ChemicalBook--->CAS DataBase List--->126766-32-3

126766-32-3

126766-32-3 Structure

126766-32-3 Structure
IdentificationBack Directory
[Name]

GR 89696 FUMARATE
[CAS]

126766-32-3
[Synonyms]

GR 89696
GR 89696 FUMARATE
GR 89696 fumarate salt solid
Methyl 4-(2-(3,4-dichlorophenyl)acetyl)-3-(pyrrolidin-1-ylmethyl)piperazine-1-carboxylate fumarate
4-((3,4-Dichlorophenyl)acetyl)-3-(1-pyrrolidinylmethyl)-1-piperazinecarboxylicacidmethylesterfumarate
4-([3,4-DICHLOROPHENYL]ACETYL)-3-(1-PYRROLIDINYLMETHYL)-1-PIPERAZINECARBOXYLIC ACID METHYL ESTER FUMARATE
[Molecular Formula]

C23H29Cl2N3O7
[MDL Number]

MFCD00274044
[MOL File]

126766-32-3.mol
[Molecular Weight]

530.4
Chemical PropertiesBack Directory
[storage temp. ]

Store at RT
[solubility ]

ethanol: 4.0 mg/mL
[form ]

solid
[color ]

off-white
[InChIKey]

ABTNETSDXZBJTE-WLHGVMLRSA-N
[SMILES]

OC(=O)\C=C\C(O)=O.COC(=O)N1CCN(C(CN2CCCC2)C1)C(=O)Cc3ccc(Cl)c(Cl)c3
Safety DataBack Directory
[WGK Germany ]

3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

GR 89696 is a selective κ-opioid receptor agonist with anti-nociceptive and neuroprotective properties.
[Biological Activity]

Highly potent and selective κ -opioid agonist (IC 50 = 0.04 nM) that may be selective for the putative κ 2 receptor. Anti-nociceptive and neuroprotective in vivo .
[in vivo]

GR 89696 (intramuscular injection, 0.01-0.1 μg/kg) attenuates the scratching response induced by intrathecal morphine (0.03mg) in a dose-dependent manner without affecting the analgesic effect of morphine[1].
GR-896960(subcutaneous injection, 1 mg/kg) reduces cerebral artery infarct volume by 38% in a rat model of permanent focal ischemia[2].

[storage]

Store at +4°C
Spectrum DetailBack Directory
[Spectrum Detail]

GR 89696 FUMARATE(126766-32-3)1HNMR
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