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)

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.

In traditional Ayurvedic and tribal medicine, the bark of Soymida febrifuga has long been employed as a febrifuge. Among Keralian Ayurvedic practitioners of southern India, a decoction made from about 30 g of dried bark boiled in 1 L of water for 20–30 minutes is taken to lower malarial fevers (Jain, 1991). In Gujarat, village healers grind fresh leaves into a poultice and apply it directly to cuts and ulcerated skin, a practice recorded among the Barda tribal community (Sharma & Patel, 2016). In the eastern state of Chhattisgarh, tribal healers prepare a root decoction of roughly 20 g of dried root simmered in 500 mL of water for 15 minutes to relieve dysenteric diarrhoea (Bennett et al., 2021). These preparations illustrate that the species is used primarily as a water‑based infusion or decoction of the bark, root and leaf.

A complementary preparation is a bark tincture used by herbalists in central Madhya Pradesh. Practitioners macerate 100 g of powdered bark in 500 mL of 45 % ethanol for 14 days, shaking the vessel daily; the resulting liquid is strained and stored in amber bottles (Raghav & Sinha, 2014). The tincture is administered at a dose of 1 mL (≈20 drops) three times daily for chronic low‑grade fever. This maceration technique is also employed for a leaf‑oil infusion, where fresh leaves are steeped in a carrier oil for 7 days and then applied topically for inflammatory skin conditions.

**Practical bark decoction recipe** – To make a fever‑reducing tea, place 30 g of dried, sliced bark into a saucepan with 1 L of cold water. Bring the mixture to a boil, reduce to a gentle simmer, and maintain the heat for 20 minutes. Remove the pot, allow the liquid to cool to a comfortably warm temperature, then strain through fine muslin. The decoction can be taken in 50 mL portions twice daily, preferably after meals. Because the bark contains potent limonoids, it is not recommended for pregnant women and should be used only under the guidance of a qualified practitioner; excess intake may cause mild gastrointestinal upset.

Modern phytochemical work on Soymida febrifuga confirms the presence of limonoids such as nimbolinin A and B, meliantriol, and several other triterpenoid limonoids, together with flavonoids (quercetin, kaempferol) and hydrolyzable tannins (Kumar et al., 2017). These constituents are known to possess antipyretic, anti‑inflammatory and antimicrobial activity, providing a plausible basis for the traditional febrifuge and wound‑healing applications. Ongoing in‑vitro studies are exploring the bark’s anti‑malarial potential, and extracts now appear in several commercial Ayurvedic preparations marketed for fever and malaria in India.

General Uses Top

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Wood and fiber:
- Wood: valued as a heavy, durable timber for construction, furniture, carriage bodies, and sleepers; works well with hand and machine tools, takes a good finish, and is considered termite-resistant. Wood also serves as fuelwood.
- Bark fiber: occasionally utilized as a coarse fiber source.

Industrial and craft applications:
- Bark tannin: source of hydrolysable tannins used in leather tanning; concentration typically ~15–20% of dry bark; used in traditional leather processing and as an adjunct in modern vegetable tanning systems.

Colorants and tanning:
- Bark extract: yields reddish-brown dye solutions used for cotton and wool; suitable as a natural brown dye on protein fibers.
- Bark tannin: facilitates leather tanning to produce firm, reddish-brown hides.

Properties relevant to use:
- Wood density ~700–900 kg/m³; good dimensional stability when seasoned; natural resistance to insect damage.
- Tannins: hydrolysable class; high reactivity with protein substrates, enabling efficient leather leathering and brown dye formation; suitable for both fast and slow tanning schedules.

Sustainability and sourcing:
- Widely distributed across the Indian subcontinent and Myanmar; IUCN Red List status not evaluated. Mature, high-quality timber is typically obtained from well-managed natural forests; bark is harvested as a secondary product from mature trees or thinning operations.
- Trade controlled under CITES Appendix II as Meliaceae spp. (exempted for small leaf samples); specific requirements for export and import of lumber and bark vary by national regulations.

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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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

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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 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 180.20 unknown https://doi.org/10.1021/NP9003323
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
(2Z)-2-hydroxyimino-1-(4-hydroxyphenyl)ethanone 6412242 Click to see 165.15 unknown via CMAUP database
4-Hydroxy-alpha-oxo-benzeneacetaldehyde aldoxime 9614328 Click to see 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 214.21 unknown https://doi.org/10.1021/NP9003323
1,2,3-Propanetriol, 1-(4-hydroxy-3-methoxyphenyl)-, (1R,2R)- 11063784 Click to see 214.21 unknown https://doi.org/10.1021/NP9003323
Guaiacylglycerol 14579 Click to see 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 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 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 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
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)83542-6
(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
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)83542-6
> Organoheterocyclic compounds / Dioxepanes / 1,4-dioxepanes
Andirobin 12306782 Click to see 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 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 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 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 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
2H-1-Benzopyran-7-ol, 3,4-dihydro-2-(4-hydroxyphenyl)-, (2S)- 158280 Click to see 242.27 unknown https://doi.org/10.1021/NP9003323
7,4'-Dihydroxy-8-methylflavan 442361 Click to see 256.30 unknown https://doi.org/10.1021/NP9003323
7,4'-Dihydroxyflavan 3500616 Click to see 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 286.32 unknown https://doi.org/10.1021/NP9003323
7,4'-Dihydroxy-5-methoxy-8-methylflavane 75033429 Click to see 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 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 286.32 unknown https://doi.org/10.1021/NP9003323
(3R)-7-hydroxy-3-(4-hydroxybenzyl)chromane 46883199 Click to see 256.30 unknown https://doi.org/10.1021/NP9003323
3-[(4-hydroxyphenyl)methyl]-8-methoxy-3,4-dihydro-2H-chromen-6-ol 75033428 Click to see 286.32 unknown https://doi.org/10.1021/NP9003323
6,4'-Dihydroxy-7-methoxyhomoisoflavan 25014549 Click to see 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
(3R)-5,7-dihydroxy-3-[(4-hydroxyphenyl)methyl]-2,3-dihydrochromen-4-one 638291 Click to see 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)-7,4'-Dihydrohomoisoflavanone 26088034 Click to see 270.28 unknown https://doi.org/10.1021/NP9003323
2,3-Dihydro-5,7-dihydroxy-3-((4-hydroxyphenyl)methyl)-4H-1-benzopyran-4-one 9971218 Click to see 286.28 unknown https://doi.org/10.1021/NP9003323
3-(4-Hydroxybenzyl)-5,7-dihydroxy-6-methoxychroman-4-one 404572 Click to see 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 270.28 unknown https://doi.org/10.1021/NP9003323
CID 46883403 46883403 Click to see 300.30 unknown https://doi.org/10.1021/NP9003323
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
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 https://doi.org/10.1021/NP9003323
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
2,2',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 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 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 302.32 unknown https://doi.org/10.1021/NP9003323
Loureirin A 5319081 Click to see 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 270.28 unknown https://doi.org/10.1021/NP9003323
4,4'-Dihydroxy-2'-methoxychalcone 5319688 Click to see 270.28 unknown https://doi.org/10.1021/NP9003323
> Phenylpropanoids and polyketides / Stilbenes
3-[2-(4-Hydroxyphenyl)ethenyl]-5-methoxyphenol 405852 Click to see 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 256.30 unknown https://doi.org/10.1021/NP9003323
Pterostilbene 5281727 Click to see 256.30 unknown https://doi.org/10.1021/NP9003323

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