566660
SAG
≥98% (HPLC), solid, smoothened agonist, Calbiochem®
别名:
平滑激动剂，SAG
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关于此项目
经验公式（希尔记法）:
C28H28ClN3OS · 2HCl · 2H2O
化学文摘社编号:
分子量:
599.01
MDL number:
UNSPSC Code:
12352200
NACRES:
NA.77
产品名称
平滑激动剂，SAG, A cell-permeable Smoothened Agonist, SAG, CAS 364590-63-6, modulates the coupling of Smo with its downstream effector by interacting with the Smo heptahelical domain (KD = 59 nM).
SMILES string
[s]1c2c(c(c1C(=O)N(C5CCC(CC5)NC)Cc3cc(ccc3)c4ccncc4)Cl)cccc2.Cl.Cl.O
InChI
1S/C28H28ClN3OS.2ClH.H2O/c1-30-22-9-11-23(12-10-22)32(28(33)27-26(29)24-7-2-3-8-25(24)34-27)18-19-5-4-6-21(17-19)20-13-15-31-16-14-20;;;/h2-8,13-17,22-23,30H,9-12,18H2,1H3;2*1H;1H2
InChI key
IYXUQUYRWPGIQL-UHFFFAOYSA-N
assay
≥98% (HPLC)
form
solid
manufacturer/tradename
Calbiochem®
storage condition
OK to freeze
desiccated (hygroscopic)
protect from light
color
light yellow
solubility
DMSO: 10 mg/mL
water: 25 mg/mL
shipped in
ambient
storage temp.
2-8°C
Quality Level
Disclaimer
毒性：标准处理（A）
General description
一种细胞渗透性Smoothened激动剂，SAG，可通过与Smo七次跨膜螺旋结构域（KD = 59 nM）相互作用，调节Smo与其下游效应器的偶联。
一种细胞渗透性苯并噻吩化合物，可通过与Smo七次跨膜螺旋结构域（KD = 59 nM）相互作用，调节Smo与其下游效应器的偶联。显示可诱导Smo内化。显示可诱导刺猬通路激活（NIH 3T3衍生Shh-LIGHT2细胞中的EC50 ∼3 nM）并抵消环巴胺-KAAD（目录号239804）对Smo的抑制。据报道，在低浓度下作为激活剂，在极高浓度下作为抑制剂。
Other Notes
Wang, J., et al. 2010.Proc.Natl.Acad.Sci. USA.107, 9323.
Meloni, A.R., et al. 2006.Mol.Cell.Biol.26, 7750.
Chen, W., et al. 2004.Science306, 2257.
Chen, J.K., et al. 2002.Proc.Natl.Acad.Sci. USA99, 14071.
Frank-Kamenetsky, M., et al. 2002.J. Biol.1, 10.
Meloni, A.R., et al. 2006.Mol.Cell.Biol.26, 7750.
Chen, W., et al. 2004.Science306, 2257.
Chen, J.K., et al. 2002.Proc.Natl.Acad.Sci. USA99, 14071.
Frank-Kamenetsky, M., et al. 2002.J. Biol.1, 10.
Packaging
用惰性气体包装
Preparation Note
复溶后，等分并冷冻保存（-20°C）。贮备溶液在-20°C下可稳定保存至多6个月。
Legal Information
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
Hazard Classifications
Eye Irrit. 2
signalword
Warning
hcodes
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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