SML3667
SR11302
≥98% (HPLC)
别名:
(E,E,Z,E)-3-Methyl-7-(4-methylphenyl)-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonatetraenoic acid, SR 11302, SR-11302
一般描述
Conformationally restricted anti-AP-1 retinoid that selectively induces receptors-mediated AP-1 inhibition, but not transcription activation.
SR11302 is a conformationally restricted anti-AP-1 retinoid that selectively induces receptors-mediated AP-1 inhibition (RARα > RARγ > RXRα = RARβ), but not transcription activation (25-fold vs no RARα enhancement by 1 μM t-RA or 10 μM SR11302, respectively). Unlike t-RA, SR11302 inhibits the proliferation of cancer cultures (1 μM; Calu-6, HeLA, T47D) without inducing the differentiation of F9 cells (0.1-1 μM).
SR11302 is a conformationally restricted anti-AP-1 retinoid that selectively induces receptors-mediated AP-1 inhibition (RARα > RARγ > RXRα = RARβ), but not transcription activation (25-fold vs no RARα enhancement by 1 μM t-RA or 10 μM SR11302, respectively). Unlike t-RA, SR11302 inhibits the proliferation of cancer cultures (1 μM; Calu-6, HeLA, T47D) without inducing the differentiation of F9 cells (0.1-1 μM).
法规信息
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历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
A Fanjul et al.
Nature, 372(6501), 107-111 (1994-11-03)
Retinoids regulate many biological processes, including differentiation, morphogenesis and cell proliferation. They are also important therapeutic agents, but their clinical usefulness is limited because of side effects. Retinoid activities are mediated by specific nuclear receptors, the RARs and RXRs, which
Xiao Han et al.
Frontiers in immunology, 13, 968639-968639 (2022-09-06)
Acinar cell death and inflammatory response are two important events which determine the severity of acute pancreatitis (AP). Endoplasmic reticulum (ER) stress and necroptosis are involved in this process, but the relationships between them remain unknown. Here, we analyzed the
Ying Lu et al.
Frontiers in molecular neuroscience, 15, 859558-859558 (2022-08-16)
TLR4 and Cx43 signaling in dorsal spinal cord has been shown to be involved in the development of neuropathic pain. However, it is not clear whether TLR4 signaling is associated with the expression of MCP-1, CXCL1, and Cx43 in LPS
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