跳转至内容
Merck

K3394

Sigma-Aldrich

KH7

≥98% (HPLC)

别名:

(E)-2-(1H-Benzo[d]imidazol-2-ylthio)-N′-(5-bromo-2-hydroxybenzylidene)propanehydrazide

登录查看公司和协议定价

选择尺寸

5 MG
$298.00
25 MG
$1,140.00

$298.00


请联系客服了解存货情况

获取大包装报价

选择尺寸

变更视图
5 MG
$298.00
25 MG
$1,140.00

About This Item

经验公式(希尔记法):
C17H15BrN4O2S
分子量:
419.30
MDL编号:
UNSPSC代码:
41106305
PubChem化学物质编号:
NACRES:
NA.77

$298.00


请联系客服了解存货情况

获取大包装报价

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。[1]
  • 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。[2]
  • 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。[3]

生化/生理作用

KH7 是可溶性腺苷酸环化酶的选择性抑制剂。
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

该化合物是受体分类及信号转导手册上腺苷酸环化酶页面上的特色化合物。想要浏览手册的其他页面, 请单击此处
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。

象形图

Skull and crossbones

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

其他客户在看

Slide 1 of 2

1 of 2

Carresse L Gerald et al.
Alcoholism, clinical and experimental research, 40(2), 273-283 (2016-02-05)
Farm workers in rural areas consume more alcohol than those who reside in urban areas. Occupational exposures such as agricultural work can pose hazards on the respiratory system. It is established that hog barn dust induces inflammation in the airway
Nanshan Song et al.
Biochemical pharmacology, 150, 245-255 (2018-02-16)
β2-Aderenergic receptor (β2AR) agonist, Salmeterol exhibits anti-inflammatory activities. However, the inhibitory effects of Salmeterol on inflammasome activation are elusive and the underlying mechanisms need to be explored. In this study, we established inflammatory model in primary bone marrow-derived macrophages (BMDM)
Frances Evans et al.
Journal of cellular physiology, 235(3), 2947-2962 (2019-09-20)
In previous work, we reported that plasma membrane potential depolarization (PMPD) provokes cortical F-actin remodeling in bovine corneal endothelial (BCE) cells in culture, which eventually leads to the appearance of intercellular gaps. In kidney epithelial cells it has been shown
Mandy Lo et al.
Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology, 191(1), 113-125 (2020-11-21)
We tested in six fish species [Pacific lamprey (Lampetra richardsoni), Pacific spiny dogfish (Squalus suckleyi), Asian swamp eel (Monopterus albus), white sturgeon (Acipenser transmontanus), zebrafish (Danio rerio), and starry flounder (Platichthys stellatus)] the hypothesis that elevated extracellular [HCO3-] protects spontaneous
Xiudan Wang et al.
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.

Questions

Reviews

No rating value

Active Filters

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持