All Stories

  1. Impact of Coumarin Hybrids upon Imperative Clinical Targets against Cancer
  2. Prospects of Treating Prostate Cancer through Apalutamide: A Mini-Review
  3. Recent Nanocarrier Approaches for Targeted Drug Delivery in Cancer Therapy
  4. Synthetic and Medicinal Perspective of Fused-Thiazoles as Anticancer Agents
  5. Copanlisib: Novel PI3K Inhibitor for the Treatment of Lymphoma
  6. Isolation of Sinapic Acid from Habenaria intermedia D. Don: A New Chemical Marker for the Identification of Adulteration and Substitution
  7. Genus Calotropis: A Hub of Medicinally Active Phytoconstituents
  8. Oxaliplatin for Colorectal Cancer Therapy: A Review
  9. Natural products and their derivatives as cyclooxygenase-2 inhibitors
  10. RP-HPLC and UV Method Development for Simultaneous Estimation of Doxofylline, Montelukast and Levocetirizine Dihydrochloride in Pharmaceutical Dosages Form
  11. First report of isolation of maleamic acid from natural source Polygonatum cirrhifolium—A potential chemical marker for identification
  12. ICP-MS: Analytical Method for Identification and Detection of Elemental Impurities
  13. Chemical and Medicinal Versatility of Substituted 1,4-Dihydropyridines
  14. Synthesis, characterization and pharmacological evaluation of (Z)-2-(5-(biphenyl-4-yl)-3-(1-(imino)ethyl)-2,3-dihydro-1,3,4-oxadiazol-2-yl)phenol derivatives as potent antimicrobial and antioxidant agents
  15. Chemistry and Bioactivities of Aristeromycins: An Overview
  16. Polysaccharides based nanomaterials for targeted anti-cancer drug delivery
  17. Impact of Artificial Neural Networks in QSAR and Computational Modeling
  18. Contributors
  19. Application of RP–HPLC method in dissolution testing and statistical evaluation by NASSAM for simultaneous estimation of tertiary combined dosages forms
  20. ChemInform Abstract: Recent Advances in the Chemistry and Biology of Benzothiazoles
  21. ChemInform Abstract: Diversity-Oriented Synthesis of Fused-Imidazole Derivatives via Groebke-Blackburn-Bienayme Reaction: A Review
  22. Recent Advances in the Chemistry and Biology of Benzothiazoles
  23. Diversity-oriented synthesis of fused-imidazole derivatives via Groebke–Blackburn–Bienayme reaction: a review
  24. A Novel Multiple Tyrosine-kinase Targeted Agent to Explore the Future Perspectives of Anti-Angiogenic Therapy for the Treatment of Multiple Solid Tumors: Cabozantinib
  25. A Novel Integrase Targeting Agent to Explore the Future Prospective of HIV Eradication: Dolutegravir
  26. A Comprehensive Review on Combretastatin Analogues as Tubulin Binding Agents
  27. Riociguat as a treatment regime for pulmonary arterial hypertension: a review
  28. The critical role of bisphosphonates to target bone cancer metastasis: an overview
  29. Chemometrics: A new scenario in herbal drug standardization
  30. Chemometrics assisted quantitative estimation of synthetic and marketed formulations
  31. Chemometrics tools used in analytical chemistry: An overview
  32. A Compendium of Techniques for the Analysis of Pharmaceutical Impurities
  33. Design, synthesis and ex-vivo release studies of colon-specific polyphosphazene–anticancer drug conjugates
  34. Design, synthesis and ex vivo evaluation of colon-specific azo based prodrugs of anticancer agents
  35. Design, Synthesis and In-Vitro Cytotoxicity of Novel Platinum (II) Complexes with Phthalate as the Leaving Group
  36. Synthesis and Characterization of 3β.-Substituted Amides of 17a-Aza-Dhomo- 4-androsten-17-one as Potent 5.α-Reductase Inhibitors and Antimicrobial Agents
  37. Simultaneous Estimation and Statistical Evaluation of Developed Validated Methods for Combined Drugs in Marketed Formulation
  38. 2′-Fluoro-6′-methylene-carbocyclic adenosine phosphoramidate (FMCAP) prodrug: In vitro anti-HBV activity against the lamivudine–entecavir resistant triple mutant and its mechanism of action
  39. Corrigendum to “Antiviral activity of novel 2′-fluoro-6′-methylene-carbocyclic adenosine against wild-type and drug-resistant hepatitis B virus mutants” [Bioorg. Med. Chem. Lett. 21 (2011) 6328–6331]
  40. ChemInform Abstract: Recent Advances in Carbocyclic Nucleosides: Synthesis and Biological Activity
  41. Antiviral activity of novel 2′-fluoro-6′-methylene-carbocyclic adenosine against wild-type and drug-resistant hepatitis B virus mutants
  42. ChemInform Abstract: Synthesis and Antiviral Activity of Cyclopropyl-Spirocarbocyclic Adenosine, (4R,5S,6R,7R)-4-(6-Amino-9H-purin-9-yl)-7-(hydroxymethyl)spiro [2.4]heptane-5,6-diol Against Hepatitis C Virus.
  43. Recent Advances in Carbocyclic Nucleosides: Synthesis and Biological Activity
  44. Synthesis and antiviral activity of cyclopropyl-spirocarbocyclic adenosine, (4R,5S,6R,7R)-4-(6-amino-9H-purin-9-yl)-7-(hydroxymethyl)spiro[2.4]heptane-5,6-diol against hepatitis C virus
  45. ChemInform Abstract: (-)-Carbodine: Enantiomeric Synthesis and in vitro Antiviral Activity Against Various Strains of Influenza Virus Including H5N1 (Avian Influenza) and Novel 2009 H1N1 (Swine Flu).
  46. Structure–activity relationships of carbocyclic 6-benzylthioinosine analogues as subversive substrates of Toxoplasma gondii adenosine kinase
  47. (−)-Carbodine: Enantiomeric synthesis and in vitro antiviral activity against various strains of influenza virus including H5N1 (avian influenza) and novel 2009 H1N1 (swine flu)
  48. Modified H5 promoter improves stability of insert genes while maintaining immunogenicity during extended passage of genetically engineered MVA vaccines
  49. ChemInform Abstract: Design and Synthesis of 2-(2,6-Dibromophenyl)-3-heteroaryl-1,3-thiazolidin-4-ones as anti-HIV Agents.
  50. Mamu-A⁎01/Kb transgenic and MHC Class I knockout mice as a tool for HIV vaccine development
  51. Design and synthesis of 2-(2,6-dibromophenyl)-3-heteroaryl-1,3-thiazolidin-4-ones as anti-HIV agents
  52. Non-nucleoside inhibitors of the hepatitis C virus NS5B RNA-dependant RNA polymerase: 2-Aryl-3-heteroaryl-1,3-thiazolidin-4-one derivatives
  53. 2-(2,6-Dihalo-phenyl)-3-heteroaryl-2-ylmethyl-1, 3-thiazolidin-4-ones: Anti-HIV agents
  54. Synthesis and Biological Evaluation of 2, 3-Diaryl substituted-1, 3-thiazolidin-4-ones as Anti-HIV Agents
  55. Synthesis and evaluation of 2-(2,6-dihalophenyl)-3-pyrimidinyl-1,3-thiazolidin-4-one analogues as anti-HIV-1 agents
  56. Molecular Surface Features in Modeling the HIV-1 RT Inhibitory Activity of 2-(2,6-Disubstituted phenyl)-3-(substituted pyrimidin-2-yl)-thiazolidin-4-ones
  57. Design, synthesis, and evaluation of 2-aryl-3-heteroaryl-1,3-thiazolidin-4-ones as anti-HIV agents
  58. 2-(2,6-Dichlorophenyl)-3-(quinolin-2-yl)thiazolidin-4-one
  59. Molecular docking studies on 4-thiazolidinones as HIV-1 RT inhibitors
  60. 2-(Aryl)-3-furan-2-ylmethyl-thiazolidin-4-ones as selective HIV-RT Inhibitors
  61. Synthesis and QSAR Studies on Thiazolidinones as Anti-HIV Agents
  62. CP-MLR/PLS Directed Structure-Activity Modeling of the HIV-1 RT Inhibitory Activity of 2,3-Diaryl-1,3-thiazolidin-4-ones
  63. An expeditious synthesis of thiazolidinones and tetathiazanones