K3394
KH7
≥98% (HPLC)
别名:
(E)-2-(1H-Benzo[d]imidazol-2-ylthio)-N′-(5-bromo-2-hydroxybenzylidene)propanehydrazide
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关于此项目
经验公式（希尔记法）:
C17H15BrN4O2S
CAS Number:
分子量:
419.30
MDL编号:
UNSPSC代码:
41106305
PubChem化学物质编号:
NACRES:
NA.77
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
相关类别
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。
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。
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
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。
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
Naveen Kumar et al.
Molecular and cellular biochemistry, 430(1-2), 115-125 (2017-02-18)
Despite the current progress in cancer research and therapy, breast cancer remains the leading cause of mortality among half a million women worldwide. Migration and invasion of cancer cells are associated with prevalent tumor metastasis as well as high mortality.
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
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Cyclic nucleotides like cAMP modulate cell function via PKA activation and ion channels.
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