Pyrazines
TARGETMOL CHEMICALS INC CCT129202 5MG
Also available in 1 mg 2 mg 10 mg 25 mg 50 mg 100 mg 500 mg and bulk. Please contact Fisher for quotes. CCT129202 is an ATP-competitive pan-Aurora inhibitor for Aurora A Aurora B and Aurora C with IC50 of 0.042 uM 0.198 uM and 0.227 uM respectively. It is less potent to FGFR3 GSK3(beta) PDGFR(beta) etc. purity: 98%
TARGETMOL CHEMICALS INC 48740 RP 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. 48740 RP (RP 55779) is an antagonist of platelet-activating factor. purity: 99%
TARGETMOL CHEMICALS INC RS102895 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. RS102895 is a potent CCR2 antagonist (IC50 360 nM) and shows no effect on CCR1. purity: 99%
TARGETMOL CHEMICALS INC EPZ004777 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. EPZ004777 is a potent selective DOT1L inhibitor with IC50 of 0.4 nM. purity: 99%
TARGETMOL CHEMICALS INC HDHODH-IN-5 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. hDHODH-IN-5 is an inhibitor of human dihydroorotate dehydrogenase (hDHODH IC50 = 0.91 uM). purity: 98%
eMolecules 6164-79-0 | Methyl 2-pyrazinecarboxylate | Synthonix - Stock | MFCD00014611 | 138.126 | C6H6N2O2 | 97.000 | COC(=O)c1cnccn1 | 5g | 525920636
Methyl 2-pyrazinecarboxylate | Synthonix - Stock | 6164-79-0 | MFCD00014611 | 138.126 | C6H6N2O2 | 97.000 | COC(=O)c1cnccn1 | 5g | 525920636
TARGETMOL CHEMICALS INC PDE4B-IN-2 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. PDE4B-IN-2 (A 33) is an orally active and selective PDE4B inhibitor with an IC50 of 15 nM. PDE4B-IN-2 inhibits PDE4D (IC50=1.7 µM). PDE4B-IN-2 exhibits potent anti-inflammatory effects. purity: 99%
eMolecules 2417-73-4 | Methyl 2-bromomethylbenzoate | Ambeed | MFCD03425900 | 229.073 | C9H9BrO2 | 95.000 | COC(=O)c1ccccc1CBr | 25g | 490552202
Methyl 2-bromomethylbenzoate | Ambeed | 2417-73-4 | MFCD03425900 | 229.073 | C9H9BrO2 | 95.000 | COC(=O)c1ccccc1CBr | 25g | 490552202
TARGETMOL CHEMICALS INC CRK12-IN-2 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg and bulk. Please contact Fisher for quotes. CRK12-IN-2 is a potent inhibitor of CRK12.CRK12-IN-2 inhibits the parasite with EC50 values of 3.2 and 0.08 nM for Trypanosoma congolense and Trypanosoma vivax respectively.CRK12-IN-2 can be used for the prevention and treatment of trypanosomiasis in animals. purity: 99%
TARGETMOL CHEMICALS INC WS3 25MG
Also available in 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. WS3 a (beta) cell proliferation inducer regulates Erb3 binding protein-1 (EBP1) and the I(kappa)B kinase pathway. purity: 98%
TARGETMOL CHEMICALS INC GINSENOSIDE F1 25MG
Also available in 5 mg 10 mg 50 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Ginsenoside F1 (20(S)-Ginsenoside F1) is an enzymatically modified derivative of ginsenoside Rg1 showing competitive inhibition of the activity of CYP3A4 and a weaker inhibition of the activity of CYP2D6. purity: 99%
![eMolecules 4042-36-8 | D-Pyr-OH | Ambeed | MFCD00066212 | 129.115 | C5H7NO3 | 98.000 | OC(=O)[C@H]1CCC(=O)N1 | 10g | 490520953](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502422108.JPG-250.jpg)
eMolecules 4042-36-8 | D-Pyr-OH | Ambeed | MFCD00066212 | 129.115 | C5H7NO3 | 98.000 | OC(=O)[C@H]1CCC(=O)N1 | 10g | 490520953
D-Pyr-OH | Ambeed | 4042-36-8 | MFCD00066212 | 129.115 | C5H7NO3 | 98.000 | OC(=O)[C@H]1CCC(=O)N1 | 10g | 490520953
TARGETMOL CHEMICALS INC PBRM1-BD2-IN-5 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. PBRM1-BD2-IN-5 is a potent PBRM1 Bromodomain inhibitor with Kd values of 1.5 uM and 3.9 uM for PBRM1-BD2 and PBRM1-BD5 respectively and an IC50 value of 0.26 uM for PBRM1-BD2. PBRM1-BD2-IN-5 reduces the binding of full-length PBRM1 within the PBAF complex in cell lysates to acetylated histone peptide. PBRM1-BD2-IN-5 can be used to research anticancer. purity: 99%