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Panobinostat-d4
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Panobinostat-d4图片
CAS NO:1185237-51-7

LBH589-d4
NVP-LBH589-d4
Panobinostat-d4 (LBH589-d4) 是 Panobinostat 的氘代物。Panobinostat (LBH589; NVP-LBH589) 是一种有效的口服非选择性HDAC抑制剂,具有抗肿瘤活性。Panobinostat 可诱导HIV-1 virus的产生,即使在较低的浓度范围 8-31 nM,也可刺激 HIV-1 在潜伏感染细胞中的表达。Panobinostat 诱导细胞凋亡 (apoptosis) 和自噬 (autopha
生物活性

Panobinostat-d4 (LBH589-d4) is the deuterium labeled Panobinostat. Panobinostat (LBH589; NVP-LBH589) is a potent and orally active non-selectiveHDACinhibitor, and has antineoplastic activities[1][2]. Panobinostat inducesHIV-1virusproduction even at low concentration range 8-31 nM, stimulatesHIV-1expression in latently infected cells[4]. Panobinostat induces cellapoptosisandautophagy. Panobinostat can be used for the study of refractory or relapsed multiple myeloma[3].

体外研究
(In Vitro)

Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].

分子量

353.45

Formula

C21H19D4N3O2

CAS 号

1185237-51-7

中文名称

帕比司他 d4

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

 
 
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