(3S)-7-hydroxy-3-(4-methoxyphenyl)-2,3-dihydrochromen-4-one

Details

Top
Internal ID 32f04fcb-20d3-4d2f-9914-0bf2b5e05a2b
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > O-methylated isoflavonoids > 4-O-methylated isoflavonoids
IUPAC Name (3S)-7-hydroxy-3-(4-methoxyphenyl)-2,3-dihydrochromen-4-one
SMILES (Canonical) COC1=CC=C(C=C1)C2COC3=C(C2=O)C=CC(=C3)O
SMILES (Isomeric) COC1=CC=C(C=C1)[C@H]2COC3=C(C2=O)C=CC(=C3)O
InChI InChI=1S/C16H14O4/c1-19-12-5-2-10(3-6-12)14-9-20-15-8-11(17)4-7-13(15)16(14)18/h2-8,14,17H,9H2,1H3/t14-/m1/s1
InChI Key INYISIYHXQDCPK-CQSZACIVSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C16H14O4
Molecular Weight 270.28 g/mol
Exact Mass 270.08920892 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 2.70
Atomic LogP (AlogP) 2.76
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (3S)-7-hydroxy-3-(4-methoxyphenyl)-2,3-dihydrochromen-4-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9918 99.18%
Caco-2 + 0.7557 75.57%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.8536 85.36%
OATP2B1 inhibitior - 0.8596 85.96%
OATP1B1 inhibitior + 0.8982 89.82%
OATP1B3 inhibitior + 0.9888 98.88%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5950 59.50%
P-glycoprotein inhibitior - 0.8960 89.60%
P-glycoprotein substrate - 0.8473 84.73%
CYP3A4 substrate + 0.5435 54.35%
CYP2C9 substrate - 0.8062 80.62%
CYP2D6 substrate - 0.7218 72.18%
CYP3A4 inhibition - 0.5998 59.98%
CYP2C9 inhibition + 0.8272 82.72%
CYP2C19 inhibition + 0.9254 92.54%
CYP2D6 inhibition - 0.9080 90.80%
CYP1A2 inhibition + 0.8838 88.38%
CYP2C8 inhibition - 0.7601 76.01%
CYP inhibitory promiscuity + 0.7191 71.91%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9313 93.13%
Carcinogenicity (trinary) Non-required 0.6079 60.79%
Eye corrosion - 0.9730 97.30%
Eye irritation - 0.4782 47.82%
Skin irritation - 0.6780 67.80%
Skin corrosion - 0.9841 98.41%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7194 71.94%
Micronuclear + 0.8159 81.59%
Hepatotoxicity - 0.7000 70.00%
skin sensitisation - 0.9584 95.84%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity - 0.6355 63.55%
Acute Oral Toxicity (c) III 0.6655 66.55%
Estrogen receptor binding + 0.8763 87.63%
Androgen receptor binding + 0.8740 87.40%
Thyroid receptor binding + 0.6789 67.89%
Glucocorticoid receptor binding + 0.5375 53.75%
Aromatase binding + 0.6061 60.61%
PPAR gamma - 0.5075 50.75%
Honey bee toxicity - 0.9182 91.82%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.8765 87.65%

Targets

Top

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 98.85% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.64% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.17% 97.09%
CHEMBL2581 P07339 Cathepsin D 94.53% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.77% 96.09%
CHEMBL4208 P20618 Proteasome component C5 91.96% 90.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.50% 85.14%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.46% 99.15%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.93% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.47% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.14% 99.17%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 86.04% 96.09%
CHEMBL2535 P11166 Glucose transporter 85.74% 98.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.71% 95.89%
CHEMBL4040 P28482 MAP kinase ERK2 85.53% 83.82%
CHEMBL3231 Q13464 Rho-associated protein kinase 1 84.30% 95.55%
CHEMBL1907 P15144 Aminopeptidase N 84.28% 93.31%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.86% 89.00%
CHEMBL340 P08684 Cytochrome P450 3A4 83.32% 91.19%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 81.76% 95.89%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 81.17% 82.67%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.15% 99.23%
CHEMBL1951 P21397 Monoamine oxidase A 80.69% 91.49%

Plants that contains it

Top
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.
Dalbergia parviflora
Eysenhardtia polystachya
Myroxylon balsamum
Zollernia paraensis

Cross-Links

Top
PubChem 46881075
NPASS NPC202981
LOTUS LTS0063169
wikiData Q105116487