Drugs of Abuse Testing Reagents
Cayman Chemical Hexafluoropropylen OxID DIm 1g
A degradation product of panaxatriols cytotoxic to P388 L1210 and K562 leukemia cells (EC50s 34 32 and 38 UM) inhibits EGFR (IC50 24.1 UM) in a cell-free assay cytotoxic to HepG2 cells from 20-100 UM
Cayman Chemical ProstaglndIn I MetabolIte AC
An analytical reference standard categorized as a benzodiazepine an active metabolite of triazolam has anticonvulsant and sedative effects in mice intended for research and forensic applications
Andwin Scientific 10-PANEL DRUG CARD TEST PK/25
The 10-panel drug test card is used to quickly test urine in order to uncover the use of drugs, such as cocaine, amphetamine, methamphetamine, marijuana, opiate 2000, phencyclidine, barbiturate, bensodiazepine, and tricyclic antidepressants.. This product is sold in a pack of 25.
Cayman Chemical AMB butnoIc ACD metabolIte 5mg
A quorum-sensing signal molecule produced by P aeruginosa in response to increasing cell density increases expression of the lasB gene which encodes the virulence factor elastase in P aeruginosa (EC50 30 UM in a reporter cell assay) increases secretion of pyocyanin and PA-IL as well as increases biofilm production in P aeruginosa populations at 60 UM an iron chelator in P aeruginosa growth media at 40 UM
Abcam PK11195, benzodiazepine receptor antagonist, 10MG
MW 352.9 Da, Purity >99%. Antagonist at the mitochondrial (peripheral) benzodiazepine receptor (translocator protein, TSPO). Acts as a chemosensitizer of tumor cells to a wide range of chemotherapeutic agents.
The product is subject to the following: Abcam Restricted Use Statement
Abcam PK11195, benzodiazepine receptor antagonist, 50MG
MW 352.9 Da, Purity >99%. Antagonist at the mitochondrial (peripheral) benzodiazepine receptor (translocator protein, TSPO). Acts as a chemosensitizer of tumor cells to a wide range of chemotherapeutic agents.
The product is subject to the following: Abcam Restricted Use Statement
Cayman Chemical ProstaglndIn I MetabolIte
A chalcone with enzyme inhibitory and anticancer activities inhibits collagenase and elastase in cell-free assays (IC50s 62.05 and 17.6 UM respectively) cytotoxic to HCT116 HT-29 MCF-7 A549 and Ca Ski cancer cells (IC50s 12.75 39 47.63 40.28 and 39.88 UM respectively) induces apoptosis and cell cycle arrest at the G1 phase in HCT116 cells at 20 40 and 60 UM reduces tumor volume and induces intratumoral necrosis and apoptosis in an HCT116 mouse xenograft model at 1 and 3 mg/kg
Cayman Chemical ProstaglndIn I MetabolIte
A chalcone with enzyme inhibitory and anticancer activities inhibits collagenase and elastase in cell-free assays (IC50s 62.05 and 17.6 UM respectively) cytotoxic to HCT116 HT-29 MCF-7 A549 and Ca Ski cancer cells (IC50s 12.75 39 47.63 40.28 and 39.88 UM respectively) induces apoptosis and cell cycle arrest at the G1 phase in HCT116 cells at 20 40 and 60 UM reduces tumor volume and induces intratumoral necrosis and apoptosis in an HCT116 mouse xenograft model at 1 and 3 mg/kg
