4-Hydroxy-3,9-dimethoxypterocarpan

Details

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Internal ID d7ed60fd-01e5-48c9-98ff-b83e45331a71
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Furanoisoflavonoids > Pterocarpans
IUPAC Name 3,9-dimethoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-4-ol
SMILES (Canonical) COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4O)OC
SMILES (Isomeric) COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4O)OC
InChI InChI=1S/C17H16O5/c1-19-9-3-4-10-12-8-21-17-11(16(12)22-14(10)7-9)5-6-13(20-2)15(17)18/h3-7,12,16,18H,8H2,1-2H3
InChI Key YHSXPHNOIMTWTH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H16O5
Molecular Weight 300.30 g/mol
Exact Mass 300.09977361 g/mol
Topological Polar Surface Area (TPSA) 57.20 Ų
XlogP 2.60
Atomic LogP (AlogP) 3.02
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Hydroxy-3,9-dimethoxypterocarpan

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9534 95.34%
Caco-2 + 0.7240 72.40%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.7347 73.47%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9297 92.97%
OATP1B3 inhibitior + 0.9747 97.47%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6246 62.46%
P-glycoprotein inhibitior - 0.7495 74.95%
P-glycoprotein substrate - 0.7178 71.78%
CYP3A4 substrate + 0.5651 56.51%
CYP2C9 substrate - 0.7778 77.78%
CYP2D6 substrate + 0.4927 49.27%
CYP3A4 inhibition + 0.6350 63.50%
CYP2C9 inhibition + 0.7306 73.06%
CYP2C19 inhibition + 0.9088 90.88%
CYP2D6 inhibition + 0.7136 71.36%
CYP1A2 inhibition + 0.8787 87.87%
CYP2C8 inhibition + 0.6809 68.09%
CYP inhibitory promiscuity + 0.8122 81.22%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.4731 47.31%
Eye corrosion - 0.9870 98.70%
Eye irritation - 0.5812 58.12%
Skin irritation - 0.7452 74.52%
Skin corrosion - 0.9679 96.79%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4913 49.13%
Micronuclear + 0.7600 76.00%
Hepatotoxicity - 0.8341 83.41%
skin sensitisation - 0.7748 77.48%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.7646 76.46%
Acute Oral Toxicity (c) III 0.5359 53.59%
Estrogen receptor binding + 0.6961 69.61%
Androgen receptor binding + 0.5966 59.66%
Thyroid receptor binding + 0.6654 66.54%
Glucocorticoid receptor binding + 0.6433 64.33%
Aromatase binding - 0.6461 64.61%
PPAR gamma + 0.5958 59.58%
Honey bee toxicity - 0.8753 87.53%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6151 61.51%
Fish aquatic toxicity + 0.7940 79.40%

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 97.22% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.76% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.69% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.15% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.83% 97.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.14% 94.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.95% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.63% 92.62%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.66% 99.15%
CHEMBL4208 P20618 Proteasome component C5 84.18% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.39% 99.17%
CHEMBL2535 P11166 Glucose transporter 82.83% 98.75%
CHEMBL240 Q12809 HERG 82.34% 89.76%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.63% 94.45%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 81.56% 100.00%
CHEMBL3231 Q13464 Rho-associated protein kinase 1 80.56% 95.55%

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.
Dalbergia odorifera
Melilotus albus
Psorothamnus spinosus

Cross-Links

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PubChem 4484393
LOTUS LTS0228602
wikiData Q105348603