Piperazines

eMolecules​ 27006-02-6 | (4-Bromo-3,5-dimethylphenyl)methanol | Ambeed | MFCD00277869 | 215.090 | C9H11BrO | 98.000 | Cc1cc(CO)cc(C)c1Br | 5g | 572943451

(4-Bromo-3,5-dimethylphenyl)methanol | Ambeed | 27006-02-6 | MFCD00277869 | 215.090 | C9H11BrO | 98.000 | Cc1cc(CO)cc(C)c1Br | 5g | 572943451

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Matrix Scientific (S)-1-BOC-2-METHYLPIPERAZIN-1G

(S)-1-Boc-2-Methylpiperazine, 98%-1g,C10H20N2O2, mw 200.28,

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Medchemexpress LLC Piperazine erastin | 1538593-71-3 | 99.1% | 645.19 | C35H41ClN6O4 | 10 MG

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Piperazine erastin is a small-molecule analog of erastin that induces an iron-dependent, non-apoptotic form of cell death called ferroptosis. It is used as a research tool to probe ferroptotic mechanisms and to evaluate therapeutic or mechanistic responses in cellular and in vivo studies.

• Induces ferroptosis in cell-based assays.
• High purity suitable for research (99.12%).
• Supplied as solids and as a 10 mM solution in DMSO.
• Soluble in DMSO at reported concentrations (~33.33 mg/mL).
• Documented storage recommendations for powder and in-solvent samples.

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Medchemexpress LLC 5-(1-Piperazinyl)-2-benzofurancarboxylic acid ethyl ester dihydrochloride hydrate | 1422956-31-7 | 99.7% | C15H22Cl2N2O4 | 10 G

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5-(1-Piperazinyl)-2-benzofurancarboxylic acid ethyl ester dihydrochloride hydrate is a drug intermediate for the synthesis of various active compounds. It is a solid appearance.

• Drug intermediate for synthesis
• Solid appearance

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Ambeed AMBEED

5000866798 4-FLUORO-35-DIMETHYLPHENYL 1GR

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Chem-Impex International, Inc. 1-[5-(Trifluoromethyl)pyrid-2-yl]piperazine | 132834-58-3 | MFCD00114708 | 25G

1-[5-(Trifluoromethyl)pyrid-2-yl]piperazine, 132834-58-3, MFCD00114708, 25G

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Apexbio Technology LLC N4-Acetylsulfamethoxazole 5mg

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N4-Acetylsulfamethoxazole (CAS 21312-10-7) is a primary metabolite of sulfamethoxazole a sulfonamide antimicrobial agent This compound results from the N4-acetylation of sulfamethoxazole during hepatic metabolism and represents the predominant excreted form in urine While N4-Acetylsulfamethoxazole does not possess intrinsic antibacterial activity it is utilized in biomedical research to investigate the pharmacokinetics metabolism and disposition of sulfonamide drugs Studies involving this metabolite aid in understanding drug biotransformation pathways and can inform the evaluation of drug safety and renal excretion profiles

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Accela Chembio Inc 1-(2-methoxyethyl)piperazine | 5g | 13484-40-7 | MFCD00191214 | 98% | D: 0.97 | Shelf Life: 1260 Days | Light Sensitive/n2

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1-(2-methoxyethyl)piperazine | 5g | 13484-40-7 | MFCD00191214 | 98% | D: 0.97 | Shelf Life: 1260 Days | Light Sensitive/n2

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Accela Chembio Inc 1-(2-methoxyethyl)piperazine | 25g | 13484-40-7 | MFCD00191214 | 98% | D: 0.97 | Shelf Life: 1260 Days | Light Sensitive/n2

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1-(2-methoxyethyl)piperazine | 25g | 13484-40-7 | MFCD00191214 | 98% | D: 0.97 | Shelf Life: 1260 Days | Light Sensitive/n2

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Ambeed AMBEED

5000866968 PIPERAZINE 14-BIS2-CHLOROE 1GR

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Aobchem AOBCHEM

5000866111 N- 2-BROMO-4 5-DIMETHYLPHENYL

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TARGETMOL CHEMICALS INC GSK-LSD1 dihydrochloride 10MG

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Also available in 1 mL, 1 mg, 2 mg, 5 mg, 25 mg, 50 mg, 100 mg, 500 mg and bulk. Please contact Fisher for quotes. GSK-LSD1 dihydrochloride (GSK-LSD1 2HCl) is a specificity irreversible LSD1 inhibitor (IC50 16 nM). The selectivity of GSK-LSD1 for LSD1 is >1000 fold over other closely related FAD utilizing enzymes (i.e. MAO-A, LSD2, MAO-B). Purity 99.22%

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Medchemexpress LLC 2- 2-AMINOETHYL AMI | 25G

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2- 2-AMINOETHYL AMI | 25G

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Apexbio Technology LLC ABT 702 dihydrochloride 1188890-28-9 10mg

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ABT 702 dihydrochloride is a small-molecule inhibitor targeting adenosine kinase (AK) It is designed to inhibit AK the primary enzyme responsible for phosphorylation and metabolic inactivation of endogenous adenosine thereby elevating extracellular adenosine levels and modulating adenosine-mediated signaling ABT 702 dihydrochloride exerts its biological activity primarily through selective inhibition of AK In vitro studies indicate that ABT 702 potently inhibits AK activity and adenosine phosphorylation in intact cells Based on these pharmacological properties ABT 702 dihydrochloride holds research potential in inflammation and pain management particularly within experimental models of inflammatory and neuropathic pain

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Selleck Chemical LLC Vanoxerine dihydrochloride

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Vanoxerine (GBR-12909) is a potent and selective inhibitor of the presynaptic dopamine uptake complex

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