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柯少勇
  • 所在单位:湖北省生物农药工程研究中心
  • 职称/职务:研究员(五级)/室主任
  • 学科专业:应用化学
  • 研究方向:药物化学生物学
  • 联系电话:02759101956
  • 电子邮箱:shaoyong.ke@nberc.com
个人简历

柯少勇,男,1978年9月出生,湖北谷城人,2009年毕业于华东理工大学应用化学专业。

1998-2002 华中师范大学化学学院,本科,获理学学士学位。

2002-2005 上海师范大学生命与环境科学学院,硕士,获理学硕士学位;

2005-2009 华东理工大学药学院,博士,获工学博士学位;期间于2008年在大连理工大学,生物化学专业学习(联培);

2009-至今 湖北省农业科学院/湖北省生物农药工程研究中心

主要社会兼职情况

华中农业大学、湖北工业大学硕士生导师,中国化学会、中国植物保护学会、美国化学会及亚洲科学编辑委员会会员、BENTHAM AMBASSADOR,国际期刊Mini-Reviews in Medicinal Chemistry编委、Molecules的Guest Editor、Current Chinese Chemistry的Associate Editor、Chemical Biology Letters、Current Chinese Science及Academia Journal of Agricultural Research编委,国家科技专家库成员,中国科技论文在线特聘专家,波兰基金项目海外评审,陕西省自然基金评审专家,武汉市科技特派员;中国化学会、英国皇家化学会、美国化学会及Springer Nature、Wiley、Elsevier、Bentham、Taylor and Francis等国际出版社主办的三十余种SCI源刊论文评审专家。

目前主要研究领域

天然资源导向的农药及药物的先导发现及化学生物学

主持及参与项目(课题)情况(主要科技项目5项)

1、 新型抗青枯菌药物筛选与评价(2021-2023),湖北省农业科技创新中心重大专项课题,主持;

2、 多样性导向纳他霉素衍生物的制备、杀菌活性及作用机制(2020-2022),湖北省自然科学基金面上项目,主持;

3、 资源导向的病媒防控药物开发(2021-2022),横向课题,主持。

4、 农业生物药物分子靶标发现与绿色药物分子设计(2017-2020),重点研发计划子课题,主持;

5、 杂环亚胺作为新型杀虫剂的先导优化及应用研究(2016-2018),武汉市应用基础研究计划项目,主持;

获得的科技奖励及专利、标准情况

任职以来,荣获湖北省科技进步一等奖、湖北省技术发明二等奖、湖北省自然科学优秀论文奖、湘鄂赣农业科研杰出青年优秀奖、中国科技论文在线优秀评审专家、湖北省农科院先进工作者、湖北省农业科学院嘉奖、湖北省农科院学术报告会一等奖、湖北省农科院青年奖励基金等,并入选湖北省农业科学院首批领军人才计划;鉴定科技成果1项,以第一发明人申报国际PCT专利2项,国内发明专利14项,获得授权专利13项。

成果奖励:

1. 天然资源导向的农用活性物质发现及产品创制,2020年湖北省科技厅鉴定成果EK2020A010497001475。

2. 基于天然产物的诺沃霉素等新型农用药物的发现与创制,2019年湖北省技术发明二等奖。

3. 基于生物农药创制的十字花科蔬菜主要病虫害生物防控关键技术与应用,2015年湖北省科技进步一等奖。

发明专利:

1. 具有杀虫活性的肟醚或酯衍生物及其制备方法与应用. 授权专利: ZL201010518800.4.

2. 含氮杂环亚胺衍生物及其制备方法和用途. 授权专利: ZL201210171077.6.

3. 共轭双烯衍生物及其制备方法与作为抗癌药物的用途. 授权专利: ZL201310350441.X.

4. 具有双腙结构的甾体衍生物作为抗病毒药物的应用. 授权专利: ZL201410053947.9.

5. 含双酰胺结构的杂环亚胺衍生物及其制备方法和用途. 授权专利: ZL201610079057.4.

6. 含α-氨基酮结构的酰胺衍生物及其制备方法和用途. 授权专利: ZL201710207603.2.

7. 一种含噻唑杂环的甾体衍生物及其制备方法与应用. 授权专利: ZL201810114536.4.

8. 一种含靛红单元的甾体衍生物及其制备方法与用途. 授权专利: ZL201910115723.9.

9. 一种咔唑生物碱衍生物及其制备方法和用途. 授权专利: ZL202011250986.X.

10. 多取代N-芳基吡咯类化合物及其制备方法. 授权专利: ZL202010355204.2.

11. 一种酰胺衍生物在制备草地贪夜蛾防控药物中的应用. 授权专利: ZL202110750517.2.

12. 一种联苯酰胺衍生物及其制备方法和用途. 申请专利: ZL202010904094.0.

13. 一种环烷基噻吩亚胺衍生物作为几丁质酶抑制剂的应用. 授权专利: ZL202010426926.2.

14. Conjugated diene derivatives, preparation method therefor, and uses thereof as anticancer drug. PCT Intl. Appl. WO2015021833A1.

15. Nitrogenous Heterocyclic Imide Derivative and Preparation Method and Use Thereof. PCT Intl. Appl. WO2013177985A1.

16. 酰胺衍生物及其制备方法和用途. 申请专利: CN201910472351.5.

17. 一种酪氨酸衍生物及其制备方法和应用. 申请专利: CN202111462490.3.

代表性著作及论文发表情况

以第一或通讯作者发表SCI论文40余篇,其中IF>5的论文16篇,参编英文著作2部,代表性论文及著作如下:

Articles

1. Muhammad I, Zhang L, Zheng B, Zhao Z, Zhou D, Wan S, Chen Z, Duan H, Li Q, Liu X, Cao S, Ke S*, Ye J*, Screening of novel synthetic derivatives of dehydroepiandrosterone for inhibitors against flaviviruses infection, Virol. Sin., 2022, 37, 94. (SCI 2区)

2. Yu Z, Huang W, Shi L, Ke S*, Xu S*, Selective probes targeting c-MYC Pu22 G-quadruplex DNA and its application in live mice imaging, Chin. Chem. Lett., 2022, 33, 1627. (SCI 2区)

3. Ke S*, HuangW, ZhangZ, Wang Y, Zhang Y, Wu Z, Fang W, Wan Z, Gong Y, Yang J, Wang K*,Shi L*, Diarylamine-guided carboxamide derivatives: Synthesis, biological evaluation and potential mechanism of action, Front. Chem., 2022, 10, 953523. (SCI 2区)

4. Huang D,Zhang Z,Li Y, Liu F, Huang W, Min Y,Wang K, Yang J, Cao C, Gong Y*, Ke S*, Carboline derivatives based on natural pityriacitrin as potential antifungal agents, Phytochem. Lett., 2022, 48, 100. (SCI 4区)

5. Zhang X, Huang W, Lu X, Liu S, Feng H, Yang W, Ye J, Li F, Ke S*, Wei D*, Identification of carbazole alkaloid derivatives with acylhydrazone as novel anti-TMV agents with the guidance of a digital fluorescence visual screening, J. Agric. Food. Chem., 2021, 69, 7458. (SCI 1区)

6. Huang W, Gao Z, Zhang Z, Fang W, Wang Z, Wan Z, Shi L*, Wang K*, Ke S*, Selective and effective cytotoxic agents: Synthesis, biological evaluation and structure-activity relationships of carbazole alkaloid derivatives, Bioorg. Chem., 2021, 113, 104991. (SCI 1区)

7. Zhang L, Zhou D, Li Q, Zhu S, Muhammad I, Duan H, Cao S, Ke S*, Ye J*, Screening and discovery of novel steroidal derivatives as antiviral agents against flaviviruses, Front. Microbiol., 2021, 12, 727236. (SCI 2区)

8. Yu Z, Huang W, Xu S*, Ke S*, Benzothiazole-based colorimetric chemosensors bearing naphthol aldehyde unit: Synthesis, characterization, selective detection of hypochlorite and its application as test strips, Microchem. J., 2021, 164, 106009. (SCI 2区)

9. Ke S*,Xu T,Min Y, Wan Z, Yang Z, Wang K*, Marine alkaloid pityriacitrin and its analogues: Discovery, structures, synthetic methods and biological properties, Mini-Rev. Med. Chem., 2021, 21, 233. (SCI 3区)

10. Shi L, Wu Z, Zhang Y, Zhang Z, Fang W, Wang Y, Wan Z, Wang K*, Ke S*,Herbicidal secondary metabolites from Actinomycetes: Structure diversity, mode of actions and their roles in the development of herbicides, J. Agric. Food. Chem., 2020, 68, 17. (SCI 1区)

11. Huang D, Wang S, Song D, Cao X*, Huang W, Ke S*, Discovery of γ-lactam alkaloids derivatives as potential fungicidal agents targeting steroid biosynthesis, J. Agric. Food. Chem., 2020, 68,14438. (SCI 1区)

12.Huang W, Wang K, Liu P, Li M, Ke S*, Gu Y*, Three-component reactions of aromatic amines, 1,3-dicarbonyl compounds and α-bromoacetaldehyde acetal to access N-aryl/hetaryl-4,5-unsubstituted pyrroles, Beilstein J. Org. Chem., 2020, 16, 2920. (SCI 3区)

13. Ke S*,Fang W, Huang W,Zhang Z, Shi L, Wan Z, Wang K, Cao C, Huang D*, Sulfur-containing natural hinduchelins derivatives as potential antifungal agents against Rhizoctonia solani, Bioorg. Med. Chem. Lett., 2020, 30, 127245. (SCI 3区)

14. Xu T, Shi L, Zhang Y, Wang K, Yang Z*, Ke S*, Synthesis and biological evaluation of marine alkaloid-oriented β-carboline analogues, Eur. J. Med. Chem., 2019, 168, 293. (SCI 1区)

15. Wang S, Bao L, Song D, Wang J, Cao X*, Ke S*, Amino acid-oriented poly-substituted heterocyclic tetramic acid derivatives as potential antifungal agents, Eur. J. Med. Chem., 2019, 179, 567. (SCI 1区)

16. Ke S*, Zhang Z, Shi L, Liu M, Fang W, Zhang Y, Wu Z, Wan Z, Long T, Wang K*, An efficient synthesis and bioactivity evaluation of oxazole-containing natural Hinduchelins A-D and their derivatives, Org. Biomol. Chem., 2019, 17, 3635. (SCI 2区)

17. Ke S*, Zhang Z, Liu M, Fang W, Huang D, Wan Z, Zhou R, Wang K, Shi L*, Synthesis and bioevaluation of novel steroidal isatin conjugates derived from epiandrosterone/androsterone, J. Enzyme Inhib. Med. Chem., 2019, 34, 1607. (SCI 2区)

18. 柯少勇, 吴兆圆, 万中义, 方伟, 张亚妮, 王开梅*, 具有农药活性的微生物源核苷类化合物, 化学进展, 2019, 31, 954. (SCI 3区)

19. Ke S*, Li N, Ke T, Shi L, Zhang Z, Fang W, Zhang Y, Wang K, Zhou R, Wan Z, Yang Z, Zhang G, Wei Y*, Synthesis and evaluation of steroidal thiazoline conjugates as potential antiviral agents, Future Med. Chem., 2018, 10, 2589. (SCI 2区)

20. Ke S*, Recent progress of novel steroid derivatives and their potential biological properties, Mini-Rev. Med. Chem., 2018, 18, 745. (SCI 3区)

21. Ke S*, Shi L, Zhang Z, Yang Z, Steroidal[17,16-d]pyrimidines derived from dehydroepiandrosterone: A convenient synthesis, antiproliferation activity, structure-activity relationships, and role of heterocyclic moiety, Sci. Rep., 2017, 7, 44439. (SCI 3区)

22. Yang Q, Mao Q, Liu M, Wang K, Wu Z, Fang W, Yang Z, Luo P,Ke S*,Shi L*, The inhibitory effect of dehydroepiandrosterone and its derivatives against influenza A virus in vitro and in vivo, Arch. Virol., 2016, 161, 3061. (SCI 4区)

23. Ke S*, Novel amide-type ligand bearing bis-pyridine cores: Synthesis, spectral characterizations and X-ray structure analyses, J. Mol. Struct., 2016, 1118, 91. (SCI 3区)

24.Ke S*,Shi L, Yang Z,Discovery of novel isatin-dehydroepiandrosterone conjugates as potential anticancer agents, Bioorg. Med. Chem. Lett., 2015, 25, 4628. (SCI 3区)

25.Ke S*, Yang Z, Zhang Z, Liang Y, Wang K, Liu M, Shi L*,Multisubstituted indole-acrylonitrile hybrids as potential cytotoxic agents, Bioorg. Med. Chem. Lett., 2014, 24, 1907. (SCI 3区)

26. Ke S*, Wei Y, Shi L, Yang Q, Yang Z*,Synthesis of novel steroid derivatives derived from dehydroisoandrosterone as potential anticancer agents, Anti-Cancer Agents Med. Chem., 2013, 13, 1291. (SCI 4区)

27. Ke S*, Wei Y, Yang Z, Wang K, Liang Y, Shi L,Novel cycloalkylthiophene-imine derivatives bearing benzothiazole scaffold: Synthesis, characterization and antiviral activity evaluation, Bioorg. Med. Chem. Lett., 2013, 23, 5131. (SCI 3区)

28. Ke S*, Shi L, Cao X, Yang Q, Liang Y, Yang Z,Heterocycle-functional gramine analogues: Solvent and catalyst-free synthesis and their inhibition activities against cell proliferation, Eur. J. Med. Chem., 2012, 54, 248. (SCI 1区)

29. Shi L, HuR, Wei Y,Liang Y, Yang Z,Ke S*,Anthranilic acid-based diamides derivatives incorporating aryl-isoxazoline pharmacophore as potential anti-cancer agents: Design, synthesis and biological evaluation, Eur. J. Med. Chem., 2012, 54, 549. (SCI 1区)

30. Li S, Cao X*, Chen C, Ke S*, Novel salicylic acid-oriented thiourea-type receptors as colorimetric chemosensor: Synthesis, characterizations and selective naked-eye recognition properties, Spectrochimica Acta Part A, 2012, 96, 18. (SCI 2区)

31. Ke S, Zhang Z, Zhang Y, Shi L, Zhou R, Jiang A, Liang Y, Yang Z, Novel ether-functional spiro-tetronic acid derivatives: Molecule design, convenient synthesis and biological evaluation, Res. Chem. Intermed., 2012, 38, 1827. (SCI 3区)

32. Cao X, Chen C, Lu W,Ke S*, Chiral β-arylalkyl-1H-1,2,4-triazoles as demethylase inhibitors: Biological evaluation and its stereoselective interaction with sterol 14α-demethylase from Penicillium digitatum, Pestic. Biochem. Phys., 2011, 99, 189. (SCI 1区)

33. Ke S*, Cao X, Liang Y, Wang K, Yang Z, Synthesis and biological properties of dihydro-oxadiazine-based heterocyclic derivatives, Mini-Rev. Med. Chem., 2011, 11, 642. (SCI 3区)

34. Ke S*, Zhang Y, Shu W, Zhang Z, Shi L, Liang Y, Wang K, Yang Z,Structural diversity-guided convenient construction of functionalized polysubstituted butenolides and lactam derivatives, C. R. Chim., 2011, 14, 1071. (SCI 4区)

35. Ke S, Qian X*, Liu F, Wang N, Fan F, Li Z, Yang Q*, Diacylhydrazine derivatives as novel potential chitin biosynthesis inhibitors: Design, synthesis, and structure-activity relationship, Eur. J. Med. Chem., 2009, 44, 2985. (SCI 1区)

36. Ke S, Qian X*, Liu F, Wang N, Yang Q*, Li Z, Novel 4H-1,3,4-oxadiazin-5(6H)-ones with hydrophobic and long alkyl chains: Design, synthesis, and bioactive diversity on inhibition of monoamine oxidase, chitin biosynthesis and tumor cell, Eur. J. Med. Chem., 2009, 44, 2113. (SCI 1区)

37. Ke S, Liu F, Wang N, Yang Q*, Qian X*, 1,3,4-Oxadiazoline derivatives as novel potential inhibitors targeting chitin biosynthesis: Design, synthesis and biological evaluation, Bioorg. Med. Chem. Lett., 2009, 19, 332. (SCI 3区)

38. Ke S, Li Z, Qian X*, 1,3,4-Oxadiazole-3(2H)-carboxamide derivatives as potential novel class of monoamine oxidase (MAO) inhibitors: Synthesis, evaluation and role of urea moiety, Bioorg. Med. Chem., 2008, 16, 7565. (SCI 3区)

Chapters in Books

1. Novel agroactive secondary metabolites from actinomycetes in the past two decades with focus on screening strategies and discovery, in Natural Products fromActinomycetes – Diversity, Ecology and Drug Discovery, Edited by Ravishankar V. Rai and Jamuna A. Bai, Pages 199-221, ISBN: 978-981-16-6131-0, Publisher: Springer Nature, 2022.

2. Updated report on synthesis and biological properties of oxadiazine-based heterocyclic derivatives, in Recent Advances in Medicinal Chemistry, Edited by Atta-ur-Rahman, Muhammad Iqbal Choudhary and George Perry, Pages 107-143, ISBN: 978-1-68108-172-4, Publisher: Bentham Science Publishers and Elsevier, 2015.

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