(2s)-5,2'-Dihydroxy-7,5'-dimethoxyflavanone

Details

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Internal ID 99842c04-f456-4adb-bd8c-a920a3963094
Taxonomy Phenylpropanoids and polyketides > Flavonoids > O-methylated flavonoids > 7-O-methylated flavonoids
IUPAC Name (2S)-5-hydroxy-2-(2-hydroxy-5-methoxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one
SMILES (Canonical) COC1=CC(=C(C=C1)O)C2CC(=O)C3=C(C=C(C=C3O2)OC)O
SMILES (Isomeric) COC1=CC(=C(C=C1)O)[C@@H]2CC(=O)C3=C(C=C(C=C3O2)OC)O
InChI InChI=1S/C17H16O6/c1-21-9-3-4-12(18)11(5-9)15-8-14(20)17-13(19)6-10(22-2)7-16(17)23-15/h3-7,15,18-19H,8H2,1-2H3/t15-/m0/s1
InChI Key XMFCMXPYIULHFX-HNNXBMFYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C17H16O6
Molecular Weight 316.30 g/mol
Exact Mass 316.09468823 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 2.70

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2s)-5,2'-Dihydroxy-7,5'-dimethoxyflavanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
No predicted properties yet!

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.18% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 96.27% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.07% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.83% 96.09%
CHEMBL4208 P20618 Proteasome component C5 91.57% 90.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.16% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 90.62% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.06% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.53% 99.17%
CHEMBL2581 P07339 Cathepsin D 89.38% 98.95%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.85% 95.89%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 87.55% 91.07%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.23% 97.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.85% 94.00%
CHEMBL1929 P47989 Xanthine dehydrogenase 85.81% 96.12%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 83.68% 94.80%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.60% 92.62%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.08% 89.00%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 82.37% 91.79%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 80.81% 93.40%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Onosma hispida

Cross-Links

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PubChem 91600795
LOTUS LTS0186131
wikiData Q105330687