(E)-N-isopentyl-1-phenylmethanimine

Details

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Internal ID 5c7ebea2-6176-4744-9a80-be1affc59e6a
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name N-(3-methylbutyl)-1-phenylmethanimine
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H17N/c1-11(2)8-9-13-10-12-6-4-3-5-7-12/h3-7,10-11H,8-9H2,1-2H3
InChI Key YYQKAYVYCNKNNT-UHFFFAOYSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C12H17N
Molecular Weight 175.27 g/mol
Exact Mass 175.136099547 g/mol
Topological Polar Surface Area (TPSA) 12.40 Ų
XlogP 3.20
Atomic LogP (AlogP) 3.15
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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SCHEMBL8415752
SCHEMBL8415756
CHEBI:220096
N-phenylmethylene-3-methylbutylamine
N-(3-methylbutyl)-1-phenylmethanimine
(e)-N-(3-methylbutyl)-1-phenylmethanimine

2D Structure

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2D Structure of (E)-N-isopentyl-1-phenylmethanimine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9886 98.86%
Caco-2 + 0.9693 96.93%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Lysosomes 0.5405 54.05%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9012 90.12%
OATP1B3 inhibitior + 0.9472 94.72%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior + 0.5250 52.50%
BSEP inhibitior - 0.9447 94.47%
P-glycoprotein inhibitior - 0.9797 97.97%
P-glycoprotein substrate - 0.8718 87.18%
CYP3A4 substrate - 0.7145 71.45%
CYP2C9 substrate - 0.7939 79.39%
CYP2D6 substrate - 0.7165 71.65%
CYP3A4 inhibition - 0.9364 93.64%
CYP2C9 inhibition - 0.9529 95.29%
CYP2C19 inhibition - 0.8707 87.07%
CYP2D6 inhibition + 0.5054 50.54%
CYP1A2 inhibition + 0.5634 56.34%
CYP2C8 inhibition - 0.9396 93.96%
CYP inhibitory promiscuity - 0.9223 92.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.7241 72.41%
Eye corrosion + 0.8733 87.33%
Eye irritation + 0.8627 86.27%
Skin irritation + 0.8160 81.60%
Skin corrosion + 0.9593 95.93%
Ames mutagenesis + 0.5446 54.46%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.8400 84.00%
Hepatotoxicity + 0.6213 62.13%
skin sensitisation + 0.7212 72.12%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.6222 62.22%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.5841 58.41%
Acute Oral Toxicity (c) III 0.5825 58.25%
Estrogen receptor binding - 0.8991 89.91%
Androgen receptor binding - 0.6442 64.42%
Thyroid receptor binding - 0.6266 62.66%
Glucocorticoid receptor binding - 0.8959 89.59%
Aromatase binding - 0.7479 74.79%
PPAR gamma - 0.7935 79.35%
Honey bee toxicity - 0.9357 93.57%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity + 0.8679 86.79%

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
CHEMBL230 P35354 Cyclooxygenase-2 95.30% 89.63%
CHEMBL2581 P07339 Cathepsin D 93.85% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.76% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.91% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.71% 95.56%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 89.46% 94.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.74% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.95% 96.09%
CHEMBL1907 P15144 Aminopeptidase N 85.44% 93.31%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 84.77% 94.08%
CHEMBL3401 O75469 Pregnane X receptor 84.17% 94.73%
CHEMBL240 Q12809 HERG 83.52% 89.76%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 82.64% 94.23%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.54% 93.56%

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 15061859
LOTUS LTS0249781
wikiData Q105368863