Quantitative Structure-Activity Relationship Analysis of Some Thiourea Derivatives with Activities Against HIV-1 (IIIB)
Author:
Publisher
Wiley
Subject
Organic Chemistry,Computer Science Applications,Drug Discovery
Reference44 articles.
1. Comparative QSAR modeling of CCR5 receptor binding affinity of substituted 1-(3,3-diphenylpropyl)-piperidinyl amides and ureas
2. Classical QSAR Modeling of Anti-HIV 2,3-Diaryl-1,3-thiazolidin-4-ones
3. Synthesis and anti-HIV activity of 4-[(1,2-dihydro-2-oxo-3H-indol-3-ylidene) amino]-N(4,6-dimethyl-2-pyrimidinyl)-benzene sulfonamide and its derivatives
4. QSAR Study on Piperidinecarboxamides as Antiretroviral Agents: An Insight Into the Structural Basis for HIV Coreceptor Antagonist Activity
5. Classical QSAR Modeling of HIV-1 Reverse Transcriptase Inhibitor 2-Amino-6-arylsulfonylbenzonitriles and Congeners
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3. Oxyhalogen-sulfur chemistry: Kinetics and mechanism of oxidation of n-acetylthiourea by aqueous bromate and acidified bromate;South African Journal of Chemistry;2016
4. Application of Multivariate Linear and Nonlinear Calibration and Classification Methods in Drug Design;Combinatorial Chemistry & High Throughput Screening;2015-09-04
5. Multivariate statistical analysis methods in QSAR;RSC Advances;2015
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