ChemicalBook--->CAS DataBase List--->1216398-09-2

1216398-09-2

1216398-09-2 Structure

1216398-09-2 Structure
IdentificationBack Directory
[Name]

6-Amino-N-cyclohexyl-N,3-dimethyl-thiazolo[3,2-a]benzimidazole-2-carboxamide hydrochloride
[CAS]

1216398-09-2
[Synonyms]

3H]-YM 298198
YM-298198 hydrochloride >=98% (HPLC)
YM298198 hydrochloride, mGlu1 antagonist
[Molecular Formula]

C18H23ClN4OS
[MDL Number]

MFCD08703122
[MOL File]

1216398-09-2.mol
[Molecular Weight]

378.92
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[solubility ]

H2O: soluble5mg/mL, clear
[form ]

powder
[color ]

white to beige
[Water Solubility ]

Soluble to 100 mM in water
[InChI]

1S/C18H22N4OS.ClH/c1-11-16(17(23)21(2)13-6-4-3-5-7-13)24-18-20-14-9-8-12(19)10-15(14)22(11)18;/h8-10,13H,3-7,19H2,1-2H3;1H
[InChIKey]

WYTJVUVCSUWZTH-UHFFFAOYSA-N
[SMILES]

Cl.CN(C1CCCCC1)C(=O)c2sc3nc4ccc(N)cc4n3c2C
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22
[WGK Germany ]

3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

YM 298198 Hydrochloride is a noncompetitive, high affinity, and selective antagonist of metabotropic glutamate receptor type 1 (mGluR-1).
[Biological Activity]

YM-298198 is an orally activenoncompetitive mGlu1 receptor antagonist. The compound inhibits glutamate-induced inositol phosphate production in NIH3T3 cells (IC50 = 16 nM). YM-298198 displays analgesic and antinociceptive properties in vivo.
[in vivo]

YM-298198 hydrochloride (30 mg/kg; p.o.) shows a significant analgesic effect in streptozotocin-induced hyperalgesic mice[1].

Animal Model:Male ICR mice[1]
Dosage:30 mg/kg
Administration:Oral administration
Result:Prolonged nociceptive response latency in streptozotocin (200 mg/kg)-induced hyperalgesic mice.
[IC 50]

mGluR 1
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