Chromatography Standards
Chromatography Standards
COD, Calibration Standard , MilliporeSigma™ Supelco™
This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.
Chem Service Inc Propamocarb, 24579-73-5, MFCD00078717, 250 mg
Molecular Formula: C9 H20 N2 O2, Molecular Weight: 188.269, Alternate Name(s): Propyl (3-(dimethylamino)propyl)carbamate.
U.S. Pharmacopeia Ibuprofen, 15687-27-1, MFCD00010393, 750mg
Molecular formula C13-H18-O2, Molecular weight 206.28 g/mol, Melting Point 167 - 171.5 °F (75 - 77.5 °C), Synonyms: p-Isobutylhydratropic acid
U.S. Pharmacopeia L-Methionine, 63-68-3, MFCD00063097, 200mg
Molecular formula C5-H11-N-O2-S, Molecular weight 149.21 g/mol, Melting Point 536 - 550.4 °F (280 - 288 °C), Boiling Point 366.8 °F (186 °C)
U.S. Pharmacopeia Ethosuximide, 77-67-8, MFCD00072123, 500mg
Molecular formula C7-H11-N-O2, Molecular weight 141.17 g/mol, Melting point/freezing point 116.6 - 125.6 °F (47 - 52 °C), Synonyms: 2-Ethyl-2-Methylsuccinimide
Selleck Chemical LLC ERG240-5mg
ERG240, a selective inhibitor of branched-chain aminotransferase 1 (BCAT1) with an IC50 of 0.1-1nM, leads to decreased oxygen consumption and glycolysis through the down regulation of IRG1 expression, which leads to decrease itaconate production in human macrophages.
TARGETMOL CHEMICALS INC ISRADIPINE 50MG
Also available in 5 mg 10 mg 25 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Isradipine (PN 200-110) is a dihydropyridine calcium channel blockers with antihypertensive and vasodilator activities. Isradipine blocks the calcium entry through the calcium ion channels of coronary and peripheral vascular smooth muscle thereby dilating coronary arteries and peripheral arterioles. This increases oxygen delivery due to an increased blood flow and reduces oxygen requirements due to decreasing in total peripheral resistance. purity: 99%
AdipoGen Metformin . HCl (1 g)
Metformin . HCl (1 g), Adipogen Life Sciences. Chemical. CAS: 1115-70-4. Formula: C4H11N5 . HCl. MW: 129.2 . 36.5. . AMPK activator. Useful agent for immunometabolism research. Reported to stimulate AMP-activated protein kinase (AMPK), leading to the reduction in acetyl-CoA carboxylase (ACC) activity and induction of fatty acid oxidation. Mitochondrial electron transport chin complex I inhibitor, reducing mitochondrial reactive oxygen species (ROS). Antidiabetic and anti-hyperglycemic agent that reduces blood glucose levels, improves insulin sensitivity and decreases insulin resistance. Its metabolic effects, including the inhibition of hepatic gluconeogenesis, are mediated in part by activation of the LKB1-AMPK pathway. Used as weight-loss agent in obesity and as insulin sensitizer in nonalcoholic fatty liver disease (NAFLD). Leptin sensitizer to mediate the weight-loss effect in the brain. Targets brown adipose tissue (BAT) in vivo and reduces oxygen consumption.
Medchemexpress LLC HY-N7117 100mg Medchemexpress, 1,4-Cineole CAS:470-67-7 Purity:>98%
Medchemexpress, HY-N7117 100mg 1,4-Cineole CAS:470-67-7 1,4-Cineole is a widely distributed, natural, oxygenated monoterpene. 1,4-Cineole, present in eucalyptus oil, activates both human TRPM8 and human TRPA1. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Chem Service Inc Metolachlor, 51218-45-2, MFCD00055293, 100 mg
Molecular Formula: C15-H22-Cl-N-O2, Molecular Weight: 283.8, Classification: Herbicide, Synonym: 2-Chloro-N-(2-ethyl-6-methylphenyl)-N-(-2-methoxy-1-methylethyl)acetamide. Metolachlor is a commonly used chloroacetamide preemergent pesticide, which can be used for weed control management in a variety of food crops. It can undergo degradation in soil via microbial transformation reactions and hydrolytic reactions.
Selleck Chemical LLC Temozolomide 10mM/1mL 85622-93-1 CCRG81045, NSC 362856,TMZ
Temozolomide (CCRG81045, NSC 362856, TMZ) is a monofunctional SN-1 alkylating agent that can modify nitrogen atoms in the DNA ring and the extracyclic oxygen group, chemically converted to MTIC and degrades to methyldiazonium cation, which transfers methyl groups to DNA at physiologic pH. A DNA damage inducer in L-1210 and L-1210/BCNU cells. Temozolomide induces apoptosis and exhibits antitumor activity. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Selleck Chemical LLC Temozolomide 100mg 85622-93-1 CCRG81045, NSC 362856,TMZ
Temozolomide (CCRG81045, NSC 362856, TMZ) is a monofunctional SN-1 alkylating agent that can modify nitrogen atoms in the DNA ring and the extracyclic oxygen group, chemically converted to MTIC and degrades to methyldiazonium cation, which transfers methyl groups to DNA at physiologic pH. A DNA damage inducer in L-1210 and L-1210/BCNU cells. Temozolomide induces apoptosis and exhibits antitumor activity. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Apexbio Technology LLC Pitavastatin Calcium, 147526-32-7, MFCD00916490, 25 mg
MF: C50H46CaF2N2O8, MW: 880.98, Solubility: 34.85mg/mL in DMSO. Pitavastatin Calcium is a competitive inhibitor of the enzyme HMGCR (HMG-CoA reductase) results in a reduction in LDL cholesterol synthesis. Alternate studies show that pitavastatin can suppress oxygen production in endothelial cells by inhibiting NADPH oxidase. In addition, pitavastatin reduces the expression of eNOS mRNA while increasing the NO dependent response stimulated by acetylcholine and the calcium ionophore, A23187. Furthermore, pitavastatin inhibits the up-regulation of conductance calcium-activated potassium channels by lowering cholesterol levels in cells.
Apexbio Technology LLC Pitavastatin Calcium, 147526-32-7, MFCD00916490, 10 mg
MF: C50H46CaF2N2O8, MW: 880.98, Solubility: 34.85mg/mL in DMSO. Pitavastatin Calcium is a competitive inhibitor of the enzyme HMGCR (HMG-CoA reductase) results in a reduction in LDL cholesterol synthesis. Alternate studies show that pitavastatin can suppress oxygen production in endothelial cells by inhibiting NADPH oxidase. In addition, pitavastatin reduces the expression of eNOS mRNA while increasing the NO dependent response stimulated by acetylcholine and the calcium ionophore, A23187. Furthermore, pitavastatin inhibits the up-regulation of conductance calcium-activated potassium channels by lowering cholesterol levels in cells.
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