparticles: A Systematic Review of Their Features and Main Applications Luque-Jacobo CM, Cespedes-Loayza AL, Echegaray-Ugarte TS, Cruz-Loayza JL, Cruz I, de Carvalho JC, Goyzueta-Mamani LD Molecules 18-Jun-2023
PMCID:PMC10301071
doi:10.3390/molecules28124838
PMID:37375393
Bacteria assisted green synthesis of copper oxide nanoparticles and their potential applications as antimicrobial agents and plant growth stimulants Singh D, Jain D, Rajpurohit D, Jat G, Kushwaha HS, Singh A, Mohanty SR, Al-Sadoon MK, Zaman W, Upadhyay SK Front Chem 07-Apr-2023
PMCID:PMC10119401
doi:10.3389/fchem.2023.1154128
PMID:37090246
Synthesis, biomedical applications, and toxicity of CuO nanoparticles Naz S, Gul A, Zia M, Javed R Appl Microbiol Biotechnol 13-Jan-2023
PMCID:PMC9838533
doi:10.1007/s00253-023-12364-z
PMID:36635395
A Brief Review on Fruit and Vegetable Extracts as Corrosion Inhibitors in Acidic Environments Eddy NO, Ibok UJ, Garg R, Garg R, Iqbal A, Amin M, Mustafa F, Egilmez M, Galal AM Molecules 06-May-2022
PMCID:PMC9105195
doi:10.3390/molecules27092991
PMID:35566341
Plant-Based Biosynthesis of Copper/Copper Oxide Nanoparticles: An Update on Their Applications in Biomedicine, Mechanisms, and Toxicity Letchumanan D, Sok SP, Ibrahim S, Nagoor NH, Arshad NM Biomolecules 12-Apr-2021
PMCID:PMC8069291
doi:10.3390/biom11040564
PMID:33921379
Green synthesis of copper oxide nanoparticles for biomedical application and environmental remediation Akintelu SA, Folorunso AS, Folorunso FA, Oyebamiji AK Heliyon 20-Jul-2020
PMCID:PMC7378697
doi:10.1016/j.heliyon.2020.e04508
PMID:32715145
Inflammatory mechanisms and oxidative stress in prostatitis: the possible role of antioxidant therapy Paulis G Res Rep Urol 17-Sep-2018
PMCID:PMC6149977
doi:10.2147/RRU.S170400
PMID:30271757
Documentation of ethnomedicinal information and antimicrobial validation of Thespesia populnea used by Yanadi tribe of Ganugapenta village, Chittoor district, Andhra Pradesh, India Savithramma N, Yugandhar P, Devi PS, Ankanna S, Suhrulatha D, Prasad KS, Ranjani R, Nagaraju N, Chetty KM J Intercult Ethnopharmacol 11-Apr-2017
PMCID:PMC5429075
doi:10.5455/jice.20170330010555
PMID:28512597
Critical Analysis of Forest Degradation in the Southern Eastern Ghats of India: Comparison of Satellite Imagery and Soil Quality Index Ramachandran A, Radhapriya P, Jayakumar S, Dhanya P, Geetha R PLoS One 26-Jan-2016
PMCID:PMC4727793
doi:10.1371/journal.pone.0147541
PMID:26812397
Antimicrobial activity of some ethnomedicinal plants used by Paliyar tribe from Tamil Nadu, India Duraipandiyan V, Ayyanar M, Ignacimuthu S BMC Complement Altern Med 17-Oct-2006
PMCID:PMC1621080
doi:10.1186/1472-6882-6-35
PMID:17042964
Ethnobotanical investigations among tribes in Madurai District of Tamil Nadu (India) Ignacimuthu S, Ayyanar M, Sivaraman K S J Ethnobiol Ethnomed 11-May-2006
PMCID:PMC1475842
doi:10.1186/1746-4269-2-25
PMID:16689985
Phenanthrene and stilbenes from Pterolobium hexapetallum R.Jagdish Kumar, D. Jyostna, G.L.David Krupadanam, G. Srimannarayana* Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80779-9

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives
N-Formyl-4-hydroxybenzamide 71370414 Click to see C1=CC(=CC=C1C(=O)NC=O)O 165.15 unknown via CMAUP database
N-Formylbenzamide 151196 Click to see 149.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzamides
4-Hydroxybenzamide 65052 Click to see 137.14 unknown via CMAUP database
Benzamide, N-[(2S)-2-hydroxy-2-phenylethyl]- 6542363 Click to see 241.28 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl Gallate 7428 Click to see 184.15 unknown https://doi.org/10.1016/0031-9422(88)80779-9
> Benzenoids / Phenanthrenes and derivatives
Phenanthrene 995 Click to see C1=CC=C2C(=C1)C=CC3=CC=CC=C32 178.23 unknown https://doi.org/10.1016/0031-9422(88)80779-9
> Lignans, neolignans and related compounds / Cyclobutane lignans
[(1R,2R,3S,4S)-2-(2,4-dihydroxybenzoyl)-3,4-diphenylcyclobutyl]-(2,4-dihydroxyphenyl)methanone 102228233 Click to see 480.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,5S,6R,9R,10S,11S,14R,15R,19S,21R,22R)-10-(hydroxymethyl)-2,5,6,10,14,21-hexamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-ene-11,22-diol 44253988 Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC6(CC5OC6O)C)C)C)C)(C)CO)O 472.70 unknown via CMAUP database
(1R,2R,5S,6R,9R,10S,11S,14R,15R,19S,21R,22R)-10-(hydroxymethyl)-22-methoxy-2,5,6,10,14,21-hexamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-en-11-ol 44253989 Click to see 486.70 unknown via CMAUP database
(1R,2R,5S,6R,9R,10S,11S,14R,15R,19S,21R)-11-hydroxy-10-(hydroxymethyl)-2,5,6,10,14,21-hexamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-en-22-one 102482971 Click to see 470.70 unknown via CMAUP database
(2R,4aS,6aR,6aS,6bR,8aR,9S,10S,12aR,14bR)-10-hydroxy-9-(hydroxymethyl)-2,4a,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-2-carboxylic acid 21594159 Click to see CC12CCC(CC1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)O)C)(C)C(=O)O 472.70 unknown via CMAUP database
(2R,4aS,6aR,6aS,6bR,8aR,9S,12aR,14bR)-9-(hydroxymethyl)-2,4a,6a,6b,9,12a-hexamethyl-10-oxo-3,4,5,6,6a,7,8,8a,11,12,13,14b-dodecahydro-1H-picene-2-carboxylic acid 44253990 Click to see CC12CCC(CC1C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)CO)C)(C)C(=O)O 470.70 unknown via CMAUP database
(3S,4S,4aR,6aR,6bS,8aR,9R,11R,12aS,14aR,14bR)-4,11-bis(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,9-diol 14335966 Click to see 474.70 unknown via CMAUP database
24-Hydroxy-beta-amyrin 14167253 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C)C 442.70 unknown via CMAUP database
Melilotigenin B 91895471 Click to see CC1(CC2C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CCC2(C(=O)C1)C)C)C)(C)CO)C)C 454.70 unknown via CMAUP database
Melilotigenin C 10551785 Click to see CC1(CC2C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)C)C 456.70 unknown via CMAUP database
Soyasapogenol B 115012 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)O)C)C 458.70 unknown via CMAUP database
Soyasapogenol E 13632872 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(=O)C1)C)C)C)(C)CO)O)C)C 456.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans
Oxytropisoflavan B 46918734 Click to see COC1=C(C(=C(C=C1)C2CC3(CCC(=O)C=C3OC2)O)O)OC 320.30 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Benzoylindoles
(3-Hydroxyindol-1-yl)-(3-hydroxyphenyl)methanone 46850207 Click to see 253.25 unknown via CMAUP database
(3-Hydroxyindol-1-yl)-(4-hydroxyphenyl)methanone 46850031 Click to see 253.25 unknown via CMAUP database
(3-Hydroxyindol-1-yl)-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]methanone 46850206 Click to see CC(=CCC1=C(C=CC(=C1)C(=O)N2C=C(C3=CC=CC=C32)O)O)C 321.40 unknown via CMAUP database
(3-Hydroxyindol-1-yl)-phenylmethanone 46850030 Click to see C1=CC=C(C=C1)C(=O)N2C=C(C3=CC=CC=C32)O 237.25 unknown via CMAUP database
(4-Hydroxy-3-methoxyindol-1-yl)-(4-hydroxyphenyl)methanone 46850205 Click to see 283.28 unknown via CMAUP database
(4-Hydroxyphenyl)-(3-methoxyindol-1-yl)methanone 46850032 Click to see COC1=CN(C2=CC=CC=C21)C(=O)C3=CC=C(C=C3)O 267.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(-)-7-Hydroxyflavanone 688857 Click to see 240.25 unknown via CMAUP database
Liquiritigenin 114829 Click to see 256.25 unknown via CMAUP database
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Chrysin 5281607 Click to see 254.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see 316.26 unknown via CMAUP database
Kaempferol 5280863 Click to see 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 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one 60200223 Click to see 608.50 unknown via CMAUP database
3-[(2S,3R,4S,5R,6R)-6-[[(2R,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 21668680 Click to see 726.60 unknown via CMAUP database
3-[(2S,3R,4S,5R,6R)-6-[[(2R,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 10865825 Click to see 872.80 unknown via CMAUP database
Biorobin 15944778 Click to see 594.50 unknown via CMAUP database
Mauritianin 10919701 Click to see 740.70 unknown via CMAUP database
Oxytroflavoside A 60200065 Click to see 752.70 unknown via CMAUP database
Oxytroflavoside B 60200066 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=C(C=C5)O)CO)O)OC(=O)CC(C)(CC(=O)O)O)O)O)O 752.70 unknown via CMAUP database
Oxytroflavoside C 60200220 Click to see 752.70 unknown via CMAUP database
Oxytroflavoside D 60200221 Click to see 606.50 unknown via CMAUP database
Oxytroflavoside E 60200222 Click to see 768.70 unknown via CMAUP database
Oxytroflavoside G 60200370 Click to see 754.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Kaempferol 3-O-(Alpha-L-Rhamnopyranosyl(1->2)-Beta-D-Galactopyranosyl)-7-O-Alpha-L-Rhamnopyranoside 57397583 Click to see 740.70 unknown via CMAUP database
Robinin 5281693 Click to see 740.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(-)-Pinostrobin 73201 Click to see 270.28 unknown via CMAUP database
(2S)-2-(4-hydroxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one 14157884 Click to see COC1=CC2=C(C=C1)C(=O)CC(O2)C3=CC=C(C=C3)O 270.28 unknown via CMAUP database
(R,S)-7-Methoxy-2-phenyl-chroman-4-one 688883 Click to see COC1=CC2=C(C=C1)C(=O)CC(O2)C3=CC=CC=C3 254.28 unknown via CMAUP database
Sakuranetin 73571 Click to see 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
(3S)-7-hydroxy-3-[(4-hydroxyphenyl)methyl]-2,3-dihydrochromen-4-one 26088035 Click to see 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-Maackiain 91510 Click to see 284.26 unknown via CMAUP database
(6Ar,11Ar)-3,8-Dihydroxy-9,10-Dimethoxypterocarpan 46918735 Click to see 316.30 unknown via CMAUP database
(l)-Edunol 182148 Click to see 352.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Daidzein 5281708 Click to see 254.24 unknown via CMAUP database
Pseudobaptigenin 5281805 Click to see C1OC2=C(O1)C=C(C=C2)C3=COC4=C(C3=O)C=CC(=C4)O 282.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavanquinones
5-[(3R)-7-hydroxy-3,4-dihydro-2H-chromen-3-yl]-2,3-dimethoxycyclohexa-2,5-diene-1,4-dione 10403457 Click to see COC1=C(C(=O)C(=CC1=O)C2CC3=C(C=C(C=C3)O)OC2)OC 316.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Daidzein-4'-glucoside 49862229 Click to see 416.40 unknown via CMAUP database
Sophoricoside 5321398 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
3'-Methoxydaidzein 5319422 Click to see COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
Isomucronulatol, (-)- 10380176 Click to see 302.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
(3R)-2',3',7-trihydroxy-4'-methoxyisoflavan 15939757 Click to see COC1=C(C(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O)O 288.29 unknown via CMAUP database
(R)-Mucronulatol 13873811 Click to see 302.32 unknown via CMAUP database
Calycosin 5280448 Click to see 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
2'-Hydroxybiochanin A 5282075 Click to see 300.26 unknown via CMAUP database
Formononetin 5280378 Click to see 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
Isoformononetin 3764 Click to see 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
2',4'-Dihydroxydihydrochalcone 586491 Click to see 242.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2,4-Dihydroxyphenyl)-3-(4-Hydroxyphenyl)Prop-2-En-1-One 425 Click to see 256.25 unknown via CMAUP database
1-(2,4-Dihydroxyphenyl)-3-phenylprop-2-en-1-one 344530 Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O 240.25 unknown via CMAUP database
2-Propen-1-one, 1-(2-hydroxy-4-methoxyphenyl)-3-(4-hydroxyphenyl)- 592216 Click to see COC1=CC(=C(C=C1)C(=O)C=CC2=CC=C(C=C2)O)O 270.28 unknown via CMAUP database
2',4'-Dihydroxychalcone 5376979 Click to see 240.25 unknown via CMAUP database
2a(2),4a(2)-Dihydroxy-4-methoxychalcone 166795 Click to see 270.28 unknown via CMAUP database
4'-Methoxy-2'-hydroxy chalcone 265720 Click to see 254.28 unknown via CMAUP database
Isoliquiritigenin 638278 Click to see 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
2',4',4-Trihydroxy-3'-prenylchalcone 193568 Click to see 324.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
1-(4-Hydroxy-2-methoxyphenyl)-3-phenylprop-2-en-1-one 71442332 Click to see 254.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
5-(2-(4-Hydroxyphenyl)Ethenyl)Benzene-1,3-Diol 5056 Click to see 228.24 unknown https://doi.org/10.1016/0031-9422(88)80779-9
Pterostilbene 5281727 Click to see 256.30 unknown https://doi.org/10.1016/0031-9422(88)80779-9
Resveratrol 445154 Click to see 228.24 unknown https://doi.org/10.1016/0031-9422(88)80779-9

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