Related content

Design, synthesis, and SAR of anthranilamide-based factor Xa inhibitors incorporating substituted biphenyl P4 motifs

By Zhang P.   Bao L.   Zuckett J.F.   Goldman E.A.   Jia Z.J.   Arfsten A.   Edwards S.   Sinha U.   Hutchaleelaha A.   Park G.   Lambing J.L.   Hollenbach S.J.   Scarborough R.M.   Zhu B.-Y.  

Bioorganic and Medicinal Chemistry Letters, Vol. 14, Iss. 4, 2004-02 ,pp. : 983-987

Elsevier

Access to resources Recommend Favorite

Design, synthesis and SAR study of hydroxychalcone inhibitors of human β-secretase (BACE1)

By Ma Lei   Yang Zhengyi   Li Chenjing   Zhu Zhiyuan   Shen Xu   Hu Lihong  

Journal of Enzyme Inhibition and Medicinal Chemistry, Vol. 26, Iss. 5, 2011-10 ,pp. : 643-648

Informa Healthcare

Access to resources Recommend Favorite

QSAR study of substituted 1-(2-naphthyl)-1H-pyrazole-5-carboxylamide factor Xa (fXa) inhibitors

By Ma X.   Zhou L.  

Molecular Simulation, Vol. 33, Iss. 15, 2007-12 ,pp. : 1213-1222

Taylor & Francis Ltd

Access to resources Recommend Favorite

Design, synthesis, and activity of HDAC inhibitors with a N-formyl hydroxylamine head group

By Wu T.Y.H.   Hassig C.   Wu Y.   Ding S.   Schultz P.G.  

Bioorganic and Medicinal Chemistry Letters, Vol. 14, Iss. 2, 2004-01 ,pp. : 449-453

Elsevier

Access to resources Recommend Favorite

3D-QSAR, docking and molecular dynamics for factor Xa inhibitors as anticoagulant agents

By Ghasemi Jahan B.   Hooshmand Shabnam  

Molecular Simulation, Vol. 39, Iss. 6, 2013-05 ,pp. : 453-471

Taylor & Francis Ltd

Access to resources Recommend Favorite