Syntheses and antiproliferative evaluation of 6-thienyl, 6-polyphenyl aryl and 6-naphthyl derivatives of 2,4-diaminopyrido[3,2-d]pyramidine as non-classical antifolate targeting DHFR
暂无分享,去创建一个
Junyi Liu | Xia Li | Xiaowei Wang | Zhili Zhang | Chao Tian | Hao Li | Ningning Fan | Meng Wang | Liangmin Xue | Jiajia Yang
[1] M. Wang,et al. Synthesis and antiproliferative activity of a series of novel 6-substituted pyrido[3,2-d]pyrimidines as potential nonclassical lipophilic antifolates targeting dihydrofolate reductase. , 2017, European journal of medicinal chemistry.
[2] Hongliang Yang,et al. Synthesis, preliminary structure-activity relationships and biological evaluation of pyridinyl-4,5-2H-isoxazole derivatives as potent antitumor agents , 2017, Chemical Research in Chinese Universities.
[3] Junyi Liu,et al. A convenient one-pot process for the synthesis of 2,4-dihydroxy-6-phenylethylenyl-8-deazapteridine derivatives , 2016 .
[4] N. Priestley,et al. Charged Nonclassical Antifolates with Activity Against Gram-Positive and Gram-Negative Pathogens. , 2016, ACS medicinal chemistry letters.
[5] Ghada S. Hassan,et al. Synthesis, biological evaluation and molecular modeling study of 2-(1,3,4-thiadiazolyl-thio and 4-methyl-thiazolyl-thio)-quinazolin-4-ones as a new class of DHFR inhibitors. , 2014, Bioorganic & medicinal chemistry letters.
[6] C. Frei,et al. Trimethoprim-Sulfamethoxazole or Clindamycin for Community-Associated MRSA (CA-MRSA) Skin Infections , 2010, The Journal of the American Board of Family Medicine.
[7] Ebtehal S. Al-Abdullah,et al. Synthesis, Antimicrobial, and Anti-inflammatory Activities of Novel 5-(1-Adamantyl)-4-arylideneamino-3-mercapto-1,2,4-triazoles and Related Derivatives , 2010, Molecules.
[8] N. Priestley,et al. Probing the Active Site of Candida glabrata Dihydrofolate Reductase with High Resolution Crystal Structures and the Synthesis of New Inhibitors , 2009, Chemical biology & drug design.
[9] Erin S. Bolstad,et al. Structure-based approach to the development of potent and selective inhibitors of dihydrofolate reductase from cryptosporidium. , 2008, Journal of medicinal chemistry.
[10] Peter E Wright,et al. Structure, dynamics, and catalytic function of dihydrofolate reductase. , 2004, Annual review of biophysics and biomolecular structure.
[11] J. Kublin,et al. Sustained clinical efficacy of sulfadoxine-pyrimethamine for uncomplicated falciparum malaria in Malawi after 10 years as first line treatment: five year prospective study , 2004, BMJ : British Medical Journal.
[12] I. Goldman,et al. Resistance to antifolates , 2003, Oncogene.
[13] Norio Miyaura,et al. Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds , 1995 .
[14] R. Schilsky,et al. Antifolates: the next generation. , 1992, Seminars in oncology.
[15] E M Berman,et al. The renewed potential for folate antagonists in contemporary cancer chemotherapy. , 1991, Journal of medicinal chemistry.
[16] R. M. Hyde,et al. 2,4-Diamino-5-benzylpyrimidines as antibacterial agents. 7. Analysis of the effect of 3,5-dialkyl substituent size and shape on binding to four different dihydrofolate reductase enzymes. , 1987, Journal of medicinal chemistry.
[17] R. Jackson. Folate Antagonists as Therapeutic Agents, vol. 1: Biochemistry, Molecular Actions, and Synthetic Design; vol. 2: Pharmacology, Experimental and Clinical Therapeutics , 1985 .
[18] A. J. Salter,et al. Trimethoprim-sulfamethoxazole: an assessment of more than 12 years of use. , 1982, Reviews of infectious diseases.
[19] M. Ouellette,et al. New mechanisms of drug resistance in parasitic protozoa. , 1995, Annual review of microbiology.