Oxytrofalcatin C

Details

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Internal ID af3b40cc-6dc0-4abb-bbe8-941eab2dd645
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Benzoylindoles
IUPAC Name (4-hydroxyphenyl)-(3-methoxyindol-1-yl)methanone
SMILES (Canonical) COC1=CN(C2=CC=CC=C21)C(=O)C3=CC=C(C=C3)O
SMILES (Isomeric) COC1=CN(C2=CC=CC=C21)C(=O)C3=CC=C(C=C3)O
InChI InChI=1S/C16H13NO3/c1-20-15-10-17(14-5-3-2-4-13(14)15)16(19)11-6-8-12(18)9-7-11/h2-10,18H,1H3
InChI Key VPCGYNIHGIGTQN-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H13NO3
Molecular Weight 267.28 g/mol
Exact Mass 267.08954328 g/mol
Topological Polar Surface Area (TPSA) 51.50 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.04
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Oxytrofalcatin C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9917 99.17%
Caco-2 + 0.9007 90.07%
Blood Brain Barrier + 0.7067 70.67%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6542 65.42%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9081 90.81%
OATP1B3 inhibitior + 0.9530 95.30%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6833 68.33%
P-glycoprotein inhibitior - 0.7510 75.10%
P-glycoprotein substrate - 0.7557 75.57%
CYP3A4 substrate + 0.5519 55.19%
CYP2C9 substrate - 0.7947 79.47%
CYP2D6 substrate - 0.8113 81.13%
CYP3A4 inhibition - 0.5962 59.62%
CYP2C9 inhibition - 0.7392 73.92%
CYP2C19 inhibition - 0.5178 51.78%
CYP2D6 inhibition - 0.9174 91.74%
CYP1A2 inhibition + 0.8951 89.51%
CYP2C8 inhibition + 0.7925 79.25%
CYP inhibitory promiscuity + 0.5422 54.22%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Warning 0.4358 43.58%
Eye corrosion - 0.9897 98.97%
Eye irritation + 0.8119 81.19%
Skin irritation - 0.8299 82.99%
Skin corrosion - 0.9691 96.91%
Ames mutagenesis + 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6126 61.26%
Micronuclear + 0.7900 79.00%
Hepatotoxicity - 0.6341 63.41%
skin sensitisation - 0.9291 92.91%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.5962 59.62%
Nephrotoxicity + 0.5110 51.10%
Acute Oral Toxicity (c) III 0.6639 66.39%
Estrogen receptor binding + 0.9136 91.36%
Androgen receptor binding + 0.6958 69.58%
Thyroid receptor binding + 0.5700 57.00%
Glucocorticoid receptor binding + 0.8971 89.71%
Aromatase binding + 0.8714 87.14%
PPAR gamma + 0.6178 61.78%
Honey bee toxicity - 0.9392 93.92%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5949 59.49%
Fish aquatic toxicity - 0.5928 59.28%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.17% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 95.37% 93.99%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.69% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.66% 86.33%
CHEMBL1255126 O15151 Protein Mdm4 91.22% 90.20%
CHEMBL2535 P11166 Glucose transporter 90.81% 98.75%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 86.95% 93.10%
CHEMBL1899 P46098 Serotonin 3a (5-HT3a) receptor 86.67% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.24% 99.17%
CHEMBL2581 P07339 Cathepsin D 84.60% 98.95%
CHEMBL4208 P20618 Proteasome component C5 83.60% 90.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.77% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.68% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.21% 85.14%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 82.01% 89.62%

Cross-Links

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PubChem 46850032
NPASS NPC27225
LOTUS LTS0264894
wikiData Q105290641