1235975-95-7

Basic information

• Product Name: [5-(2,4-dimethoxy-benzyloxycarbamoyl)-pentyl]-carbamic acid 9H-fluoren-9-yl methyl ester
• Synonyms: [5-(2,4-dimethoxy-benzyloxycarbamoyl)-pentyl]-carbamic acid 9H-fluoren-9-yl methyl ester
• CAS NO: 1235975-95-7
• Molecular Weight: 518.61
• Mol File: 1235975-95-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: [5-(2,4-dimethoxy-benzyloxycarbamoyl)-pentyl]-carbamic acid 9H-fluoren-9-yl methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: [5-(2,4-dimethoxy-benzyloxycarbamoyl)-pentyl]-carbamic acid 9H-fluoren-9-yl methyl ester(1235975-95-7)
• EPA Substance Registry System: [5-(2,4-dimethoxy-benzyloxycarbamoyl)-pentyl]-carbamic acid 9H-fluoren-9-yl methyl ester(1235975-95-7)

Safety Data

• Hazardous Substances Data: 1235975-95-7(Hazardous Substances Data)

Upstream product

• 88574-06-5 6-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}hexanoic acid 
• 216067-66-2 O-(2,4-dimethoxy-benzyl)-hydroxylamine 

Relevant articles and documents

Acylurea connected straight chain hydroxamates as novel histone deacetylase inhibitors: Synthesis, SAR, and in vivo antitumor activity

Thirty-six novel acylurea connected straight chain hydroxamates were designed and synthesized. Structure-activity relationships (SAR) were established for the length of linear chain linker and substitutions on the benzoylurea group. Compounds 5g, 5i, 5n, and 19 showed 10-20-fold enhanced HDAC1 potency compared to SAHA. In general, the cellular potency pIC50 (COLO205) correlates with enzymatic potency pIC50 (HDAC1). Compound 5b (SB207), a structurally simple and close analogue to SAHA, is more potent against HDAC1 and HDAC6 compared to the latter. As a representative example of this series, good in vitro enzymatic and cellular potency plus an excellent pharmacokinetic profile has translated into better efficacy than SAHA in both prostate cancer (PC3) and colon cancer (HCT116) xenograft models.