Pyrazines
TARGETMOL CHEMICALS INC RANOLAZINE 200MG
Also available in 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Ranolazine (RS 43285-003) is a calcium uptake inhibitor via the sodium/calcium channel used to treat chronic angina. It affects the sodium-dependent calcium channels during myocardial ischemia in rabbits by altering the intracellular sodium level. purity: 98%
TARGETMOL CHEMICALS INC RS 15385-198 5MG
Also available in 1mg 10mg 25mg 50mg 100mg 500mg and bulk. Please contact Fisher for quotes. RS 15385-198 is a less active isomer of Delequamine. Delequamine is a selective alpha2-adrenergic receptor antagonist. purity: 98%
TARGETMOL CHEMICALS INC ISATORIBINE 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg and bulk. Please contact Fisher for quotes. Isatoribine(ANA245) free base is a potent TLR7 receptor agonist with anti-hepatitis C virus infection activity for the study of HCV infection. purity: 99%
TARGETMOL CHEMICALS INC DPTIP 5MG
Also available in 1 mg 2 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. DPTIP is an effective inhibitor of neutral sphingomyelinase 2 with an IC50 value of 30 nM. purity: 98%
TARGETMOL CHEMICALS INC YO-01027 10MG
Also available in 1 mg 2 mg 5 mg 25 mg 50 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. YO-01027 (DBZ) is a potent (gamma)-secretase inhibitor. purity: 99%
TARGETMOL CHEMICALS INC GOLVATINIB 25MG
Also available in 2 mg 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Golvatinib (E-7050) is an orally bioavailable dual kinase inhibitor of c-Met (hepatocyte growth factor receptor) and VEGFR-2 (vascular endothelial growth factor receptor-2) tyrosine kinases with potential antineoplastic activity. c-Met/VEGFR kinase inhibitor E7050 binds to and inhibits the activities of both c-Met and VEGFR-2 which may inhibit tumor cell growth and survival of tumor cells that overexpress these receptor tyrosine kinases. c-Met and VEGFR-2 are upregulated in a variety of tumor cell types and play important roles in tumor cell growth migration and angiogenesis. purity: 98%
TARGETMOL CHEMICALS INC TELAPREVIR 10MG
Also available in 1 mg 5 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Telaprevir (Incivek) (VX-950) is an effective inhibitor of HCV NS3-4A serine protease (IC50 0.35 uM). purity: 96%
TARGETMOL CHEMICALS INC TRANS-TRANILAST 25MG
Also available in 5 mg 10 mg 50 mg 100 mg 200 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Trans-Tranilast is an antiallergic drug developed by Kissei Pharmaceuticals. It was approved in 1982 for use in Japan and South Korea for bronchial asthma. Indications for keloid and hypertrophic scar were added in 1993. It has been used for the treatment of allergic disorders such as asthma allergic rhinitis and atopic dermatitis. purity: 99%
TARGETMOL CHEMICALS INC ERG240 5MG
Also available in 1mg 5mg and bulk. Please contact Fisher for quotes. ERG240 is an inhibitor of branched-chain amino acid aminotransferase 1 (BCAT1). ERG240 can be used for the research of rheumatoid arthritis cancer and bone disease. purity: 99%
Accela Chembio Inc 5-methyl-2-pyrazinecarboxylic Acid | 100g | 5521-55-1 | MFCD00068241 | 98% | Shelf Life: 1440 Days | Regular
5-methyl-2-pyrazinecarboxylic Acid | 100g | 5521-55-1 | MFCD00068241 | 98% | Shelf Life: 1440 Days | Regular
Cell Signaling Technology Phospho-Tau Ser416 Matched A
Phospho-Tau (Ser416) Matched Antibody Pair 1 Kit
eMolecules 381-98-6 | 2-(Trifluoromethyl)acrylic acid | Combi-Blocks | MFCD00042424 | 140.061 | C4H3F3O2 | 97.000 | OC(=O)C(=C)C(F)(F)F | 1g | 205389902
2-(Trifluoromethyl)acrylic acid | Combi-Blocks | 381-98-6 | MFCD00042424 | 140.061 | C4H3F3O2 | 97.000 | OC(=O)C(=C)C(F)(F)F | 1g | 205389902
TARGETMOL CHEMICALS INC IXAZOMIB 10MG
Also available in 1 mg 5 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Ixazomib (MLN2238) a second generation boron-containing peptide proteasome inhibitor (PI) inhibits the chymotrypsin-like proteolytic ((beta)5) site of the 20S proteasome (IC50/Ki 3.4/0.93 nM in cell-free assays) also inhibits the caspase-like ((beta)1) and trypsin-like ((beta)2) proteolytic sites (IC50 31/3500 nM). purity: 98%
eMolecules 333-27-7 | Methyl trifluoromethanesulfonate | Combi-Blocks | MFCD00000409 | 164.100 | C2H3F3O3S | 96.000 | COS(=O)(=O)C(F)(F)F | 100g | 117556956
Methyl trifluoromethanesulfonate | Combi-Blocks | 333-27-7 | MFCD00000409 | 164.100 | C2H3F3O3S | 96.000 | COS(=O)(=O)C(F)(F)F | 100g | 117556956