Sophoraisoflavanone A

Details

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Internal ID 7c0d9963-be28-4bfc-a08c-0ca577175a34
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflavans > Isoflavanones > 3-prenylated isoflavanones
IUPAC Name 5,7-dihydroxy-3-[4-hydroxy-2-methoxy-3-(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one
SMILES (Canonical) CC(=CCC1=C(C=CC(=C1OC)C2COC3=CC(=CC(=C3C2=O)O)O)O)C
SMILES (Isomeric) CC(=CCC1=C(C=CC(=C1OC)C2COC3=CC(=CC(=C3C2=O)O)O)O)C
InChI InChI=1S/C21H22O6/c1-11(2)4-5-14-16(23)7-6-13(21(14)26-3)15-10-27-18-9-12(22)8-17(24)19(18)20(15)25/h4,6-9,15,22-24H,5,10H2,1-3H3
InChI Key AALISTBXLBQUEH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H22O6
Molecular Weight 370.40 g/mol
Exact Mass 370.14163842 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 4.50
Atomic LogP (AlogP) 3.68
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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69573-59-7
DTXSID00331962
LMPK12050480

2D Structure

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2D Structure of Sophoraisoflavanone A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9860 98.60%
Caco-2 + 0.7576 75.76%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7651 76.51%
OATP2B1 inhibitior - 0.7190 71.90%
OATP1B1 inhibitior + 0.9283 92.83%
OATP1B3 inhibitior + 0.8322 83.22%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.6545 65.45%
P-glycoprotein inhibitior - 0.5350 53.50%
P-glycoprotein substrate - 0.6685 66.85%
CYP3A4 substrate + 0.5972 59.72%
CYP2C9 substrate + 0.5973 59.73%
CYP2D6 substrate - 0.7963 79.63%
CYP3A4 inhibition - 0.6732 67.32%
CYP2C9 inhibition + 0.8400 84.00%
CYP2C19 inhibition + 0.8963 89.63%
CYP2D6 inhibition - 0.6342 63.42%
CYP1A2 inhibition + 0.9215 92.15%
CYP2C8 inhibition + 0.5752 57.52%
CYP inhibitory promiscuity + 0.9174 91.74%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7643 76.43%
Eye corrosion - 0.9888 98.88%
Eye irritation - 0.5484 54.84%
Skin irritation - 0.8072 80.72%
Skin corrosion - 0.9557 95.57%
Ames mutagenesis + 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5116 51.16%
Micronuclear - 0.5200 52.00%
Hepatotoxicity + 0.6017 60.17%
skin sensitisation - 0.8184 81.84%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.6637 66.37%
Acute Oral Toxicity (c) III 0.6981 69.81%
Estrogen receptor binding + 0.8630 86.30%
Androgen receptor binding + 0.8284 82.84%
Thyroid receptor binding + 0.6462 64.62%
Glucocorticoid receptor binding + 0.8935 89.35%
Aromatase binding - 0.4933 49.33%
PPAR gamma + 0.7920 79.20%
Honey bee toxicity - 0.8198 81.98%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9889 98.89%

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 99.80% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.66% 94.45%
CHEMBL2581 P07339 Cathepsin D 96.64% 98.95%
CHEMBL1929 P47989 Xanthine dehydrogenase 94.26% 96.12%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.62% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.55% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.68% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 91.15% 99.15%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.03% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.71% 99.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.60% 100.00%
CHEMBL240 Q12809 HERG 88.58% 89.76%
CHEMBL3401 O75469 Pregnane X receptor 87.81% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.65% 99.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.64% 97.09%
CHEMBL2535 P11166 Glucose transporter 87.53% 98.75%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 87.20% 93.40%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.72% 93.99%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 86.69% 92.68%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.77% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.03% 92.62%
CHEMBL340 P08684 Cytochrome P450 3A4 84.07% 91.19%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.81% 85.14%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.26% 94.80%
CHEMBL1951 P21397 Monoamine oxidase A 80.59% 91.49%

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.
Sophora flavescens
Sophora fraseri
Sophora koreensis
Sophora tomentosa

Cross-Links

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PubChem 442822
NPASS NPC19615
LOTUS LTS0070810
wikiData Q104397314