864953-29-7 Usage
Uses
Used in Pharmaceutical Industry:
BMS 663068 is used as an antiviral agent for the treatment of HIV/AIDS. It works by inhibiting the HIV-1 envelope glycoprotein gp120, preventing the virus from entering human cells and thus reducing viral replication and spread.
Used in HIV/AIDS Research:
BMS 663068 is used as a research tool in the study of HIV/AIDS, particularly in understanding the mechanisms of viral entry and the development of resistance to current antiretroviral drugs. Its strong antiviral activity against a broad range of HIV-1 strains makes it a valuable asset in the search for new and more effective treatments.
Used in Clinical Trials:
BMS 663068 is being evaluated in clinical trials as a potential component of combination therapy for HIV infection. Its unique mechanism of action and efficacy against drug-resistant strains of HIV-1 make it a promising candidate for improving treatment outcomes and addressing the unmet needs of individuals with HIV/AIDS.
Used in Drug Development:
BMS 663068 represents a new class of HIV entry inhibitors, which has implications for the development of new antiviral drugs and therapeutic strategies. Its discovery and ongoing evaluation in clinical trials contribute to the advancement of HIV/AIDS treatment options and the ongoing fight against the virus.
Check Digit Verification of cas no
The CAS Registry Mumber 864953-29-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,4,9,5 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 864953-29:
(8*8)+(7*6)+(6*4)+(5*9)+(4*5)+(3*3)+(2*2)+(1*9)=217
217 % 10 = 7
So 864953-29-7 is a valid CAS Registry Number.
864953-29-7Relevant articles and documents
Prodrugs of piperazine and substituted piperidine antiviral agents
-
Page/Page column 46; 48; 54; 55, (2010/02/14)
This invention provides for prodrug Compounds I, pharmaceutical compositions thereof, and their use in treating HIV infection. wherein: X is C or N with the proviso that when X is N, R1 does not exist; W is C or N with the proviso that when W is N, R2 does not exist; V is C; E is hydrogen or a pharmaceutically acceptable salt thereof; and Y is selected from the group consisting of Also, this invention provides for intermediate Compounds II useful in making prodrug Compounds I. wherein: L and M are independently selected from the group consisting of C1-C6 alkyl, phenyl, benzyl, trialkylsilyl, -2,2,2-trichloroethoxy and 2-trimethylsilylethoxy.