别名盐酸4-脱氧吡哆醇 英文别名NSC61770 | 2,4-DIMETHYL-3-HYDROXY-5-HYDROXYMETHYLPYRIDINE HYDROCHLORIDE | 4-Deoxypyridoxine, HCl | Desoxypyridoxime hydrochloride | 3-Pyridinemethanol, 4,6-dimethyl-5-hydroxy-, hydrochloride | 4-Desoxypyridoxine hydrochloride | SB52336 | SK 591 | 4-DOP hy ...
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别名: 4-脱氧吡哆醇盐酸盐 分子式: C8H11NO2?HCl 分子量: 189.6 纯度: >98% 溶解度: DMSO: 10 mg/ml,PBS (pH 7.2): 10 mg/ml 储存: Store at -20°C 库存: 现货 Background 4-Deoxypyridoxine (4-DPD) is a vitamin B6 antimetabolite with diverse biological activities. It inhibits...
中文名称: 5-(羟甲基)-2,4-二甲基吡啶-3-醇 中文同义词: 5-(羟甲基)-2,4-二甲基吡啶-3-醇;维生素B6 EP杂质2;维生素B6杂质2(维生素B6 EP杂质B);吡哆醇盐酸盐杂质B;维生素B61 英文名称: 4-deoxypyridoxine 英文同义词: 4-deoxypyridoxine;DEOXYPYRIDOXINE;4,6-DIMETHYL-5-HYDROXY-3-PYRIDINEMETHANOL;4-...
原料品名4-Deoxypyridoxine hydrochloride 原料中文名称4-脱氧吡哆醇盐酸盐 中文别名盐酸吡哆辛杂质B;盐酸普莫卡因杂质B;2,4-二甲基-3-羟基-羟甲基吡啶盐酸盐;4-脱氧吡哆醇盐酸盐;盐酸-4-脱氧维生素B6;4-脱氧基维生素 B6 盐酸盐;吡哆嗪EP杂质B;吡RID醇杂质B HCL ...
4-Deoxypyridoxine 5'-phosphate inhibits ornithine decarboxylase activity with a Ki of 06 mM. 4-Deoxypyridoxine 5'-phosphate is a competitive inhibitor of the activation of glutamate apodecarboxylase by Pyridoxal 5'-phosphate (Ki of 0.27 μM) and strongly inhibits glutamate-dependent labeling of ...
产品活性:4-Deoxypyridoxine 5'-phosphate 是一种 Pyridoxal 5'-phosphate 的类似物,也是一种鞘氨醇1-磷酸酯 (S1P) 抑制剂。4-Deoxypyridoxine 5'-phosphate 抑制鸟氨酸脱羧酶 (ornithine decarboxylase) 活性,Ki 为60 μM。4-Deoxypyridoxine 5'-phosphate 是 Pyridoxal 5'-phosphate 激活谷氨酸脱羧酶 (glutamate...
4-Deoxypyridoxine phosphate MedKoo 是超高质量的实验室药物供应商。它于2009年由获得博士学位的Qingqi Chen博士创立。北京大学合成化学专业,并在约翰内斯-开普勒大学林茨(与 Heinz Falk 博士)、内华达里诺大学(与 David Lightner 博士)和不列颠哥伦比亚大学(与 David Dolphin 博士)接受博士后培训。
4-deoxypyridoxine improves the viability of isolated pancreatic islets ex vivo 来自 Taylor & Francis 喜欢 0 阅读量: 20 作者:H Lee,H Seon Park,S Hee Hong,O Kyung Choi,SD Cho,J Park,J Eun Oh,S Soo Chung,HS Jung,KS Park 摘要: The successful islet transplantation, for the treatment of ...
Synthesis for 4'-deoxypyridoxine-3-(ethyl carbonate), 4'-deoxypyridoxine 5'-acetate, 4'-deoxy-3-0-(2-sulfoethyl)-pyridoxine, and the metabolites are presented. These synthesis were facilitated by using ethylchloroformate conjugates and N-methylpiperazine hydrolysis to block and unblock the phenol...