共 279 条
- [21] Jamal F(2011)Structure-guided fragment-based in silico drug design of dengue protease inhibitors J Comput Aided Mol Des 167 28-930
- [22] Masoodi T(2016)The ways and means of fragment-based drug design Pharmacol Ther 38 117-10
- [23] Uddin S(2017)Combinatorial chemistry in drug discovery Curr Opin Chem Biol 103 893-215
- [24] Singh M(2003)The combinatorial synthesis of bicyclic privileged structures or privileged substructures Chem Rev 48 7-120
- [25] Haris M(2012)Heterocycles in drugs and drug discovery Chem Heterocycl Compd 8 205-2300
- [26] Macha M(2013)Heterocycles as nonclassical bioisosteres of α-amino acids ChemMedChem 176 93-667
- [27] Bhat AA(2015)Synthesis of fluorinated oxygen- and sulfur-containing heteroaromatics J Fluor Chem 45 2287-212
- [28] Yan X(2019)Synthesis, characterization, and antimicrobial activity of novel hydrazone-bearing tricyclic quinazolines Res Chem Intermed 193 656-50
- [29] Yang L(2018)Design, synthesis, and toward a side-ring optimization of tricyclic thieno[2,3-d]pyrimidin-4(3H)-ones and their effect on melanin synthesis in murine B16 cells Phosphorus Sulfur Silicon Relat Elem 2 207-6843
- [30] Feng G(2018)A convenient one-pot synthesis of 2,3-disubstituted thieno[2,3- d ]pyrimidin-4(3 H)-ones from 2 H-thieno[2,3- d ][1,3]oxazine-2,4(1 H)-diones, aromatic aldehydes and amines SynOpen 24 43-66