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Scutellaria discolor

Scutellaria discolor - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Scutellaria discolor - 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 UUID643fec8d68043476794410
Scientific name Scutellaria discolor
Authority Colebr.
First published in Pl. Asiat. Rar. 1: 66 1830

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 追天花根
Chinese 挖耳草
Chinese 熊胆草
Chinese 夜
Chinese 一支箭
Chinese 紫背草
Chinese 土黄芩
Chinese 异色黄芩
Chinese 四天红
Chinese 行草

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Scutellaria discolor var. cyrtopoda (Miq.) Adelb. Fl. Java 201: 14 (1954)
Scutellaria discolor var. discolor Unknown

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
    • Papuasia
      • New Guinea

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000307774
KEW urn:lsid:ipni.org:names:458248-1
The Plant List kew-189059
Open Tree Of Life 5793077
NCBI Taxonomy 1383557
IPNI 458248-1
iNaturalist 473626
GBIF 5609597
EPPO SCDDI
EOL 2894238

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
Treatment Effects of Natural Products on Inflammatory Bowel Disease In Vivo and Their Mechanisms: Based on Animal Experiments Zhou Y, Wang D, Yan W Nutrients 18-Feb-2023
PMCID:PMC9967064
doi:10.3390/nu15041031
PMID:36839389
The Involvement of Natural Polyphenols in the Chemoprevention of Cervical Cancer Drețcanu G, Iuhas CI, Diaconeasa Z Int J Mol Sci 16-Aug-2021
PMCID:PMC8396230
doi:10.3390/ijms22168812
PMID:34445518
Emerging cellular and molecular mechanisms underlying anticancer indications of chrysin Talebi M, Talebi M, Farkhondeh T, Simal-Gandara J, Kopustinskiene DM, Bernatoniene J, Samarghandian S Cancer Cell Int 15-Apr-2021
PMCID:PMC8050922
doi:10.1186/s12935-021-01906-y
PMID:33858433
Broad-Spectrum Preclinical Antitumor Activity of Chrysin: Current Trends and Future Perspectives Moghadam ER, Ang HL, Asnaf SE, Zabolian A, Saleki H, Yavari M, Esmaeili H, Zarrabi A, Ashrafizadeh M, Kumar AP Biomolecules 27-Sep-2020
PMCID:PMC7600196
doi:10.3390/biom10101374
PMID:32992587
Ethnomedicine study on traditional medicinal plants in the Wuliang Mountains of Jingdong, Yunnan, China Gao L, Wei N, Yang G, Zhang Z, Liu G, Cai C J Ethnobiol Ethnomed 19-Aug-2019
PMCID:PMC6699132
doi:10.1186/s13002-019-0316-1
PMID:31426826
Quantitative Ethnobotany of Medicinal Plants Used by Indigenous Communities in the Bandarban District of Bangladesh Faruque MO, Uddin SB, Barlow JW, Hu S, Dong S, Cai Q, Li X, Hu X Front Pharmacol 06-Feb-2018
PMCID:PMC5808248
doi:10.3389/fphar.2018.00040
PMID:29467652
A new species of Scutellaria (Scutellarioideae, Lamiaceae) from Sichuan Province in southwest China Zhao F, Liu ED, Peng H, Xiang CL PeerJ 08-Aug-2017
PMCID:PMC5550825
doi:10.7717/peerj.3624
PMID:28804694
Clerodane diterpenes: sources, structures, and biological activities Li R, Morris-Natschke SL, Lee KH Nat Prod Rep 18-Jul-2016
PMCID:PMC5154363
doi:10.1039/c5np00137d
PMID:27433555
A Drug-Target Network-Based Approach to Evaluate the Efficacy of Medicinal Plants for Type II Diabetes Mellitus Gu J, Chen L, Yuan G, Xu X Evid Based Complement Alternat Med 10-Oct-2013
PMCID:PMC3810496
doi:10.1155/2013/203614
PMID:24223610
Medicinal plants, traditional medicine, markets and management in far-west Nepal Kunwar RM, Mahat L, Acharya RP, Bussmann RW J Ethnobiol Ethnomed 12-Apr-2013
PMCID:PMC3643841
doi:10.1186/1746-4269-9-24
PMID:23587109
Studies on Nepalese Crude Drugs. XXI. On the Diterpenoid Constituents of the Aerial Part of Scutellaria discolor COLEBR. Akiko OHNO, Haruhisa KIZU, Tsuyoshi TOMIMORI Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.44.1540
Studies on the nepalese crude drugs. XI. On the flavonoid constituents of the aerial parts of Scutellaria discolor COLEBR. TSUYOSHI TOMIMORI, YUKINORI MIYAICHI, YOSHITAKA IMOTO, HARUHISA KIZU, TSUNEO NAMBA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.36.3654
Studies on the Nepalese crude drugs. VI. On the flavonoid constituents of the root of Scutellaria discolor Colebr. (2). TSUYOSHI TOMIMORI, YUKINORI MIYAICHI, YOSHITAKA IMOTO, HARUHISA KIZU, TSUNEO NAMBA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.34.406
Studies on Nepalese crude drugs. V. On the flavonoid constituents of the root of Scutellaria discolor COLEBR. TSUYOSHI TOMIMORI, YUKINORI MIYAICHI, YOSHITAKA IMOTO, HARUHISA KIZU, TSUNEO NAMBA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.33.4457
Traditional herbal medicine in Far-west Nepal: a pharmacological appraisal Kunwar RM, Shrestha KP, Bussmann RW J Ethnobiol Ethnomed 13-Dec-2010
PMCID:PMC3012020
doi:10.1186/1746-4269-6-35
PMID:21144003

Phytochemical Profile Top

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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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-Epioleanolic acid 11869658 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1248/CPB.44.1540
3-Epiursolic acid 7163177 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1248/CPB.44.1540
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1248/CPB.44.1540
Super Squalene; trans-Squalene;AddaVax 1105 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1248/CPB.44.1540
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
24-Methylene-cycloartanol 9547213 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 440.70 unknown https://doi.org/10.1248/CPB.44.1540
24-Methylenecycloartanol 94204 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 440.70 unknown https://doi.org/10.1248/CPB.44.1540
3-Epicycloeucalenol 543796 Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1O)C)C(C)CCC(=C)C(C)C)C 426.70 unknown https://doi.org/10.1248/CPB.44.1540
Cycloeucalenol 101690 Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1O)C)C(C)CCC(=C)C(C)C)C 426.70 unknown https://doi.org/10.1248/CPB.44.1540
> Organoheterocyclic compounds / Furofurans
[(1R,2S,4R,5S,6R,8R,11R)-5-[(3aS,5S,6aS)-3a,4,5,6a-tetrahydrofuro[2,3-b]furan-5-yl]-10-hydroxy-4,5-dimethylspiro[9-oxatricyclo[6.2.2.01,6]dodecane-11,2'-oxirane]-2-yl] acetate 10621348 Click to see CC1CC(C23C(C1(C)C4CC5C=COC5O4)CC(CC26CO6)OC3O)OC(=O)C 406.50 unknown https://doi.org/10.1248/CPB.44.1540
[(1S,2S,4R,5S,6R,8S,10S,11R)-5-[(3aS,5S,6aS)-3a,4,5,6a-tetrahydrofuro[2,3-b]furan-5-yl]-10-hydroxy-4,5-dimethylspiro[9-oxatricyclo[6.2.2.01,6]dodecane-11,2'-oxirane]-2-yl] acetate 162936315 Click to see CC1CC(C23C(C1(C)C4CC5C=COC5O4)CC(CC26CO6)OC3O)OC(=O)C 406.50 unknown https://doi.org/10.1248/CPB.44.1540
[(4R,4aR,5S,7R,8S,8aR)-8-[(2S,3aS,5R,6aR)-5-ethoxy-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-2-yl]-5-acetyloxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 10600777 Click to see CCOC1CC2CC(OC2O1)C3(C(CC(C4(C3CCCC45CO5)COC(=O)C)OC(=O)C)C)C 480.60 unknown https://doi.org/10.1248/CPB.44.1540
[(4R,4aR,5S,7R,8S,8aR)-8-[(2S,3aS,5R,6aR)-5-hydroxy-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-2-yl]-5-acetyloxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 44566824 Click to see CC1CC(C2(C(C1(C)C3CC4CC(OC4O3)O)CCCC25CO5)COC(=O)C)OC(=O)C 452.50 unknown https://doi.org/10.1248/CPB.44.1540
[(4R,4aR,5S,7R,8S,8aR)-8-[(2S,3aS,5S,6aR)-5-ethoxy-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-2-yl]-5-acetyloxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 10719524 Click to see CCOC1CC2CC(OC2O1)C3(C(CC(C4(C3CCCC45CO5)COC(=O)C)OC(=O)C)C)C 480.60 unknown https://doi.org/10.1248/CPB.44.1540
[10-Hydroxy-5-(5-hydroxy-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-2-yl)-4,5-dimethylspiro[9-oxatricyclo[6.2.2.01,6]dodecane-11,2'-oxirane]-2-yl] acetate 162984410 Click to see CC1CC(C23C(C1(C)C4CC5CC(OC5O4)O)CC(CC26CO6)OC3O)OC(=O)C 424.50 unknown https://doi.org/10.1248/CPB.44.1540
[5-(3a,4,5,6a-Tetrahydrofuro[2,3-b]furan-5-yl)-10-acetyloxy-4,5-dimethylspiro[9-oxatricyclo[6.2.2.01,6]dodecane-11,2'-oxirane]-2-yl] acetate 75069279 Click to see CC1CC(C23C(C1(C)C4CC5C=COC5O4)CC(CC26CO6)OC3OC(=O)C)OC(=O)C 448.50 unknown https://doi.org/10.1248/CPB.44.1540
[5-(3a,4,5,6a-Tetrahydrofuro[2,3-b]furan-5-yl)-10-hydroxy-4,5-dimethylspiro[9-oxatricyclo[6.2.2.01,6]dodecane-11,2'-oxirane]-2-yl] acetate 74001039 Click to see CC1CC(C23C(C1(C)C4CC5C=COC5O4)CC(CC26CO6)OC3O)OC(=O)C 406.50 unknown https://doi.org/10.1248/CPB.44.1540
[5-acetyloxy-8-(5-ethoxy-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-2-yl)-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 14543113 Click to see CCOC1CC2CC(OC2O1)C3(C(CC(C4(C3CCCC45CO5)COC(=O)C)OC(=O)C)C)C 480.60 unknown https://doi.org/10.1248/CPB.44.1540
[5-acetyloxy-8-(5-hydroxy-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-2-yl)-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 13559428 Click to see CC1CC(C2(C(C1(C)C3CC4CC(OC4O3)O)CCCC25CO5)COC(=O)C)OC(=O)C 452.50 unknown https://doi.org/10.1248/CPB.44.1540
[8-(2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-5-yl)-5-acetyloxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 13559425 Click to see CC1CC(C2(C(C1(C)C3CC4CCOC4O3)CCCC25CO5)COC(=O)C)OC(=O)C 436.50 unknown https://doi.org/10.1248/CPB.44.1540
[8-(3a,4,5,6a-tetrahydrofuro[2,3-b]furan-5-yl)-5-acetyloxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl acetate 5088213 Click to see CC1CC(C2(C(C1(C)C3CC4C=COC4O3)CCCC25CO5)COC(=O)C)OC(=O)C 434.50 unknown https://doi.org/10.1248/CPB.44.1540
14,15-Dihydroclerodin 11812163 Click to see CC1CC(C2(C(C1(C)C3CC4CCOC4O3)CCCC25CO5)COC(=O)C)OC(=O)C 436.50 unknown https://doi.org/10.1248/CPB.44.1540
3-Deoxycaryoptinol 124059 Click to see CC1CC(C2(C(C1(C)C3CC4C=COC4O3)CCCC25CO5)COC(=O)C)OC(=O)C 434.50 unknown https://doi.org/10.1248/CPB.44.1540
Clerodin 442014 Click to see CC1CC(C2(C(C1(C)C3CC4C=COC4O3)CCCC25CO5)COC(=O)C)OC(=O)C 434.50 unknown https://doi.org/10.1248/CPB.44.1540
Jodrellin A 162978727 Click to see CC1CC(C23C(C1(C)C4CC5C=COC5O4)CC(CC26CO6)OC3OC(=O)C)OC(=O)C 448.50 unknown https://doi.org/10.1248/CPB.44.1540
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1248/CPB.34.406
> 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 https://doi.org/10.1248/CPB.36.3654
Chrysin 5281607 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 254.24 unknown https://doi.org/10.1248/CPB.36.3654
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 https://doi.org/10.1248/CPB.36.3654
Norwogonin 5281674 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)O 270.24 unknown https://doi.org/10.1055/S-2002-36351
https://doi.org/10.1248/CPB.33.4457
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Oroxindin 3084961 Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)O)OC4C(C(C(C(O4)C(=O)O)O)O)O 460.40 unknown https://doi.org/10.1248/CPB.33.4457
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-8-O-glucuronides
6-(5,7-Dihydroxy-4-oxo-2-phenylchromen-8-yl)oxy-3,4,5-trihydroxyoxane-2-carboxylic acid 14180784 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O 446.40 unknown https://doi.org/10.1248/CPB.36.3654
Norwogonin-8-O-glucuronide 14180785 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O 446.40 unknown https://doi.org/10.1248/CPB.36.3654
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-5-hydroxy-2-(2-hydroxy-6-methoxyphenyl)-6,7-dimethoxy-2,3-dihydrochromen-4-one 162908392 Click to see COC1=CC=CC(=C1C2CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 346.30 unknown https://doi.org/10.1248/CPB.33.4457
5,2'-Dihydroxy-6,7,6'-trimethoxyflavanone 13889020 Click to see COC1=CC=CC(=C1C2CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 346.30 unknown https://doi.org/10.1248/CPB.33.4457
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
(2s)-5,2'-Dihydroxy-7,8,6'-trimethoxyflavanone 129829819 Click to see COC1=CC=CC(=C1C2CC(=O)C3=C(O2)C(=C(C=C3O)OC)OC)O 346.30 unknown https://doi.org/10.1248/CPB.33.4457
(2s)-5,7-Dihydroxy-8,2'-dimethoxyflavanone 101669621 Click to see COC1=CC=CC=C1C2CC(=O)C3=C(O2)C(=C(C=C3O)O)OC 316.30 unknown https://doi.org/10.1248/CPB.33.4457
[(2S,3R,4S,5S,6R)-2-[2-(5,7-dihydroxy-8-methoxy-4-oxochromen-2-yl)-3-hydroxyphenoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 14180788 Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=C(C=CC=C3OC4C(C(C(C(O4)CO)O)O)OC(=O)C=CC5=CC(=C(C=C5)O)O)O)O)O 640.50 unknown https://doi.org/10.1248/CPB.36.3654
[2-[2-(5,7-Dihydroxy-8-methoxy-4-oxochromen-2-yl)-3-hydroxyphenoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 163045252 Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=C(C=CC=C3OC4C(C(C(C(O4)CO)O)O)OC(=O)C=CC5=CC(=C(C=C5)O)O)O)O)O 640.50 unknown https://doi.org/10.1248/CPB.36.3654
5,2'-Dihydroxy-7,8,6'-trimethoxyflavanone 13889019 Click to see COC1=CC=CC(=C1C2CC(=O)C3=C(O2)C(=C(C=C3O)OC)OC)O 346.30 unknown https://doi.org/10.1248/CPB.33.4457
5,7-Dihydroxy-8,2'-dimethoxyflavanone 21636235 Click to see COC1=CC=CC=C1C2CC(=O)C3=C(O2)C(=C(C=C3O)O)OC 316.30 unknown https://doi.org/10.1248/CPB.33.4457
5,7-Dihydroxy-8,2',6'-trimethoxyflavone 14180789 Click to see COC1=C(C(=CC=C1)OC)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC 344.30 unknown https://doi.org/10.1248/CPB.34.406
7-Hydroxy-2',5,8-trimethoxyflavanone 21636238 Click to see COC1=CC=CC=C1C2CC(=O)C3=C(C=C(C(=C3O2)OC)O)OC 330.30 unknown https://doi.org/10.1248/CPB.33.4457
7-Hydroxy-5,8,2'-trimethoxyflavanone 21721829 Click to see COC1=CC=CC=C1C2CC(=O)C3=C(C=C(C(=C3O2)OC)O)OC 330.30 unknown https://doi.org/10.1248/CPB.33.4457
7-Hydroxy-5,8,2'-trimethoxyflavone 21637563 Click to see COC1=CC=CC=C1C2=CC(=O)C3=C(C=C(C(=C3O2)OC)O)OC 328.30 unknown https://doi.org/10.1248/CPB.34.406
Wogonin 5281703 Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)O)O 284.26 unknown https://doi.org/10.1248/CPB.36.3654
https://doi.org/10.1248/CPB.33.4457
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
2-Propen-1-one,1-(2,4-dihydroxy-3,6-dimethoxyphenyl)-3-(2-methoxyphenyl)-,(E)- 73817552 Click to see COC1=CC=CC=C1C=CC(=O)C2=C(C=C(C(=C2O)OC)O)OC 330.30 unknown https://doi.org/10.1248/CPB.33.4457
2',4'-Dihydroxy-2,3',6'-trimethoxychalcone 21636239 Click to see COC1=CC=CC=C1C=CC(=O)C2=C(C=C(C(=C2O)OC)O)OC 330.30 unknown https://doi.org/10.1248/CPB.33.4457

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