共 304516 个产品
- 货号:197331CAS:810659-53-1包装:5 MG分子式:C24H21N3O6S2纯度规格:The Bcl-2 Inhibitor II, YC137, also referenced under CAS 810659-53-1, controls the biological activity of Bcl-2. This small molecule/inhibitor is primarily used for Activators/Inducers applications.分子量:511.57
- 货号:203646CAS:1206711-16-1包装:5 MG分子式:C24H20N4O纯度规格:The BMP Inhibitor II, DMH1, also referenced under CAS 1206711-16-1, controls the biological activity of BMP. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.分子量:380.44
- 货号:203694CAS:包装:5 MG分子式:K[VO(O2)2C10H8N2] · 3H2O纯度规格:A potent inhibitor of phosphotyrosine phosphatase (Ki = 100 nM for insulin receptor dephosphorylation).分子量:
- 货号:203987CAS:487-52-5包装:5 MG分子式:C15H12O5纯度规格:A cell-permeable, reversible, substrate competitive, plant polyphenol that acts as a specific protein tyrosine kinase inhibitor.分子量:272.25
- 货号:215900CAS:包装:5 MG分子式:C13H12N4O5S纯度规格:The Carbonic Anhydrase IX/XII Inhibitor controls the biological activity of Carbonic Anhydrase IX/XII. This small molecule/inhibitor is primarily used for Cancer applications.分子量:336.32
- 货号:215901CAS:包装:5 MG分子式:C13H12FN3O3S纯度规格:The Carbonic Anhydrase IX/XII Inhibitr II, U-104 controls the biological activity of Carbonic Anhydrase IX/XII. This small molecule/inhibitor is primarily used for Cancer applications.分子量:309.32
- 货号:400012CAS:178603-78-6包装:5 MG分子式:C24H33ClN4O8纯度规格:The Caspase-1 Inhibitor II, also referenced under CAS 178603-78-6, controls the biological activity of Caspase-1. This small molecule/inhibitor is primarily used for Cancer applications.分子量:540.99
- 货号:688225CAS:219137-85-6包装:5 MG分子式:C33H36F3N5O10纯度规格:Fluorogenic caspase-1 substrate.分子量:719.66
- 货号:218739CAS:包装:5 MG分子式:C38H40N8O11纯度规格:A fluorogenic substrate for detecting caspase-1 (ICE), caspase-4, and caspase-5 activity.分子量:784.77
- 货号:218763CAS:包装:5 MG分子式:C38H44F3N5O12纯度规格:A fluorogenic substrate for caspase-6 (Mch2).分子量:819.78
- 货号:217699CAS:包装:5 MG分子式:C18H13N3OS2纯度规格:RO-3306 is a cell-permeable, potent and ATP-competitive inhibitor of Cdk1 (Ki = 35 nM and 110 nM for Cdk1/B1 and Cdk1/A, respectively).分子量:351.45
- 货号:219671CAS:328541-79-3包装:5 MG分子式:C19H15Br2N3O3纯度规格:CFTR Inhibitor II, GlyH-101, CAS 328541-79-3, is a cell-permeable potent, selective and reversible open-channel blocker of CFTR (Ki = 4.3 μM in CFTR-expressing FRT cells).分子量:493.15
- 货号:220005CAS:75450-34-9包装:5 MG分子式:C15H11Cl2NOS纯度规格:A cell-permeable benzothiazepine derivative of clonazepam that acts as a specific and potent inhibitor of the mitochondrial Na+/Ca2+ exchanger (IC50 = 360 nM).分子量:324.22
- 货号:229103CAS:1001478-90-5包装:5 MG分子式:C20H22N4OS纯度规格:The Choline Kinase-α Inhibitor, CK37, also referenced under CAS 1001478-90-5, controls the biological activity of Choline Kinase-α. This small molecule/inhibitor is primarily used for Phosphorylation & Dephosphorylation applications.分子量:366.48
- 货号:230950CAS:74772-77-3包装:5 MG分子式:C18H23NO3S纯度规格:A potent thiazolinedione (TDZ) type anti-hyperglycemic agent and a selective PPARγ agonist (EC50 = 3 μM).分子量:333.45
- 货号:236005CAS:130717-51-0包装:5 MG分子式:C23H25N3O3S · xHCl纯度规格:The COX-1 Inhibitor, FR122047, also referenced under CAS 130717-51-0, controls the biological activity of COX-1. This small molecule/inhibitor is primarily used for Cell Signaling applications.分子量:423.53 (free base basis)
- 货号:236015CAS:116686-15-8包装:5 MG分子式:C15H13F2NO4S纯度规格:The COX-2 Inhibitor V, FK3311, also referenced under CAS 116686-15-8, controls the biological activity of COX-2. This small molecule/inhibitor is primarily used for Cell Signaling applications.分子量:341.33
- 货号:238395CAS:9001-15-4包装:5 KU分子式:纯度规格:Creatine Phosphokinase, Porcine Heart, CAS 9001-15-4, is a native creatine phosphokinase that catalyzes the reversible conversion of creatine and ATP to creatine phosphate and ADP.分子量:
- 货号:376650CAS:124753-97-5包装:5 MG分子式:C24H47NO3纯度规格:Biologically active, cell-permeable, non-physiological ceramide analog.分子量:397.63
- 货号:165304CAS:79055-68-8包装:5 MG分子式:C5H12NO5P纯度规格:Active enantiomer of DL-2-amino-5-phosphonopentanoic acid (AP5) that is a commonly used as a competitive NMDA receptor antagonist.分子量:197.13
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