Vestitol, (-)-

Details

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Internal ID 99084e3b-924c-4f6e-9aa5-9e7eaafbc51b
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > O-methylated isoflavonoids > 4-O-methylated isoflavonoids
IUPAC Name (3R)-3-(2-hydroxy-4-methoxyphenyl)-3,4-dihydro-2H-chromen-7-ol
SMILES (Canonical) COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O
SMILES (Isomeric) COC1=CC(=C(C=C1)[C@H]2CC3=C(C=C(C=C3)O)OC2)O
InChI InChI=1S/C16H16O4/c1-19-13-4-5-14(15(18)8-13)11-6-10-2-3-12(17)7-16(10)20-9-11/h2-5,7-8,11,17-18H,6,9H2,1H3/t11-/m0/s1
InChI Key XRVFNNUXNVWYTI-NSHDSACASA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C16H16O4
Molecular Weight 272.29 g/mol
Exact Mass 272.10485899 g/mol
Topological Polar Surface Area (TPSA) 58.90 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.83
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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35878-41-2
(R)-Vestitol
Vestitol, (-)-
(R)-(-)-Vestitol
UNII-9JHS2AVR43
9JHS2AVR43
CHEBI:80392
(3R)-3-(2-hydroxy-4-methoxyphenyl)-3,4-dihydro-2H-chromen-7-ol
(3R)-3-(2-hydroxy-4-methoxyphenyl)-3,4-dihydro-2H-1-benzopyran-7-ol
2H-1-BENZOPYRAN-7-OL, 3,4-DIHYDRO-3-(2-HYDROXY-4-METHOXYPHENYL)-, (3R)-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Vestitol, (-)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9591 95.91%
Caco-2 + 0.8368 83.68%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8652 86.52%
OATP2B1 inhibitior - 0.8537 85.37%
OATP1B1 inhibitior + 0.9300 93.00%
OATP1B3 inhibitior + 0.9870 98.70%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.4595 45.95%
P-glycoprotein inhibitior - 0.8349 83.49%
P-glycoprotein substrate + 0.5064 50.64%
CYP3A4 substrate + 0.5701 57.01%
CYP2C9 substrate - 0.6025 60.25%
CYP2D6 substrate + 0.5974 59.74%
CYP3A4 inhibition - 0.7320 73.20%
CYP2C9 inhibition + 0.8596 85.96%
CYP2C19 inhibition + 0.9268 92.68%
CYP2D6 inhibition - 0.7038 70.38%
CYP1A2 inhibition + 0.8452 84.52%
CYP2C8 inhibition - 0.5655 56.55%
CYP inhibitory promiscuity + 0.8433 84.33%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8913 89.13%
Carcinogenicity (trinary) Non-required 0.6142 61.42%
Eye corrosion - 0.9868 98.68%
Eye irritation + 0.7303 73.03%
Skin irritation - 0.7497 74.97%
Skin corrosion - 0.9595 95.95%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5805 58.05%
Micronuclear + 0.7000 70.00%
Hepatotoxicity - 0.6560 65.60%
skin sensitisation - 0.9546 95.46%
Respiratory toxicity + 0.5556 55.56%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.7841 78.41%
Acute Oral Toxicity (c) III 0.4928 49.28%
Estrogen receptor binding + 0.7173 71.73%
Androgen receptor binding + 0.6981 69.81%
Thyroid receptor binding + 0.7131 71.31%
Glucocorticoid receptor binding + 0.5383 53.83%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.5261 52.61%
Honey bee toxicity - 0.8923 89.23%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9090 90.90%

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 98.34% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.78% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 92.12% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.98% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 91.13% 95.89%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 90.90% 91.79%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.04% 99.17%
CHEMBL4208 P20618 Proteasome component C5 89.77% 90.00%
CHEMBL2581 P07339 Cathepsin D 89.12% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.01% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.61% 93.99%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.02% 97.09%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.67% 95.89%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 86.12% 93.40%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.82% 94.00%
CHEMBL236 P41143 Delta opioid receptor 85.62% 99.35%
CHEMBL267 P12931 Tyrosine-protein kinase SRC 85.60% 95.69%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.10% 94.45%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 83.64% 100.00%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 82.90% 100.00%
CHEMBL1951 P21397 Monoamine oxidase A 82.76% 91.49%
CHEMBL2535 P11166 Glucose transporter 82.08% 98.75%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.83% 92.62%
CHEMBL226 P30542 Adenosine A1 receptor 81.53% 95.93%
CHEMBL3085 P43003 Excitatory amino acid transporter 1 81.06% 94.67%

Cross-Links

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PubChem 182259
NPASS NPC50315
LOTUS LTS0191687
wikiData Q27149418