143288-21-5

Basic information

• Product Name: Glycine, N-[4-(aminosulfonyl)benzoyl]-
• CAS NO: 143288-21-5
• Molecular Formula: C9H10N2O5S
• Molecular Weight: 258.255
• Mol File: 143288-21-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Glycine, N-[4-(aminosulfonyl)benzoyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Glycine, N-[4-(aminosulfonyl)benzoyl]-(143288-21-5)
• EPA Substance Registry System: Glycine, N-[4-(aminosulfonyl)benzoyl]-(143288-21-5)

Safety Data

• Hazardous Substances Data: 143288-21-5(Hazardous Substances Data)

Upstream product

• 56-40-6 glycine 
• 154715-61-4 4-uulfamoyl-benzoic acid 2,5-dioxo-pyrrolidin-1-yl ester 
• 138-41-0 4-(aminosulfonyl)-benzoic acid 

Downstream Products

• 176170-33-5 (4-Sulfamoyl-benzoylamino)-acetic acid 2,5-dioxo-pyrrolidin-1-yl ester 
• 176170-34-6 {2-[2-(4-Sulfamoyl-benzoylamino)-acetylamino]-acetylamino}-acetic acid 2,5-dioxo-pyrrolidin-1-yl ester 

Relevant articles and documents

A versatile polypeptide platform for integrated recognition and reporting: Affinity arrays for protein-ligand interaction analysis

A molecular platform for protein detection and quantification is reported in which recognition has been integrated with direct monitoring of target-protein binding. The platform is based on a versatile 42-residue helix-loop-helix polypeptide that dimerize

Benzenesulfonamide-peptide conjugates as probes for secondary binding sites near the active site of carbonic anhydrase

Libraries of N-(4-sulfamoylbenzoyl)oligoglycines terminated with different L-amino acids were screened to identify tight binding inhibitors of human carbonic anhydrase II. Inhibitors terminated with hydrophobic amino acids showed significant enhancements in binding compared to the corresponding glycine derivatives. No enhancements were observed due to polar interactions.