PeptideDB

RU28362

CAS: 74915-64-3 F: C23H28O3 W: 352.47

RU28362 is a potent and selective glucocorticoid agonist. RU28362 increases the Bnip3 mRNA levels in neurons. RU28362 in
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Bioactivity RU28362 is a potent and selective glucocorticoid agonist. RU28362 increases the Bnip3 mRNA levels in neurons. RU28362 inhibits adrenocorticotrophic hormone (ACTH) and corticosterone secretion[1][2].
Invitro RU28362 (0.1、1、5、10 nM; 72 小时) 会以剂量依赖性方式增加神经元中的 Bnip3 mRNA 水平[1]。 RT-PCR[1] Cell Line:
In Vivo RU28362 (150 µg/kg;腹腔注射) 可抑制促肾上腺皮质激素 (ACTH) 和皮质酮的分泌,并选择性抑制应激诱导的垂体前叶 POMC hnRNA 增加[2]。 Animal Model:
Name RU28362
CAS 74915-64-3
Formula C23H28O3
Molar Mass 352.47
Transport Room temperature in continental US; may vary elsewhere.
Storage

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

Reference [1]. Sandau US, et al. Glucocorticoids exacerbate hypoxia-induced expression of the pro-apoptotic gene Bnip3 in the developing cortex. Neuroscience. 2007 Jan 19;144(2):482-94. [2]. Ginsberg AB, et al. Specific and time-dependent effects of glucocorticoid receptor agonist RU28362 on stress-induced pro-opiomelanocortin hnRNA, c-fos mRNA and zif268 mRNA in the pituitary. J Neuroendocrinol. 2006 Feb;18(2):129-38.