CID 54686380

Details

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Internal ID f6cd79ad-7a27-4aab-a2a9-b06b3c824df4
Taxonomy Organoheterocyclic compounds > Quinolines and derivatives > Quinolones and derivatives > Hydroquinolones
IUPAC Name 4-hydroxy-3-[[3-(2-hydroxyethyl)-1H-indol-2-yl]-(4-hydroxyphenyl)methyl]-1-methylquinolin-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H24N2O4/c1-29-22-9-5-3-7-20(22)26(32)24(27(29)33)23(16-10-12-17(31)13-11-16)25-19(14-15-30)18-6-2-4-8-21(18)28-25/h2-13,23,28,30-32H,14-15H2,1H3
InChI Key VAIDRVODZNHJKE-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C27H24N2O4
Molecular Weight 440.50 g/mol
Exact Mass 440.17360725 g/mol
Topological Polar Surface Area (TPSA) 96.80 Ų
XlogP 3.60
Atomic LogP (AlogP) 4.15
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 54686380

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9404 94.04%
Caco-2 - 0.7054 70.54%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.7945 79.45%
OATP2B1 inhibitior - 0.5782 57.82%
OATP1B1 inhibitior - 0.3209 32.09%
OATP1B3 inhibitior + 0.9419 94.19%
MATE1 inhibitior - 0.6200 62.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.8695 86.95%
P-glycoprotein inhibitior + 0.6333 63.33%
P-glycoprotein substrate + 0.5690 56.90%
CYP3A4 substrate + 0.6522 65.22%
CYP2C9 substrate + 0.6095 60.95%
CYP2D6 substrate - 0.8407 84.07%
CYP3A4 inhibition - 0.7264 72.64%
CYP2C9 inhibition - 0.8786 87.86%
CYP2C19 inhibition - 0.8834 88.34%
CYP2D6 inhibition - 0.8084 80.84%
CYP1A2 inhibition - 0.5062 50.62%
CYP2C8 inhibition - 0.5817 58.17%
CYP inhibitory promiscuity - 0.6965 69.65%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5568 55.68%
Eye corrosion - 0.9923 99.23%
Eye irritation - 0.9321 93.21%
Skin irritation - 0.8426 84.26%
Skin corrosion - 0.9532 95.32%
Ames mutagenesis + 0.5263 52.63%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear + 0.8300 83.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.9222 92.22%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity - 0.7313 73.13%
Acute Oral Toxicity (c) III 0.6571 65.71%
Estrogen receptor binding + 0.7738 77.38%
Androgen receptor binding + 0.7924 79.24%
Thyroid receptor binding + 0.7555 75.55%
Glucocorticoid receptor binding + 0.8667 86.67%
Aromatase binding + 0.6554 65.54%
PPAR gamma + 0.8182 81.82%
Honey bee toxicity - 0.7764 77.64%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity - 0.8515 85.15%

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
CHEMBL2581 P07339 Cathepsin D 99.37% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.99% 95.56%
CHEMBL255 P29275 Adenosine A2b receptor 97.49% 98.59%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.62% 91.11%
CHEMBL5103 Q969S8 Histone deacetylase 10 94.61% 90.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.04% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.77% 89.00%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 93.72% 91.71%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.45% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.05% 85.14%
CHEMBL3192 Q9BY41 Histone deacetylase 8 90.30% 93.99%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 85.07% 94.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.88% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 84.36% 94.75%
CHEMBL3401 O75469 Pregnane X receptor 84.11% 94.73%
CHEMBL226 P30542 Adenosine A1 receptor 82.61% 95.93%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.23% 94.00%
CHEMBL1978 P11511 Cytochrome P450 19A1 81.77% 91.76%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.42% 94.45%
CHEMBL3310 Q96DB2 Histone deacetylase 11 81.24% 88.56%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.22% 86.92%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 80.64% 94.23%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.26% 99.23%

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 54686380
LOTUS LTS0178751
wikiData Q104199148