Bauhiniastatin 4

Details

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Internal ID ab65e800-8167-4949-9bc1-df4d9b7d7c82
Taxonomy Organoheterocyclic compounds > Benzoxepines > Dibenzoxepines
IUPAC Name 1-methoxy-2-methylbenzo[b][1]benzoxepine-3,7-diol
SMILES (Canonical) CC1=C(C=C2C=CC3=C(C=CC=C3OC2=C1OC)O)O
SMILES (Isomeric) CC1=C(C=C2C=CC3=C(C=CC=C3OC2=C1OC)O)O
InChI InChI=1S/C16H14O4/c1-9-13(18)8-10-6-7-11-12(17)4-3-5-14(11)20-16(10)15(9)19-2/h3-8,17-18H,1-2H3
InChI Key IAKYVWSFYNMJDD-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H14O4
Molecular Weight 270.28 g/mol
Exact Mass 270.08920892 g/mol
Topological Polar Surface Area (TPSA) 58.90 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.69
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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CHEMBL480649
InChI=1/C16H14O4/c1-9-13(18)8-10-6-7-11-12(17)4-3-5-14(11)20-16(10)15(9)19-2/h3-8,17-18H,1-2H

2D Structure

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2D Structure of Bauhiniastatin 4

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9827 98.27%
Caco-2 + 0.7390 73.90%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.4838 48.38%
OATP2B1 inhibitior - 0.8494 84.94%
OATP1B1 inhibitior + 0.9185 91.85%
OATP1B3 inhibitior + 0.9749 97.49%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.5681 56.81%
P-glycoprotein inhibitior - 0.8057 80.57%
P-glycoprotein substrate - 0.8687 86.87%
CYP3A4 substrate + 0.5346 53.46%
CYP2C9 substrate + 0.6108 61.08%
CYP2D6 substrate - 0.6908 69.08%
CYP3A4 inhibition + 0.5000 50.00%
CYP2C9 inhibition - 0.6461 64.61%
CYP2C19 inhibition + 0.7908 79.08%
CYP2D6 inhibition - 0.6578 65.78%
CYP1A2 inhibition + 0.8229 82.29%
CYP2C8 inhibition + 0.6475 64.75%
CYP inhibitory promiscuity + 0.8358 83.58%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8951 89.51%
Carcinogenicity (trinary) Non-required 0.4784 47.84%
Eye corrosion - 0.9802 98.02%
Eye irritation + 0.9233 92.33%
Skin irritation - 0.6436 64.36%
Skin corrosion - 0.9336 93.36%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6420 64.20%
Micronuclear + 0.8200 82.00%
Hepatotoxicity - 0.5926 59.26%
skin sensitisation - 0.7500 75.00%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.8254 82.54%
Acute Oral Toxicity (c) II 0.4862 48.62%
Estrogen receptor binding + 0.9212 92.12%
Androgen receptor binding + 0.7947 79.47%
Thyroid receptor binding + 0.8314 83.14%
Glucocorticoid receptor binding + 0.8923 89.23%
Aromatase binding + 0.8140 81.40%
PPAR gamma + 0.7304 73.04%
Honey bee toxicity - 0.9493 94.93%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9629 96.29%

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 97.18% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 97.04% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.18% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 90.74% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.40% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.18% 94.45%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.18% 99.15%
CHEMBL2535 P11166 Glucose transporter 86.99% 98.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.90% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.41% 86.33%
CHEMBL2581 P07339 Cathepsin D 85.18% 98.95%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 84.10% 93.65%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.23% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.88% 99.23%

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.
Alnus cordata
Aloe deltoideodonta
Bauhinia purpurea
Crinum latifolium
Hemionitis aschenborniana
Leitneria floridana
Thermopsis mollis

Cross-Links

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PubChem 11666202
NPASS NPC229231
LOTUS LTS0125197
wikiData Q105036178