K3394
KH7
≥98% (HPLC)
别名:
(E)-2-(1H-Benzo[d]imidazol-2-ylthio)-N′-(5-bromo-2-hydroxybenzylidene)propanehydrazide
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选择尺寸
关于此项目
经验公式（希尔记法）:
C17H15BrN4O2S
化学文摘社编号:
分子量:
419.30
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
41106305
MDL number:
产品名称
KH7, ≥98% (HPLC)
InChI key
WILMXUAKQKGGCC-DJKKODMXSA-N
SMILES string
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+
assay
≥98% (HPLC)
form
powder
solubility
DMSO: >20 mg/mL
storage temp.
2-8°C
Quality Level
相关类别
Application
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。
Biochem/physiol Actions
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。
Features and Benefits
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。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Cyclic nucleotides like cAMP modulate cell function via PKA activation and ion channels.
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