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Merck
CN

495320

ODQ

≥98% (TLC and HPLC), nitric oxide (NO)-sensitive guanylyl cyclase inhibitor, powder

别名:

ODQ

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关于此项目

经验公式(希尔记法):
C9H5N3O2
化学文摘社编号:
分子量:
187.15
UNSPSC Code:
12352200
NACRES:
NA.77
MDL number:
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产品名称

ODQ, A cell-permeable, potent and selective inhibitor of nitric oxide (NO)-sensitive guanylyl cyclase (IC50 = 20 nM).

SMILES string

[n]21c(n[o][c]2=O)cnc3c1cccc3

InChI

1S/C9H5N3O2/c13-9-12-7-4-2-1-3-6(7)10-5-8(12)11-14-9/h1-5H

InChI key

LZMHWZHOZLVYDL-UHFFFAOYSA-N

assay

≥98% (TLC and HPLC)

form

powder

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze
protect from light

color

light yellow

solubility

DMSO: 25 mg/mL

shipped in

ambient

storage temp.

−20°C

Quality Level

Biochem/physiol Actions

主要靶标
(NO)-敏感性鸟苷酸环化酶
产物不与ATP竞争。
可逆性:是
细胞可渗透性:具有
靶标IC50:一氧化氮(NO)敏感性鸟苷酸环化酶为20 nM

Disclaimer

毒性:刺激性(B)

General description

一氧化氮(NO)敏感性鸟苷酸环化酶(IC50=20 nM)的强效和选择性抑制剂。在培养的小脑切片中,ODQ可逆地抑制对谷氨酸受体激动剂的NO依赖性cGMP反应,而不会影响NOS活性。它不会化学灭活NO。但是,它确实抑制了响应NO供体的cGMP生成。ODQ未能抑制NO介导的巨噬细胞毒性(与cGMP无关的现象),也不会影响颗粒状鸟苷酸环化酶或腺苷酸环化酶的活性。
一氧化氮(NO)敏感性鸟苷酸环化酶(IC50=20 nM)的细胞可渗透,强效和选择性抑制剂。在培养的小脑切片中,ODQ可逆地抑制对谷氨酸受体激动剂的NO依赖性cGMP反应,而不会影响NOS活性。它不会化学灭活NO。但是,它确实抑制了响应NO供体的cGMP生成。ODQ不会抑制NO介导的巨噬细胞毒性(与cGMP无关的现象),也不会影响颗粒状鸟苷酸环化酶或腺苷酸环化酶的活性。

Other Notes

Wang, D., et al. 1998.J. Biol. Chem. 273, 33027.
Southam, E., et al. 1996.Br. J. Pharmacol.119, 527.
Brunner, F., et al. 1995.FEBS Lett.376, 262.
Garthwaite, J., et al. 1995.Mol.Pharmacol.48, 184.

Preparation Note

复溶后,等分并冷冻保存(-20°C)。贮备液在-20°C下可稳定保存至多6个月。

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Maria Peleli et al.
Acta physiologica (Oxford, England), 239(1), e14021-e14021 (2023-08-09)
In extracerebral vascular beds cystathionine-gamma lyase (CSE) activity plays a vasodilatory role but the role of this hydrogen sulfide (H2 S) producing enzyme in the intracerebral arterioles remain poorly understood. We hypothesized a similar function in the intracerebral arterioles. Intracerebral

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