Pyrazines
Cell Signaling Technology Acetyl-Histone H3 Lys27 Matc
Acetyl-Histone H3 (Lys27) Matched Antibody Pair 1 Kit
Cell Signaling Technology Total PDGF Receptor alpha Matc
Total PDGF Receptor alpha Matched Antibody Pair 1 Kit
TARGETMOL CHEMICALS INC SKF83959 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. SKF83959 a benzazepine analog is a selective and potent partial agonist of the dopamine D1 receptor with Ki values of 1.18 7.56 920 and 399 nM for rat D1 D5 D2 and D3 receptors respectively.SKF83959 is a potent variant modulator of the sigma ((sigma))-1 receptor which ameliorates cognitive dysfunction for the study depression and Alzheimer's disease. purity: 98%
TARGETMOL CHEMICALS INC VPC-18005 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. VPC-18005 is a luciferase inhibitor. VPC-18005 inhibits ERG-induced transcription and interacts directly with the ERG-ETS domain thereby disrupting the ERG binding to DNA. purity: 98%
TARGETMOL CHEMICALS INC ODM-203 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. ODM-203 a Selective Inhibitor of FGFR and VEGFR Shows Strong Antitumor Activity and Induces Antitumor Immunitypurity: 98%
eMolecules 24484-98-8 | 2,3-Diamino-4-chloropyridine | Synthonix - Stock | MFCD13181777 | 143.570 | C5H6ClN3 | 95.000 | Nc1nccc(Cl)c1N | 250mg | 525914234
2,3-Diamino-4-chloropyridine | Synthonix - Stock | 24484-98-8 | MFCD13181777 | 143.570 | C5H6ClN3 | 95.000 | Nc1nccc(Cl)c1N | 250mg | 525914234
Cambridge Isotope Laboratories Oxydemeton-methyl (unlabeled) 100 ug/mL in acetonitrile 1 2 mL
Oxydemeton-methyl (unlabeled) 100 ug/mL in acetonitrile 1 2 mL
eMolecules 333-27-7 | Methyl trifluoromethanesulfonate | Combi-Blocks | MFCD00000409 | 164.100 | C2H3F3O3S | 96.000 | COS(=O)(=O)C(F)(F)F | 500g | 117556957
Methyl trifluoromethanesulfonate | Combi-Blocks | 333-27-7 | MFCD00000409 | 164.100 | C2H3F3O3S | 96.000 | COS(=O)(=O)C(F)(F)F | 500g | 117556957
TARGETMOL CHEMICALS INC ALPHA-CYPERONE 25MG
Also available in 5 mg 50 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. 1. alpha-Cyperone ((alpha)-Cyperone) is a promising inhibitor of Hla production by S. aureus and protects lung cells from this bacterium. 2. alpha-Cyperone significantly inhibited PGE2 production by suppressing the LPS-induced expression of inducible COX-2 at both the mRNA and the protein levels downregulated the production and mRNA expression of the inflammatory cytokine IL-6. 3. alpha-Cyperone inhibited actin cytoskeleton polymerization induced by APEC-O78 through down regulating the expression of Nck-2 Cdc42 and Rac1. purity: 99%
TARGETMOL CHEMICALS INC VP-4604 50MG
Also available in 100 mg 500 mg and bulk. Please contact Fisher for quotes. VP-4604 is a potent anti-methicillin-resistant Staphylococcus aureus (MRSA) compound. VP-4604 exhibited significant microbial growth inhibition against S. aureus with an MIC of 4-8 ug/mL. VP-4604 inhibited the growth of methicillin-resistant S. aureus with a growth inhibition rate of over 95%. purity: 99%
TARGETMOL CHEMICALS INC CDK1/2 INHIBITOR III 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg and bulk. Please contact Fisher for quotes. Cdk1/2 Inhibitor III is a selective Cdk1/2 inhibitor with an IC50 value of 2.1 uM against CDK1/cyclin B. purity: 99%
TARGETMOL CHEMICALS INC CF53 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. CF53 is a highly potent selective and orally active inhibitor of BET protein with a Ki of <1 nM Kd of 2.2 nM and an IC50 of 2 nM for BRD4 BD1. CF53 binds to both the BD1 and BD2 domains of BRD2 BRD3 BRD4 and BRDT BET proteins with high affinities very selective over non-BET bromodomain-containing proteins. CF53 shows potent anti-tumor activity both in vitro and in vivo. purity: 100%
Medchemexpress LLC 5-Bromo-2,4-diamino-6-hydroxypyrimidine | 6312-72-7 | 205.01 | 1 G
5-Bromo-2,4-diamino-6-hydroxypyrimidine is a biochemical reagent with a molecular weight of 205.01 and a chemical formula of C4H5BrN4O. It is intended for research use only.
- For research use only
- Not sold to patients
TARGETMOL CHEMICALS INC AS1949490 10MG
Also available in 1 mg 2 mg 5 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. AS1949490 activated glucose metabolism via up-regulation of GLUT1 gene in L6 myotubes[1][2]. AS1949490 is a potent and selective SHIP-2 (SH2 domain-containing inositol 5′ phosphatase 2) inhibitor with an IC50 of 620 nM. purity: 99%
TARGETMOL CHEMICALS INC INS3-54-A26 5MG
Also available in 1 mg 2 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. inS3-54-A26 is an inhibitor of the DNA-binding domain of STAT3. inS3-54-A26 suppresses tumor growth metastasis and the gene expression of STAT3. purity: 98%