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Cas Index 2

• 2101700-15-4 | Pirtobrutinib (Catalog# : 20618)
• 2904682-19-3 | PDS-0330 (Catalog# : 231106)PDS0330 is a new claudin-1 inhibitor in Colorectal Cancer.
• 2253123-16-7 | Pimicotinib ( ABSK02 ) (Catalog# : 20548)Pimicotinib is a novel small molecule inhibitor of CSF-1R, which is orally available,
• 260415-63-2 | PD-173955 (Catalog# : 20499)PD-173955 is a src tyrosine kinase inhibitor. PD173955 inhibited Bcr-Abl-dependent ce
• 217171-01-2 | PD-173212 (Catalog# : 20468)PD-173212 is a small molecule N-type calcium channel blocker. PD173212 fully reduced
• 2172870-89-0 | Paltusotine ( CRN-00808 ) (Catalog# : 20294)Paltusotine is a new class of oral, selective, nonpeptide, somatostatin receptor type
• 2230198-02-2 | PF-06882961 (Catalog# : 21251)PF-06882961 is a potent, orally bioavailable agonist of the glucagon-like peptide-1 r
• 26305-03-3 | Pepstatin (Catalog# : 2071607)Pepstatin inhibits the aspartic protease endothiapepsin.
• 2227425-05-8 | PF-06869206 (Catalog# : 2071506)PF-06869206 is an Orally Bioavailable Selective Inhibitors of the Sodium-Phosphate Co
• 26033-20-5 | 3-PHENYL-1H-PYRAZOLE-4-CARBALDEHYDE (Catalog# : 2062020)
• 248282-01-1 | Paquinimod (Catalog# : 2061706)Paquinimod, also known as ABR‑215757, is a S100A9 inhibitor preventing S100A9 bindi
• 2170608-82-7 | PZ-2891 (Catalog# : 193282)PZ-2891 is a potent and selective, orally active Pantothenate kinase (PANK) modulator
• 2185857-97-8 | PF-06873600 (Catalog# : 191145)PF-06873600 is an orally bioavailable, cyclin-dependent kinase (CDK) inhibitor, with
• 2070014-93-4 | PF-CBP1 HCl (Catalog# : 179112)PF-CBP1, also known as PF-06670910, is potent and highly-selective inhibitor of the b
• 25606-41-1 | Propamocarb hydrochloride (Catalog# : 2017080115)Propamocarb hydrochloride is an efficient, broad-spectrum, carbamate fungicide safe. 
• 257933-82-7 | Pelitinib (Catalog# : 17022702)Pelitinib (EKB-569; WAY-EKB 569) is a potent irreversible EGFR inhibitor with IC50 of
• 202350-68-3 | PNU-159682 (Catalog# : 16071409)PNU-159682 is a major active metabolite of nemorubicin (MMDX) in human liver microsom
• 269718-84-5 | Pardoprunox (Catalog# : 122523)Pardoprunox is a novel partial dopamine D2 and D3 receptor agonist and serotonin 5-HT
• 219580-11-7 | PD173074 (Catalog# : 122212)PD173074 is a small-molecule FGFR3-selective tyrosine kinase inhibitor (TKI), as a th
• 269718-83-4 | Pardoprunox hydrochloride (Catalog# : 111010)Pardoprunox hydrochloride is a novel partial dopamine D2 and D3 receptor agonist and
• 20062-91-3 | 3-(4-phenoxyphenyl)propanoic acid (Catalog# : 90709)Coming soon!
• 212844-53-6 | Purvalanol A (Catalog# : 52564)Purvalanol A(NG-60) is a potent, cell-permeable, and selective inhibitor of cyclin-de
• 212844-54-7 | Purvalanol B (Catalog# : 52559)Purvalanol B(NG-95) is a cyclin-dependent kinase inhibitor with IC50 values of 6, 6,
• 2645-32-1 | PR-619 (Catalog# : 52227)PR-619 is a broad-range DUB inhibitor with potential for further development as a che
• 2794934-49-7 | RGT-018 (Catalog# : 24148)RGT-018 is a potent and orally active SOS1 inhibitor with anti-tumor effects.
• 2204289-53-0 | (Rac)-SHIN2 (Catalog# : 24136)(Rac)-SHIN2 is a serine hydroxymethyltransferase (SHMT) inhibitor having 1,4-dihydrop
• 2642037-07-6 | RMC-4998 (Catalog# : 20666)RMC-4998 is a tri-complex inhibitor and KRASG12C inhibitor. RMC-4998 targets the acti
• 2503036-46-0 | RNK-05047 (Catalog# : 24008)RNK-05047 is a PROTAC degrader of BRD4 which displays significant tumor growth inhibi
• 2750709-91-0 | Resigratinib (Catalog# : 20627)Resigratinib is a fibroblast growth factor receptor tyrosine kinase inhibitor and ant
• 2031185-00-7 | Risvodetinib (Catalog# : 20621)Risvodetinib, also known as IkT-148009., is a brain-penetrant c-Abl inhibitor with a