4-hydroxy-3-oxo-N-phenylpentanamide

Details

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Internal ID 04c48baa-4927-4eaa-8c5f-272089babc6b
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 4-hydroxy-3-oxo-N-phenylpentanamide
SMILES (Canonical) CC(C(=O)CC(=O)NC1=CC=CC=C1)O
SMILES (Isomeric) CC(C(=O)CC(=O)NC1=CC=CC=C1)O
InChI InChI=1S/C11H13NO3/c1-8(13)10(14)7-11(15)12-9-5-3-2-4-6-9/h2-6,8,13H,7H2,1H3,(H,12,15)
InChI Key WJAJOBHLCGERKV-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H13NO3
Molecular Weight 207.23 g/mol
Exact Mass 207.08954328 g/mol
Topological Polar Surface Area (TPSA) 66.40 Ų
XlogP 1.30
Atomic LogP (AlogP) 0.97
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-hydroxy-3-oxo-N-phenylpentanamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9602 96.02%
Caco-2 + 0.6245 62.45%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.7480 74.80%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9325 93.25%
OATP1B3 inhibitior + 0.9495 94.95%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9030 90.30%
P-glycoprotein inhibitior - 0.9854 98.54%
P-glycoprotein substrate - 0.9388 93.88%
CYP3A4 substrate - 0.6886 68.86%
CYP2C9 substrate - 0.6147 61.47%
CYP2D6 substrate - 0.7846 78.46%
CYP3A4 inhibition - 0.9817 98.17%
CYP2C9 inhibition - 0.8753 87.53%
CYP2C19 inhibition - 0.8417 84.17%
CYP2D6 inhibition - 0.9634 96.34%
CYP1A2 inhibition - 0.7142 71.42%
CYP2C8 inhibition - 0.9606 96.06%
CYP inhibitory promiscuity - 0.9049 90.49%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7400 74.00%
Carcinogenicity (trinary) Non-required 0.7218 72.18%
Eye corrosion - 0.9885 98.85%
Eye irritation - 0.6518 65.18%
Skin irritation - 0.7953 79.53%
Skin corrosion - 0.9671 96.71%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8668 86.68%
Micronuclear + 0.7500 75.00%
Hepatotoxicity - 0.5662 56.62%
skin sensitisation - 0.9234 92.34%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity + 0.4501 45.01%
Acute Oral Toxicity (c) III 0.6284 62.84%
Estrogen receptor binding - 0.6228 62.28%
Androgen receptor binding + 0.5955 59.55%
Thyroid receptor binding - 0.7398 73.98%
Glucocorticoid receptor binding - 0.5783 57.83%
Aromatase binding - 0.6403 64.03%
PPAR gamma + 0.5945 59.45%
Honey bee toxicity - 0.9907 99.07%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity - 0.6116 61.16%

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
CHEMBL3401 O75469 Pregnane X receptor 89.86% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.44% 95.56%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 88.22% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 87.38% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.66% 91.11%
CHEMBL2782 P35610 Acyl coenzyme A:cholesterol acyltransferase 1 85.43% 91.65%
CHEMBL2581 P07339 Cathepsin D 84.87% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.61% 96.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.71% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.16% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.43% 96.00%
CHEMBL2535 P11166 Glucose transporter 80.08% 98.75%
CHEMBL4973 P43004 Excitatory amino acid transporter 2 80.06% 98.75%
CHEMBL3308 P55212 Caspase-6 80.02% 97.56%

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 163189970
LOTUS LTS0029240
wikiData Q105306642