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1.
Piperidine-3,4-diol and piperidine-3-ol derivatives of pyrrolo[2,1-f][1,2,4]triazine as inhibitors of anaplastic lymphoma kinase.
Bioorg Med Chem Lett
; 25(5): 1047-52, 2015 Mar 01.
Article
in English
| MEDLINE | ID: mdl-25655723
2.
Correction to "Synthesis and Crystal Structure of an Enantiomerically Pure, Internally Coordinated Alkylchloroborane. The Boron-Centered Anomeric Affect".
J Am Chem Soc
; 2018 Jun 08.
Article
in English
| MEDLINE | ID: mdl-29883109
3.
4-phenoxypiperidine pyridazin-3-one histamine H(3) receptor inverse agonists demonstrating potent and robust wake promoting activity.
Bioorg Med Chem Lett
; 22(4): 1504-9, 2012 Feb 15.
Article
in English
| MEDLINE | ID: mdl-22290075
4.
Structure activity relationships of 5-, 6-, and 7-methyl-substituted azepan-3-one cathepsin K inhibitors.
J Med Chem
; 49(5): 1597-612, 2006 Mar 09.
Article
in English
| MEDLINE | ID: mdl-16509577
5.
3,4-Diaza-bicyclo[4.1.0]hept-4-en-2-one phenoxypropylamine analogs of irdabisant (CEP-26401) as potent histamine-3 receptor inverse agonists with robust wake-promoting activity.
Eur J Med Chem
; 95: 349-56, 2015 May 05.
Article
in English
| MEDLINE | ID: mdl-25827402
6.
Design, synthesis, and anaplastic lymphoma kinase (ALK) inhibitory activity for a novel series of 2,4,8,22-tetraazatetracyclo[14.3.1.1³,7.19,¹³]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaene macrocycles.
J Med Chem
; 55(1): 449-64, 2012 Jan 12.
Article
in English
| MEDLINE | ID: mdl-22172029
7.
Discovery of an orally efficacious inhibitor of anaplastic lymphoma kinase.
J Med Chem
; 55(10): 4580-93, 2012 May 24.
Article
in English
| MEDLINE | ID: mdl-22564207
8.
The first coordination complexes of selenones: a structural comparison with complexes of sulfones.
Inorg Chem
; 42(22): 7098-105, 2003 Nov 03.
Article
in English
| MEDLINE | ID: mdl-14577777
9.
Design and synthesis of conformationally restricted eight-Membered ring diketones as potential serine protease inhibitors.
Bioorg Med Chem Lett
; 12(17): 2359-62, 2002 Sep 02.
Article
in English
| MEDLINE | ID: mdl-12161133
10.
Phenylbutyrates as potent, orally bioavailable vitronectin receptor (integrin alphavbeta3) antagonists.
Bioorg Med Chem Lett
; 13(8): 1483-6, 2003 Apr 17.
Article
in English
| MEDLINE | ID: mdl-12668017
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