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Diphemanil mesylate | CAS:62-97-5
Diphemanil mesylate
  • 名称:甲硫二苯马尼; 二苯马尼甲硫酸盐; N,N-二甲基-4-哌啶亚基-1,1-二苯甲烷甲基硫酸盐 | Diphemanil mesylate
  • CAS号:62-97-5
  • 别名:Diphemanil methylsulfate; N,N-Dimethyl-4-piperidylidene-1,1-diphenylmethane methylsulfate
  • 分子式:C20H24N.CH3O4S
  • 分子量:389.51
  • EINESC号:200-552-4

产品描述

物理化学性质

熔点 194-195 ºC

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1-Aminocyclobutane-1-carboxylate (ACBC): a specific antagonist of the N-methyl-D-aspartate receptor coupled glycine receptor.W F Hood et al.European journal of pharmacology, 161(2-3), 281-282 (1989-02-28) Kinetic basis of partial agonism at NMDA receptors.Cassandra L Kussius et al.Nature neuroscience, 12(9), 1114-1120 (2009-08-04) 1-Aminocyclobutanecarboxylic acid derivatives as novel structural elements in bioactive peptides: application to tuftsin analogs.E Gershonov et al.Journal of medicinal chemistry, 39(24), 4833-4843 (1996-11-22) 1-aminocyclobutane[11C]carboxylic acid, a potential tumor-seeking agent.L C Washburn et al.Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 20(10), 1055-1061 (1979-10-01) Neuropharmacological characterization of 1-aminocyclopropane-1-carboxylate and 1-aminocyclobutane-1-carboxylate, ligands of the N-methyl-D-aspartate-associated glycine receptor.T S Rao et al.Neuropharmacology, 29(3), 305-309 (1990-03-01) Evidence for a functional coupling of the NMDA and glycine recognition sites in synaptic plasma membranes.R P Compton et al.European journal of pharmacology, 188(1), 63-70 (1990-01-23) Conformational studies on model peptides with 1-aminocyclobutane 1-carboxylic acid residues.V N Balaji et al.Peptide research, 8(3), 178-186 (1995-05-01) Insulin-induced phospho-oligosaccharide stimulates amino acid transport in isolated rat hepatocytes.I Varela et al.The Biochemical journal, 267(2), 541-544 (1990-04-15) Synthesis, NMDA receptor antagonist activity, and anticonvulsant action of 1-aminocyclobutanecarboxylic acid derivatives.Y Gaoni et al.Journal of medicinal chemistry, 37(25), 4288-4296 (1994-12-09) Mechanism of partial agonist action at the NR1 subunit of NMDA receptors.Atsushi Inanobe et al.Neuron, 47(1), 71-84 (2005-07-06) Dietary N-3 fatty acids inhibit ischaemic and excitotoxic brain damage in the rat.J K Relton et al.Brain research bulletin, 32(3), 223-226 (1993-01-01) Modulation of [3H]3-((+-)-2-carboxypiperazin-4-yl)propyl-1-phosphonic acid ([3H]CPP) binding by ligands acting at the glycine and the polyamine sites of the rat brain NMDA receptor complex.R H Porter et al.European journal of pharmacology, 227(1), 83-88 (1992-09-01) Inhibition by 1-aminocyclobutane-1-carboxylate of the activity of 1-aminocyclopropane-1-carboxylate oxidase obtained from senescing petals of carnation (Dianthus caryophyllus L.) flowers.Y Kosugi et al.Plant & cell physiology, 38(3), 312-318 (1997-03-01) Conformational characterization of the 1-aminocyclobutane-1-carboxylic acid residue in model peptides.M Gatos et al.Journal of peptide science : an official publication of the European Peptide Society, 3(2), 110-122 (1997-03-01) Tumor detection with 1-aminocyclopentane and 1-aminocyclobutane C-11-carboxylic acid using positron emission computerized tomography.K F Hübner et al.Clinical nuclear medicine, 6(6), 249-252 (1981-06-01) [Change in the level of 1-aminochloropropane-1-carbonic acid. Activity of a protein inhibitor of polygalacturonase, intensity of formation of oligouronides in apples during ripening and treatment with haloethane derivatives and aminoethoxyvinylglycine].E A Bulantseva et al.Prikladnaia biokhimiia i mikrobiologiia, 39(4), 461-464 (2003-10-03) Pharmacological characteristics of cyclic homologues of glycine at the N-methyl-D-aspartate receptor-associated glycine site.G B Watson et al.Neuropharmacology, 29(8), 727-730 (1990-08-01) Ethylene biosynthesis: processing of a substrate analog supports a radical mechanism for the ethylene-forming enzyme.M C Pirrung et al.Chemistry & biology, 5(1), 49-57 (1998-02-28) Glycine antagonist action of 1-aminocyclobutane-1-carboxylate (ACBC) in Xenopus oocytes injected with rat brain mRNA.G B Watson et al.European journal of pharmacology, 167(2), 291-294 (1989-08-22)
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