CAS 402849-27-8
:4-Chlorobenzoic acid 2-(4-chlorobenzoyl)-1-(4-methoxyphenyl)hydrazide
- Benzoic acid, 4-chloro-, 2-(4-chlorobenzoyl)-1-(4-methoxyphenyl)hydrazide
- 4-Chlorobenzoic acid 2-(4-chlorobenzoyl)-1-(4-methoxyphenyl)hydrazide
- 4-Chloro-N''-(4-chlorobenzoyl)-N-(4-methoxyphenyl)benzohydrazide
- Indomethacin (Indometacin) EP Impurity F
- Indometacin Impurity 14
- Indometacin EP Impurity F
- Indometacin 1,2-Propylene Glycol Esters (Mixture of Isomers)
- Indomethacin impurity 5/Indomethacin EP Impurity F/2-(4-Chlorobenzoyl)-1-(4-methoxyphenyl)hydrazide-4-chloro-benzoic acid
- Indomethacin EP Impurity F
- Indomethacin Impurity 6(Indomethacin EP Impurity F)
- Indapamide EP Impurity F
- Indometacin (Indomethacin) EP Impurity F
- 4-Chloro-2-(4-chlorobenzoyl)-1-(4-Methoxyphenyl)hydrazide Benzoic Acid
- See more synonyms
Indomethacin Hydrazine Analog (1-(4-Chlorobenzoyl)-1-(4-methoxyphenyl)-2-(4-chlorobenzoyl)hydrazide)
CAS:Aromatic organic derivatives of hydrazine or of hydroxylamineFormula:C21H16Cl2N2O3Color and Shape:White PowderMolecular weight:414.0538Indomethacin (Indometacin) EP Impurity F
CAS:Formula:C21H16Cl2N2O3Color and Shape:White To Off-White SolidMolecular weight:415.274-Chloro-2-(4-chlorobenzoyl)-1-(4-methoxyphenyl)hydrazide Benzoic Acid
CAS:Applications An impurity of the anti-inflammatory drug indomnethacin (I641000). Indomethacin inhibits cyclooxygenase (IC50=0.1uM) selectively over liposygenases (IC50=100uM for 5-,12- and 15-LO). A clinically useful NAISD.
References Salari, H., et al.: Prostagland. Leukotrienes Med., 13, 53 (1984), Lehmann, J.M., et al.: J. Biol. Chem., 272, 3406 (1997)Formula:C21H16Cl2N2O3Color and Shape:NeatMolecular weight:415.274-Chloro-2-(4-chlorobenzoyl)-1-(4-methoxyphenyl)hydrazide benzoic acid
CAS:4-Chloro-2-(4-chlorobenzoyl)-1-(4-methoxyphenyl)hydrazide benzoic acid is an activator. It has a CAS number of 402849-27-8 and is available for sale as a research tool. 4-Chloro-2-(4-chlorobenzoyl)-1-(4-methoxyphenyl)hydrazide benzoic acid activates the ligand receptor system by binding to specific receptors, thereby triggering cellular responses such as changes in ion channel activity and protein synthesis. 4CBAB is used in pharmacological research to study the function of ion channels, antibodies, peptides and other cell biology molecules. It can also be used to study protein interactions.
Formula:C21H16Cl2N2O3Purity:Min. 95%Molecular weight:415.3 g/mol





