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58471-30-0

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58471-30-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58471-30-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,4,7 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 58471-30:
(7*5)+(6*8)+(5*4)+(4*7)+(3*1)+(2*3)+(1*0)=140
140 % 10 = 0
So 58471-30-0 is a valid CAS Registry Number.

58471-30-0Relevant academic research and scientific papers

Novel HIV-1 Non-nucleoside Reverse Transcriptase Inhibitor Agents: Optimization of Diarylanilines with High Potency against Wild-Type and Rilpivirine-Resistant E138K Mutant Virus

Liu, Na,Wei, Lei,Huang, Li,Yu, Fei,Zheng, Weifan,Qin, Bingjie,Zhu, Dong-Qin,Morris-Natschke, Susan L.,Jiang, Shibo,Chen, Chin-Ho,Lee, Kuo-Hsiung,Xie, Lan

, p. 3689 - 3704 (2016)

Three series (6, 13, and 14) of new diarylaniline (DAAN) analogues were designed, synthesized, and evaluated for anti-HIV potency, especially against the E138K viral strain with a major mutation conferring resistance to the new-generation non-nucleoside reverse transcriptase inhibitor drug rilpivirine (1b). Promising new compounds were then assessed for physicochemical and associated pharmaceutical properties, including aqueous solubility, log P value, and metabolic stability, as well as predicted lipophilic parameters of ligand efficiency, ligand lipophilic efficiency, and ligand efficiency-dependent lipophilicity indices, which are associated with ADME property profiles. Compounds 6a, 14c, and 14d showed high potency against the 1b-resistant E138K mutated viral strain as well as good balance between anti-HIV-1 activity and desirable druglike properties. From the perspective of optimizing future NNRTI compounds as clinical trial candidates, computational modeling results provided valuable information about how the R1 group might provide greater efficacy against the E138K mutant.

HIV INHIBITING 1,2,4-TRIAZIN-6-ONE DERIVATIVES

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Page/Page column 62, (2008/06/13)

The present invention relates to HIV replication inhibitors of formula (I) a N-oxide, a pharmaceutically acceptable addition salt, a quaternary amine or a stereochemically isomeric form thereof, wherein ring A and ring B represent phenyl, pyridyl, pyridaz

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