AL-438

Modify Date: 2024-01-16 08:59:41

AL-438 structure	Common Name	AL-438
	CAS Number	239066-73-0	Molecular Weight	347.45
	Density	N/A	Boiling Point	N/A
	Molecular Formula	C₂₃H₂₅NO₂	Melting Point	N/A
	MSDS	N/A	Flash Point	N/A

Use of AL-438

AL-438 is a potent, selective and orally active glucocorticoid receptor modulator with Kis of 2.5, 1786, 53, 1440, >1000 nM for glucocorticoid receptor, progesterone receptor, mineralocorticoid receptor, androgen receptor, estrogen receptor, respectively. AL-438 shows antiinflammatory activity[1][2].

Name	AL-438

Description	AL-438 is a potent, selective and orally active glucocorticoid receptor modulator with Kis of 2.5, 1786, 53, 1440, >1000 nM for glucocorticoid receptor, progesterone receptor, mineralocorticoid receptor, androgen receptor, estrogen receptor, respectively. AL-438 shows antiinflammatory activity[1][2].
Related Catalog	Research Areas >> Inflammation/Immunology Signaling Pathways >> GPCR/G Protein >> Glucocorticoid Receptor
Target	Ki: 2.5 nM (glucocorticoid receptor)[1]
In Vitro	AL-438 (1 µM) 降低 ATDC5 细胞中 LPS 诱导的 IL-6 的生成[1]。 AL-438 (0-1 µM; 1 h+24 h) 抑制 HSKF1501 细胞中 IL-1β (2 ng/ml) 诱导的 IL-6 表达[2]。
In Vivo	AL-438 (1, 10, 100 mg/kg; p.o.) 在大鼠体内显示出抗炎活性[2]。 Animal Model: Male Sprague Dawley rats (carrageenan paw edema model)[2] Dosage: 1, 10, 100 mg/kg Administration: P.o. Result: Showed antiinflammatory activity with ED50 value of 11 mg/kg in acute inflammation assay.
References	[1]. Owen HC, et al. The growth plate sparing effects of the selective glucocorticoid receptor modulator, AL-438. Mol Cell Endocrinol. 2007 Jan 29;264(1-2):164-70. [2]. Coghlan MJ, et al. A novel antiinflammatory maintains glucocorticoid efficacy with reduced side effects. Mol Endocrinol. 2003 May;17(5):860-9.

Molecular Formula	C₂₃H₂₅NO₂
Molecular Weight	347.45

AL-438

Use of AL-438

Names

AL-438 Biological Activity

Chemical & Physical Properties