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表单
powder
质量水平
作用机制
cell membrane | interferes
enzyme | inhibits
储存温度
−20°C
SMILES字符串
Cl[H].NCCCCCCNS(=O)(=O)c1cccc2c(Cl)cccc12
InChI
1S/C16H21ClN2O2S.ClH/c17-15-9-5-8-14-13(15)7-6-10-16(14)22(20,21)19-12-4-2-1-3-11-18;/h5-10,19H,1-4,11-12,18H2;1H
InChI key
OMMOSRLIFSCDBL-UHFFFAOYSA-N
基因信息
human ... CAMK2A(815) , CAMK2B(816)
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应用
N-(6-氨基己基)-5-氯-1-萘磺酰胺盐酸盐已用于研究其对被膜小窝染色的作用。
生化/生理作用
N-(6-氨基己基)-5-氯-1-萘磺酰胺盐酸盐(W-7)是一种钙调素拮抗剂,可抑制磷脂敏感性钙依赖蛋白激酶。
特点和优势
该化合物是环核苷酸研究的特色产品。点击此处,发现更多特色环核苷酸产品。如需了解有关生物活性小分子在其他研究领域的更多信息,请访问sigma.com/ discover-bsm。
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
历史批次信息供参考:
FEBS letters, 442(2-3), 173-177 (1999-02-03)
Small-angle X-ray scattering and nuclear magnetic resonance were used to investigate the structural change of calcium-bound calmodulin (Ca2+/CaM) in solution upon binding to its antagonist, N-(6-aminohexyl)-5-chloro-1-naphthalenesulfonamide (W-7). The radius of gyration was 17.4+/-0.3 A for Ca2+/CaM-W-7 with a molar ratio
N-(6-Aminohexyl)-5-chloro-1-naphthalenesulfonamide (W-7), a calmodulin antagonist, also inhibits phospholipid sensitive calcium-dependent protein kinase
Biochimica et biophysica acta. General subjects, 755(1), 144-147 (1983)
Channels (Austin, Tex.), 5(4), 308-313 (2011-06-10)
NHE3 is regulated via alterations in membrane surface charge. This is achieved through altered binding of cationic regions in the cytosolic-terminus of the exchanger with the inner leaflet of the plasma membrane. Calmodulin antagonists, including W-7, regulate surface potential and
Mis-assembly of clathrin lattices on endosomes reveals a regulatory switch for coated pit formation.
The Journal of cell biology, 123(5), 1107-1117 (1993-12-01)
The clathrin-coated pit lattice is held onto the plasma membrane by an integral membrane protein that binds the clathrin AP-2 subunit with high affinity. In vitro studies have suggested that this protein controls the assembly of the pit because membrane
The American journal of pathology, 183(3), 996-1009 (2013-07-11)
Several observations suggest the expansion of a distinct medial smooth muscle cell (SMC) subset in atherosclerosis and restenosis. We characterized the phenotypic features of SMC subsets in cultures derived from human carotid endarterectomy specimens. Specimens comprised an undiseased portion (thin
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