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质量水平
方案
≥98% (HPLC)
表单
powder
溶解性
DMSO: >20 mg/mL
储存温度
2-8°C
SMILES字符串
CC(Sc1nc2ccccc2[nH]1)C(=O)N\N=C\c3cc(Br)ccc3O
InChI
1S/C17H15BrN4O2S/c1-10(25-17-20-13-4-2-3-5-14(13)21-17)16(24)22-19-9-11-8-12(18)6-7-15(11)23/h2-10,23H,1H3,(H,20,21)(H,22,24)/b19-9+
InChI key
WILMXUAKQKGGCC-DJKKODMXSA-N
应用
KH7已被用于:
- 作为可溶性腺苷酸环化酶(sAC)拮抗剂,用于研究其对精子细胞中1型瞬时受体(TRPV1)作用介导的信号通路的影响。
- 作为选择性sAC拮抗剂,用于研究其对精子细胞中质子门控通道(HV1)诱导作用的信号通路的影响。
- 作为sAC抑制剂,用于研究其对单磷酸化肌球蛋白轻链(pMLC)中cAMP增加的影响。
生化/生理作用
KH7 是可溶性腺苷酸环化酶的选择性抑制剂。可溶性腺苷酸环化酶(sAC)泛表达,是cAMP 信号传递的重要组成部分。
特点和优势
这种化合物是环核苷酸研究的特色产品。点击此处查看更多特色环核苷酸产品。登录sigma.com/discover-bsm可了解更多关于其他研究领域中关于生物活性小分子的消息。
适用性
在洗涤剂的作用下,KH7 对 sAC 无活性。当用于细胞实验时,KH7 在50μM以上的浓度下显示出非特异性膜破坏效应。
警示用语:
Danger
危险声明
危险分类
Acute Tox. 3 Oral
储存分类代码
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
从最新的版本中选择一种:
分析证书(COA)
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Biochemical pharmacology, 150, 245-255 (2018-02-16)
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Journal of cellular physiology, 235(3), 2947-2962 (2019-09-20)
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Molecular and cellular biochemistry, 430(1-2), 115-125 (2017-02-18)
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Fish & shellfish immunology, 66, 140-147 (2017-05-10)
Ocean acidification (OA) has deleterious impacts on immune response and energy homeostasis status of Mollusca. In the present study, the apoptosis ratio of hemocytes and the adenosine triphosphate (ATP) allocation in gill tissues were determined after Pacific oysters Crassostrea gigas
商品
Cyclic nucleotides like cAMP modulate cell function via PKA activation and ion channels.
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