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2-(4-chlorophenyl)-2,3-dihydro-1H-pyrrolo[3,4-b]quinolin-1-one, also known as JNJ-63533054, is a heterocyclic compound characterized by a pyrroloquinolinone core structure. This molecule features a 4-chlorophenyl group that contributes to its specific interactions with target enzymes, potentially enhancing its potency and selectivity. It has been the subject of research for its potential as a kinase inhibitor in cancer treatment, with ongoing studies to explore its pharmacological properties and therapeutic applications.

180161-75-5

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180161-75-5 Usage

Uses

Used in Pharmaceutical Industry:
2-(4-chlorophenyl)-2,3-dihydro-1H-pyrrolo[3,4-b]quinolin-1-one is used as a kinase inhibitor for its potential role in cancer treatment. The presence of the 4-chlorophenyl group allows for specific interactions with target enzymes, which may improve the compound's potency and selectivity in inhibiting the activity of enzymes that contribute to cancer cell growth and proliferation. Ongoing research aims to further understand its pharmacological properties and evaluate its potential therapeutic uses in oncology.

Check Digit Verification of cas no

The CAS Registry Mumber 180161-75-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,1,6 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 180161-75:
(8*1)+(7*8)+(6*0)+(5*1)+(4*6)+(3*1)+(2*7)+(1*5)=115
115 % 10 = 5
So 180161-75-5 is a valid CAS Registry Number.

180161-75-5Relevant academic research and scientific papers

Synthesis and structure-activity relationship studies in peripheral benzodiazepine receptor ligands related to alpidem

Cappelli, Andrea,Giuliani, Germano,Valenti, Salvatore,Anzini, Maurizio,Vomero, Salvatore,Giorgi, Gianluca,Sogliano, Cristiana,Maciocco, Elisabetta,Biggio, Giovanni,Concas, Alessandra

, p. 3428 - 3437 (2008/09/20)

The exploration of the structure-affinity relationships concerning a new class of peripheral benzodiazepine receptor (PBR) ligands related to alpidem has been pursued in order to evaluate the consistency of the structure-affinity relationships among diffe

Molecular basis of peripheral vs central benzodiazepine receptor selectivity in a new class of peripheral benzodiazepine receptor ligands related to alpidem

Anzini, Maurizio,Cappelli, Andrea,Vomero, Salvatore,Giorgi, Gianluca,Langer, Thierry,Bruni, Giancarlo,Romeo, Maria R.,Basile, Anthony S.

, p. 4275 - 4284 (2007/10/03)

Alpidem (1), the anxiolytic imidazopyridine, has nanomolar binding affinity for both the central benzodiazepine receptor (cbr) and the peripheral benzodiazepine receptor (pbr). A novel class of pbr ligands related to alpidem has been designed by comparing

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