8-Hydroxy-3,4,9,10-tetramethoxypterocarpan

Details

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Internal ID a20b920d-0978-4de6-8d08-431a06fc3ef5
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Furanoisoflavonoids > Pterocarpans
IUPAC Name 3,4,9,10-tetramethoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-8-ol
SMILES (Canonical) COC1=C(C2=C(C=C1)C3C(CO2)C4=CC(=C(C(=C4O3)OC)OC)O)OC
SMILES (Isomeric) COC1=C(C2=C(C=C1)C3C(CO2)C4=CC(=C(C(=C4O3)OC)OC)O)OC
InChI InChI=1S/C19H20O7/c1-21-13-6-5-9-14-11(8-25-15(9)18(13)23-3)10-7-12(20)17(22-2)19(24-4)16(10)26-14/h5-7,11,14,20H,8H2,1-4H3
InChI Key AAAQSJHHXMDZCO-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H20O7
Molecular Weight 360.40 g/mol
Exact Mass 360.12090297 g/mol
Topological Polar Surface Area (TPSA) 75.60 Ų
XlogP 2.50
Atomic LogP (AlogP) 3.04
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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LMPK12070088

2D Structure

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2D Structure of 8-Hydroxy-3,4,9,10-tetramethoxypterocarpan

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9751 97.51%
Caco-2 + 0.8480 84.80%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7400 74.00%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9393 93.93%
OATP1B3 inhibitior + 0.9645 96.45%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5056 50.56%
P-glycoprotein inhibitior - 0.6807 68.07%
P-glycoprotein substrate - 0.7222 72.22%
CYP3A4 substrate + 0.5402 54.02%
CYP2C9 substrate - 0.7778 77.78%
CYP2D6 substrate + 0.4927 49.27%
CYP3A4 inhibition + 0.5059 50.59%
CYP2C9 inhibition - 0.5764 57.64%
CYP2C19 inhibition + 0.8118 81.18%
CYP2D6 inhibition + 0.5073 50.73%
CYP1A2 inhibition + 0.8819 88.19%
CYP2C8 inhibition + 0.6093 60.93%
CYP inhibitory promiscuity + 0.7209 72.09%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.4737 47.37%
Eye corrosion - 0.9874 98.74%
Eye irritation - 0.8142 81.42%
Skin irritation - 0.7853 78.53%
Skin corrosion - 0.9772 97.72%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5292 52.92%
Micronuclear + 0.7300 73.00%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation - 0.7751 77.51%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.8102 81.02%
Acute Oral Toxicity (c) III 0.4787 47.87%
Estrogen receptor binding + 0.7637 76.37%
Androgen receptor binding + 0.5730 57.30%
Thyroid receptor binding + 0.7845 78.45%
Glucocorticoid receptor binding + 0.7039 70.39%
Aromatase binding - 0.5939 59.39%
PPAR gamma + 0.5615 56.15%
Honey bee toxicity - 0.8924 89.24%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5751 57.51%
Fish aquatic toxicity + 0.7937 79.37%

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 96.93% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.05% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.00% 86.33%
CHEMBL2535 P11166 Glucose transporter 89.66% 98.75%
CHEMBL4040 P28482 MAP kinase ERK2 89.03% 83.82%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 87.54% 89.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.98% 95.89%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.87% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.37% 97.09%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 83.37% 100.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.31% 92.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.12% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.42% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.35% 99.17%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.67% 97.14%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.55% 99.15%

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.
Swartzia laevicarpa

Cross-Links

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PubChem 44257463
LOTUS LTS0045980
wikiData Q103815946