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1H-Imidazole-5-carboxylic acid, 1-((1R)-1-phenylethyl)-, 1-(methoxycarbonyl)cyclopropyl ester , GABA-A receptor; anion channel agonist, CAS No.1446482-29-6, GABA-A receptor; anion channel agonist
Basic Description
Synonyms
ABP-700 | Q27283258 | 1H-Imidazole-5-carboxylic acid, 1-((1R)-1-phenylethyl)-, 1-(methoxycarbonyl)cyclopropyl ester | LZ0835OW2M | DTXSID801025960 | SCHEMBL15125263 | UNII-LZ0835OW2M | DB15411 | CPMM | CHEMBL4297255 | Cyclopropyl-methoxycarbonyl metomidat
Specifications & Purity
Moligand™, ≥98%
Storage Temp
Store at -20°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Grade
Moligand™
Action Type
AGONIST
Mechanism of action
GABA-A receptor; anion channel agonist
Product Description
ABP-700, an Etomidate analog and anesthetic, is a γ-aminobutyric acid type receptor agonist.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Azoles
Subclass
Imidazoles
Intermediate Tree Nodes
Substituted imidazoles
Direct Parent
Carbonylimidazoles
Alternative Parents
N-substituted imidazoles Cyclopropanecarboxylic acids and derivatives Benzene and substituted derivatives Methyl esters Heteroaromatic compounds Monocarboxylic acids and derivatives Azacyclic compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Imidazole-4-carbonyl group - Monocyclic benzene moiety - Cyclopropanecarboxylic acid or derivatives - N-substituted imidazole - Benzenoid - Heteroaromatic compound - Methyl ester - Carboxylic acid ester - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Azacycle - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Carbonyl group - Organonitrogen compound - Organooxygen compound - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as carbonylimidazoles. These are substituted imidazoles in which the imidazole ring bears a carbonyl group.
External Descriptors
Not available
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Names and Identifiers
IUPAC Name
(1-methoxycarbonylcyclopropyl) 3-[(1R)-1-phenylethyl]imidazole-4-carboxylate
INCHI
InChI=1S/C17H18N2O4/c1-12(13-6-4-3-5-7-13)19-11-18-10-14(19)15(20)23-17(8-9-17)16(21)22-2/h3-7,10-12H,8-9H2,1-2H3/t12-/m1/s1
InChIKey
DRAFVCKNYNQOKR-GFCCVEGCSA-N
Smiles
CC(C1=CC=CC=C1)N2C=NC=C2C(=O)OC3(CC3)C(=O)OC
Isomeric SMILES
C[C@H](C1=CC=CC=C1)N2C=NC=C2C(=O)OC3(CC3)C(=O)OC
PubChem CID
71481187
Molecular Weight
314.34
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
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