Carboxylic acids and derivatives

U.S. Pharmacopeia Cholesteryl caprylate | 1182-42-9 | MFCD00003642 | 200 mg

Cholesteryl caprylate | Mol Wt: 512.85 | 1182-42-9 | MFCD00003642 | 200 mg

Medchemexpress LLC Pacritinib citrate | 1228923-42-9 | 99.7% | 664.70 | 5 MG

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Pacritinib citrate is a potent inhibitor of both wild-type JAK2 (IC50=23 nM) and JAK2V617F mutant (IC50=19 nM). It also inhibits FLT3 (IC50=22 nM) and its mutant FLT3D835Y (IC50=6 nM). Pacritinib citrate can be used for the research of acute myeloid leukemia (AML) and myelofibrosis (MF).

• Potent inhibitor of wild-type JAK2 (IC50=23 nM)
• Potent inhibitor of JAK2V617F mutant (IC50=19 nM)
• Inhibits FLT3 (IC50=22 nM)
• Inhibits FLT3D835Y mutant (IC50=6 nM)
• Can be used for the research of acute myeloid leukemia (AML)
• Can be used for the research of myelofibrosis (MF)

Medchemexpress LLC Pacritinib (citrate) | 1228923-42-9 | 99.7% | 664.70 | 1 ML

Small and Specialty Supplier Partner
Small and/or specialty supplier based on Federal laws and SBA requirements.
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Pacritinib (SB1518) citrate is a potent inhibitor of both wild-type JAK2 (IC50=23 nM) and JAK2V617F mutant (IC50=19 nM). It also inhibits FLT3 (IC50=22 nM) and its mutant FLT3D835Y (IC50=6 nM). This compound can be used for the research of acute myeloid leukemia (AML) and myelofibrosis (MF).

• Potent inhibitor of wild-type JAK2 (IC50=23 nM)
• Potent inhibitor of JAK2V617F mutant (IC50=19 nM)
• Inhibits FLT3 (IC50=22 nM)
• Inhibits FLT3D835Y mutant (IC50=6 nM)
• Used for research in acute myeloid leukemia (AML) and myelofibrosis (MF)

eMolecules​ Tetrakis(decyl)ammonium bromide | 14937-42-9 | MFCD00043166 | 25g

Combi-Blocks | Tetrakis(decyl)ammonium bromide | 25g | 267196004 | QD-8053 | 97.000 | 14937-42-9 | MFCD00043166 | 659.023 | C40H84BrN

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Sigma Aldrich Fine Chemicals Biosciences Cholesteryl caprylate United States Pharmacopeia (USP) Reference Standard | 1182-42-9 | MFCD00003642 | 200MG

Cholesteryl caprylate United States Pharmacopeia (USP) Reference Standard | Mol Wt: 512.85 | 1182-42-9 | MFCD00003642 | 200MG

eMolecules​ Ambeed / Z-D-Lys(Boc)-OH / 1g / 552534496 / A112843 / / 66845-42-9 / MFCD00065699 / 380.441 / C19H28N2O6

Ambeed / Z-D-Lys(Boc)-OH / 1g / 552534496 / A112843 / / 66845-42-9 / MFCD00065699 / 380.441 / C19H28N2O6

Selleck Chemical LLC Pimethixene maleate S3913-5mg

Pimethixene (Pimetixene) maleate an antihistamine anntimigraine agent and antiserotonergic compound is a highly potent antagonist of a broad range of monoamine receptors including a variety of serotonin receptors Pimethixene maleate inhibits 5-HT2A 5-HT2B 5-HT2C 5-HT1A 5-HT1B 5-HT6 5-HT7 Adrenergic -1A Dopamine D1 Receptor Dopamine D2 Receptor Dopamine D4 4 Receptor Histamine H1 Receptor Muscarinic M1 and Muscarinic M2 with pKi of 10 22 10 44 8 42 7 63 5 7 30 7 28 7 61 6 37 8 19 7 54 10 14 8 61 and 9 38 respectively