The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
26820555 |
87 |
Synthesis and evaluation of colletoic acid core derivatives. |
St. Jude Children'S Research Hospital |
26187704 |
63 |
Discovery of 11ß-hydroxysteroid dehydrogenase type 1 inhibitor. |
Incheon National University |
25590374 |
23 |
Hupehenols A-E, selective 11ß-hydroxysteroid dehydrogenase type 1 (11ß-HSD1) inhibitors from Viburnum hupehense. |
Chinese Academy Of Sciences |
25800116 |
62 |
Synthesis and optimization of picolinamide derivatives as a novel class of 11ß-hydroxysteroid dehydrogenase type 1 (11ß-HSD1) inhibitors. |
Seoul National University |
25050169 |
52 |
Optimization of 1,2,4-Triazolopyridines as Inhibitors of Human 11ß-Hydroxysteroid Dehydrogenase Type 1 (11ß-HSD-1). |
Bristol-Myers Squibb |
24294985 |
42 |
Medicinal chemistry of inhibitors of 11ß-hydroxysteroid dehydrogenase type 1 (11ß-HSD1). |
Astrazeneca |
24074876 |
17 |
Synthesis of sterically encumbered 11ß-aminoprogesterone derivatives and evaluation as 11ß-hydroxysteroid dehydrogenase inhibitors and mineralocorticoid receptor antagonists. |
University Of Alberta |
23747808 |
51 |
Discovery and structure-activity relationships of ent-Kaurene diterpenoids as potent and selective 11ß-HSD1 inhibitors: potential impact in diabetes. |
Chinese Academy Of Sciences |
23659858 |
17 |
Evaluation of selective inhibitors of 11ß-HSD1 for the treatment of hypertension. |
Merck |
23478147 |
42 |
Discovery of SAR184841, a potent and long-lasting inhibitor of 11ß-hydroxysteroid dehydrogenase type 1, active in a physiopathological animal model of T2D. |
Sanofi R & D |
24900572 |
54 |
Discovery of HSD-621 as a Potential Agent for the Treatment of Type 2 Diabetes. |
Pfizer |
23153367 |
92 |
Free-Wilson and structural approaches to co-optimizing human and rodent isoform potency for 11ß-hydroxysteroid dehydrogenase type 1 (11ß-HSD1) inhibitors. |
Astrazeneca |
23088558 |
36 |
Novel acidic 11ß-hydroxysteroid dehydrogenase type 1 (11ß-HSD1) inhibitor with reduced acyl glucuronide liability: the discovery of 4-[4-(2-adamantylcarbamoyl)-5-tert-butyl-pyrazol-1-yl]benzoic acid (AZD8329). |
Astrazeneca |
23013933 |
59 |
Optimisation of pharmacokinetic properties in a neutral series of 11ß-HSD1 inhibitors. |
Astrazeneca |
24900382 |
41 |
Discovery of 2-Alkyl-1-arylsulfonylprolinamides as 11ß-Hydroxysteroid Dehydrogenase Type 1 Inhibitors. |
TBA |
22691057 |
32 |
Discovery of a potent, selective, and orally bioavailable acidic 11ß-hydroxysteroid dehydrogenase type 1 (11ß-HSD1) inhibitor: discovery of 2-[(3S)-1-[5-(cyclohexylcarbamoyl)-6-propylsulfanylpyridin-2-yl]-3-piperidyl]acetic acid (AZD4017). |
Astrazeneca |
22901389 |
28 |
Structure-based design of 7-azaindole-pyrrolidine amides as inhibitors of 11ß-hydroxysteroid dehydrogenase type I. |
Merck Serono |
22360639 |
12 |
Cycloartane and friedelane triterpenoids from the leaves of Caloncoba glauca and their evaluation for inhibition of 11ß-hydroxysteroid dehydrogenases. |
Chinese Academy Of Sciences |
22440625 |
44 |
Synthesis and evaluation of piperidine urea derivatives as efficacious 11ß-hydroxysteroid dehydrogenase type 1 inhibitors in diabetic ob/ob mice. |
Chinese Academy Of Sciences |
19564108 |
48 |
4-(Phenylsulfonamidomethyl)benzamides as potent and selective inhibitors of the 11beta-hydroxysteroid dehydrogenase type 1 with efficacy in diabetic ob/ob mice. |
Chinese Academy Of Sciences |
18553955 |
43 |
Discovery of novel, potent benzamide inhibitors of 11beta-hydroxysteroid dehydrogenase type 1 (11beta-HSD1) exhibiting oral activity in an enzyme inhibition ex vivo model. |
Amgen |
18440812 |
113 |
Phenylcyclobutyl triazoles as selective inhibitors of 11beta-hydroxysteroid dehydrogenase type I. |
Merck Research Laboratories |
18434143 |
96 |
Bis-aryl triazoles as selective inhibitors of 11beta-hydroxysteroid dehydrogenase type 1. |
Merck |
17490884 |
39 |
beta-Keto sulfones as inhibitors of 11beta-hydroxysteroid dehydrogenase type I and the mechanism of action. |
Wyeth Research |
22148241 |
3 |
Cyclopeptide Alkaloids from Ziziphus apetala. |
Kunming Institute Of Botany |
21983444 |
78 |
Discovery of 3-hydroxy-4-cyano-isoquinolines as novel, potent, and selective inhibitors of human 11ß-hydroxydehydrogenase 1 (11ß-HSD1). |
Bristol-Myers Squibb Research & Development |
21873057 |
13 |
Potent and novel 11ß-HSD1 inhibitors identified from shape and docking based virtual screening. |
Shanghai Pharmaceutical Holding |
21786805 |
130 |
Structure-based design and synthesis of 1,3-oxazinan-2-one inhibitors of 11ß-hydroxysteroid dehydrogenase type 1. |
Vitae Pharmaceuticals |
21689935 |
55 |
Generation of 3,8-substituted 1,2,4-triazolopyridines as potent inhibitors of human 11ß-hydroxysteroid dehydrogenase type 1 (11ß-HSD-1). |
Bristol-Myers Squibb |
21334894 |
218 |
Substituted phenyl triazoles as selective inhibitors of 11 β-Hydroxysteroid Dehydrogenase Type 1. |
Merck |
21439819 |
49 |
Pyrrolidine-pyrazole ureas as potent and selective inhibitors of 11β-hydroxysteroid-dehydrogenase type 1. |
Sanofi-Aventis R&D |
21421311 |
135 |
Bicyclo[2.2.2]octyltriazole inhibitors of 11β-hydoxysteroid dehydrogenase type 1. Pharmacological agents for the treatment of metabolic syndrome. |
Merck Research Laboratories |
21376605 |
26 |
Synthesis of new glycyrrhetinic acid derived ring A azepanone, 29-urea and 29-hydroxamic acid derivatives as selective 11ß-hydroxysteroid dehydrogenase 2 inhibitors. |
University Of Technology |
20864344 |
110 |
Discovery and optimization of adamantyl carbamate inhibitors of 11ß-HSD1. |
Vitae Pharmaceuticals |
20851614 |
22 |
Synthesis of novel 3-amino and 29-hydroxamic acid derivatives of glycyrrhetinic acid as selective 11ß-hydroxysteroid dehydrogenase 2 inhibitors. |
University Of Natural Resources And Applied Life Sciences |
20465278 |
27 |
Discovery of a potent, orally active 11beta-hydroxysteroid dehydrogenase type 1 inhibitor for clinical study: identification of (S)-2-((1S,2S,4R)-bicyclo[2.2.1]heptan-2-ylamino)-5-isopropyl-5-methylthiazol-4(5H)-one (AMG 221). |
Amgen |
20363126 |
50 |
The development and SAR of pyrrolidine carboxamide 11beta-HSD1 inhibitors. |
Pfizer |
20064717 |
64 |
Spirocyclic ureas: orally bioavailable 11beta-HSD1 inhibitors identified by computer-aided drug design. |
Vitae Pharmaceuticals |
19395260 |
29 |
Discovery and structure-activity relationships of pentanedioic acid diamides as potent inhibitors of 11beta-hydroxysteroid dehydrogenase type I. |
Merck Serono |
19181519 |
71 |
Synthesis and optimization of arylsulfonylpiperazines as a novel class of inhibitors of 11 beta-hydroxysteroid dehydrogenase type 1 (11 beta-HSD1). |
TBA |
19053753 |
67 |
Further studies with the 2-amino-1,3-thiazol-4(5H)-one class of 11beta-hydroxysteroid dehydrogenase type 1 inhibitors: reducing pregnane X receptor activity and exploring activity in a monkey pharmacodynamic model. |
Amgen |
18440811 |
207 |
4-Methyl-5-phenyl triazoles as selective inhibitors of 11beta-hydroxysteroid dehydrogenase type I. |
Merck Research Laboratories |
17919905 |
56 |
The discovery of 2-anilinothiazolones as 11beta-HSD1 inhibitors. |
Amgen |
17600707 |
48 |
Oxazolones as potent inhibitors of 11beta-hydroxysteroid dehydrogenase type 1. |
Biovitrum |
17442567 |
27 |
Piperidine amides as 11beta-hydroxysteroid dehydrogenase type 1 inhibitors. |
Biovitrum |
17201418 |
105 |
Discovery and metabolic stabilization of potent and selective 2-amino-N-(adamant-2-yl) acetamide 11beta-hydroxysteroid dehydrogenase type 1 inhibitors. |
Abbott Laboratories |
17070044 |
102 |
Adamantane sulfone and sulfonamide 11-beta-HSD1 Inhibitors. |
Abbott Laboratories |
17000111 |
127 |
Discovery of potent and selective inhibitors of 11beta-HSD1 for the treatment of metabolic syndrome. |
Abbott Laboratories |
16996734 |
93 |
Adamantane 11-beta-HSD-1 inhibitors: Application of an isocyanide multicomponent reaction. |
Abbott Laboratories |
16931002 |
73 |
Discovery of orally active butyrolactam 11beta-HSD1 inhibitors. |
Abbott Laboratories |
16899366 |
85 |
Synthesis and biological evaluation of heterocycle containing adamantane 11beta-HSD1 inhibitors. |
Abbott Laboratories |
16890427 |
81 |
Synthesis and structural activity relationship of 11beta-HSD1 inhibitors with novel adamantane replacements. |
Abbott Laboratories |
16759088 |
38 |
The discovery of new 11beta-hydroxysteroid dehydrogenase type 1 inhibitors by common feature pharmacophore modeling and virtual screening. |
University Of Innsbruck |
16185866 |
53 |
Discovery of 4-heteroarylbicyclo[2.2.2]octyltriazoles as potent and selective inhibitors of 11beta-HSD1: novel therapeutic agents for the treatment of metabolic syndrome. |
Merck |
15911270 |
19 |
Synthesis and biological evaluation of sulfonamidooxazoles and beta-keto sulfones: selective inhibitors of 11beta-hydroxysteroid dehydrogenase type I. |
Wyeth Research |
21337480 |
17 |
Design and synthesis of conformationally constrained cyclophilin inhibitors showing a cyclosporin-A phenotype in C. elegans. |
The University Of Edinburgh |
20187655 |
12 |
Development of GlcNAc-inspired iminocyclitiols as potent and selective N-acetyl-beta-hexosaminidase inhibitors. |
Academia Sinica |