5-butyl-2-chloro-1H-imidazole-4-carbaldehyde

Details

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Internal ID a2bfd52c-fdf9-44ce-9bc3-04550bb23165
Taxonomy Organoheterocyclic compounds > Azoles > Imidazoles > Trisubstituted imidazoles > 2,4,5-trisubstituted imidazoles
IUPAC Name 5-butyl-2-chloro-1H-imidazole-4-carbaldehyde
SMILES (Canonical) CCCCC1=C(N=C(N1)Cl)C=O
SMILES (Isomeric) CCCCC1=C(N=C(N1)Cl)C=O
InChI InChI=1S/C8H11ClN2O/c1-2-3-4-6-7(5-12)11-8(9)10-6/h5H,2-4H2,1H3,(H,10,11)
InChI Key YRYJVCIVKUGXFG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C8H11ClN2O
Molecular Weight 186.64 g/mol
Exact Mass 186.0559907 g/mol
Topological Polar Surface Area (TPSA) 45.80 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.22
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-butyl-2-chloro-1H-imidazole-4-carbaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.7480 74.80%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.4673 46.73%
OATP2B1 inhibitior - 0.8548 85.48%
OATP1B1 inhibitior + 0.8893 88.93%
OATP1B3 inhibitior + 0.9401 94.01%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.8314 83.14%
P-glycoprotein inhibitior - 0.9763 97.63%
P-glycoprotein substrate - 0.8163 81.63%
CYP3A4 substrate - 0.5338 53.38%
CYP2C9 substrate - 0.5824 58.24%
CYP2D6 substrate - 0.8745 87.45%
CYP3A4 inhibition - 0.5560 55.60%
CYP2C9 inhibition - 0.6373 63.73%
CYP2C19 inhibition + 0.5677 56.77%
CYP2D6 inhibition - 0.8082 80.82%
CYP1A2 inhibition + 0.7762 77.62%
CYP2C8 inhibition - 0.7549 75.49%
CYP inhibitory promiscuity + 0.6261 62.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7500 75.00%
Carcinogenicity (trinary) Non-required 0.6598 65.98%
Eye corrosion - 0.9749 97.49%
Eye irritation - 0.6231 62.31%
Skin irritation - 0.7407 74.07%
Skin corrosion - 0.8278 82.78%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5124 51.24%
Micronuclear + 0.5700 57.00%
Hepatotoxicity + 0.6375 63.75%
skin sensitisation - 0.8015 80.15%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.8079 80.79%
Acute Oral Toxicity (c) III 0.4886 48.86%
Estrogen receptor binding - 0.7485 74.85%
Androgen receptor binding - 0.7858 78.58%
Thyroid receptor binding - 0.5467 54.67%
Glucocorticoid receptor binding - 0.5862 58.62%
Aromatase binding - 0.6707 67.07%
PPAR gamma - 0.7165 71.65%
Honey bee toxicity - 0.9713 97.13%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.6148 61.48%
Fish aquatic toxicity + 0.7636 76.36%

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 93.71% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.52% 94.45%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 89.68% 92.29%
CHEMBL3401 O75469 Pregnane X receptor 89.17% 94.73%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 87.56% 89.34%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 87.42% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.75% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 86.55% 89.63%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.04% 97.25%
CHEMBL255 P29275 Adenosine A2b receptor 85.98% 98.59%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 85.80% 85.94%
CHEMBL1781 P11387 DNA topoisomerase I 83.45% 97.00%
CHEMBL1952 P04818 Thymidylate synthase 82.51% 93.53%
CHEMBL1937 Q92769 Histone deacetylase 2 81.33% 94.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.21% 95.56%

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.
Jatropha curcas
Jatropha multifida

Cross-Links

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PubChem 11469508
LOTUS LTS0092716
wikiData Q105028250