1. lin, s.#; du, t.#; zhang, j.#; wu, d.; tian, h.; zhang, k.; jiang, l.; lu, d.; sheng, l.; li, y.; ji, m.*; chen, x.*; xu, h.* optimization of benzamide derivatives as potent and orally active tubulin inhibitors targeting the colchicine binding site. j. med. chem. 2022, 65, 16372–16391. (# co-first authors;封面文章)
2. zhang, j.#; jiang, h.#; lin, s.#; wu, d.; tian, h.; jiang, l.; cui, y.; jin, j.*; chen, x.*; xu, h.* design and optimization of thienopyrimidine derivatives as potent and selective pi3kδ inhibitors for the treatment of b-cell malignancies. j. med. chem. 2022, 65, 8011–8028. (# co-first authors;封面文章)
3. lin, s.#; jin, j.#; liu, y.#; tian, h.; zhang, y.; fu, r.; zhang, j.; wang, m.; du, t.; ji, m.; wu, d.; zhang, k.; sheng, l.; li, y.; chen, x.*; xu, h.* discovery of 4-methylquinazoline based pi3k inhibitors for the potential treatment of idiopathic pulmonary fibrosis. j. med. chem. 2019, 62, 8873-8879. (# co-first authors;封面文章)
4. lin, s.#; wang, c.#; ji, m.; wu, d.; lv, y.; zhang, k.; dong, y.; jin, j.; chen, j.; zhang, j.; sheng, l.; li, y.; chen, x.*; xu, h.* discovery and optimization of 2-amino-4-methylquinazoline derivatives as highly potent phosphatidylinositol 3-kinase inhibitors for cancer treatment. j. med. chem. 2018, 61, 6087–6109. (# co-first authors)
5. lin, s.#; wang, c.#; ji, m.; wu, d.; lv, y.; sheng, l.; han, f.; dong, y.; zhang, k.; yang, y.; li, y,; chen, x.*; xu, h.* discovery of new thienopyrimidine derivatives as potent and orally efficacious phosphoinositide 3-kinase inhibitors. bioorg. med. chem. 2018, 26, 637–646. (# co-first authors)
6. lin, s.#; li, y.#; zheng, y.; luo, l.; sun, q.*; ge, z.; cheng, t.; li, r.* design, synthesis and biological evaluation of quinazoline–phosphoramidate mustard conjugates as anticancer drugs. eur. j. med. chem. 2017, 127, 442-458 (# co-first authors)
7. han, f.#; lin, s.#; liu, p.; liu, x.; tao, j.; deng, x.; yi, c.; xu, h.* discovery of a novel series of thienopyrimidine as highly potent and selective pi3k inhibitors. acs med. chem. lett., 2015, 6, 434-438. (# co-first authors)
8. lin, s.#; han, f.#; liu, p.; tao, j.; zhong, x.; liu, x.; yi, c.*; xu, h.* identification of novel 7-amino-5-methyl-1,6-naphthyridin-2(1h)-one derivatives as potent pi3k/mtor dual inhibitors. bioorg. med. chem. lett. 2014, 24, 790-793. (# co-first authors)
9. han, f.#; lin, s.#; liu, p.; tao, j.; yi, c.*; xu, h.* synthesis and structure–activity relationships of pi3k/mtor dual inhibitors from a series of 2-amino-4-methylpyrido[2,3-d]pyrimidine derivatives. bioorg. med. chem. lett. 2014, 24, 4538-4541. (# co-first authors)
10. lin, s.; wang, n.; zhao, s.; sun, q.; zhang, w.; ye, j.; cheng, t.; li, r.* synthesis and analgesic evaluation of a series of proline-typed spiro cyclic quaternary ammoniums. med. chem. res. 2014, 23, 862-869.