1H-Imidazole-5-propanoic acid

Details

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Internal ID e247ecbd-fcd6-456a-94f8-02d35a9ba72f
Taxonomy Organoheterocyclic compounds > Azoles > Imidazoles > Substituted imidazoles > Imidazolyl carboxylic acids and derivatives
IUPAC Name 3-(1H-imidazol-5-yl)propanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H8N2O2/c9-6(10)2-1-5-3-7-4-8-5/h3-4H,1-2H2,(H,7,8)(H,9,10)
InChI Key ZCKYOWGFRHAZIQ-UHFFFAOYSA-N
Popularity 43 references in papers

Physical and Chemical Properties

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Molecular Formula C6H8N2O2
Molecular Weight 140.14 g/mol
Exact Mass 140.058577502 g/mol
Topological Polar Surface Area (TPSA) 66.00 Ų
XlogP -0.30
Atomic LogP (AlogP) 0.43
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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1H-Imidazole-4-propanoic acid
Imidazolylpropionic acid
5-Imidazolepropionic acid
NSC-66737
8B1241598D
DTXSID30148040
1H-Imidazole-5-propanoic acid
RefChem:908336
DTXCID9070531
214-045-0
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1H-Imidazole-5-propanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9956 99.56%
Caco-2 + 0.7430 74.30%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.6021 60.21%
OATP2B1 inhibitior - 0.8586 85.86%
OATP1B1 inhibitior + 0.8738 87.38%
OATP1B3 inhibitior + 0.9481 94.81%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9080 90.80%
P-glycoprotein inhibitior - 0.9935 99.35%
P-glycoprotein substrate - 0.9585 95.85%
CYP3A4 substrate - 0.7470 74.70%
CYP2C9 substrate - 0.7829 78.29%
CYP2D6 substrate - 0.8911 89.11%
CYP3A4 inhibition - 0.8185 81.85%
CYP2C9 inhibition - 0.9007 90.07%
CYP2C19 inhibition - 0.9537 95.37%
CYP2D6 inhibition - 0.9375 93.75%
CYP1A2 inhibition - 0.9560 95.60%
CYP2C8 inhibition - 0.8093 80.93%
CYP inhibitory promiscuity - 0.9675 96.75%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6540 65.40%
Eye corrosion - 0.9635 96.35%
Eye irritation + 0.8474 84.74%
Skin irritation - 0.5963 59.63%
Skin corrosion - 0.7102 71.02%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6342 63.42%
Micronuclear + 0.5700 57.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.9125 91.25%
Respiratory toxicity + 0.8333 83.33%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.8426 84.26%
Acute Oral Toxicity (c) III 0.6940 69.40%
Estrogen receptor binding - 0.8912 89.12%
Androgen receptor binding - 0.8990 89.90%
Thyroid receptor binding - 0.8377 83.77%
Glucocorticoid receptor binding - 0.7567 75.67%
Aromatase binding - 0.7649 76.49%
PPAR gamma - 0.6966 69.66%
Honey bee toxicity - 0.9664 96.64%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.8574 85.74%
Fish aquatic toxicity - 0.9708 97.08%

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 94.12% 96.09%
CHEMBL1255126 O15151 Protein Mdm4 87.91% 90.20%
CHEMBL2581 P07339 Cathepsin D 83.32% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.01% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 82.56% 89.63%
CHEMBL3976 Q9UHL4 Dipeptidyl peptidase II 82.56% 92.29%
CHEMBL1781 P11387 DNA topoisomerase I 81.98% 97.00%
CHEMBL4296013 Q5VWK5 Interleukin-23 receptor 81.75% 88.00%
CHEMBL255 P29275 Adenosine A2b receptor 81.27% 98.59%
CHEMBL1835 P24557 Thromboxane-A synthase 80.21% 98.00%

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 70630
LOTUS LTS0109595
wikiData Q27140293