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CGS 9895

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For Research Use Only | Not For Clinical Use
CATAP77779501
CAS77779-50-1
Structure
MDL NumberMFCD23704790
Molecular Weight291.30
InChI KeyKSKRJZMRHSNRBX-UHFFFAOYSA-N
Description≥98% (HPLC)
SolubilityDMSO: >2 mg/mL (warmed)
Assay≥98% (HPLC)
Colorlight yellow to light brown
Formpowder
Size5MG, 25MG
Storage Conditions2-8°C
1

Benzodiazepine Receptor Modulation of [35S]TBPS Binding to the Chloride Channel. Noncompetitive Inhibition of Classical Benzodiazepines and Competitive Inhibition of the Partial Agonist, CGS 9895, by CGS 8216

P Loo, A Braunwalder, P L Wood

Neuropharmacology. 1987 Jul;26(7A):775-8.

PMID: 2442653

1

Benzodiazepine-induced Hyperphagia: Stereospecificity and Antagonism by Pyrazoloquinolines, CGS 9895 and CGS 9896

S J Cooper, R E Yerbury

Psychopharmacology (Berl). 1986;89(4):462-6.

PMID: 3018825

1

Comparison of a New Class of Pyrrole Containing Benzodiazepine Ligands to the Pyrazoloquinolinones CGS 9896, 9895, and 8216

L T Schove, J J Perez, P A Maguire, G H Loew

Med Chem Res. 1994;4(5):307-14.

PMID: 11539383

1

Differential Diazepam-Antagonist Effects of the Benzodiazepine Receptor Ligand CGS 9895 in Rodents

N J Katzman, H E Shannon

J Pharmacol Exp Ther. 1985 Dec;235(3):589-95.

PMID: 3001268

1

Molecular Mode of Action of CGS 9895 at α1 β2 γ2 GABAA Receptors

Maria C Maldifassi, Roland Baur, Erwin Sigel

J Neurochem. 2016 Sep;138(5):722-30.

PMID: 27319298

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