Pyrazines

Aromatic organic heterocyclic compounds that consist of a six-membered ring with four carbon atoms and two nitrogen atoms at opposite positions of the ring, making this ring symmetrical.

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1,051 – 1,065 of 2,793 results

1,051

Bioss Mono-Methyl-Histone H3 Lys27

Mono-Methyl-Histone H3 Lys27 Monoclonal Antibody

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1,052

Bioss Mono-Methyl-Histone H3 Lys36

Mono-Methyl-Histone H3 Lys36 Monoclonal Antibody

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1,053

TARGETMOL CHEMICALS INC PYR3 5MG

Also available in 1 mg 2 mg 10 mg 25 mg 50 mg 100 mg 200 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Pyr3 is a selective transient receptor potential canonical channel 3 inhibitor. Pyr3 inhibits TRPC3-mediated Ca2+ influx in a dose-dependent manner(IC50 = 700 nM). purity: 99%

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1,054

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%

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1,055

TARGETMOL CHEMICALS INC GAVESTINEL 5MG

Also available in 1 mg 10 mg 25 mg 50 mg 100 mg and bulk. Please contact Fisher for quotes. Gavestinel (GV 150526) is a non-competitive NMDA receptor antagonist that is potent selective and orally active.Gavestinel binds to the glycine site of the NMDA receptor with a binding affinity (pKi value) of 8.5.Gavestinel is used in acute ischaemic stroke studies. purity: 99%

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1,056

TARGETMOL CHEMICALS INC RELDESEMTIV 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. Reldesemtiv (CK-2127107) is a selective activator of fast skeletal muscle troponin with an EC50 of 3.4 uM. Reldesemtiv increases exercise performance in the heart failure model. purity: 95%

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1,057

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%

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1,058

TARGETMOL CHEMICALS INC UNC1999 25MG

Also available in 1 mg 2 mg 5 mg 10 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. UNC1999 is a orally bioavailable effective and specific inhibitor of EZH2 (IC50=2 nM) and EZH1 (IC50=45). purity: 99%

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1,059

TARGETMOL CHEMICALS INC ML400 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. ML400 (CID73050863) is an allosteric inhibitor of LMPTP with an EC50 of 1uM. ML400 displays good cell-based activity and rodent pharmacokinetics. purity: 99%

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1,060

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%

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1,061

TARGETMOL CHEMICALS INC E-FECP-OXINDOLE 5MG

Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg and bulk. Please contact Fisher for quotes. (E)-FeCP-oxindole is an inhibitor of VEGFR2 with IC50 of 214 nM. purity: 99%

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1,062

eMolecules 1380571-72-1 | 6-Oxa-1-azaspiro[3.3]heptane hemioxalate | ChemScene | MFCD22373634 | 288.300 | C12H20N2O6 | 97.000 | OC(=O)C(O)=O.C1CC2(COC2)N1.C1CC2(COC2)N1 | 1g | 572309274

6-Oxa-1-azaspiro[3.3]heptane hemioxalate | ChemScene | 1380571-72-1 | MFCD22373634 | 288.300 | C12H20N2O6 | 97.000 | OC(=O)C(O)=O.C1CC2(COC2)N1.C1CC2(COC2)N1 | 1g | 572309274