Pyrazines

eMolecules​ Methyl 6-iodopyrazine-2-carboxylate | 1603172-68-4 | | 1g

Synthonix - Stock | Methyl 6-iodopyrazine-2-carboxylate | 1g | 499993976 | M63354 | | 1603172-68-4 | | 264.022 | C6H5IN2O2

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eMolecules​ Accela ChemBio (ASD) (S)-3-(2-Morpholinyl)propanoic Acid Hydrochloride 5g 475561089 SY261758 95.000 1787250-02-5 [null] 195.640 C7H14ClNO3

Accela ChemBio (ASD) (S)-3-(2-Morpholinyl)propanoic Acid Hydrochloride 5g 475561089 SY261758 95.000 1787250-02-5 [null] 195.640 C7H14ClNO3

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TARGETMOL CHEMICALS INC GLOBALAGLIATIN 5MG

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Also available in 1 mg 10 mg 25 mg 50 mg and bulk. Please contact Fisher for quotes. Globalagliatin (LY2608204) has been used in trials studying the treatment of Diabetes Mellitus Type 2. purity: 99%

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TARGETMOL CHEMICALS INC TAMIBAROTENE 200MG

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Also available in 10 mg 25 mg 50 mg 100 mg 500 mg 1000 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Tamibarotene (Amnolake) is an orally active synthetic retinoid developed to overcome all-trans retinoic acid (ATRA) resistance with potential antineoplastic activity. purity: 98%

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Chemscene ChemScene | Methyl 6-chloropyrazine-2-carboxylate | 10G | CS-W003732 | 0.98 | 23611-75-8| MFCD10686598 | 172.57

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ChemScene | Methyl 6-chloropyrazine-2-carboxylate | 10G | CS-W003732 | 0.98 | 23611-75-8| MFCD10686598 | 172.57

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TARGETMOL CHEMICALS INC MENIN-MLL INHIBITOR MI-2 10MG

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Also available in 1 mg 2 mg 5 mg 25 mg 50 mg 100 mg 200 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Menin-MLL inhibitor MI-2 (MI2) is a potent menin-MLL interaction inhibitor with IC50 of 446 nM. purity: 97%

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TARGETMOL CHEMICALS INC DMAT 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. DMAT (Casein kinase II Inhibitor) is a potent and specific inhibitor of CK2(IC50 value of 130 nM). purity: 99%

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TARGETMOL CHEMICALS INC BYK204165 25MG

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Also available in 1 mg 5 mg 10 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. BYK204165 (RT-017290) is a potent PARP inhibitor (PARP1; IC50 = 44.67 nM for human recombinant PARP1 in an enzyme assay)purity: 99%

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Medchemexpress LLC 2,4-diamino-6-hydroxypyrimidine | 56-06-4 | MFCD00006098 | >98.0% | 126.12 g/mol | C4H6N4O | 1 G

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2,4-diamino-6-hydroxypyrimidine is a small-molecule research reagent used primarily as an inhibitor of GTP cyclohydrolase I (GCH1). It is supplied as a solid and is used in biochemical and enzymatic studies to probe folate and pteridine biosynthesis pathways.

• acts as a GTP cyclohydrolase I (GCH1) inhibitor
• molecular weight 126.12 g/mol
• CAS number 56-06-4
• purity greater than 98.0% (HPLC)
• appearance off-white to light yellow solid
• suitable for enzymatic assays and biochemical research

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TARGETMOL CHEMICALS INC AZD1940 5MG

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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. AZD1940 (UNII-0J0035E9FT) is a high affinity CB(1)/CB(2) receptor agonist of the cannabinoid with oral activity. Application in the study of orofacial pain. purity: 99%

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TARGETMOL CHEMICALS INC RO 67-7476 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. Ro 67-7476 is a positive allosteric modulator of mGlu1 receptors. No activity at human mGlu1 receptors. Potentiates glutamate-induced calcium release with EC 50 of 60.1 nM. purity: 99%

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TARGETMOL CHEMICALS INC SAR-260301 5MG

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Also available in 1mg 10mg 25mg 50mg 100mg 500mg and bulk. Please contact Fisher for quotes. SAR-260301 is an orally available and selective inhibitor of PI3Kβ (IC50: 23 nM). purity: 98%

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TARGETMOL CHEMICALS INC Research Chemical 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. Pifithrin-(alpha), p-Nitro, Cyclic (PFN-(alpha)) (PFN-(alpha)) is cell-permeable and active-form inhibitor of p53. purity: 99%

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TARGETMOL CHEMICALS INC 4E1RCAT 25MG

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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. 4E1RCat is a dual inhibitor of eIF4EeIF4 g and eIF4E4E-BP1 interaction. And it inhibits the binding of eIF4 g to eIF4E with IC50 of 3.2 uM. purity: 99%

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Sigma Aldrich Fine Chemicals Biosciences 2,3-Pyrazinedicarboxylic anhydride 97% | 4744-50-7 | MFCD00179418 | 25G

2,3-Pyrazinedicarboxylic anhydride 97% | Purity: 97% | Mol Wt: 150.09 | 4744-50-7 | MFCD00179418 | 25G

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