Maccari et al., 2012 - Google Patents
Low molecular weight phosphotyrosine protein phosphatases as emerging targets for the design of novel therapeutic agentsMaccari et al., 2012
- Document ID
- 10525518876728311862
- Author
- Maccari R
- Ottanà R
- Publication year
- Publication venue
- Journal of medicinal chemistry
External Links
Snippet
Protein phosphorylation represents a key post-translational modification that is critical to the control of many cellular functions. The reversible phosphorylation of tyrosine residues of proteins is a significant regulatory event in eukaryotes compared to other protein …
- 239000003814 drug 0 title description 24
Classifications
-
- 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)
- C12N9/16—Hydrolases (3) acting on ester bonds (3.1)
-
- 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
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
-
- 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
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/5005—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
- G01N33/5008—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics
- G01N33/502—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells for testing or evaluating the effect of chemical or biological compounds, e.g. drugs, cosmetics for testing non-proliferative effects
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Maccari et al. | Low molecular weight phosphotyrosine protein phosphatases as emerging targets for the design of novel therapeutic agents | |
Yu et al. | Regulatory mechanisms and novel therapeutic targeting strategies for protein tyrosine phosphatases | |
DeLaBarre et al. | Full-length human glutaminase in complex with an allosteric inhibitor | |
Menchise et al. | Carbonic anhydrase inhibitors: stacking with Phe131 determines active site binding region of inhibitors as exemplified by the X-ray crystal structure of a membrane-impermeant antitumor sulfonamide complexed with isozyme II | |
Assimon et al. | CB-6644 is a selective inhibitor of the RUVBL1/2 complex with anticancer activity | |
Jackson et al. | Molecular reactions of protein phosphatases insights from structure and chemistry | |
Evans et al. | Discovery of a selective phosphoinositide-3-kinase (PI3K)-γ inhibitor (IPI-549) as an immuno-oncology clinical candidate | |
Lu et al. | SHAFTS: a hybrid approach for 3D molecular similarity calculation. 2. Prospective case study in the discovery of diverse p90 ribosomal S6 protein kinase 2 inhibitors to suppress cell migration | |
Combs | Recent advances in the discovery of competitive protein tyrosine phosphatase 1B inhibitors for the treatment of diabetes, obesity, and cancer | |
Johnson | The regulation of protein phosphorylation | |
Sarmiento et al. | Structural basis of plasticity in protein tyrosine phosphatase 1B substrate recognition | |
Tonks | Protein tyrosine phosphatases: from genes, to function, to disease | |
Morgan et al. | Characterization of two distinct structural classes of selective aldehyde dehydrogenase 1A1 inhibitors | |
Palomo et al. | 5-imino-1, 2, 4-thiadiazoles: first small molecules as substrate competitive inhibitors of glycogen synthase kinase 3 | |
Parajuli et al. | Selective ALDH3A1 inhibition by benzimidazole analogues increase mafosfamide sensitivity in cancer cells | |
Lavecchia et al. | Discovery of new inhibitors of Cdc25B dual specificity phosphatases by structure-based virtual screening | |
Hoegenauer et al. | Discovery and pharmacological characterization of novel quinazoline-based PI3K delta-selective inhibitors | |
Davidovich et al. | Discovery of novel isatin-based p53 inducers | |
Zhang et al. | A highly selective and potent PTP-MEG2 inhibitor with therapeutic potential for type 2 diabetes | |
Ong et al. | Rational design of selective organoruthenium inhibitors of protein tyrosine phosphatase 1B | |
Schmitt et al. | Hydroxybenzothiophene ketones are efficient pre-mRNA splicing modulators due to dual inhibition of Dyrk1A and Clk1/4 | |
Souza et al. | From immune response to cancer: a spot on the low molecular weight protein tyrosine phosphatase | |
Hoylaerts et al. | Mammalian alkaline phosphatase catalysis requires active site structure stabilization via the N-terminal amino acid microenvironment | |
Sergienko et al. | Inhibition of hematopoietic protein tyrosine phosphatase augments and prolongs ERK1/2 and p38 activation | |
Gkeka et al. | Exploring a non-ATP pocket for potential allosteric modulation of PI3Kα |