Strepantibin C

Details

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Internal ID 17f4eb7b-e99b-49cb-a0c7-43e2d1f8ec77
Taxonomy Hydrocarbon derivatives > Tropones
IUPAC Name 2-acetyl-3-hydroxy-6-methoxy-4,7-diphenylcyclohepta-2,4,6-trien-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H18O4/c1-14(23)19-21(24)17(15-9-5-3-6-10-15)13-18(26-2)20(22(19)25)16-11-7-4-8-12-16/h3-13,24H,1-2H3
InChI Key CUOXCUWYCBQGCZ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H18O4
Molecular Weight 346.40 g/mol
Exact Mass 346.12050905 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 3.90
Atomic LogP (AlogP) 4.30
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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Strepantibin C
BDBM50505249

2D Structure

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2D Structure of Strepantibin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9921 99.21%
Caco-2 + 0.8162 81.62%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.9411 94.11%
OATP2B1 inhibitior - 0.8594 85.94%
OATP1B1 inhibitior + 0.9101 91.01%
OATP1B3 inhibitior + 0.9405 94.05%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.8311 83.11%
P-glycoprotein inhibitior - 0.4630 46.30%
P-glycoprotein substrate - 0.8569 85.69%
CYP3A4 substrate + 0.5051 50.51%
CYP2C9 substrate - 0.6065 60.65%
CYP2D6 substrate - 0.8220 82.20%
CYP3A4 inhibition - 0.8075 80.75%
CYP2C9 inhibition - 0.8510 85.10%
CYP2C19 inhibition + 0.6301 63.01%
CYP2D6 inhibition - 0.8758 87.58%
CYP1A2 inhibition + 0.6584 65.84%
CYP2C8 inhibition + 0.5889 58.89%
CYP inhibitory promiscuity - 0.6026 60.26%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6663 66.63%
Carcinogenicity (trinary) Non-required 0.6532 65.32%
Eye corrosion - 0.9797 97.97%
Eye irritation + 0.8472 84.72%
Skin irritation - 0.7418 74.18%
Skin corrosion - 0.9482 94.82%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5562 55.62%
Micronuclear + 0.6533 65.33%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.9671 96.71%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity + 0.6134 61.34%
Acute Oral Toxicity (c) III 0.5224 52.24%
Estrogen receptor binding + 0.8646 86.46%
Androgen receptor binding + 0.7971 79.71%
Thyroid receptor binding + 0.5250 52.50%
Glucocorticoid receptor binding + 0.6282 62.82%
Aromatase binding + 0.7800 78.00%
PPAR gamma + 0.7178 71.78%
Honey bee toxicity - 0.9360 93.60%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.6049 60.49%
Fish aquatic toxicity + 0.9867 98.67%

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 98.06% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.93% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.48% 86.33%
CHEMBL2002 P12268 Inosine-5'-monophosphate dehydrogenase 2 93.82% 98.21%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.25% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.57% 96.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 91.21% 95.50%
CHEMBL1255126 O15151 Protein Mdm4 87.72% 90.20%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.10% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.75% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.06% 99.15%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.59% 96.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.55% 85.14%
CHEMBL2095172 P14867 GABA-A receptor; alpha-1/beta-2/gamma-2 81.55% 92.67%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.93% 94.00%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 80.87% 95.64%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.57% 99.23%
CHEMBL340 P08684 Cytochrome P450 3A4 80.06% 91.19%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 145720922
LOTUS LTS0102764
wikiData Q103818062