PlantaeDB Logo
Login Sign-up

Butea monosperma

Butea monosperma - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Upload a new image!

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 UUID643fd93ca8b7e691752349
Scientific name Butea monosperma
Authority (Lam.) Kuntze
First published in Revis. Gen. Pl.1: 202 (1891)

Description Top

Suggest a correction or write a new one!
, Delhi, 1998, ISBN 81-208-1097-0

Butea monosperma, also known as flame-of-the-forest, dhak, palash, and bastard teak, is a slow-growing tree native to tropical and sub-tropical regions of South and Southeast Asia. It can be found in countries such as Bangladesh, India, Nepal, Pakistan, Sri Lanka, Myanmar, Thailand, Laos, Cambodia, Vietnam, Malaysia, and western Indonesia. The tree is highly revered by Hindus and is often used in religious ceremonies. It is also prized for its vibrant orange-red flowers and is cultivated as an ornamental tree. Butea monosperma is a small-sized deciduous tree that can grow up to 15 meters tall. Its leaves are pinnate with three leaflets, and it produces bright orange-red flowers in racemes up to 15 cm long. The tree is used for timber, resin, fodder, medicine, and dye, and is also important for lac production and leather production. In addition, its flowers are used in traditional Holi colors and as a dye for fabric. Butea monosperma is also associated with cultural and religious traditions in various regions, and is considered a symbol

Synonyms Top

Scientific name Authority First published in
Erythrina monosperma Lam. Encycl.1: 391 (1785)
Butea frondosa Roxb.
Plaso monosperma Kuntze Revis. Gen. Pl.1: 202 (1891)
Butea braamiana DC. Prodr.2: 415 (1825)
Butea frondosa var. lutea (Witt.) Maheshw.
Plaso monosperma var. flava Kuntze
Plaso monosperma var. rubra Kuntze
Rudolphia frondosa (Roxb.) Poir. J.B.A.M.de Lamarck, Encycl.6: 333 (1804)
Butea braamania DC.
Plaso frondosa (Roxb.) A.Lyons Pl. Nam., ed. 2: 363 (1907)
Corallodendron monospermum (Lam.) Kuntze Revis. Gen. Pl.1: 173 (1891)
Kennedia monosperma Steud. Nomencl. Bot., ed. 2, 1: 845 (1840)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English bastard teak
English flame-of-the-forest
English palash
English bengal kino
Assamese পলাশ
Bengali পলাশ
German malabar-lackbaum
Persian درخت شعله جنگل
Finnish bengalinleiskupuu
gom पळस - butea monosperma
Gujarati ખાખરો
Hindi पलाश
Indonesian palasa
Japanese ハナモツヤクノキ
Japanese パラッシュ
jv plasa
Kannada ಪಲಾಶ
lo ດອກຈານ
Malayalam പ്ലാശ്
Marathi पळस
Malay pokok palasa
Burmese ပေါက်
Nepali पलाँसको बोट
Oriya ପଳାଶ
Punjabi ਕੇਸੂ
Punjab کیسو
Russian Бутея односемянная
sa पलाशवृक्षः
sat ᱢᱩᱨᱩᱫ ᱫᱟᱨᱮ
Sinhala ගස් කෑල
su plasa
Tamil புரசு
tcy ಪಲಾಶ
Telugu మోదుగ
Thai ทองกวาว
Vietnamese gièng gièng
Chinese 紫铆树
Chinese 紫矿
Chinese 三品一枝花
Chinese 紫铆
Chinese 紫矿（紫铆）

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000184561
UNII BV3214055Q
USDA Plants BUMO5
Tropicos 13057461
KEW urn:lsid:ipni.org:names:482566-1
The Plant List ild-30638
Missouri Botanical Garden 280658
Open Tree Of Life 170163
NCBI Taxonomy 56060
IUCN Red List 62485
IPNI 1150441-2
iNaturalist 68681
GBIF 2940416
Freebase /m/02p754c
EPPO BUAMO
EOL 643039
USDA GRIN 8177
Wikipedia Butea_monosperma

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
Unveiling the molecular mechanisms: dietary phytosterols as guardians against cardiovascular diseases El Omari N, Bakrim S, Khalid A, Abdalla AN, Iesa MA, El Kadri K, Tang SY, Goh BH, Bouyahya A Nat Prod Bioprospect 09-May-2024
PMCID:PMC11082103
doi:10.1007/s13659-024-00451-1
PMID:38722432
Unleashing the promise of emerging nanomaterials as a sustainable platform to mitigate antimicrobial resistance Rahman S, Sadaf S, Hoque ME, Mishra A, Mubarak NM, Malafaia G, Singh J RSC Adv 01-May-2024
PMCID:PMC11062400
doi:10.1039/d3ra05816f
PMID:38694553
Targeting interleukin-6 as a treatment approach for peritoneal carcinomatosis Dadgar N, Sherry C, Zimmerman J, Park H, Lewis C, Donnenberg A, Zaidi AH, Fan Y, Xiao K, Bartlett D, Donnenberg V, Wagner PL J Transl Med 30-Apr-2024
PMCID:PMC11061933
doi:10.1186/s12967-024-05205-8
PMID:38689325
Antioxidant and Hypoglycemic Potential of Phytogenic Selenium Nanoparticle- and Light Regime-Mediated In Vitro Caralluma tuberculata Callus Culture Extract Ali A, Mashwani ZU, Raja NI, Mohammad S, Ahmad MS, Luna-Arias JP ACS Omega 24-Apr-2024
PMCID:PMC11079897
doi:10.1021/acsomega.3c10222
PMID:38737082
Lectins as the prominent potential to deliver bioactive metal nanoparticles by recognizing cell surface glycans Bala Subramaniyan S, Veerappan A Heliyon 11-Apr-2024
PMCID:PMC11024627
doi:10.1016/j.heliyon.2024.e29394
From Flora to Pharmaceuticals: 100 new additions to angiosperms of Gafargaon subdistrict in Bangladesh and unraveling antidiabetic drug candidates targeting DPP4 through in silico approach Ahmed SS, Rahman MO PLoS One 29-Mar-2024
PMCID:PMC10980240
doi:10.1371/journal.pone.0301348
PMID:38551991
Spatial and temporal assessment of snake encounters in urban Delhi, India Barhadiya G, Purkayastha J, Saha AK, Ghosh C Sci Rep 06-Mar-2024
PMCID:PMC10917809
doi:10.1038/s41598-023-50373-0
PMID:38448500
Plant-Derived Senotherapeutics for the Prevention and Treatment of Intervertebral Disc Degeneration and Aging Mavrogonatou E, Kletsas D Metabolites 28-Feb-2024
PMCID:PMC10971879
doi:10.3390/metabo14030146
PMID:38535306
Bio-mordants: a review Benli H Environ Sci Pollut Res Int 23-Feb-2024
PMCID:PMC10948525
doi:10.1007/s11356-024-32174-8
PMID:38396176
Biogenic synthesis of silver nanoparticles using Rubus fruticosus extract and their antibacterial efficacy against Erwinia caratovora and Ralstonia solanacearum phytopathogens Khan A, Ahmad N, Fazal H, Ali M, Akbar F, Khan I, Tayyab M, Uddin MN, Ahmad N, Abdel-Maksoud MA, Saleh IA, Zomot N, AbdElgawad H, Rauf K, Iqbal B, Teixeira Filho MC, El-Tayeb MA, Jalal A RSC Adv 14-Feb-2024
PMCID:PMC10864949
doi:10.1039/d3ra06723h
PMID:38362085
Deciphering the Plastomic Code of Chinese Hog-Peanut (Amphicarpaea edgeworthii Benth., Leguminosae): Comparative Genomics and Evolutionary Insights within the Phaseoleae Tribe Xiang YN, Wang XQ, Ding LL, Bai XY, Feng YQ, Qi ZC, Sun YT, Yan XL Genes (Basel) 11-Jan-2024
PMCID:PMC10815570
doi:10.3390/genes15010088
PMID:38254977
Osteoarthritis in the Elderly Population: Preclinical Evidence of Nutrigenomic Activities of Flavonoids Naselli F, Bellavia D, Costa V, De Luca A, Raimondi L, Giavaresi G, Caradonna F Nutrients 28-Dec-2023
PMCID:PMC10780745
doi:10.3390/nu16010112
PMID:38201942
Pest categorisation of Pestalotiopsis microspora Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Migheli Q, Vloutoglou I, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 21-Dec-2023
PMCID:PMC10733803
doi:10.2903/j.efsa.2023.8493
PMID:38130321
Enhancing wool dyeing with clove bud (Syzygium aromaticum) based natural dye via microwave treatment using a central composite design Yameen M, Asghar F, Adeel S, Haider MZ, Özomay M, Aftab M, Mia R Sci Prog 22-Nov-2023
PMCID:PMC10666708
doi:10.1177/00368504231215593
PMID:37993993
Renogrit attenuates Vancomycin-induced nephrotoxicity in human renal spheroids and in Sprague-Dawley rats by regulating kidney injury biomarkers and creatinine/urea clearance Balkrishna A, Sharma S, Gohel V, Kumari A, Rawat M, Maity M, Sinha S, Dev R, Varshney A PLoS One 08-Nov-2023
PMCID:PMC10631690
doi:10.1371/journal.pone.0293605
PMID:37939153

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,4-Dihydroxybenzoic acid 1491 Click to see C1=CC(=C(C=C1O)O)C(=O)O 154.12 unknown https://doi.org/10.3987/COM-11-12275
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl gallate 7428 Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O 184.15 unknown https://doi.org/10.3987/COM-11-12275
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown https://doi.org/10.1007/S10600-010-9521-9
Dotriacontanoic acid 19255 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 480.80 unknown https://doi.org/10.1007/S10600-010-9521-9
Nonacosanoic acid 20245 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 438.80 unknown https://doi.org/10.1016/S0031-9422(00)00136-9
Octacosanoic acid 10470 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 424.70 unknown https://doi.org/10.1007/S10600-010-9521-9
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(E,2R,14R)-1-cyclohexyl-2,14-dihydroxy-11,12,15,15-tetramethylhexadec-11-en-8-one 154495969 Click to see CC(=C(C)CC(C(C)(C)C)O)CCC(=O)CCCCCC(CC1CCCCC1)O 408.70 unknown https://doi.org/10.1016/S0031-9422(00)00136-9
(E,2S,14S)-1-cyclohexyl-2,14-dihydroxy-11,12-dimethyloctadec-11-en-8-one 162881222 Click to see CCCCC(CC(=C(C)CCC(=O)CCCCCC(CC1CCCCC1)O)C)O 408.70 unknown https://doi.org/10.1016/S0031-9422(00)00136-9
2,14-Dihydroxy-11,12-dimethyl-8-oxo-octadec-11-enylcyclohexane 68909959 Click to see CCCCC(CC(=C(C)CCC(=O)CCCCCC(CC1CCCCC1)O)C)O 408.70 unknown https://doi.org/10.1016/S0031-9422(00)00136-9
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
2-[4,5-Dihydroxy-2-(hydroxymethyl)-6-[[4-(6-methylhept-5-en-2-yl)cyclohexyl]methoxy]oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 162949755 Click to see CC(CCC=C(C)C)C1CCC(CC1)COC2C(C(C(C(O2)CO)OC3C(C(C(C(O3)CO)O)O)O)O)O 548.70 unknown https://doi.org/10.1007/S10600-010-9521-9
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4-hydroxy-3,5-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]oxane-2-carboxylic acid 101941082 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)OC7C(C(C(C(O7)CO)O)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C2C1)C)C(=O)OC9C(C(C(C(O9)CO)O)O)O)C 1119.20 unknown https://doi.org/10.1007/S10600-010-9521-9
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,5R,8R,9S,10R,13S,14R,17S)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylhept-6-en-2-yl]-2,3,5,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 15552165 Click to see CC(CCCC(=C)C)C1CCC2(C1(CCC3C2CCC4C3(CCC(C4(C)C)O)C)C)C 428.70 unknown https://doi.org/10.1016/S0031-9422(00)00136-9
4,4,10,13,14-pentamethyl-17-(6-methylhept-6-en-2-yl)-2,3,5,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 73198261 Click to see CC(CCCC(=C)C)C1CCC2(C1(CCC3C2CCC4C3(CCC(C4(C)C)O)C)C)C 428.70 unknown https://doi.org/10.1016/S0031-9422(00)00136-9
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.4038/JNSFSR.V18I2.8195
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.4038/JNSFSR.V18I2.8195
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
(3S,8S,9R,10R,13R,14S,17R)-4,4,9,13,14-pentamethyl-17-[(Z,2R)-6-methyl-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyhept-5-en-2-yl]-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 163192216 Click to see CC(CCC=C(C)COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)C3CCC4(C3(CC(=O)C5(C4CC=C6C5CCC(C6(C)C)OC7C(C(C(C(O7)CO)O)O)O)C)C)C 943.10 unknown https://doi.org/10.1016/S0031-9422(00)85390-X
https://doi.org/10.1248/CPB.57.428
https://doi.org/10.3987/COM-11-12275
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(2S,3R,4S,5R)-2-[[(3S,8S,9S,10R,13R,14S,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-yl]oxy]oxane-3,4,5-triol 162970463 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(CO5)O)O)O)C)C)C(C)C 546.80 unknown https://doi.org/10.1007/S10600-010-9521-9
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-5-Ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 12314479 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)00136-9
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)00136-9
https://doi.org/10.1016/J.FITOTE.2008.12.002
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/10.4038/JNSFSR.V18I2.8195
2-[[17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73072970 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown https://doi.org/10.1016/S0031-9422(00)00136-9
2-[[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-yl]oxy]oxane-3,4,5-triol 78407243 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(CO5)O)O)O)C)C)C(C)C 546.80 unknown https://doi.org/10.1007/S10600-010-9521-9
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/J.FITOTE.2008.12.002
https://doi.org/10.1016/S0031-9422(00)00136-9
Stigmasterol glucoside 6602508 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown https://doi.org/10.1016/S0031-9422(00)00136-9
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
7,8-Dihydroxychromen-4-one 21853376 Click to see C1=CC(=C(C2=C1C(=O)C=CO2)O)O 178.14 unknown https://doi.org/10.3987/COM-11-12275
> Organoheterocyclic compounds / Pyrrolidines / Phenylpyrrolidines
4,7-Epoxy-1H-isoindole-1,3(2H)-dione, hexahydro-3a-methyl-2-phenyl-, [3aR-(3aalpha,4beta,7beta,7aalpha)]- 605122 Click to see CC12C3CCC(C1C(=O)N(C2=O)C4=CC=CC=C4)O3 257.28 unknown https://doi.org/10.1016/0031-9422(90)85059-O
> Phenylpropanoids and polyketides / Aurone flavonoids
(2Z)-6-hydroxy-2-[[4-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methylidene]-1-benzofuran-3-one 54597953 Click to see C1=CC(=C(C=C1C=C2C(=O)C3=C(O2)C=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.3987/COM-11-12275
6-hydroxy-2-[[4-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methylidene]-1-benzofuran-3-one 162874926 Click to see C1=CC(=C(C=C1C=C2C(=O)C3=C(O2)C=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.3987/COM-11-12275
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.3987/COM-11-12275
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(5R,6S,6aR,12aS)-6-(2,4-dihydroxybenzoyl)-5-(3,4-dihydroxyphenyl)-2,3,10-trihydroxy-5,6,6a,12a-tetrahydrobenzo[c]xanthen-7-one 54597999 Click to see C1=CC(=C(C=C1C2C(C3C(C4=CC(=C(C=C24)O)O)OC5=C(C3=O)C=CC(=C5)O)C(=O)C6=C(C=C(C=C6)O)O)O)O 542.50 unknown https://doi.org/10.3987/COM-11-12275
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2S,3R)-2-(3,4-dihydroxyphenyl)-3-[(2S,3R)-2-(3,4-dihydroxyphenyl)-7-hydroxy-4-oxo-2,3-dihydrochromen-3-yl]-7-hydroxy-2,3-dihydrochromen-4-one 56600458 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)C4C(OC5=C(C4=O)C=CC(=C5)O)C6=CC(=C(C=C6)O)O)O)O 542.50 unknown https://doi.org/10.3987/COM-11-12275
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S,3R)-3-[4,5-dihydroxy-2-[(6-hydroxy-3-oxo-1-benzofuran-2-ylidene)methyl]phenyl]-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydrochromen-4-one 162985635 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)C4=CC(=C(C=C4C=C5C(=O)C6=C(O5)C=C(C=C6)O)O)O)O)O 540.50 unknown https://doi.org/10.3987/COM-11-12275
(2S,3R)-3-[4,5-dihydroxy-2-[(Z)-(6-hydroxy-3-oxo-1-benzofuran-2-ylidene)methyl]phenyl]-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydrochromen-4-one 56600459 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)C4=CC(=C(C=C4C=C5C(=O)C6=C(O5)C=C(C=C6)O)O)O)O)O 540.50 unknown https://doi.org/10.3987/COM-11-12275
3',4',7-Trihydroxyflavanone 3496769 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC(=C(C=C3)O)O 272.25 unknown https://doi.org/10.3987/COM-11-12275
https://doi.org/10.1248/CPB.57.428
https://doi.org/10.1039/CT9048501459
4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)- 1889 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O 256.25 unknown https://doi.org/10.1248/CPB.57.428
Butin 92775 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC(=C(C=C3)O)O 272.25 unknown https://doi.org/10.1016/0378-8741(86)90046-2
https://doi.org/10.1039/CT9048501459
https://doi.org/10.3987/COM-11-12275
https://doi.org/10.1248/CPB.57.428
https://doi.org/10.1007/BF03172444
Liquiritigenin 114829 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O 256.25 unknown https://doi.org/10.1248/CPB.57.428
> Phenylpropanoids and polyketides / Flavonoids / Flavones
7,3',4'-Trihydroxyflavone 5322065 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C=C3)O)O)O 270.24 unknown https://doi.org/10.1248/CPB.57.428
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferide 5281666 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.3987/COM-11-12275
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2R)-7-hydroxy-2-[4-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydrochromen-4-one 162864430 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC(=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 434.40 unknown https://doi.org/10.1248/CPB.57.428
(2S)-7-hydroxy-2-[4-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydrochromen-4-one 162864428 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC(=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 434.40 unknown https://doi.org/10.3987/COM-11-12275
(2S)-7-hydroxy-2-[4-hydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydrochromen-4-one 162864429 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC(=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 434.40 unknown https://doi.org/10.1016/S0031-9422(00)85390-X
(E)-1-[2-hydroxy-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-[4-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-en-1-one 163189476 Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 596.50 unknown https://doi.org/10.1016/S0031-9422(00)85390-X
(E)-3-(3,4-dihydroxyphenyl)-1-[2-hydroxy-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-en-1-one 163189337 Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 434.40 unknown https://doi.org/10.1016/S0031-9422(00)85390-X
1-(2,4-dihydroxyphenyl)-3-[4-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propan-1-one 42604492 Click to see C1=CC(=C(C=C1CCC(=O)C2=C(C=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)O 436.40 unknown https://doi.org/10.1248/CPB.57.428
1-(2,4-Dihydroxyphenyl)-3-[4-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propan-1-one 74817736 Click to see C1=CC(=C(C=C1CCC(=O)C2=C(C=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)O 436.40 unknown https://doi.org/10.1248/CPB.57.428
1-[2-Hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-[4-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-en-1-one 4481621 Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 596.50 unknown https://doi.org/10.1016/S0031-9422(00)85390-X
https://doi.org/10.3987/COM-11-12275
3-(3,4-Dihydroxyphenyl)-1-[2-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-en-1-one 57168663 Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 434.40 unknown https://doi.org/10.1016/S0031-9422(00)85390-X
https://doi.org/10.3987/COM-11-12275
7-Hydroxy-2-[4-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydrochromen-4-one 74819344 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC(=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 434.40 unknown https://doi.org/10.1248/CPB.57.428
https://doi.org/10.1016/S0031-9422(00)85390-X
Coreopsin 12303943 Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 434.40 unknown https://doi.org/10.3987/COM-11-12275
Isobutrin 5281256 Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 596.50 unknown https://doi.org/10.1016/J.PHYMED.2004.11.007
https://doi.org/10.1055/S-2007-969083
https://doi.org/10.3987/COM-11-12275
Isomonospermoside 42607822 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC(=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 434.40 unknown https://doi.org/10.1248/CPB.57.428
Monospermoside 42607524 Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)O 434.40 unknown https://doi.org/10.1016/S0031-9422(00)85390-X
https://doi.org/10.1248/CPB.57.428
https://doi.org/10.3987/COM-11-12275
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Aurone O-glycosides
(2E)-2-[(3,4-dihydroxyphenyl)methylidene]-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1-benzofuran-3-one 163190455 Click to see C1=CC(=C(C=C1C=C2C(=O)C3=C(O2)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(00)85390-X
2-[(3,4-dihydroxyphenyl)methylidene]-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1-benzofuran-3-one 162908827 Click to see C1=CC(=C(C=C1C=C2C(=O)C3=C(O2)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(00)85390-X
2-[(3,4-Dihydroxyphenyl)methylidene]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1-benzofuran-3-one 73981741 Click to see C1=CC(=C(C=C1C=C2C(=O)C3=C(O2)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.3987/COM-11-12275
Sulfurein 10071442 Click to see C1=CC(=C(C=C1C=C2C(=O)C3=C(O2)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.3987/COM-11-12275
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-2-(3,4-dihydroxyphenyl)-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 162901595 Click to see C1C(OC2=C(C1=O)C=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O 434.40 unknown https://doi.org/10.1016/S0031-9422(00)85390-X
(2S)-2-[4-hydroxy-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 162963379 Click to see C1C(OC2=C(C1=O)C=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC5C(C(C(C(O5)CO)O)O)O 596.50 unknown https://doi.org/10.1016/S0031-9422(00)85390-X
(2S)-2-[4-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-7-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 162963380 Click to see C1C(OC2=C(C1=O)C=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC5C(C(C(C(O5)CO)O)O)O 596.50 unknown https://doi.org/10.1248/CPB.57.428
2-[4-Hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 3496770 Click to see C1C(OC2=C(C1=O)C=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC5C(C(C(C(O5)CO)O)O)O 596.50 unknown https://doi.org/10.1248/CPB.57.428
https://doi.org/10.1016/S0031-9422(00)85390-X
https://doi.org/10.1007/BF03049298
Butrin 164630 Click to see C1C(OC2=C(C1=O)C=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC5C(C(C(C(O5)CO)O)O)O 596.50 unknown https://doi.org/10.1016/J.PHYMED.2004.11.007
https://doi.org/10.1248/CPB.57.428
https://doi.org/10.1007/BF03049298
https://doi.org/10.1055/S-2007-969083
CID 12309899 12309899 Click to see C1C(OC2=C(C1=O)C=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O 434.40 unknown https://doi.org/10.1016/S0031-9422(00)85390-X
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2872957/
Isocoreopsin 193124 Click to see C1C(OC2=C(C1=O)C=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O 434.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2872957/
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R,3R)-3,6-dihydroxy-7-methoxy-2-phenyl-2,3-dihydrochromen-4-one 163195581 Click to see COC1=C(C=C2C(=C1)OC(C(C2=O)O)C3=CC=CC=C3)O 286.28 unknown https://doi.org/10.1016/J.BMCL.2008.12.064
3,6-Dihydroxy-7-methoxy-2-phenyl-2,3-dihydrochromen-4-one 163007770 Click to see COC1=C(C=C2C(=C1)OC(C(C2=O)O)C3=CC=CC=C3)O 286.28 unknown https://doi.org/10.1016/J.BMCL.2008.12.064
> Phenylpropanoids and polyketides / Isoflavonoids
(12R)-16-methoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-1(20),2,4(8),9,13(18),14,16-heptaene 162959799 Click to see COC1=CC2=C(C=C1)C3C(=CO2)C4=CC5=C(C=C4O3)OCO5 296.27 unknown https://doi.org/10.1016/J.BMCL.2008.12.064
16-Methoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-1(20),2,4(8),9,13(18),14,16-heptaene 57857193 Click to see COC1=CC2=C(C=C1)C3C(=CO2)C4=CC5=C(C=C4O3)OCO5 296.27 unknown https://doi.org/10.1016/J.BMCL.2008.12.064
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
(20-Oxo-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-1(12),2,4(8),9,13(18),14,16-heptaen-16-yl) acetate 15454269 Click to see CC(=O)OC1=CC2=C(C=C1)C3=C(C4=CC5=C(C=C4O3)OCO5)C(=O)O2 338.30 unknown https://doi.org/10.1016/J.BMCL.2008.12.064
16-Hydroxy-15-(3-methylbut-2-enyl)-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-1(12),2,4(8),9,13(18),14,16-heptaen-20-one 162864788 Click to see CC(=CCC1=CC2=C(C=C1O)OC(=O)C3=C2OC4=CC5=C(C=C43)OCO5)C 364.30 unknown https://doi.org/10.1016/J.BMCL.2008.12.064
16-Methyl-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-1(12),2,4(8),9,13(18),14,16-heptaen-20-one 163049152 Click to see CC1=CC2=C(C=C1)C3=C(C4=CC5=C(C=C4O3)OCO5)C(=O)O2 294.26 unknown https://doi.org/10.1016/J.BMCL.2008.12.064
4,9-Dihydroxy-3,8-dimethoxy-[1]benzofuro[3,2-c]chromen-6-one 162868360 Click to see COC1=C(C2=C(C=C1)C3=C(C4=CC(=C(C=C4O3)O)OC)C(=O)O2)O 328.27 unknown https://doi.org/10.1016/J.BMCL.2008.12.064
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
9-Methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-3-ol 623060 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O 270.28 unknown https://doi.org/10.1016/J.BMCL.2008.12.064
Medicarpin 336327 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O 270.28 unknown https://doi.org/10.4038/JNSFSR.V18I2.8195
https://doi.org/10.1016/J.BMCL.2008.12.064
https://doi.org/10.1016/0378-8741(89)90046-9
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
2'-Hydroxygenistein 5282074 Click to see C1=CC(=C(C=C1O)O)C2=COC3=CC(=CC(=C3C2=O)O)O 286.24 unknown https://doi.org/10.1016/J.BMCL.2008.12.064
Daidzein 5281708 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)O)O 254.24 unknown https://doi.org/10.1016/J.BMCL.2008.12.064
Genistein 5280961 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O 270.24 unknown https://doi.org/10.1016/J.BMCL.2008.12.064
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3-(4-Methoxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 3733033 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O 430.40 unknown https://doi.org/10.1016/J.BMCL.2008.12.064
https://doi.org/10.1248/CPB.57.428
6-hydroxy-3-(4-methoxyphenyl)-7-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 162929787 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1248/CPB.57.428
Ononin 442813 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O 430.40 unknown https://doi.org/10.1248/CPB.57.428
https://doi.org/10.1016/J.BMCL.2008.12.064
Texasin 7-O-glucoside 44257243 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O 446.40 unknown https://doi.org/10.1248/CPB.57.428
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
3-(3,4-dimethoxyphenyl)-7-hydroxy-4H-chromen-4-one 5748605 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)OC 298.29 unknown https://doi.org/10.1016/J.BMCL.2008.12.064
7-hydroxy-3-(4-methoxyphenyl)-2-methyl-4H-chromen-4-one 5400231 Click to see CC1=C(C(=O)C2=C(O1)C=C(C=C2)O)C3=CC=C(C=C3)OC 282.29 unknown https://doi.org/10.1016/J.BMCL.2008.12.064
Afrormosin 5281704 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=C(C=C3C2=O)OC)O 298.29 unknown https://doi.org/10.1248/CPB.57.428
https://doi.org/10.3987/COM-11-12275
Formononetin 5280378 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O 268.26 unknown https://doi.org/10.1248/CPB.57.428
https://doi.org/10.1016/J.BMCL.2008.12.064
https://doi.org/10.3987/COM-11-12275
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
Cajanin 5281706 Click to see COC1=CC(=C2C(=C1)OC=C(C2=O)C3=C(C=C(C=C3)O)O)O 300.26 unknown https://doi.org/10.1016/J.BMCL.2008.12.064
Isoformononetin 3764 Click to see COC1=CC2=C(C=C1)C(=O)C(=CO2)C3=CC=C(C=C3)O 268.26 unknown https://doi.org/10.1016/J.BMCL.2008.12.064
Prunetin 5281804 Click to see COC1=CC(=C2C(=C1)OC=C(C2=O)C3=CC=C(C=C3)O)O 284.26 unknown https://doi.org/10.4038/JNSFSR.V18I2.8195
https://doi.org/10.1016/J.BMCL.2008.12.064
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2,4-Dihydroxyphenyl)-3-(3,4-dihydroxyphenyl)prop-2-en-1-one 2483 Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O)O 272.25 unknown https://doi.org/10.1039/CT9048501459
https://doi.org/10.3987/COM-11-12275
https://doi.org/10.1248/CPB.57.428
Butein 5281222 Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O)O 272.25 unknown https://doi.org/10.1039/CT9048501459
https://doi.org/10.3987/COM-11-12275
https://doi.org/10.1248/CPB.57.428
GU17;ISL;Isoliquiritigen 425 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1248/CPB.57.428
Trihydroxychalcone 638278 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1248/CPB.57.428

Biological Material Top ebay Auctions

Please wait .. loading items ..

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.