3,9,10-Trimethoxypterocarpan

Details

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Internal ID a0ac7a2b-cd94-4739-94f1-234905236eb0
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Furanoisoflavonoids > Pterocarpans
IUPAC Name (6aR,11aR)-3,9,10-trimethoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene
SMILES (Canonical) COC1=CC2=C(C=C1)C3C(CO2)C4=C(O3)C(=C(C=C4)OC)OC
SMILES (Isomeric) COC1=CC2=C(C=C1)[C@H]3[C@@H](CO2)C4=C(O3)C(=C(C=C4)OC)OC
InChI InChI=1S/C18H18O5/c1-19-10-4-5-12-15(8-10)22-9-13-11-6-7-14(20-2)18(21-3)17(11)23-16(12)13/h4-8,13,16H,9H2,1-3H3/t13-,16-/m0/s1
InChI Key RFFNFQZKHNKOPO-BBRMVZONSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H18O5
Molecular Weight 314.30 g/mol
Exact Mass 314.11542367 g/mol
Topological Polar Surface Area (TPSA) 46.20 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.32
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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3,9,10-TRIMETHOXYPTEROCARPAN
Q63399224

2D Structure

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2D Structure of 3,9,10-Trimethoxypterocarpan

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9863 98.63%
Caco-2 + 0.9253 92.53%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6732 67.32%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9472 94.72%
OATP1B3 inhibitior + 0.9805 98.05%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.5880 58.80%
P-glycoprotein inhibitior - 0.5227 52.27%
P-glycoprotein substrate - 0.7835 78.35%
CYP3A4 substrate + 0.5530 55.30%
CYP2C9 substrate - 0.8090 80.90%
CYP2D6 substrate + 0.5058 50.58%
CYP3A4 inhibition + 0.5707 57.07%
CYP2C9 inhibition - 0.5170 51.70%
CYP2C19 inhibition + 0.8891 88.91%
CYP2D6 inhibition + 0.5717 57.17%
CYP1A2 inhibition + 0.9444 94.44%
CYP2C8 inhibition + 0.5598 55.98%
CYP inhibitory promiscuity + 0.8654 86.54%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4706 47.06%
Eye corrosion - 0.9810 98.10%
Eye irritation - 0.8321 83.21%
Skin irritation - 0.7957 79.57%
Skin corrosion - 0.9784 97.84%
Ames mutagenesis + 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7622 76.22%
Micronuclear + 0.6700 67.00%
Hepatotoxicity - 0.7625 76.25%
skin sensitisation - 0.7276 72.76%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.6851 68.51%
Acute Oral Toxicity (c) III 0.4917 49.17%
Estrogen receptor binding + 0.7447 74.47%
Androgen receptor binding + 0.6381 63.81%
Thyroid receptor binding + 0.7888 78.88%
Glucocorticoid receptor binding + 0.6950 69.50%
Aromatase binding - 0.7144 71.44%
PPAR gamma - 0.6351 63.51%
Honey bee toxicity - 0.8479 84.79%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.7200 72.00%
Fish aquatic toxicity + 0.8444 84.44%

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
CHEMBL4040 P28482 MAP kinase ERK2 95.32% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.37% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.51% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.34% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.36% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.23% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.77% 95.89%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 87.47% 97.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.23% 94.00%
CHEMBL2535 P11166 Glucose transporter 86.59% 98.75%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 86.25% 92.62%
CHEMBL1907 P15144 Aminopeptidase N 85.36% 93.31%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 85.26% 94.80%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 84.73% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.01% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.30% 99.17%
CHEMBL4208 P20618 Proteasome component C5 81.18% 90.00%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 80.71% 94.03%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.67% 100.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.43% 93.99%
CHEMBL4349 Q02083 N-acylsphingosine-amidohydrolase 80.03% 93.00%

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.
Astragalus mongholicus

Cross-Links

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PubChem 15689655
NPASS NPC211242
LOTUS LTS0082226
wikiData Q63399224