Drug Standards
Sigma Aldrich Fine Chemicals Biosciences Antazoline Related Compound A United States Pharmacopeia (USP) Reference Standard | 26953-37-7 | 15MG
Antazoline Related Compound A United States Pharmacopeia (USP) Reference Standard | Mol Wt: 283.37 | 26953-37-7 | 15MG
Sigma Aldrich Fine Chemicals Biosciences Valaciclovir impurity S European Pharmacopoeia (EP) Reference Standard | 502421-44-5 |
Valaciclovir impurity S European Pharmacopoeia (EP) Reference Standard | Mol Wt: 424.45 | 502421-44-5 |
Apexbio Technology LLC Gemcitabine HCl 122111-03-9 10mM (in 1mL H2O)
Gemcitabine HCl (CAS 122111-03-9) is a small molecule inhibitor of DNA synthesis commonly employed in biomedical research targeting cancer cell proliferation It acts by impeding DNA replication exerting cytotoxic effects in various cancer cell models When evaluated in vitro IC50 values have been reported as 240 4 29 0 M (CCRF-CEM/dCK/) 14 7 2 8 M (TC-1) 36 7 5 1 M (TC-1-GR) 50 nM (PANC 1) and 49 7 17 7 nM (MIA PACA-2) Additionally preclinical studies have demonstrated enhanced apoptosis and growth inhibition in pancreatic cancer models (COLO 357 L3 6pl) highlighting Gemcitabine HCl s significance as a valuable research tool for investigating tumor biology and therapeutic interventions
eMolecules Ambeed / (3S4R)-rel-tert-Butyl 3-fluoro-4-(hydroxymethyl)piperidine-1-carboxylate / 100mg / 687212259 / A104034 / / 882033-93-4 / MFCD19439662 / 233.283 / C11H20FNO3
Ambeed / (3S4R)-rel-tert-Butyl 3-fluoro-4-(hydroxymethyl)piperidine-1-carboxylate / 100mg / 687212259 / A104034 / / 882033-93-4 / MFCD19439662 / 233.283 / C11H20FNO3
Cambridge Isotope Laboratories N,N-DIMETHYLANILINE (D11, 98%), 1 G, 85785-00-8
N,N-DIMETHYLANILINE (D11, 98%), 1 G, 85785-00-8
TARGETMOL CHEMICALS INC THEAFLAVIN-3-GALLATE 5MG
Also available in 10 mg 20 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Theaflavin-3-gallate (Theaflavine-3-Gallate) can play a role in decreased intestinal cholesterol absorption via inhibition of micelle formation. Theaflavin-3-gallate has anticancer and apoptotic effects in non-small cell lung carcinoma it acts as prooxidants and induce oxidative stress with carcinoma cells more sensitive than normal fibroblasts. purity: 99%
Apexbio Technology LLC Topoisomerase 1 inhibitor. Topotecan 10mg. 162808-62-0. MFCD09837756
Topoisomerase 1 inhibitor. Topotecan 10mg. 162808-62-0. MFCD09837756
Apexbio Technology LLC potent, cell permeable PKC inhibitor 62996-74-1. MFCD00077402
potent, cell permeable PKC inhibitor 62996-74-1. MFCD00077402
Sigma Aldrich Fine Chemicals Biosciences Mycophenolate sodium United States Pharmacopeia (USP) Reference Standard | 37415-62-6 | 200MG
Mycophenolate sodium United States Pharmacopeia (USP) Reference Standard | Mol Wt: 342.32 | 37415-62-6 | 200MG
Sigma Aldrich Fine Chemicals Biosciences Glycopyrrolate Related Com50MG
Pharmaceutical secondary standards for application in quality control provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards
Medchemexpress LLC Afatinib impurity 83 | 1360430-70-1 | 95.1% | 50mg
Afatinib impurity 83 is an impurity of Afatinib (HY-10261)
Medchemexpress LLC Benzoic acid, 2-methoxy-5-methyl-, methyl ester | 63113-79-1 | MFCD06411343 | 10g
Ilurodoline impurity 10 is an impurity of Ilurodoline
Sigma Aldrich Fine Chemicals Biosciences Lopinavir for peak identification European Pharmacopoeia (EP) Reference Standard | 192725-17-0 |
Lopinavir for peak identification European Pharmacopoeia (EP) Reference Standard | Mol Wt: 628.8 | 192725-17-0 |
Apexbio Technology LLC Milrinone 78415-72-2 50mg
Milrinone (CAS 78415-72-2) is a selective inhibitor of phosphodiesterase 3 (PDE3) demonstrating an IC50 of 56 12 nM for PDE3 inhibition It acts on both PDE3A localized predominantly in cardiac tissue vascular smooth muscle and platelets and PDE3B found in adipose tissue liver and pancreatic islets Milrinone increases intracellular cAMP levels in platelets with an EC50 of 5329 970 nM leading to enhanced contractility and vasodilation effects This profile supports its utility in cardiovascular research and metabolic studies involving cAMP-mediated signaling pathways
Cayman Chemical Montelukast sodium salt
A CysLT1 receptor antagonist (IC50 = 4.9 nM in HEK293 cell membranes expressing the human receptor); selective for CysLT1 over CysLT2 receptors (IC50 = >10,000 nM in COS-7 cell membranes expressing the human receptor); inhibits LTD4-induced bronchoconstriction in anesthetized guinea pigs (ED50 = 69 nmol/kg, p.o.); inhibits ovalbumin-induced airway hyperresponsiveness and increases in the number of total cells and eosinophils in BALF in a mouse model of allergic asthma at 3 and 10 mg/kg