3D-FP37625 - piperazine-adipate
Désolé, aucun produit avec la référence 3D-FP37625 n'a été trouvé, cependant nous vous invitons à consulter les produits similaires suivants:
Piperazine Adipate
CAS :Formule :C4H10N2·C6H10O4Degré de pureté :>98.0%(T)Couleur et forme :White to Almost white powder to crystalMasse moléculaire :232.28Piperazine adipate
CAS :Formule :C4H10N2·C6H10O4Degré de pureté :98.0 - 102.0 % (anhydrous basis)Couleur et forme :White or almost white crystalline powderMasse moléculaire :232.28Piperazine adipate
CAS :Piperazine adipate is a potent broad spectrum anthelmintic.Formule :C10H20N2O4Degré de pureté :99.9%Couleur et forme :256-257°C Dissolves Slowly Ph (0 2-0 01 Molar Aqueous Solutions) 5 45 Ph (5% Solution) 5 - 6 (NtpMasse moléculaire :232.28PIPERAZINE ADIPATE CRS
CAS :PIPERAZINE ADIPATE CRSFormule :C10H20N2O4Couleur et forme :PowderMasse moléculaire :232.2768Hexanedioic acid, compd. with piperazine (1:1)
CAS :Degré de pureté :≥98%(T)Masse moléculaire :232.2799988Piperazine Adipate (DISCONTINUED)
CAS :Compounds containing a pyrimidine ring (whether or notFormule :C6H10O4·C4H10N2Couleur et forme :PowderMasse moléculaire :232.14231Piperazine 2HCl
CAS :Piperazine (2HCl) is gamma-aminobutyric acid (GABA) agonists and its major effects appear to be on the central nervous system. Piperazine was the anthelmintic with the greatest number of reports of toxicoses and suspected toxicoses in cats. Piperazine neurotoxicity in cats and dogs usually was manifested by muscle tremors, ataxia, and/or behavioral disturbances within 24 hours after estimated daily dose(s) between 20 and 110 mg/kg[1]. For di-substituted derivatives, ciprofloxacin was selected and hybrids were synthesized via substitution at piperazinyl-N4. The reaction of piperazinyl-NH of ciprofloxacin with selected drugs resulted in pronounced growth inhibition of standard as well as resistant bacterial strains[2]. The parent piperazine 6 was found to exhibit a reasonable activity toward the HeLa and MDA MB 231 tumor cell lines (IC50= 9.2 and 8.4 μΜ, respectively)[3]. Piperazine adipate (10 mM) causes mortality of A. galli and H. gallinae after a maximum of 30 min exposure, inhibits malate oxidation by 78%, and inhibits aldolase activity in both parasites. Piperazine adipate (10 mM) also inhibits cholinesterase activity by 96% in Ascaridia galli (A. galli) and 93% in Heterakis gallinae (H. gallinae). Piperazine adipate inhibits oxaloacetate reduction by 26% and 55% in A. galli and H. gallinae, resepctively[4].Formule :C4H12Cl2N2Couleur et forme :SolidMasse moléculaire :159.05











