153182-39-9 Usage
Description
(4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-1,3-bis(4-methoxybenzyl)-1,3-diazepan-2-one is a complex organic molecule characterized by its diazepan ring structure. It is highly functionalized, containing two benzyl groups, two hydroxyl groups, and two methoxybenzyl groups. The specific arrangement of these groups gives the compound its stereochemistry, with the R and S designations indicating the spatial orientation of its substituents.
Uses
Used in Medicinal Chemistry:
(4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-1,3-bis(4-methoxybenzyl)-1,3-diazepan-2-one is used as a potential candidate in medicinal chemistry for its diverse biological activities. (4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-1,3-bis(4-methoxybenzyl)-1,3-diazepan-2-one's unique structure and functional groups make it an interesting target for further synthetic studies and biological evaluations.
Used in Central Nervous System Depressants:
In the pharmaceutical industry, (4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-1,3-bis(4-methoxybenzyl)-1,3-diazepan-2-one is used as a central nervous system depressant due to its diazepan derivative nature, which is known to exhibit such activity.
Used in Antimicrobial Agents:
(4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-1,3-bis(4-methoxybenzyl)-1,3-diazepan-2-one is also used as an antimicrobial agent in the pharmaceutical industry, leveraging its potential biological activities against various microorganisms.
Used in Synthetic Studies:
In the field of chemical research and development, (4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-1,3-bis(4-methoxybenzyl)-1,3-diazepan-2-one is used as a subject for synthetic studies to explore its potential applications and to understand its chemical behavior and reactivity.
Used in Biological Evaluations:
(4R,5S,6S,7R)-4,7-dibenzyl-5,6-dihydroxy-1,3-bis(4-methoxybenzyl)-1,3-diazepan-2-one is utilized in biological evaluations to assess its efficacy and safety in various biological systems, which can help in determining its suitability for different applications in the medical and pharmaceutical fields.
Check Digit Verification of cas no
The CAS Registry Mumber 153182-39-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,1,8 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 153182-39:
(8*1)+(7*5)+(6*3)+(5*1)+(4*8)+(3*2)+(2*3)+(1*9)=119
119 % 10 = 9
So 153182-39-9 is a valid CAS Registry Number.
153182-39-9Relevant articles and documents
Cyclic HIV protease inhibitors: Synthesis, conformational analysis, P2/P2' structure-activity relationship, and molecular recognition of cyclic ureas
Lam, Patrick Y. S.,Ru, Yu,Jadhav, Prabhakar K.,Aldrich, Paul E.,DeLucca, George V.,Eyermann, Charles J.,Chang, Chong-Hwan,Emmett, George,Holler, Edward R.,Daneker, Wayne F.,Li, Liangzhu,Confalone, Pat N.,McHugh, Robert J.,Han, Qi,Li, Renhua,Markwalder, Jay A.,Seitz, Steven P.,Sharpe, Thomas R.,Bacheler, Lee T.,Rayner, Marlene M.,Klabe, Ronald M.,Shum, Linyee,Winslow, Dean L.,Kornhauser, David M.,Jackson, David A.,Erickson-Viitanen, Susan,Hodge, C. Nicholas
, p. 3514 - 3525 (2007/10/03)
High-resolution X-ray structures of the complexes of HIV-1 protease (HIV-1PR) with peptidomimetic inhibitors reveal the presence of a structural water molecule which is hydrogen bonded to both the mobile flaps of the enzyme and the two carbonyls flanking
