Singaram et al., 2023 - Google Patents
Targeting lipid–protein interaction to treat Syk-mediated acute myeloid leukemiaSingaram et al., 2023
View PDF- Document ID
- 6524058669096070296
- Author
- Singaram I
- Sharma A
- Pant S
- Lihan M
- Park M
- Pergande M
- Buwaneka P
- Hu Y
- Mahmud N
- Kim Y
- Cologna S
- Gevorgyan V
- Khan I
- Tajkhorshid E
- Cho W
- Publication year
- Publication venue
- Nature chemical biology
External Links
Snippet
Membrane lipids control the cellular activity of kinases containing the Src homology 2 (SH2) domain through direct lipid–SH2 domain interactions. Here we report development of new nonlipidic small molecule inhibitors of the lipid–SH2 domain interaction that block the …
Classifications
-
- 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
-
- 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
- G01N33/53—Immunoassay; Biospecific binding assay
-
- 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
- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
- G01N33/6803—General methods of protein analysis not limited to specific proteins or families of proteins
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/90—Enzymes; Proenzymes
- G01N2333/91—Transferases (2.)
- G01N2333/912—Transferases (2.) transferring phosphorus containing groups, e.g. kinases (2.7)
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2500/00—Screening for compounds of potential therapeutic value
- G01N2500/04—Screening involving studying the effect of compounds C directly on molecule A (e.g. C are potential ligands for a receptor A, or potential substrates for an enzyme A)
-
- 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
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Guo et al. | Enhancing intracellular accumulation and target engagement of PROTACs with reversible covalent chemistry | |
Ferguson et al. | Discovery of a selective inhibitor of doublecortin like kinase 1 | |
Chen et al. | Mutation-induced impacts on the switch transformations of the GDP-and GTP-bound K-ras: Insights from multiple replica Gaussian accelerated molecular dynamics and free energy analysis | |
Ayaz et al. | Structural mechanism of a drug-binding process involving a large conformational change of the protein target | |
Spyrakis et al. | The roles of water in the protein matrix: a largely untapped resource for drug discovery | |
Wang et al. | Small-molecule inhibitor targeting the Hsp90-Cdc37 protein-protein interaction in colorectal cancer | |
Singaram et al. | Targeting lipid–protein interaction to treat Syk-mediated acute myeloid leukemia | |
Ball et al. | An isothermal shift assay for proteome scale drug-target identification | |
McMillin et al. | Structural basis of M3 muscarinic receptor dimer/oligomer formation | |
Okuzumi et al. | Inhibitor hijacking of Akt activation | |
Zhou et al. | KRASQ61H preferentially signals through MAPK in a RAF dimer-dependent manner in non–small cell lung cancer | |
Wang et al. | A dynamic charge-charge interaction modulates PP2A: B56 substrate recruitment | |
Lu et al. | Designed covalent allosteric modulators: an emerging paradigm in drug discovery | |
Kok et al. | Discovery of small-molecule enzyme activators by activity-based protein profiling | |
Kaneshige et al. | A selective small-molecule STAT5 PROTAC degrader capable of achieving tumor regression in vivo | |
Boulton et al. | Mechanism of selective enzyme inhibition through uncompetitive regulation of an allosteric agonist | |
Feng et al. | K-RasG12D has a potential allosteric small molecule binding site | |
Lee et al. | Structure-based discovery of novel small molecule Wnt signaling inhibitors by targeting the cysteine-rich domain of frizzled | |
Yan et al. | Structures of AMP-activated protein kinase bound to novel pharmacological activators in phosphorylated, non-phosphorylated, and nucleotide-free states | |
Hauseman et al. | Structure of the MRAS–SHOC2–PP1C phosphatase complex | |
Zech et al. | Novel small molecule inhibitors of choline kinase identified by fragment-based drug discovery | |
Xu et al. | Precision therapeutic targeting of human cancer cell motility | |
Cheeseman et al. | Exploiting protein conformational change to optimize adenosine-derived inhibitors of HSP70 | |
Sheng et al. | Lipids regulate Lck protein activity through their interactions with the Lck Src homology 2 domain | |
Granovsky et al. | Raf kinase inhibitory protein function is regulated via a flexible pocket and novel phosphorylation-dependent mechanism |