Drug Standards

Sigma Aldrich Fine Chemicals Biosciences Amisulpride British Pharmacopoeia (BP) Reference Standard | 71675-85-9 | MFCD00866691 |

Amisulpride British Pharmacopoeia (BP) Reference Standard | Mol Wt: 369.48 | 71675-85-9 | MFCD00866691 |

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Medchemexpress LLC Tofacitinib Impurity | 100MG

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Tofacitinib Impurity | 100MG

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Medchemexpress LLC Cytidine, 2'-deoxy-2',2'-difluoro-, hydrochloride | 122111-03-9 | 99.9% | C9H12ClF2N3O4 | 1 ML

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Gemcitabine hydrochloride is a pyrimidine nucleoside analog antimetabolite and an antineoplastic agent. It inhibits DNA synthesis and repair, leading to autophagy and apoptosis.

• Targets DNA/RNA synthesis
• Functions as a nucleoside antimetabolite/analog
• Induces autophagy and apoptosis
• Used in cancer research

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Selleck Chemical LLC Mitoxantrone 2HCl 10mM/1mL 70476-82-3 NSC-301739

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Mitoxantrone 2HCl (NSC-301739) is a dihydrochloride salt of Mitoxantrone. Mitoxantrone is an inhibitor of type II topoisomerase and protein kinase C (PKC) with IC50 of 8.5 ?M for PKC. Mitoxantrone inhibits cell proliferative growth of MCF-7/wt cells with IC50 of 0.42 ?M. Mitoxantrone also induces apoptosis. *For Research & Development use only.  Product is not intended for drug, household, or human consumption.

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Cerilliant Corporation MULTI COMPONENT ALCOHOL MIX

Multicomponent Alcohol Mix - 500 �g/mL ea. analyte; 1.2 mL/ampoule

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Cayman Chemical DIclofenac ethyl ester 25mg

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An esterified form of diclofenac; has been used as a precursor in the synthesis of diclofenac derivatives with anti-inflammatory and analgesic activity and decreased ulcerogenicity

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Sigma Aldrich Fine Chemicals Biosciences Gonadorelin hydrochloride United States Pharmacopeia (USP) Reference Standard | 33515-09-2 (free base) | 6.53MG

Gonadorelin hydrochloride United States Pharmacopeia (USP) Reference Standard | Mol Wt: 1255.21 | 33515-09-2 (free base) | 6.53MG

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Medchemexpress LLC Oprozomib | 935888-69-0 | 99.8% | 1MG

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Oprozomib | 935888-69-0 | 99.8% | 1MG

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Medchemexpress LLC Oxibendazole | 20559-55-1 | MFCD00133728 | 99.6% | 249.27 | C12H15N3O3 | 10 MG

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Oxibendazole is a benzimidazole anthelmintic research compound (CAS 20559-55-1) with reported apoptosis-inducing, anti-cancer, and anti-inflammatory activities. It is supplied for laboratory research in solid form or as DMSO solutions, with a reported purity of approximately 99.6% and a molecular weight of 249.27 g/mol.

• Effective benzimidazole anthelmintic against nematode infections.
• Induces apoptosis in preclinical studies, indicating potential anti-cancer activity.
• Available as solid or ready-to-use DMSO solution for experimental flexibility.
• High reported purity suitable for research applications.
• Well-defined chemical identity: molecular weight 249.27 g/mol, CAS 20559-55-1.

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Cayman Chemical Hydroxy CelecoxIb 25mg

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An inactive metabolite of celecoxib

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Sigma Aldrich Fine Chemicals Biosciences Phenylbutazone impurity B European Pharmacopoeia (EP) Reference Standard | 16860-43-8 |

Phenylbutazone impurity B European Pharmacopoeia (EP) Reference Standard | Mol Wt: 324.37 | 16860-43-8 |

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Sigma Aldrich Fine Chemicals Biosciences Cefmetazole United States Pharmacopeia (USP) Reference Standard | 56796-20-4 | 200MG

Cefmetazole United States Pharmacopeia (USP) Reference Standard | Mol Wt: 471.53 | 56796-20-4 | 200MG

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Sigma Aldrich Fine Chemicals Biosciences Chlorobenzhydryl Piperazine United States Pharmacopeia (USP) Reference Standard | 300543-56-0 | 75MG

Chlorobenzhydryl Piperazine United States Pharmacopeia (USP) Reference Standard | Mol Wt: 286.8 | 300543-56-0 | 75MG

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Selleck Chemical LLC Cefetamet pivoxil hydrochloride S4865-25mg

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Cefetamet pivoxil hydrochloride is the hydrochloride salt form of cefetamet pivoxil which is an oral third-generation cephalosporin antibiotic

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Apexbio Technology LLC Flavopiridol hydrochloride 131740-09-5 10mM (in 1mL DMSO)

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Flavopiridol hydrochloride is a selective inhibitor of cyclin-dependent kinases (CDKs) specifically targeting CDK1 CDK2 CDK4 and CDK6 with reported IC50 values approximately 41 nM and CDK7 with an IC50 of about 300 nM Additionally it has been observed to inhibit EGFR and protein kinase A at micromolar concentrations By inhibiting CDK activity flavopiridol hydrochloride disrupts cell cycle progression inducing G1 phase arrest as demonstrated in breast cancer cell lines Furthermore its capacity to inhibit phosphorylation of Rb protein and suppress anti-apoptotic proteins such as Mcl-1 and XIAP facilitates apoptosis in lymphoma cell models Flavopiridol hydrochloride is utilized in preclinical studies of cell cycle regulation apoptosis signaling and cancer research including experiments using xenograft tumor models in mice

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