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Soymida febrifuga

Soymida febrifuga - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID6440493b7d932573651587
Scientific name Soymida febrifuga
Authority (Roxb.) A.Juss.
First published in Mém. Mus. Hist. Nat. 19: 251 (1830 publ. 1831)

Description Top

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Synonyms Top

Scientific name Authority First published in
Swietenia obtusifolia Stokes Bot. Mat. Med. 2: 480 (1812)
Swietenia soymida A.Duncan Swietenia soymida : 16 (1794)
Swietenia febrifuga Roxb. Pl. Coromandel 1(1): 18, t. 17. 1795 [May 1795]

Common names Top

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Language Common/alternative name
Tamil சே மரம்

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-tropical
    • Indian Subcontinent
      • Bangladesh
      • India
      • Sri Lanka
    • Indo-China
      • Myanmar

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001083425
UNII 1N1019269G
Tropicos 20400003
KEW urn:lsid:ipni.org:names:941499-1
The Plant List tro-20400003
Open Tree Of Life 5747871
NCBI Taxonomy 1672007
IPNI 941499-1
iNaturalist 541110
GBIF 3850622
USDA GRIN 35174
CMAUP NPO20812

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
History of safe use of herbs - Approaches for documenting evidence Narayana DB, Brindavanam NB, Shirsekar S J Ayurveda Integr Med 09-Jan-2024
PMCID:PMC10792638
doi:10.1016/j.jaim.2023.100849
PMID:38194856
Pimpinella pruatjan Molk: LC-MS/MS-QTFT Analysis of Bioactive Compounds from Decoction and Ethanol Extract of Aerial Parts Timotius KH, Rahayu I, Nurcahyanti AD J Pharm Bioallied Sci 15-Aug-2023
PMCID:PMC10496851
doi:10.4103/jpbs.jpbs_183_22
PMID:37705859
The Spectrum of Pharmacological Actions of Syringetin and Its Natural Derivatives—A Summary Review Chmiel M, Stompor-Gorący M Nutrients 04-Dec-2022
PMCID:PMC9739508
doi:10.3390/nu14235157
PMID:36501187
Inventorization and Consensus Analysis of Ethnoveterinary Medicinal Knowledge Among the Local People in Eastern India: Perception, Cultural Significance, and Resilience Mandal SK, Rahaman CH Front Pharmacol 29-Apr-2022
PMCID:PMC9099233
doi:10.3389/fphar.2022.861577
PMID:35571138
Prunus armeniaca Gum-Alginate Polymeric Microspheres to Enhance the Bioavailability of Tramadol Hydrochloride: Formulation and Evaluation Noureen S, Noreen S, Ghumman SA, Batool F, Hameed H, Hasan S, Noreen F, Elsherif MA, Bukhari SN Pharmaceutics 22-Apr-2022
PMCID:PMC9144292
doi:10.3390/pharmaceutics14050916
PMID:35631501
Nanotechnology-Based Bioactive Antifeedant for Plant Protection Melanie M, Miranti M, Kasmara H, Malini DM, Husodo T, Panatarani C, Joni IM, Hermawan W Nanomaterials (Basel) 14-Feb-2022
PMCID:PMC8879102
doi:10.3390/nano12040630
PMID:35214959
Antifungal Activities of Wood and Non-Wood Kraft Handsheets Treated with Melia azedarach Extract Using SEM and HPLC Analyses Salem MZ, Alotaibi SS, Elgat WA, Taha AS, Fares YG, El-Shehawi AM, Ghareeb RY Polymers (Basel) 20-Jun-2021
PMCID:PMC8235202
doi:10.3390/polym13122012
PMID:34203016
Green synthesis of silver nanoparticles using plant extracts and their antimicrobial activities: a review of recent literature Vanlalveni C, Lallianrawna S, Biswas A, Selvaraj M, Changmai B, Rokhum SL RSC Adv 13-Jan-2021
PMCID:PMC8694026
doi:10.1039/d0ra09941d
PMID:35424248
Promising Roles of Alternative Medicine and Plant-Based Nanotechnology as Remedies for Urinary Tract Infections Chandra H, Singh C, Kumari P, Yadav S, Mishra AP, Laishevtcev A, Brisc C, Brisc MC, Munteanu MA, Bungau S Molecules 28-Nov-2020
PMCID:PMC7731396
doi:10.3390/molecules25235593
PMID:33260701
Shoot tip necrosis of in vitro plant cultures: a reappraisal of possible causes and solutions Teixeira da Silva JA, Nezami-Alanagh E, Barreal ME, Kher MM, Wicaksono A, Gulyás A, Hidvégi N, Magyar-Tábori K, Mendler-Drienyovszki N, Márton L, Landín M, Gallego PP, Driver JA, Dobránszki J Planta 03-Sep-2020
PMCID:PMC7471112
doi:10.1007/s00425-020-03449-4
PMID:32885282
Biosynthesized Silver Nanoparticles by Aqueous Stem Extract of Entada spiralis and Screening of Their Biomedical Activity Wan Mat Khalir WK, Shameli K, Jazayeri SD, Othman NA, Che Jusoh NW, Hassan NM Front Chem 19-Aug-2020
PMCID:PMC7466720
doi:10.3389/fchem.2020.00620
PMID:32974269
Plant-Based Phytochemicals as Possible Alternative to Antibiotics in Combating Bacterial Drug Resistance AlSheikh HM, Sultan I, Kumar V, Rather IA, Al-Sheikh H, Tasleem Jan A, Haq QM Antibiotics (Basel) 04-Aug-2020
PMCID:PMC7460449
doi:10.3390/antibiotics9080480
PMID:32759771
A review on biosynthesis of silver nanoparticles and their biocidal properties Siddiqi KS, Husen A, Rao RA J Nanobiotechnology 16-Feb-2018
PMCID:PMC5815253
doi:10.1186/s12951-018-0334-5
PMID:29452593
Infrequent use of medicinal plants from India in snakebite treatment Upasani MS, Upasani SV, Beldar VG, Beldar CG, Gujarathi PP Integr Med Res 06-Nov-2017
PMCID:PMC5884010
doi:10.1016/j.imr.2017.10.003
PMID:29629287
Ethnomedicinal plants used for snakebite in India: a brief overview Upasani SV, Beldar VG, Tatiya AU, Upasani MS, Surana SJ, Patil DS Integr Med Res 20-Mar-2017
PMCID:PMC5478250
doi:10.1016/j.imr.2017.03.001
PMID:28664135

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 / Benzoic acid esters
Diethylhexylphthalate 7057919 Click to see CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC 390.60 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1021/NP9003323
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Propylparaben 7175 Click to see CCCOC(=O)C1=CC=C(C=C1)O 180.20 unknown https://doi.org/10.1021/NP9003323
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
(E)-2-(4-Hydroxyphenyl)-2-oxoacetaldehyde oxime 6412242 Click to see C1=CC(=CC=C1C(=O)C=NO)O 165.15 unknown via CMAUP database
4-Hydroxy-alpha-oxo-benzeneacetaldehyde aldoxime 9614328 Click to see C1=CC(=CC=C1C(=O)C=NO)O 165.15 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
(1S,2S)-1-(4-hydroxy-3-methoxyphenyl)propane-1,2,3-triol 12310249 Click to see COC1=C(C=CC(=C1)C(C(CO)O)O)O 214.21 unknown https://doi.org/10.1021/NP9003323
Guaiacylglycerol 14579 Click to see COC1=C(C=CC(=C1)C(C(CO)O)O)O 214.21 unknown https://doi.org/10.1021/NP9003323
threo-Guaiacylglycerol 11063784 Click to see COC1=C(C=CC(=C1)C(C(CO)O)O)O 214.21 unknown https://doi.org/10.1021/NP9003323
> Lipids and lipid-like molecules / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
[3,7,17-Triacetyloxy-19-(furan-3-carbonyl)-21-(2-methoxy-2-oxoethyl)-2,5,15,19-tetramethyl-10-oxo-9,14,16,20-tetraoxaheptacyclo[10.4.3.12,5.112,15.01,13.03,7.08,13]henicosan-6-yl] 2,3-dimethyloxirane-2-carboxylate 163192819 Click to see CC1C(O1)(C)C(=O)OC2C3(CC4(C2(C5C67C8(CC(=O)O5)C(CC(C6(C4(C3CC(=O)OC)C)OC(O8)(O7)C)OC(=O)C)(C)C(=O)C9=COC=C9)OC(=O)C)OC(=O)C)C 814.80 unknown https://doi.org/10.1016/S0031-9422(00)83542-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
[(1R,6R,7R,10S,15R,16S,17S,18S,19S,20S)-19,20-diacetyloxy-6-(furan-3-yl)-16-(2-methoxy-2-oxoethyl)-7,12,15,17-tetramethyl-4-oxo-5,11,13,21-tetraoxaheptacyclo[10.8.1.114,17.01,10.02,7.010,15.014,19]docos-2-en-18-yl] 2,3-dimethyloxirane-2-carboxylate 101321330 Click to see CC1C(O1)(C)C(=O)OC2C3(CC45C2(C(C67C8=CC(=O)OC(C8(CCC6(C4(C3CC(=O)OC)C)OC(O5)(O7)C)C)C9=COC=C9)OC(=O)C)OC(=O)C)C 740.70 unknown https://doi.org/10.1016/S0031-9422(00)83542-6
[(5S,6S,8R,9R,10R,13R,17S)-17-(furan-3-yl)-17-hydroxy-4,4,8,10,13-pentamethyl-3,16-dioxo-5,6,7,9,11,12-hexahydrocyclopenta[a]phenanthren-6-yl] acetate 162907799 Click to see CC(=O)OC1CC2(C(CCC3(C2=CC(=O)C3(C4=COC=C4)O)C)C5(C1C(C(=O)C=C5)(C)C)C)C 466.60 unknown https://doi.org/10.1016/S0031-9422(00)83542-6
[17-(Furan-3-yl)-17-hydroxy-4,4,8,10,13-pentamethyl-3,16-dioxo-5,6,7,9,11,12-hexahydrocyclopenta[a]phenanthren-6-yl] acetate 162907798 Click to see CC(=O)OC1CC2(C(CCC3(C2=CC(=O)C3(C4=COC=C4)O)C)C5(C1C(C(=O)C=C5)(C)C)C)C 466.60 unknown https://doi.org/10.1016/S0031-9422(00)83542-6
Angolensic acid methyl ester 419676 Click to see CC1(C(C2(C3CCC4(C(OC(=O)CC4(C3=C)OC2CC1=O)C5=COC=C5)C)C)CC(=O)OC)C 470.60 unknown https://doi.org/10.1016/S0031-9422(00)83542-6
Methyl angolensate 21596327 Click to see CC1(C(C2(C3CCC4(C(OC(=O)CC4(C3=C)OC2CC1=O)C5=COC=C5)C)C)CC(=O)OC)C 470.60 unknown https://doi.org/10.1016/S0031-9422(00)83542-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-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 11870456 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/S0031-9422(00)90134-1
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/S0031-9422(00)90134-1
https://doi.org/10.1016/S0031-9422(00)83542-6
24-Ethylcholest-5-en-3beta-ol 22012 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/S0031-9422(00)83542-6
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/S0031-9422(00)83542-6
> Organoheterocyclic compounds / Dioxepanes / 1,4-dioxepanes
Andirobin 12306782 Click to see CC1(C(C(C=CC1=O)(C)C2CCC3(C(OC(=O)C4C3(C2=C)O4)C5=COC=C5)C)CC(=O)OC)C 468.50 unknown https://doi.org/10.1016/S0031-9422(00)83542-6
methyl 2-[2-[4-(furan-3-yl)-4a-methyl-8-methylidene-2-oxo-4,5,6,7-tetrahydro-1aH-oxireno[2,3-d]isochromen-7-yl]-2,6,6-trimethyl-5-oxocyclohex-3-en-1-yl]acetate 4425075 Click to see CC1(C(C(C=CC1=O)(C)C2CCC3(C(OC(=O)C4C3(C2=C)O4)C5=COC=C5)C)CC(=O)OC)C 468.50 unknown https://doi.org/10.1016/S0031-9422(00)83542-6
> Organoheterocyclic compounds / Indoles and derivatives / Pyrroloindoles
(+)-Yatakemycin 11721692 Click to see COC1=C(C=C2C=C(NC2=C1)C(=O)N3CC4CC45C3=CC(=O)C6=C5C=C(N6)C(=O)N7CCC8=C9C=C(NC9=C(C(=C87)O)OC)C(=O)SC)O 679.70 unknown https://doi.org/10.1021/NP9003323
> Organoheterocyclic compounds / Naphthopyrans
[(1R,2S,5R,6R,10S,13S,14R,16S)-6-(furan-3-yl)-16-(2-methoxy-2-oxoethyl)-1,5,15,15-tetramethyl-8,17-dioxo-7-oxatetracyclo[11.3.1.02,11.05,10]heptadec-11-en-14-yl] (E)-2-methylbut-2-enoate 101717452 Click to see CC=C(C)C(=O)OC1C2C=C3C(CCC4(C3CC(=O)OC4C5=COC=C5)C)C(C2=O)(C(C1(C)C)CC(=O)OC)C 552.70 unknown https://doi.org/10.1016/S0031-9422(00)83542-6
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
Deoxyandirobin 6708516 Click to see CC1(C(C(C=CC1=O)(C)C2CCC3(C(OC(=O)C=C3C2=C)C4=COC=C4)C)CC(=O)OC)C 452.50 unknown https://doi.org/10.1016/S0031-9422(00)83542-6
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
6-Hydroxy-3-[(4-hydroxyphenyl)methyl]-7-methoxychromen-2-one 44479225 Click to see COC1=C(C=C2C=C(C(=O)OC2=C1)CC3=CC=C(C=C3)O)O 298.29 unknown https://doi.org/10.1021/NP9003323
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
3-(4-Hydroxybenzyl)-6-methoxy-7-hydroxy-2H-1-benzopyran-2-one 44479224 Click to see COC1=C(C=C2C(=C1)C=C(C(=O)O2)CC3=CC=C(C=C3)O)O 298.29 unknown https://doi.org/10.1021/NP9003323
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
5,7-Dihydroxyflavanone 238782 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1021/NP9003323
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1021/NP9003323
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
(2r)-4',7-Dihydroxy-8-methylflavane 46883348 Click to see CC1=C(C=CC2=C1OC(CC2)C3=CC=C(C=C3)O)O 256.30 unknown https://doi.org/10.1021/NP9003323
2-(4-hydroxyphenyl)-8-methyl-3,4-dihydro-2H-chromen-7-ol 3500619 Click to see CC1=C(C=CC2=C1OC(CC2)C3=CC=C(C=C3)O)O 256.30 unknown https://doi.org/10.1021/NP9003323
3,4-Dihydro-2-(4-hydroxyphenyl)-2H-1-benzopyran-7-ol 3500616 Click to see C1CC2=C(C=C(C=C2)O)OC1C3=CC=C(C=C3)O 242.27 unknown https://doi.org/10.1021/NP9003323
7,4'-Dihydroxy-8-methylflavan 442361 Click to see CC1=C(C=CC2=C1OC(CC2)C3=CC=C(C=C3)O)O 256.30 unknown https://doi.org/10.1021/NP9003323
7,4'-Dihydroxyflavan 158280 Click to see C1CC2=C(C=C(C=C2)O)OC1C3=CC=C(C=C3)O 242.27 unknown https://doi.org/10.1021/NP9003323
Tupichinol C 11064571 Click to see C1CC2=C(C=C(C=C2)O)OC1C3=CC=C(C=C3)O 242.27 unknown https://doi.org/10.1021/NP9003323
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
(2R)-2-(4-hydroxyphenyl)-5-methoxy-8-methyl-3,4-dihydro-2H-chromen-7-ol 44479223 Click to see CC1=C2C(=C(C=C1O)OC)CCC(O2)C3=CC=C(C=C3)O 286.32 unknown https://doi.org/10.1021/NP9003323
2-(4-hydroxyphenyl)-5-methoxy-8-methyl-3,4-dihydro-2H-chromen-7-ol 75033429 Click to see CC1=C2C(=C(C=C1O)OC)CCC(O2)C3=CC=C(C=C3)O 286.32 unknown https://doi.org/10.1021/NP9003323
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4-(7-Methoxy-3,4-dihydro-2H-chromen-2-yl)phenol 11276880 Click to see COC1=CC2=C(CCC(O2)C3=CC=C(C=C3)O)C=C1 256.30 unknown https://doi.org/10.1021/NP9003323
4'-Hydroxy-7-methoxyflavan 185609 Click to see COC1=CC2=C(CCC(O2)C3=CC=C(C=C3)O)C=C1 256.30 unknown https://doi.org/10.1021/NP9003323
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans
(3R)-3-(4-Hydroxybenzyl)-6-hydroxy-8-methoxy-3,4-dihydro-2H-1-benzopyran 44479222 Click to see COC1=CC(=CC2=C1OCC(C2)CC3=CC=C(C=C3)O)O 286.32 unknown https://doi.org/10.1021/NP9003323
(3R)-3-[(4-hydroxyphenyl)methyl]-7-methoxy-3,4-dihydro-2H-chromen-6-ol 46883147 Click to see COC1=C(C=C2CC(COC2=C1)CC3=CC=C(C=C3)O)O 286.32 unknown https://doi.org/10.1021/NP9003323
(3R)-7-hydroxy-3-(4-hydroxybenzyl)chromane 46883199 Click to see C1C(COC2=C1C=CC(=C2)O)CC3=CC=C(C=C3)O 256.30 unknown https://doi.org/10.1021/NP9003323
3-[(4-hydroxyphenyl)methyl]-7-methoxy-3,4-dihydro-2H-chromen-6-ol 25014549 Click to see COC1=C(C=C2CC(COC2=C1)CC3=CC=C(C=C3)O)O 286.32 unknown https://doi.org/10.1021/NP9003323
3-[(4-hydroxyphenyl)methyl]-8-methoxy-3,4-dihydro-2H-chromen-6-ol 75033428 Click to see COC1=CC(=CC2=C1OCC(C2)CC3=CC=C(C=C3)O)O 286.32 unknown https://doi.org/10.1021/NP9003323
7-Hydroxy-3-(4-hydroxybenzyl)chroman 11708657 Click to see C1C(COC2=C1C=CC(=C2)O)CC3=CC=C(C=C3)O 256.30 unknown https://doi.org/10.1021/NP9003323
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
(-)-5,7-Dihydroxy-3-(4-hydroxybenzyl)-4-chromanone 9971218 Click to see C1C(C(=O)C2=C(C=C(C=C2O1)O)O)CC3=CC=C(C=C3)O 286.28 unknown https://doi.org/10.1021/NP9003323
(3R)-5,7-dihydroxy-3-[(4-hydroxyphenyl)methyl]-2,3-dihydrochromen-4-one 638291 Click to see C1C(C(=O)C2=C(C=C(C=C2O1)O)O)CC3=CC=C(C=C3)O 286.28 unknown https://doi.org/10.1021/NP9003323
(3R)-5,7-dihydroxy-3-[(4-hydroxyphenyl)methyl]-6-methoxy-2,3-dihydrochromen-4-one 638288 Click to see COC1=C(C2=C(C=C1O)OCC(C2=O)CC3=CC=C(C=C3)O)O 316.30 unknown https://doi.org/10.1021/NP9003323
(3R)-5,7-dihydroxy-3-[(4-methoxyphenyl)methyl]-2,3-dihydrochromen-4-one 46883403 Click to see COC1=CC=C(C=C1)CC2COC3=CC(=CC(=C3C2=O)O)O 300.30 unknown https://doi.org/10.1021/NP9003323
(3R)-7,4 inverted exclamation mark-Dihydrohomoisoflavanone 26088034 Click to see C1C(C(=O)C2=C(O1)C=C(C=C2)O)CC3=CC=C(C=C3)O 270.28 unknown https://doi.org/10.1021/NP9003323
3-(4-Hydroxybenzyl)-5,7-dihydroxy-6-methoxychroman-4-one 404572 Click to see COC1=C(C2=C(C=C1O)OCC(C2=O)CC3=CC=C(C=C3)O)O 316.30 unknown https://doi.org/10.1021/NP9003323
3,9-Dihydroeucomin 11415348 Click to see COC1=CC=C(C=C1)CC2COC3=CC(=CC(=C3C2=O)O)O 300.30 unknown https://doi.org/10.1021/NP9003323
7,4'-Dihydroxyhomoisoflavanone 3759709 Click to see C1C(C(=O)C2=C(O1)C=C(C=C2)O)CC3=CC=C(C=C3)O 270.28 unknown https://doi.org/10.1021/NP9003323
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
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 https://doi.org/10.1021/NP9003323
2-Propen-1-one, 1-(2,4-dihydroxyphenyl)-3-phenyl- 344530 Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O 240.25 unknown https://doi.org/10.1021/NP9003323
2,2',4'-Trihydroxychalcone 5811533 Click to see C1=CC=C(C(=C1)C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1021/NP9003323
2',4'-Dihydroxychalcone 5376979 Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O 240.25 unknown https://doi.org/10.1021/NP9003323
2',4',2-Trihydroxychalcone 213726 Click to see C1=CC=C(C(=C1)C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1021/NP9003323
4,2'-Dihydroxy-4'-methoxychalcone 6537040 Click to see COC1=CC(=C(C=C1)C(=O)C=CC2=CC=C(C=C2)O)O 270.28 unknown https://doi.org/10.1021/NP9003323
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Retro-dihydrochalcones
2,4,4'-Trihydroxydihydrochalcone 10801179 Click to see C1=CC(=CC=C1C(=O)CCC2=C(C=C(C=C2)O)O)O 258.27 unknown https://doi.org/10.1021/NP9003323
2,4'-Dihydroxy-4-methoxydihydrochalcone 14157883 Click to see COC1=CC(=C(C=C1)CCC(=O)C2=CC=C(C=C2)O)O 272.29 unknown https://doi.org/10.1021/NP9003323
3-(4-Hydroxy-2,6-dimethoxyphenyl)-1-(4-methoxyphenyl)propan-1-one 46883374 Click to see COC1=CC=C(C=C1)C(=O)CCC2=C(C=C(C=C2OC)O)OC 316.30 unknown https://doi.org/10.1021/NP9003323
4,4'-Dihydroxy-2,6-dimethoxydihydrochalcone 10424988 Click to see COC1=CC(=CC(=C1CCC(=O)C2=CC=C(C=C2)O)OC)O 302.32 unknown https://doi.org/10.1021/NP9003323
Loureirin A 5319081 Click to see COC1=CC(=C(C=C1)CCC(=O)C2=CC=C(C=C2)O)OC 286.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
1-(4-Hydroxy-2-methoxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one 25201046 Click to see COC1=C(C=CC(=C1)O)C(=O)C=CC2=CC=C(C=C2)O 270.28 unknown https://doi.org/10.1021/NP9003323
2'-O-Methylisoliquiritigenin 5319688 Click to see COC1=C(C=CC(=C1)O)C(=O)C=CC2=CC=C(C=C2)O 270.28 unknown https://doi.org/10.1021/NP9003323
> Phenylpropanoids and polyketides / Stilbenes
3-[2-(4-Hydroxyphenyl)ethenyl]-5-methoxyphenol 405852 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=C(C=C2)O 242.27 unknown https://doi.org/10.1021/NP9003323
3-Methoxy-4',5-dihydroxy-trans-stilbene 5473050 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=C(C=C2)O 242.27 unknown https://doi.org/10.1021/NP9003323
4-[2-(3,5-Dimethoxyphenyl)ethenyl]phenol 160517 Click to see COC1=CC(=CC(=C1)C=CC2=CC=C(C=C2)O)OC 256.30 unknown https://doi.org/10.1021/NP9003323
Pterostilbene 5281727 Click to see COC1=CC(=CC(=C1)C=CC2=CC=C(C=C2)O)OC 256.30 unknown https://doi.org/10.1021/NP9003323

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