1007310-67-9

Basic information

• Product Name: C₂₇H₃₁FN₆O₄S
• Synonyms: C₂₇H₃₁FN₆O₄S
• CAS NO: 1007310-67-9
• Molecular Weight: 554.645
• Mol File: 1007310-67-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₂₇H₃₁FN₆O₄S(CAS DataBase Reference)
• NIST Chemistry Reference: C₂₇H₃₁FN₆O₄S(1007310-67-9)
• EPA Substance Registry System: C₂₇H₃₁FN₆O₄S(1007310-67-9)

Safety Data

• Hazardous Substances Data: 1007310-67-9(Hazardous Substances Data)

Upstream product

• 139756-22-2 5-(5-Chlorosulphonyl-2-ethoxyphenyl)-1-methyl-3-n-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one 
• 1011-15-0 1-(o-fluorophenyl)piperazine 

Relevant articles and documents

Synthesis and pharmacological evaluations of sildenafil analogues for treatment of erectile dysfunction

The 5-[2-ethoxy-5-(4-methylpiperazin-1-ylsulfonyl)phenyl]-1-methyl-3- propyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one, sildenafil, is a cGMP-specific phosphodiesterase-5 (PDE5) inhibitor used for penile erectile dysfunction. In the search for more potent and selective PDE5 inhibitors, new sildenafil analogues (6a-v), characterized by the presence on the sulfonyl group in the 5′ position of novel N-4-substituted piperazines or ethylenediamine moiety, were prepared by traditional and microwave-assisted synthesis and tested in rabbit isolated aorta and corpus cavernosum. Similarly to sildenafil, several analogues showed IC50 values in the nanomolar range. In the in vitro studies, all the tested compounds caused concentration-dependent relaxations in both rabbit isolated aorta and corpus cavernosum. All sildenafil analogues potentiated the nitric oxide-dependent vasodilation in endothelium-intact rabbit aorta. Compound 6f exhibited great pEC50 value in corpus cavernosum, and compounds 6r and 6u in isolated aorta were found as potent as sildenafil for inhibiting PDE5. Because several analogues were significantly more lipophilic than sildenafil, these compounds may offer a new lead for development of new sildenafil analogues.