Bauhinoxepin G

Details

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Internal ID 2fa549d9-d397-480a-8248-266575807687
Taxonomy Organoheterocyclic compounds > Benzoxepines > Dibenzoxepines
IUPAC Name 1-methoxy-2-methyl-5,6-dihydrobenzo[b][1]benzoxepine-3,6-diol
SMILES (Canonical) CC1=C(C=C2CC(C3=CC=CC=C3OC2=C1OC)O)O
SMILES (Isomeric) CC1=C(C=C2CC(C3=CC=CC=C3OC2=C1OC)O)O
InChI InChI=1S/C16H16O4/c1-9-12(17)7-10-8-13(18)11-5-3-4-6-14(11)20-16(10)15(9)19-2/h3-7,13,17-18H,8H2,1-2H3
InChI Key SIOAIWJGWNUSDR-UHFFFAOYSA-N
Popularity 1 reference 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 2.60
Atomic LogP (AlogP) 3.09
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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CHEMBL227741

2D Structure

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2D Structure of Bauhinoxepin G

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9625 96.25%
Caco-2 + 0.5052 50.52%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.4979 49.79%
OATP2B1 inhibitior - 0.8559 85.59%
OATP1B1 inhibitior + 0.8972 89.72%
OATP1B3 inhibitior + 0.9668 96.68%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.6408 64.08%
P-glycoprotein inhibitior - 0.8935 89.35%
P-glycoprotein substrate - 0.8388 83.88%
CYP3A4 substrate + 0.5945 59.45%
CYP2C9 substrate - 0.7818 78.18%
CYP2D6 substrate + 0.5000 50.00%
CYP3A4 inhibition - 0.6914 69.14%
CYP2C9 inhibition - 0.7574 75.74%
CYP2C19 inhibition + 0.6311 63.11%
CYP2D6 inhibition - 0.5685 56.85%
CYP1A2 inhibition + 0.7333 73.33%
CYP2C8 inhibition + 0.6472 64.72%
CYP inhibitory promiscuity - 0.5374 53.74%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8708 87.08%
Carcinogenicity (trinary) Non-required 0.5219 52.19%
Eye corrosion - 0.9868 98.68%
Eye irritation - 0.6589 65.89%
Skin irritation - 0.6838 68.38%
Skin corrosion - 0.9380 93.80%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4829 48.29%
Micronuclear + 0.7159 71.59%
Hepatotoxicity - 0.5727 57.27%
skin sensitisation - 0.8501 85.01%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.9105 91.05%
Acute Oral Toxicity (c) III 0.4307 43.07%
Estrogen receptor binding + 0.5313 53.13%
Androgen receptor binding + 0.5715 57.15%
Thyroid receptor binding + 0.6483 64.83%
Glucocorticoid receptor binding + 0.7364 73.64%
Aromatase binding + 0.6398 63.98%
PPAR gamma + 0.6161 61.61%
Honey bee toxicity - 0.8803 88.03%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.7771 77.71%

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 99.26% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 94.45% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.48% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.73% 93.99%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.18% 96.09%
CHEMBL2581 P07339 Cathepsin D 88.94% 98.95%
CHEMBL2535 P11166 Glucose transporter 87.79% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.31% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.91% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.39% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.00% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.92% 99.23%
CHEMBL2056 P21728 Dopamine D1 receptor 82.58% 91.00%
CHEMBL2041 P07949 Tyrosine-protein kinase receptor RET 82.33% 91.79%
CHEMBL3401 O75469 Pregnane X receptor 81.71% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.63% 94.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.22% 93.56%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.00% 93.65%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.18% 92.62%

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.
Bauhinia purpurea

Cross-Links

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PubChem 16679965
LOTUS LTS0050547
wikiData Q105253889