2-(1-methyl-1H-imidazol-4-yl)acetic acid

Details

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Internal ID 9128ff95-fc67-4f02-801c-fd225340ed5c
Taxonomy Organoheterocyclic compounds > Azoles > Imidazoles > Substituted imidazoles > Imidazolyl carboxylic acids and derivatives
IUPAC Name 2-(1-methylimidazol-4-yl)acetic acid
SMILES (Canonical) CN1C=C(N=C1)CC(=O)O
SMILES (Isomeric) CN1C=C(N=C1)CC(=O)O
InChI InChI=1S/C6H8N2O2/c1-8-3-5(7-4-8)2-6(9)10/h3-4H,2H2,1H3,(H,9,10)
InChI Key ZHCKPJGJQOPTLB-UHFFFAOYSA-N
Popularity 140 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) 55.10 Ų
XlogP -0.50
Atomic LogP (AlogP) 0.05
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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Methylimidazoleacetic acid
1H-Imidazole-4-acetic acid, 1-methyl-
1-METHYLIMIDAZOLEACETIC ACID
EKP351892F
DTXSID30180884
RefChem:818627
DTXCID70103375
2-(1-methyl-1H-imidazol-4-yl)acetic acid
2-(1-methylimidazol-4-yl)acetic acid
(1-METHYL-1H-IMIDAZOL-4-YL)-ACETIC ACID
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-(1-methyl-1H-imidazol-4-yl)acetic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9781 97.81%
Caco-2 + 0.6267 62.67%
Blood Brain Barrier + 0.8317 83.17%
Human oral bioavailability + 0.8429 84.29%
Subcellular localzation Mitochondria 0.5702 57.02%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9578 95.78%
OATP1B3 inhibitior + 0.9457 94.57%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior - 0.9424 94.24%
P-glycoprotein inhibitior - 0.9855 98.55%
P-glycoprotein substrate - 0.9528 95.28%
CYP3A4 substrate - 0.7441 74.41%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9106 91.06%
CYP3A4 inhibition - 0.9411 94.11%
CYP2C9 inhibition - 0.9440 94.40%
CYP2C19 inhibition - 0.9678 96.78%
CYP2D6 inhibition - 0.9268 92.68%
CYP1A2 inhibition - 0.9634 96.34%
CYP2C8 inhibition - 0.9780 97.80%
CYP inhibitory promiscuity - 0.9795 97.95%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.4976 49.76%
Eye corrosion - 0.8870 88.70%
Eye irritation + 0.6891 68.91%
Skin irritation - 0.5953 59.53%
Skin corrosion - 0.7411 74.11%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7307 73.07%
Micronuclear + 0.6200 62.00%
Hepatotoxicity + 0.7625 76.25%
skin sensitisation - 0.9153 91.53%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.8270 82.70%
Acute Oral Toxicity (c) III 0.5555 55.55%
Estrogen receptor binding - 0.9368 93.68%
Androgen receptor binding - 0.8773 87.73%
Thyroid receptor binding - 0.7678 76.78%
Glucocorticoid receptor binding - 0.6837 68.37%
Aromatase binding - 0.8545 85.45%
PPAR gamma - 0.6431 64.31%
Honey bee toxicity - 0.9911 99.11%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.8300 83.00%
Fish aquatic toxicity - 0.9667 96.67%

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 97.63% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.22% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.97% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.93% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.43% 95.56%
CHEMBL4208 P20618 Proteasome component C5 84.86% 90.00%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 81.99% 81.11%

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 75810
LOTUS LTS0017801
wikiData Q27105479