Chromatography Standards
Apexbio Technology LLC Alprostadil(Synonyms: Prostaglandin E1, PGE1, Alprostadilum, Edex, Caverject, Muse, Prostin VR, Liprostin), 10mM (in 1mL DMSO), CAS: 745-65-3.
Alprostadil (CAS 745-65-3) also known as prostaglandin E1 is an endogenous prostaglandin analog that exerts potent vasodilatory activity by binding and activating prostaglandin E-type (EP) receptors primarily EP2 and EP4 Upon receptor activation intracellular cyclic adenosine monophosphate (cAMP) levels rise mediating smooth muscle relaxation and vasodilation Clinically Alprostadil is investigated and utilized in research contexts addressing vascular biology erectile dysfunction mechanisms and cardiovascular function offering insights into prostaglandin signaling pathways
Medchemexpress LLC Tofacitinib citrate | 540737-29-9 | 99.94% | 50 MG
Tofacitinib citrate is an orally available JAK3/2/1 inhibitor with IC50s of 1, 20, and 112 nM, respectively. It also exhibits antibacterial, antifungal, and antiviral activities.
- Orally available JAK3/2/1 inhibitor
- Antibacterial activity
- Antifungal activity
- Antiviral activity
U.S. Pharmacopeia Carbamazepine, 298-46-4, MFCD00005073, 100 mg
Empirical Formula (Hill Notation): C15H12N2O, Molecular Weight: 236.27, mp: 191-192 °C, Synonym: 5H-Dibenz[b,f]azepine-5-carboxamide.
Medchemexpress LLC Pinaverium impurity 1 | 54370-00-2 | MFCD02093896 | 96.5% | 247.09 g/mol | C9H11BrO3 | 250 MG
Pinaverium impurity 1 is a characterized impurity of pinaverium supplied as an analytical reference for laboratory research and method development. It is intended for research use only and is not for human or clinical use. The substance has chemical formula C9H11BrO3, CAS 54370-00-2, and a molecular weight of 247.09 g/mol. Store under conditions specified on the certificate of analysis.
- Suitable as an analytical reference standard for impurity profiling and method validation.
- Provides confirmed chemical identifiers (CAS, formula, molecular weight).
- Intended for research use only, not for clinical applications.
- Certificate of analysis available for storage and purity details.
- Supplied for laboratory and analytical workflows.
Apexbio Technology LLC Lapatinib Ditosylate 388082-77-7 100mg
Lapatinib Ditosylate (CAS 388082-77-7) is a reversible dual inhibitor of the ErbB-2 (HER2) and epidermal growth factor receptor (EGFR) tyrosine kinases It competitively binds to the ATP-binding sites of these receptors preventing activation and downstream signaling In vitro Lapatinib Ditosylate exhibits potent inhibition with IC50 values of 9 2 nM for ErbB-2 and 10 8 nM for EGFR and demonstrates over 300-fold selectivity compared to kinases such as MEK and ERK The compound suppresses proliferation and downstream phosphorylation events (Erk1/2 AKT) in cancer cell lines overexpressing ErbB-2/EGFR and induces G1 cell cycle arrest In vivo it reduces tumor growth in xenograft mouse models Lapatinib Ditosylate is widely utilized in studies exploring receptor tyrosine kinase function and targeted cancer therapies
Sigma Aldrich Fine Chemicals Biosciences Itraconazole United States Pharmacopeia (USP) Reference Standard | 84625-61-6 | MFCD00870168 | 100MG
Itraconazole United States Pharmacopeia (USP) Reference Standard | Mol Wt: 705.63 | 84625-61-6 | MFCD00870168 | 100MG
MOLTOX Molecular Toxicology Inc Mitomycin C, 10 ug/vial, 5 vials/pack, Store in Refrigerator
For use in Ames test with TA102 tester strain. Dose 0.5 µg/plate. Reconstitute with organic solvents such as DMSO or sterile dH2O as applicable. Direct acting mutagens do not require the use of S9 metabolic activation to cause mutagenicity. CONTROLCHEM™ chemicals are obtained from major suppliers of research chemicals and are employed without further characterization or purification. Packaged quantities are precise within 1%. Please Note: CONTROLCHEM™ chemicals are known mutagens/carcinogens/toxins and are sold only to those experienced in the safe handling and disposal of hazardous materials. Consult your Institutional Safety Officer before ordering.
Selleck Chemical LLC Ponatinib (AP24534) 10mg 943319-70-8
Ponatinib (AP24534) is a novel, potent multi-target inhibitor of Abl, PDGFR?, VEGFR2, FGFR1 and Src with IC50 of 0.37 nM, 1.1 nM, 1.5 nM, 2.2 nM and 5.4 nM in cell-free assays, respectively. Ponatinib (AP24534) inhibits autophagy. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Sigma Aldrich Fine Chemicals Biosciences Moxidectin for system suitability European Pharmacopoeia (EP) Reference Standard | 113507-06-5 | MFCD00866560
Moxidectin for system suitability European Pharmacopoeia (EP) Reference Standard | Mol Wt: 639.82 | 113507-06-5 | MFCD00866560
Medchemexpress LLC Edoxaban impurity 65 | 50mg
Edoxaban Impurity 65 is an impurity of Edoxaban (HY-10264)
TARGETMOL CHEMICALS INC IMATINIB 1000MG
Also available in 100 mg 200 mg 500 mg 5000 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Imatinib (STI571) is an inhibitor of the receptor tyrosine kinases c-Abl Bcr-Abl PDGFR and c-Kit (IC50 600/100/100 nM). purity: 99%
Sigma Aldrich Fine Chemicals Biosciences 3-Benzyl-4-heptanone United States Pharmacopeia (USP) Reference Standard | 7492-37-7 | 5X0.5ML
3-Benzyl-4-heptanone United States Pharmacopeia (USP) Reference Standard | Mol Wt: 204.31 | 7492-37-7 | 5X0.5ML
Med Vet International Fluconazole Tablets 200mg, 100 Tablets
VET LICENSE NEEDS TO BE PROVIDED IN 3-4 BUSINESS DAYS OR ORDER WILL BE CANCELLED
Fluconazole Tablets 200mg, 100 tablets
Sigma Aldrich Fine Chemicals Biosciences Flubendazol European Pharmacopoeia (EP) Reference StandardPurity: | MW: 313.28 | 31430-15-6 | MFCD00871999 | 0
Flubendazol European Pharmacopoeia (EP) Reference StandardPurity: | MW: 313.28 | 31430-15-6 | MFCD00871999 | 0
Sigma Aldrich Fine Chemicals Biosciences Benazepril Related Compound D United States Pharmacopeia (USP) Reference Standard | 112110-48-2 (free base) | 15MG
Benazepril Related Compound D United States Pharmacopeia (USP) Reference Standard | Mol Wt: 467 | 112110-48-2 (free base) | 15MG