3-Hydroxymethyl-4-(3-methyl-3h-imidazol-4-yl)-1-phenyl-butan-1-one

Details

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Internal ID bca40a94-41d5-4519-99b3-3ca6ed47b055
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Phenylketones > Alkyl-phenylketones
IUPAC Name 3-(hydroxymethyl)-4-(3-methylimidazol-4-yl)-1-phenylbutan-1-one
SMILES (Canonical) CN1C=NC=C1CC(CC(=O)C2=CC=CC=C2)CO
SMILES (Isomeric) CN1C=NC=C1CC(CC(=O)C2=CC=CC=C2)CO
InChI InChI=1S/C15H18N2O2/c1-17-11-16-9-14(17)7-12(10-18)8-15(19)13-5-3-2-4-6-13/h2-6,9,11-12,18H,7-8,10H2,1H3
InChI Key ZJEJAGFGZYSLRB-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H18N2O2
Molecular Weight 258.32 g/mol
Exact Mass 258.136827821 g/mol
Topological Polar Surface Area (TPSA) 55.10 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.84
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Hydroxymethyl-4-(3-methyl-3h-imidazol-4-yl)-1-phenyl-butan-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9943 99.43%
Caco-2 + 0.9042 90.42%
Blood Brain Barrier + 0.7567 75.67%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.6753 67.53%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9313 93.13%
OATP1B3 inhibitior + 0.9461 94.61%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.6184 61.84%
P-glycoprotein inhibitior - 0.8921 89.21%
P-glycoprotein substrate - 0.8135 81.35%
CYP3A4 substrate - 0.6338 63.38%
CYP2C9 substrate - 0.7683 76.83%
CYP2D6 substrate - 0.8458 84.58%
CYP3A4 inhibition - 0.6648 66.48%
CYP2C9 inhibition - 0.9004 90.04%
CYP2C19 inhibition - 0.8168 81.68%
CYP2D6 inhibition - 0.8656 86.56%
CYP1A2 inhibition - 0.7271 72.71%
CYP2C8 inhibition - 0.8534 85.34%
CYP inhibitory promiscuity - 0.8382 83.82%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.6010 60.10%
Eye corrosion - 0.9836 98.36%
Eye irritation - 0.8417 84.17%
Skin irritation - 0.6855 68.55%
Skin corrosion - 0.8969 89.69%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5761 57.61%
Micronuclear + 0.7300 73.00%
Hepatotoxicity - 0.5393 53.93%
skin sensitisation - 0.8927 89.27%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity - 0.6007 60.07%
Acute Oral Toxicity (c) III 0.6097 60.97%
Estrogen receptor binding - 0.5704 57.04%
Androgen receptor binding - 0.7308 73.08%
Thyroid receptor binding - 0.6389 63.89%
Glucocorticoid receptor binding - 0.5243 52.43%
Aromatase binding + 0.7419 74.19%
PPAR gamma - 0.6533 65.33%
Honey bee toxicity - 0.9530 95.30%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity - 0.8684 86.84%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.77% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.09% 86.33%
CHEMBL2581 P07339 Cathepsin D 93.63% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 92.44% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.71% 95.56%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 86.11% 81.11%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 84.53% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.78% 96.00%

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.
Pilocarpus microphyllus

Cross-Links

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PubChem 101452193
LOTUS LTS0165391
wikiData Q105377841