王召印

王召印,男,中國科學院大學專職教師。

基本介紹

  • 中文名:王召印
  • 畢業院校:美國耶魯大學
  • 學位/學歷:博士
  • 職業:教師
人物經歷,科研成果,專利成果,發表論文,

人物經歷

2012-04~現在, 南京奧昭生物科技有限公司, 創始人,總裁
2010-11~現在, 加拿大貝達藥業公司, 創始人,總裁
2008-07~2010-06,默克加拿大分部, 高級科學家
2002-07~2008-06,默克加拿大分部, 部門主任
1988-08~2002-06,默克加拿大分部, 高級研究化學家
1982-09~1988-08,美國耶魯大學, 博士
1978-09~1982-06,蘭州大學, 學士

科研成果

專利成果

( 1 ) 一種含氮烷基化和芳基化亞碸亞胺的吲哚胺-2,3-雙加氧酶抑制劑, 2017, 第 1 作者, 專利號: PCT/CN2017/076160
( 2 ) 一種作為吲哚胺-2,3-雙加氧酶抑制劑的氨基磺酸脂及其製備方法和用途, 2017, 第 1 作者, 專利號: PCT/CN2017/072730
( 3 ) 一種吲哚胺-2,3-雙加氧酶抑制劑及其製備方法, 2014, 第 1 作者, 專利號: PCT/CN2015/089666
( 4 ) Cyclic molecules as bruton’s tyrosine kinase inhibitors, 2013, 第 1 作者, 專利號: WO2013113097
( 5 ) Novel heterocyclic compounds as HDAC6 inhibitors, 2013, 第 1 作者, 專利號: WO2013078544
( 6 ) Heterocyclic molecules as apoptosis inducers, 2013, 第 1 作者, 專利號: WO2013053045
( 7 ) Spirocyclic molecules as protein kinase inhibitors, 2013, 第 1 作者, 專利號: WO2013013308
( 8 ) Novel ureas for the treatment and prevention of cancer, 2012, 第 1 作者, 專利號: WO2012094451
( 9 ) Indole derivatives as CRTH2 receptor antagonists, 2009, 第 1 作者, 專利號: US7696222
( 10 ) Indole amide derivatives as EP4 receptor antagonists, 2009, 第 3 作者, 專利號: US7968578

發表論文

(1) Discovery of MK-7246, a selective CRTH2 antagonist for the treatment of respiratory diseases, Bioorg. Med. Chem. Lett., 2011, 通訊作者
(2) The identification of substituted benzothiophene derivatives as PGE2 subtype 4 receptor antagonists: From acid to non-acid, Bioorg. Med. Chem. Lett., 2011, 通訊作者
(3) An activity-based probe for high-throughput measurements of triacylglycerol lipases, Anal. Biochem. , 2011, 第 3 作者
(4) Identification of prostaglandin D2 receptor antagonists based on tetrahydropyridoneindole scaffold, Bioorg. Med. Chem. Lett., 2008, 第 3 作者
(5) Practical [14C]-Synthesis of molecules containing an acetic acid moiety: Application to [14C]-labeled DP1 Antagonists., Journal of Labelled Compounds and Radiopharmaceuticals, 2007, 第 2 作者
(6) The development of potent non-peptidic PTP-1B inhibitors, Bioorg. Med. Chem. Lett., 2004, 第 3 作者
(7) Benzimidazoles as New Potent and Selective DP Antagonists for the treatment of Allergic Rhinitis, Bioorg. Med. Chem. Lett., 2004, 第 2 作者
(8) A mild and efficient new synthesis of aryl sulfones from boronic acids and sulfinic acid salts, Tetrahedron Lett. , 2004, 第 2 作者
(9) A mild, convenient synthesis of sulfinates and sulfonamides from alkyl and aryl halides, Tetrahedron Lett., 2002, 第 2 作者
(10) An Efficient Copper Catalyst for the Formation of Sulfones from Sulfinic Acid Salts and Aryl Iodides, Org. Lett., 2002, 第 2 作者
(11) Discovery of a potent and selective COX-2 inhibitor in the alkoxy lactone series with optimized metabolic profile, Bioorg. Med. Chem. Lett., 2002, 第 3 作者
(12) MK 966, Vioxx, 4-(4-Methylsulfonylphenyl)-3-Phenyl-2(5H)-Furanone: the Discovery of a Selective and Orally Active Cyclooxygenase-2 Inhibitor, Bioorg. Med. Chem. Lett., 1999, 第 2 作者
(13) Lewis acid-catalyzed intramolecular reaction between silyl enol ethers and ortho esters: an efficient approach to 1,6-anhydropyranoses., Synlett., 1994, 第 3 作者
(14) Synthesis of a radioactive photoaffinity archidonic acid analog, Tetrahedron Lett., 1994, 第 3 作者
(15) Lewis Acid-catalyzed intramolecular reaction between silyl enol esters and ortho esters: an efficient approach to 1,6-anhydropyranoses., Synlett., 1994, 第 3 作者
(16) A straightforward approach to the synthesis of the tricyclic core of taxanes, J. Org. Chem. , 1993, 通訊作者
(17) Enantiospecific synthesis via sequential diastereofacial and diastereotopic group selective reactions: enantiodivergent synthesis of syn-1,3-polyols, J. Am. Chem. Soc., 1992, 通訊作者
(18) Synthetic studies towards the immunosuppressant FK-506: synthesis of the C10-C34 fragment, Tetrahedron Lett., 1991, 通訊作者
(19) The asymmetric epoxidation of divinyl carbinols: theory and applications, Tetrahedron , 1990, 第 2 作者
(20) Selectivity in ozonolyses of cyclic 1,3-dienes, Tetrahedron Lett., 1990, 通訊作者
(21) Stereoselective synthesis of the C10-C24 fragment of FK-506, Tetrahedron Lett., 1989, 通訊作者
(22) Stereoselective synthesis of the C10-C24 fragment of FK-506., Tetrahedron Lett., 1989, 第 2 作者

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