p-nitrophenacyl bromide

p-nitrophenacyl bromide Structure
p-nitrophenacyl bromide structure
Common Name p-nitrophenacyl bromide
CAS Number 99-81-0 Molecular Weight 244.042
Density 1.7±0.1 g/cm3 Boiling Point 325.2±17.0 °C at 760 mmHg
Molecular Formula C8H6BrNO3 Melting Point 94-99 °C(lit.)
MSDS Chinese USA Flash Point 150.5±20.9 °C
Symbol GHS05
GHS05
Signal Word Danger

QSAR study and conformational analysis of 4-arylthiazolylhydrazones derived from 1-indanones with anti-Trypanosoma cruzi activity.

Eur. J. Pharm. Sci. 78 , 190-7, (2015)

A set of 4-arylthiazolylhydrazones derived from 1-indanones (TZHs) previously synthesized and assayed against Trypanosoma cruzi, the causative agent of Chagas disease, were explored in terms of conformational analysis. We found that TZHs can adopt four minimu...

Active site of bee venom phospholipase A2: the role of histidine-34, aspartate-64 and tyrosine-87.

Biochemistry 35(14) , 4591-601, (1996)

In bee venom phospholipase A2, histidine-34 probably functions as a Brønsted base to deprotonate the attacking water. Aspartate-64 and tyrosine-87 form a hydrogen bonding network with histidine-34. We have prepared mutants at these positions and studied their...

Chemical modification and inactivation of rat liver microsomal cytochrome P-450c by 2-bromo-4'-nitroacetophenone.

J. Biol. Chem. 261(25) , 11478-86, (1986)

The alkylating agent 2-bromo-4'-nitroacetophenone (BrNAP) binds covalently to each of 10 isozymes of purified rat liver microsomal cytochrome P-450 (P-450a-P-450j) but substantially inhibits the catalytic activity of only cytochrome P-450c. Regardless of pH, ...

[Amphoteric ion intermediates in the pyrazine series. II. The action of p-nitrophenacyl bromide on pyrazine].

Rev. Med. Chir. Soc. Med. Nat. Iasi. 94(1) , 157-60, (1990)

Continuing to present the results of the investigations carried out on the amphoteric ions intermediates of the N-heteroatomic system with 2 natrium atoms in positions 1, 4, new pyrasine derivatives synthetized with p-nitro-phenacyl bromide are described. The...

Use of an imperfect neutral diluent and outer vesicle layer scooting mode hydrolysis to analyze the interfacial kinetics, inhibition, and substrate preferences of bee venom phospholipase A2.

Biochemistry 36(13) , 3870-81, (1997)

Interfacial catalytic constants for bee venom phospholipase A2 (bvPLA2) have been obtained for its action on vesicles of the anionic phospholipid 1,2-dimyristoylphosphatidylmethanol (DMPM) in the highly processive scooting mode. Spectroscopic measurements whi...

Mechanism of inactivation of rat liver microsomal cytochrome P-450c by 2-bromo-4'-nitroacetophenone.

J. Biol. Chem. 261(25) , 11487-95, (1986)

The mechanism by which 2-bromo-4'-nitroacetophenone (BrNAP) inactivates cytochrome P-450c, which involves alkylation primarily at Cys-292, is shown in the present study to involve an uncoupling of NADPH utilization and oxygen consumption from product formatio...