Hooft van Huijsduijnen et al., 2004 - Google Patents
Prospects for inhibitors of protein tyrosine phosphatase 1B as antidiabetic drugsHooft van Huijsduijnen et al., 2004
- Document ID
- 2819359150029554595
- Author
- Hooft van Huijsduijnen R
- Sauer W
- Bombrun A
- Swinnen D
- Publication year
- Publication venue
- Journal of medicinal chemistry
External Links
Snippet
Protein tyrosine phosphatase 1B (PTP1B) emerged only 4 years ago as a new drug target for the treatment of diabetes and, possibly, obesity. The enzyme belongs to the family of tyrosine phosphatases, which consists of∼ 90 members. 1-3 Interestingly, this target had a …
- 108010015847 Non-Receptor Type 1 Protein Tyrosine Phosphatase 0 title abstract description 338
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/428—Thiazoles condensed with carbocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic, hydroximic acids
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICRO-ORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING OR MAINTAINING MICRO-ORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/14—Hydrolases (3)
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Hooft van Huijsduijnen et al. | Prospects for inhibitors of protein tyrosine phosphatase 1B as antidiabetic drugs | |
Jin et al. | Azo-PROTAC: novel light-controlled small-molecule tool for protein knockdown | |
Singh et al. | DcpS as a therapeutic target for spinal muscular atrophy | |
Philip et al. | Cyclin-dependent kinase 8: A new hope in targeted cancer therapy? Miniperspective | |
Conti et al. | Cyclic AMP-specific PDE4 phosphodiesterases as critical components of cyclic AMP signaling | |
Seno et al. | Pyrrolidine inhibitors of human cytosolic phospholipase A2 | |
Scott et al. | Discovery of a 3-(4-pyrimidinyl) indazole (MLi-2), an orally available and selective leucine-rich repeat kinase 2 (LRRK2) inhibitor that reduces brain kinase activity | |
Hoover et al. | Indole-2-carboxamide inhibitors of human liver glycogen phosphorylase | |
Tonks | PTP1B: from the sidelines to the front lines! | |
Desideri et al. | Homoisoflavonoids: natural scaffolds with potent and selective monoamine oxidase-B inhibition properties | |
Davies et al. | Monoacidic inhibitors of the Kelch-like ECH-associated protein 1: nuclear factor erythroid 2-related factor 2 (KEAP1: NRF2) protein–protein interaction with high cell potency identified by fragment-based discovery | |
Tang et al. | Discovery and development of small-molecule inhibitors of glycogen synthase | |
von Geldern et al. | Pyrrolidine-3-carboxylic acids as endothelin antagonists. 4. Side chain conformational restriction leads to ETB selectivity | |
Ndubaku et al. | Design of selective PAK1 inhibitor G-5555: improving properties by employing an unorthodox low-p K a polar moiety | |
Lovera et al. | The different flexibility of c-Src and c-Abl kinases regulates the accessibility of a druggable inactive conformation | |
Granchi et al. | A patent review of Monoacylglycerol Lipase (MAGL) inhibitors (2013-2017) | |
Gómez-Galeno et al. | A potent and selective AMPK activator that inhibits de novo lipogenesis | |
Ebdrup et al. | Synthesis and Structure− Activity relationship for a novel class of potent and selective carbamoyl-triazole based inhibitors of hormone sensitive lipase | |
Donella-Deana et al. | Unique substrate specificity of anaplastic lymphoma kinase (ALK): development of phosphoacceptor peptides for the assay of ALK activity | |
Chaikuad et al. | An unusual binding model of the methyl 9-anilinothiazolo [5, 4-f] quinazoline-2-carbimidates (EHT 1610 and EHT 5372) confers high selectivity for dual-specificity tyrosine phosphorylation-regulated kinases | |
Amato et al. | N-pyridyl and pyrimidine benzamides as KCNQ2/Q3 potassium channel openers for the treatment of epilepsy | |
Maccari et al. | Low molecular weight phosphotyrosine protein phosphatases as emerging targets for the design of novel therapeutic agents | |
Huber et al. | Novel 3-arylideneindolin-2-ones as inhibitors of NAD+-dependent histone deacetylases (sirtuins) | |
Robertson et al. | The rhodadyns, a new class of small molecule inhibitors of dynamin GTPase activity | |
Charlier et al. | Structural insights into human 5-lipoxygenase inhibition: combined ligand-based and target-based approach |