Pyrazines
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Filtered Search Results
eMolecules 5780-66-5 | Pyrazine-2-carbaldehyde | Combi-Blocks | MFCD02179278 | 108.100 | C5H4N2O | 98.000 | O=Cc1cnccn1 | 1g | 117563116
Pyrazine-2-carbaldehyde | Combi-Blocks | 5780-66-5 | MFCD02179278 | 108.100 | C5H4N2O | 98.000 | O=Cc1cnccn1 | 1g | 117563116
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TARGETMOL CHEMICALS INC CADAZOLID 10MG
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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. Cadazolid (ACT-179811) is an oxazolidinone-type antibiotic with activity against gram-positive bacteria including Clostridium difficile. purity: 99%
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TARGETMOL CHEMICALS INC CORRECTOR C4 5MG
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Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg and bulk. Please contact Fisher for quotes. Corrector C4 a corrector commonly used to study cystic fibrosis mutants works by alleviating the interaction between CFTR transmembrane domain mutants and protein homeostasis. purity: 98%
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Bioss Histone H3mono methyl K79 Mono
Histone H3mono methyl K79 Monoclonal Antibody
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Cambridge Isotope Laboratories 1 4 5 8-TetraCN (PCN-46) (unlabeled) 100 ug/mL in nonane 1 mL
1 4 5 8-TetraCN (PCN-46) (unlabeled) 100 ug/mL in nonane 1 mL
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STEMCELL Technologies PFI-3
Epigenetic modifier; Inhibits SMARCA2 and SMARCA4 - 5 Mg
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TARGETMOL CHEMICALS INC AF-353 10MG
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Also available in 1 mg 2 mg 5 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. AF-353 (Ro-4) an effective and orally bioavailable antagonist of the P2X3/P2X2/3 receptor inhibits human and rat P2X3 (pIC50= 8.0). purity: 98%
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TARGETMOL CHEMICALS INC RECILISIB 10MG
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Also available in 1 mg 2 mg 5 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Recilisib (ON 01210) is a radioprotectantcan activate AKT PI3K activities in cells. purity: 99%
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TARGETMOL CHEMICALS INC PEIMINE 25MG
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Also available in 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. 1. Peimine (Wanpeinine A) has good anti-inflammatory effects in vivo. 2. Peimine is an inhibitor to inhibit LPS-induced production of inflammatory cytokines by blocking the MAPKs and NF-(kappa)B signaling pathway. purity: 99%
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Cell Signaling Technology Total S6 Ribosomal Protein Mat
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Total S6 Ribosomal Protein Matched Antibody Pair 1 Kit
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Cell Signaling Technology Phospho-EGF Receptor panTyr
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Phospho-EGF Receptor (panTyr) Matched Antibody Pair 1 Kit
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TARGETMOL CHEMICALS INC LDCA 5MG
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Also available in 10 mg 25 mg 50 mg 100 mg 500 mg and bulk. Please contact Fisher for quotes. LDCA is a double-hit metabolic regulator that exhibits potent anti-proliferative activity. lDCA competitively inhibits LDH-A enzyme activity alters mitochondrial hyperpolarization and simultaneously subverts apoptosis. lDCA has a pronounced effect in cancer cells and does not show toxicity. purity: 98%
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TARGETMOL CHEMICALS INC CPSI-1306 10MG
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Also available in 25 mg 50 mg 100 mg 200 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. (±)-CPSI-1306 (2-(3-(24-Difluorophenyl)-45-dihydroisoxazol-5-yl)-1-morpholinoethan-1-one) is a macrophage migration inhibitory factor (MIF) antagonist and can be used in studies about non-insulin-dependent diabetes mellitus (NIDDM) and the prevention of the deleterious cutaneous effects of acute and chronic UVB exposure. purity: 97%
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TARGETMOL CHEMICALS INC KURARINONE 5MG
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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. Kurarinone a flavanoid derived from shrub Sophora flavescensKurarinone exhibits anti-tumor estrogenic and anti-inflammatory activities it also shows strong inhibitory effect on immune responses. Kurarinone may ameliorate chronic inflammatory skin diseases through the suppression of pathogenic CD4(+) T-cell differentiation and the overall immune response. purity: 99%
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TARGETMOL CHEMICALS INC CE-224535 5MG
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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. CE-224535 (PF-04905428) is a selective antagonist of P2X7 receptor. CE-224535 can be used in disease-modifying antirheumatic studies. purity: 98%
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