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"2H-1,4-Benzodiazepin-2-one, 1,3-dihydro-5-phenyl-, 4-oxide" is a complex organic compound belonging to the benzodiazepine class. It is characterized by a benzodiazepine core structure, which is a fused ring system consisting of a diazepine ring (a seven-membered ring with two nitrogen atoms) and a benzene ring. The compound features a 1,3-dihydro substitution, indicating the presence of two hydrogen atoms attached to carbon atoms 1 and 3, and a 5-phenyl group, which is a phenyl ring attached to the 5th carbon of the benzodiazepine core. The 4-oxide functional group suggests that an oxygen atom is attached to the 4th carbon, forming an oxide. This specific chemical structure is known for its potential applications in the pharmaceutical industry, particularly in the development of drugs targeting the central nervous system.

3967-09-7

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3967-09-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3967-09-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,6 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3967-09:
(6*3)+(5*9)+(4*6)+(3*7)+(2*0)+(1*9)=117
117 % 10 = 7
So 3967-09-7 is a valid CAS Registry Number.

3967-09-7Relevant academic research and scientific papers

1,4-Benzodiazepines as inhibitors of respiratory syncytial virus

Carter, Malcolm C.,Alber, Dagmar G.,Baxter, Robert C.,Bithell, Sian K.,Budworth, Jo,Chubb, Ann,Cockerill, G. Stuart,Dowdell, Verity C. L.,Henderson, Elisa A.,Keegan, Sally J.,Kelsey, Richard D.,Lockyer, Michael J.,Stables, Jeremy N.,Wilson, Lara J.,Powell, Kenneth L.

, p. 2311 - 2319 (2007/10/03)

Respiratory syncytial virus (RSV) is the cause of one-fifth of all lower respiratory tract infections worldwide and is increasingly being recognized as a serious threat to patient groups with poorly functioning immune systems. Our approach to finding a novel inhibitor of this virus was to screen a 20 000-member diverse library in a whole cell XTT assay. Parallel assays were carried out in the absence of virus in order to quantify any associated cell toxicity. This identified 100 compounds with IC50's less than 50 μM. A-33903 (18), a 1,4-benzodiazepine analogue, was chosen as the starting point for lead optimization. This molecule was moderately active and demonstrated good pharmacokinetic properties. The most potent compounds identified from this work were A-58568 (47), A-58569 (44), and A-62066 (46), where modifications to the aromatic substitution enhanced potency, and A-58175 (42), where the amide linker was modified.

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