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Neuropathiazol - ≥98%(HPLC), high purity , CAS No.880090-88-0
Selective inducer of neuronal differentiation in hippocampal neural progenitors
Basic Description Synonyms AKOS015919526 | BCPP000150 | Ethyl 4-(methyl(2-phenylthiazol-4-yl)amino)benzoate;Neuropathiazol | SCHEMBL8238620 | BCP02467 | A14058 | DTXSID80470323 | Ethyl 4-(methyl(2-phenylthiazol-4-yl)amino)benzoate | FT-0727742 | HB3105 | Ethyl 4-[methyl-(2-phenyl-1 Specifications & Purity ≥98%(HPLC) Biochemical and Physiological Mechanisms Selective inducer of neuronal differentiation in cultured hippocampal neural progenitor cells (NPCs). Selectively suppresses astrocyte differentiation when induced by LIF, BMP2 and FBS compared to retinoic acid. Enhances maturation of NPC derived neurons. Storage Temp Store at -20°C Shipped In Ice chest + Ice pads Product Description Product description：
Neuropathiazol, a neuronal differentiation inducer, selectively induces neuronal differentiation of multipotent hippocampal neural progenitor cells.
Associated Targets(Human) Associated Targets(non-human) Names and Identifiers Pubchem Sid 488197653 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488197653 IUPAC Name ethyl 4-[methyl-(2-phenyl-1,3-thiazol-4-yl)amino]benzoate INCHI InChI=1S/C19H18N2O2S/c1-3-23-19(22)15-9-11-16(12-10-15)21(2)17-13-24-18(20-17)14-7-5-4-6-8-14/h4-13H,3H2,1-2H3 InChi Key MGKYEWWFHSESJN-UHFFFAOYSA-N Canonical SMILES CCOC(=O)C1=CC=C(C=C1)N(C)C2=CSC(=N2)C3=CC=CC=C3 Isomeric SMILES CCOC(=O)C1=CC=C(C=C1)N(C)C2=CSC(=N2)C3=CC=CC=C3 PubChem CID 11667240 Molecular Weight 338.42
Chemical and Physical Properties Solubility Solvent:DMSO, Max Conc. mg/mL: 33.84, Max Conc. mM: 100; Solvent:ethanol, Max Conc. mg/mL: 6.77, Max Conc. mM: 20
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D23141887