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Sophora exigua

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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 UUID643fd9a1757db740796227
Scientific name Sophora exigua
Authority Craib
First published in Bull. Misc. Inform. Kew1927: 71 (1927)

Description Top

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Synonyms Top

Scientific name Authority First published in
Sophora violacea var. pilosa Gagnep.
Sophora violacea subsp. pilosa (Gagnep.) Yakovlev

Common names Top

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Language Common/alternative name
Arabic صفيراء عجفاء
Thai พิษนาศน์

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Sophora exigua var. elatior P.C.Tsoong Acta Phytotax. Sin.18: 73 (1980)
Sophora exigua var. exigua Unknown

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000186510
Tropicos 13044685
KEW urn:lsid:ipni.org:names:518828-1
The Plant List ild-32976
Open Tree Of Life 3919853
IPNI 518828-1
GBIF 2959070
EOL 643999
CMAUP NPO24630

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)!
Title Authors Publication Released IDs
Antibacterial activity of flavanone isolated from <i>Sophora exigua</i> against methicillin‐resistant <i>Staphylococcus aureus</i> and its combination with antibiotics M. Sato, H. Tsuchiya, I. Takase, H. Kureshiro, S. Tanigaki, M. Iinuma Wiley 18-Oct-2006
doi:10.1002/PTR.2650090709
Occurrence of prenylated flavonoids and oligostilbenes and its significance for chemotaxonomy of genus Sophora (Leguminosae) Masayoshi Ohyama, Toshiyuki Tanaka, Junji Yokoyama, Munekazu Iinuma Elsevier BV 12-May-2003
doi:10.1016/0305-1978(95)00056-9
Lupin alkaloids fromSophora exigua Satoshi Takamatsu, Kazuki Saito, Shigeru Ohmiya, Nijsiri Ruangrungsi, Isamu Murakoshi Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)80112-E
Seven phenolic compounds in the roots of Sophora exigua Munekazu Iinuma, Junji Yokoyama, Masayoshi Ohyama, Toshiyuki Tanaka, Mizuo Mizuno, Nijsiri Ruangrungsi Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(93)85423-O
Three flavanones with a lavandulyl group in the roots of Sophora exigua Nijsiri Ruangrungsi, Munekazu Iinuma, Toshiyuki Tanaka, Masayoshi Ohyama, Junji Yokoyama, Mizuo Mizuno Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)80056-K
Eight phenolic compounds in root of Sophora exigua Munekazu Iinuma, Junji Yokoyama, Masayoshi Ohyama, Toshiyuki Tanaka, Nijsiri Ruangrungsi Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)90606-X
Three flavanones with a lavandulyl group in the roots of Sophora exigua N Ruangrungsi Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)80202-P
Flavanones with potent antibacterial activity against methicillin-resistant Staphylococcus aureus. Iinuma M, Tsuchiya H, Sato M, Yokoyama J, Ohyama M, Ohkawa Y, Tanaka T, Fujiwara S, Fujii T J Pharm Pharmacol 01-Nov-1994
doi:10.1111/J.2042-7158.1994.TB05709.X
PMID:7897594
Inhibition of the growth of cariogenic bacteria in vitro by plant flavanones. Tsuchiya H, Sato M, Iinuma M, Yokoyama J, Ohyama M, Tanaka T, Takase I, Namikawa I Experientia 15-Sep-1994
doi:10.1007/BF01956469
PMID:7925853

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
> Alkaloids and derivatives / Lupin alkaloids / Anagyrine-type alkaloids
(+)-Thermopsine 682648 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1016/0031-9422(91)80112-E
(10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 10246 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1016/0031-9422(91)80112-E
(1R,9R,10R,12R)-12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 15939858 Click to see C1CN2CC3CC(C2CC1O)CN4C3=CC=CC4=O 260.33 unknown https://doi.org/10.1016/0031-9422(91)80112-E
12-Hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 621307 Click to see C1CN2CC3CC(C2CC1O)CN4C3=CC=CC4=O 260.33 unknown https://doi.org/10.1016/0031-9422(91)80112-E
Anagyrine 5351589 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1016/0031-9422(91)80112-E
Thermopsine 92768 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1016/0031-9422(91)80112-E
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
(1R,9R)-11-methyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 1747617 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1016/0031-9422(91)80112-E
(1R)-1,2,3,4,5,6-Hexahydro-1,5-methano-8H-pyrido[1,2-a][1,5]diazocin-8-one 1278189 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1016/0031-9422(91)80112-E
(1S,5R)-3,4,5,6-tetrahydro-1H-1,5-methanopyrido[1,2-a][1,5]diazocin-8(2H)-one 6713952 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1016/0031-9422(91)80112-E
(1S,9S)-11-hydroxy-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 15939873 Click to see C1C2CN(CC1C3=CC=CC(=O)N3C2)O 206.24 unknown https://doi.org/10.1016/0031-9422(91)80112-E
11-Hydroxy-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 4416733 Click to see C1C2CN(CC1C3=CC=CC(=O)N3C2)O 206.24 unknown https://doi.org/10.1016/0031-9422(91)80112-E
12-Cytisineacetamide 15939882 Click to see C1C2CN(CC1C3=CC=CC(=O)N3C2)CC(=O)N 247.29 unknown https://doi.org/10.1016/0031-9422(91)80112-E
2-(8-oxo-1,5,6,8-tetrahydro-2H-1,5-methanopyrido[1,2-a][1,5]diazocin-3(4H)-yl)acetamide 3439560 Click to see C1C2CN(CC1C3=CC=CC(=O)N3C2)CC(=O)N 247.29 unknown https://doi.org/10.1016/0031-9422(91)80112-E
Citizin 22407 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1016/0031-9422(91)80112-E
Cytisine, N-formyl- 589870 Click to see C1C2CN(CC1C3=CC=CC(=O)N3C2)C=O 218.25 unknown https://doi.org/10.1016/0031-9422(91)80112-E
Cytisinicline 10235 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1016/0031-9422(91)80112-E
N-Formylcytisine, (-)- 6604689 Click to see C1C2CN(CC1C3=CC=CC(=O)N3C2)C=O 218.25 unknown https://doi.org/10.1016/0031-9422(91)80112-E
N-Methylcytisine 234566 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1016/0031-9422(91)80112-E
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
Hydrorhombinine 7018997 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1016/0031-9422(91)80112-E
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
5,7-Dihydroxy-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)chromen-4-one 162844304 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)C=CO2)C(=C)C)C 314.40 unknown https://doi.org/10.1016/0031-9422(93)85423-O
5,7-dihydroxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]chromen-4-one 162844305 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)C=CO2)C(=C)C)C 314.40 unknown https://doi.org/10.1016/0031-9422(93)85423-O
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
5-Hydroxy-8,8-dimethylpyrano[2,3-h]chromen-4-one 13545811 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC=CC3=O)O)C 244.24 unknown https://doi.org/10.1016/S0031-9422(00)90606-X
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S)-5-hydroxy-8,8-dimethyl-6-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2-(2,4,6-trihydroxyphenyl)-2,3-dihydropyrano[2,3-h]chromen-4-one 163046981 Click to see CC(=CCC(CC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=C(C=C(C=C4O)O)O)O)C(=C)C)C 506.60 unknown https://doi.org/10.1016/S0031-9422(00)90606-X
(2S)-5,7-dihydroxy-6-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2-(2,4,6-trihydroxyphenyl)-2,3-dihydrochromen-4-one 162846150 Click to see CC(=CCC(CC1=C(C2=C(C=C1O)OC(CC2=O)C3=C(C=C(C=C3O)O)O)O)C(=C)C)C 440.50 unknown https://doi.org/10.1016/0031-9422(93)85423-O
5,7-Dihydroxy-6-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2-(2,4,6-trihydroxyphenyl)-2,3-dihydrochromen-4-one 74819410 Click to see CC(=CCC(CC1=C(C2=C(C=C1O)OC(CC2=O)C3=C(C=C(C=C3O)O)O)O)C(=C)C)C 440.50 unknown https://doi.org/10.1016/0031-9422(93)85423-O
Exiguaflavanone C 42608028 Click to see CC(=CCC(CC1=C(C2=C(C=C1O)OC(CC2=O)C3=C(C=C(C=C3O)O)O)O)C(=C)C)C 440.50 unknown https://doi.org/10.1016/0031-9422(93)85423-O
https://doi.org/10.1016/0305-1978(95)00056-9
Exiguaflavanone I 42608048 Click to see CC(=CCC(CC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=C(C=C(C=C4O)O)O)O)C(=C)C)C 506.60 unknown https://doi.org/10.1016/S0031-9422(00)90606-X
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R)-2-(2,6-dihydroxyphenyl)-5-hydroxy-7-methoxy-8-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 162845586 Click to see CC(=CCC(CC1=C(C=C(C2=C1OC(CC2=O)C3=C(C=CC=C3O)O)O)OC)C(=C)C)C 438.50 unknown https://doi.org/10.1016/0031-9422(92)80202-P
(2R)-5,7-dihydroxy-2-(2-hydroxyphenyl)-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 133612505 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3O)C(=C)C)C 408.50 unknown https://doi.org/10.1016/0031-9422(93)85423-O
(2S,9R)-2-(2,6-dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-9-(3-methylbut-2-enyl)-2,3,9,10-tetrahydropyrano[2,3-h]chromen-4-one 162920114 Click to see CC(=CCC1CC2=C(C=C(C3=C2OC(CC3=O)C4=C(C=CC=C4O)O)O)OC1(C)C)C 424.50 unknown https://doi.org/10.1016/S0031-9422(00)90606-X
(2S)-2-(2,4-dihydroxy-5-methoxyphenyl)-5-hydroxy-7-methoxy-8-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 162843967 Click to see CC(=CCC(CC1=C(C=C(C2=C1OC(CC2=O)C3=CC(=C(C=C3O)O)OC)O)OC)C(=C)C)C 468.50 unknown https://doi.org/10.1016/0031-9422(93)85423-O
(2S)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 6565899 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C 424.50 unknown https://doi.org/10.1016/0031-9422(92)80056-K
(2S)-2-(2,6-dihydroxy-4-methoxyphenyl)-5,7-dihydroxy-6-(3-methylbut-2-enyl)-8-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 101676612 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=C(C=C(C=C3O)OC)O)CC(CC=C(C)C)C(=C)C)O)C 522.60 unknown https://doi.org/10.1111/J.2042-7158.1994.TB05709.X
https://doi.org/10.1016/0031-9422(93)85423-O
(2S)-2-(2,6-dihydroxyphenyl)-5-hydroxy-7-methoxy-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3-dihydrochromen-4-one 101625134 Click to see CC(=CCC(CC1=C(C=C(C2=C1OC(CC2=O)C3=C(C=CC=C3O)O)O)OC)C(=C)C)C 438.50 unknown https://doi.org/10.1016/0031-9422(92)80202-P
https://doi.org/10.1111/J.2042-7158.1994.TB05709.X
(2S)-2-(2,6-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 163012390 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=CC=C3O)O)C(=C)C)C 424.50 unknown https://doi.org/10.1016/0031-9422(92)80056-K
(2S)-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 14258999 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC(=C(C=C3)O)OC)C 370.40 unknown https://doi.org/10.1016/S0031-9422(00)90606-X
(2S)-5,7-dihydroxy-6-(3-methylbut-2-enyl)-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2-(2,4,6-trihydroxyphenyl)-2,3-dihydrochromen-4-one 162896348 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=C(C=C(C=C3O)O)O)CC(CC=C(C)C)C(=C)C)O)C 508.60 unknown https://doi.org/10.1016/S0031-9422(00)90606-X
(2S)-5,7-dihydroxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2-(2,4,6-trihydroxyphenyl)-2,3-dihydrochromen-4-one 162918685 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3O)O)O)C(=C)C)C 440.50 unknown https://doi.org/10.1016/S0031-9422(00)90606-X
(8S)-5-hydroxy-2,2-dimethyl-10-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-8-(2,4,6-trihydroxyphenyl)-7,8-dihydropyrano[3,2-g]chromen-6-one 163006484 Click to see CC(=CCC(CC1=C2C(=C(C3=C1OC(CC3=O)C4=C(C=C(C=C4O)O)O)O)C=CC(O2)(C)C)C(=C)C)C 506.60 unknown https://doi.org/10.1016/S0031-9422(00)90606-X
2-(2,6-Dihydroxyphenyl)-5-hydroxy-7-methoxy-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3-dihydrochromen-4-one 10455800 Click to see CC(=CCC(CC1=C(C=C(C2=C1OC(CC2=O)C3=C(C=CC=C3O)O)O)OC)C(=C)C)C 438.50 unknown https://doi.org/10.1016/0031-9422(92)80056-K
2-(2,6-Dihydroxyphenyl)-5,7-dihydroxy-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3-dihydrochromen-4-one 10070990 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=CC=C3O)O)C(=C)C)C 424.50 unknown https://doi.org/10.1016/0031-9422(92)80056-K
Exiguaflavanone A 15735861 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=CC=C3O)O)C(=C)C)C 424.50 unknown https://doi.org/10.1016/0031-9422(92)80202-P
https://doi.org/10.1007/BF01956469
https://doi.org/10.1016/0031-9422(92)80056-K
Exiguaflavanone B 15735862 Click to see CC(=CCC(CC1=C(C=C(C2=C1OC(CC2=O)C3=C(C=CC=C3O)O)O)OC)C(=C)C)C 438.50 unknown https://doi.org/10.1016/0031-9422(92)80056-K
Exiguaflavanone D 10392009 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=C(C=C(C=C3O)OC)O)CC(CC=C(C)C)C(=C)C)O)C 522.60 unknown https://doi.org/10.1016/0031-9422(93)85423-O
Exiguaflavanone E 42608029 Click to see CC(=CCC(CC1=C(C=C(C2=C1OC(CC2=O)C3=CC(=C(C=C3O)O)OC)O)OC)C(=C)C)C 468.50 unknown https://doi.org/10.1016/0031-9422(93)85423-O
Exiguaflavanone F 42607845 Click to see CC(=CCC(CC1=C(C=C(C2=C1OC(CC2=O)C3=C(C=CC(=C3)O)O)O)OC)C(=C)C)C 438.50 unknown https://doi.org/10.1016/0031-9422(93)85423-O
Exiguaflavanone G 42608030 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3O)O)O)C(=C)C)C 440.50 unknown https://doi.org/10.1016/S0031-9422(00)90606-X
Exiguaflavanone H 42608047 Click to see CC(=CCC(CC1=C2C(=C(C3=C1OC(CC3=O)C4=C(C=C(C=C4O)O)O)O)C=CC(O2)(C)C)C(=C)C)C 506.60 unknown https://doi.org/10.1016/S0031-9422(00)90606-X
Exiguaflavanone J 42608031 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=C(C=C(C=C3O)O)O)CC(CC=C(C)C)C(=C)C)O)C 508.60 unknown https://doi.org/10.1016/S0031-9422(00)90606-X
Exiguaflavanone K 11036041 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC(=C(C=C3)O)OC)C 370.40 unknown https://doi.org/10.1016/S0031-9422(00)90606-X
Exiguaflavanone L 42607848 Click to see CC(=CCC1CC2=C(C=C(C3=C2OC(CC3=O)C4=C(C=CC=C4O)O)O)OC1(C)C)C 424.50 unknown https://doi.org/10.1016/S0031-9422(00)90606-X
Exiguaflavanone M 42607846 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=CC=C3O)O)C(C)(C)O)C 442.50 unknown https://doi.org/10.1016/S0031-9422(00)90606-X
Marini 73198 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C 424.50 unknown https://doi.org/10.1016/0031-9422(92)80056-K
Sophoraflavanone G 72936 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C 424.50 unknown https://doi.org/10.1016/0031-9422(92)80202-P
https://doi.org/10.1002/PTR.2650090709
https://doi.org/10.1007/BF01956469
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 3-prenylated flavones
2-[3-[(1S,5S,6S)-6-(2,4-dihydroxybenzoyl)-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-2,4-dihydroxyphenyl]-3,7-dihydroxychromen-4-one 162921495 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C=C(C=C3)O)O)C4=C(C=CC(=C4O)C5=C(C(=O)C6=C(O5)C=C(C=C6)O)O)O 624.60 unknown https://doi.org/10.1016/0031-9422(93)85423-O
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
2-(2,6-Dihydroxy-4-methoxy-phenyl)-5,7-dihydroxy-8-(2-isopropenyl-5-methyl-hex-4-enyl)-6-(3-methylbut-2-enyl)chromen-4-one 471702 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=C(C=C(C=C3O)OC)O)CC(CC=C(C)C)C(=C)C)O)C 520.60 unknown https://doi.org/10.1111/J.2042-7158.1994.TB05709.X
https://doi.org/10.1016/0031-9422(93)85423-O
2-(2,6-Dihydroxyphenyl)-5-hydroxy-8-(2-isopropenyl-5-methyl-hex-4-enyl)-7-methoxy-chromen-4-one 471700 Click to see CC(=CCC(CC1=C(C=C(C2=C1OC(=CC2=O)C3=C(C=CC=C3O)O)O)OC)C(=C)C)C 436.50 unknown https://doi.org/10.1016/0031-9422(92)80202-P
https://doi.org/10.1111/J.2042-7158.1994.TB05709.X
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5,3',4'-Tetrahydroxy-6,7,8-trimethoxyflavone 44260067 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)O)OC)OC 376.30 unknown via CMAUP database
3,5,7,3',4'-Pentahydroxy-6,8-dimethoxyflavone 14483219 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)O)OC)O 362.30 unknown via CMAUP database
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Limocitrol 12311234 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)O)O 376.30 unknown via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 13871824 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)O)O 432.40 unknown via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 57511421 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown via CMAUP database
Vitexin 5280441 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Cacticin 5318644 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin 5280681 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 316.26 unknown via CMAUP database
5,7,8,4'-Tetrahydroxy-3-methoxyflavone 5319442 Click to see COC1=C(OC2=C(C1=O)C(=CC(=C2O)O)O)C3=CC=C(C=C3)O 316.26 unknown via CMAUP database
Gossypetin 3-methyl ether 5386958 Click to see COC1=C(OC2=C(C1=O)C(=CC(=C2O)O)O)C3=CC(=C(C=C3)O)O 332.26 unknown via CMAUP database
Gossypetin 3,3'-dimethyl ether 21676153 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)O)OC)O 346.30 unknown via CMAUP database
Quercetagetin 3-methyl ether 5320475 Click to see COC1=C(OC2=C(C1=O)C(=C(C(=C2)O)O)O)C3=CC(=C(C=C3)O)O 332.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
4',5,7-Trihydroxy-3,6-dimethoxyflavone 5352032 Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O 330.29 unknown via CMAUP database
5,7,2'-Trihydroxy-3,6,4',5'-tetramethoxyflavone 44259895 Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O)OC 390.30 unknown via CMAUP database
5,7,3'-Trihydroxy-3,6,4',5'-tetramethoxyflavone 44258045 Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC 390.30 unknown via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,5'-trimethoxyflavone 44258041 Click to see COC1=CC(=CC(=C1O)O)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC 376.30 unknown via CMAUP database
5,7,3',4',5'-Pentahydroxy-3,6-dimethoxyflavone 44259884 Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC(=C(C(=C3)O)O)O)O 362.30 unknown via CMAUP database
5,7,8,3',4'-Pentahydroxy-3,6-dimethoxyflavone 21676156 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)O)O 362.30 unknown via CMAUP database
5,7,8,4'-Tetrahydroxy-3,6-dimethoxyflavone 44260054 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)OC)O)O 346.30 unknown via CMAUP database
Axillarin 5281603 Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O 346.30 unknown via CMAUP database
Jaceidin 5464461 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Benthamitin 44259900 Click to see COC1=CC(=C(C=C1C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)OC)OC)OC)OC 432.40 unknown via CMAUP database
Casticin 5315263 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O 374.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
3',4',5,7-Tetrahydroxy-3,8-dimethoxyflavone 5748553 Click to see COC1=C(C=C(C2=C1OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)O 346.30 unknown via CMAUP database
4H-1-Benzopyran-4-one, 5,7-dihydroxy-2-(4-hydroxyphenyl)-3,6,8-trimethoxy- 5386960 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)OC)OC)O 360.30 unknown via CMAUP database
5-Hydroxy-3,6,7,8,3',4',5'-heptamethoxyflavone 44260077 Click to see COC1=CC(=CC(=C1OC)OC)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC 448.40 unknown via CMAUP database
5,2'-Dihydroxy-3,6,7,8,4',5'-hexamethoxyflavone 44260086 Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O)OC 434.40 unknown via CMAUP database
5,3'-Dihydroxy-3,6,7,8,4'-pentamethoxyflavone 369954 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O 404.40 unknown via CMAUP database
5,3',4'-Trihydroxy-3,6,7,8-tetramethoxyflavone 54799 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)OC)OC 390.30 unknown via CMAUP database
5,3',5'-Trihydroxy-3,6,7,8,4'-pentamethoxyflavone 44260074 Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O 420.40 unknown via CMAUP database
5,4'-Dihydroxy-3,6,7,8,3'-pentamethoxyflavone 100625 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O 404.40 unknown via CMAUP database
5,6,3',5'-Tetrahydroxy-3,7,8,4'-tetramethoxyflavone 44260073 Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)O)O)OC)O 406.30 unknown via CMAUP database
5,7-Dihydroxy-2-(4-hydroxy-3-methoxy-phenyl)-3,6,8-trimethoxy-chromen-4-one 5386959 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O 390.30 unknown via CMAUP database
5,7-Dihydroxy-3,6,8,3',4',5'-hexamethoxyflavone 5386963 Click to see COC1=CC(=CC(=C1OC)OC)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC 434.40 unknown via CMAUP database
5,7,2'-Trihydroxy-3,6,8,4',5'-pentamethoxyflavone 5487077 Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O)OC 420.40 unknown via CMAUP database
5,7,2',4'-Tetrahydroxy-3,6,8,5'-tetramethoxyflavone 21676158 Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O)O 406.30 unknown via CMAUP database
5,7,2',4'-Tetrahydroxy-3,8,5'-trimethoxyflavone 44260043 Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O)O 376.30 unknown via CMAUP database
5,7,2',4'-Tetrahydroxy-8,5'-dimethoxyflavone 44258626 Click to see COC1=C(C=C(C(=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC)O)O 346.30 unknown via CMAUP database
5,7,2',5'-Tetrahydroxy-3,6,8,4'-tetramethoxyflavone 44260085 Click to see COC1=C(C=C(C(=C1)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O 406.30 unknown via CMAUP database
5,7,3'-Trihydroxy-3,6,8,4'-Tetramethoxyflavone 21599528 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O 390.30 unknown via CMAUP database
5,7,3'-Trihydroxy-3,6,8,4',5'-pentamethoxyflavone 5352085 Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC 420.40 unknown via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,8-trimethoxyflavone 5386962 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)OC)O 376.30 unknown via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,8,5'-tetramethoxyflavone 44260072 Click to see COC1=CC(=CC(=C1O)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC 406.30 unknown via CMAUP database
5,7,3',4',5'-Pentahydroxy-3,6,8-trimethoxyflavone 11383767 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C(=C3)O)O)O)OC)OC)O 392.30 unknown via CMAUP database
5,7,3',5'-Tetrahydroxy-3,6,8,4'-tetramethoxyflavone 44260071 Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O 406.30 unknown via CMAUP database
5,7,4'-Trihydroxy-3,6,8,3',5'-pentamethoxyflavone 21676159 Click to see COC1=CC(=CC(=C1O)OC)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC 420.40 unknown via CMAUP database
5,7,4'-Trihydroxy-3,8-dimethoxyflavone 13983738 Click to see COC1=C(C=C(C2=C1OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O)O 330.29 unknown via CMAUP database
Agecorynin D 14162688 Click to see COC1=C(C=C(C(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O)O 390.30 unknown via CMAUP database
Calycopterin 10429470 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)OC)OC)OC 374.30 unknown via CMAUP database
Conyzatin 13916282 Click to see COC1=CC(=CC(=C1OC)OC)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC 404.40 unknown via CMAUP database
Digicitrin 10071564 Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC 434.40 unknown via CMAUP database
Gossypetin 3,8,3'-trimethyl ether 5386961 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O 360.30 unknown via CMAUP database
Hibiscetin 3,8,4'-trimethyl ether 44260037 Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O 376.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
3-Hydroxy-8,9-methylenedioxypterocarpane 363863 Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5 284.26 unknown https://doi.org/10.1016/0031-9422(93)85423-O

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