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2-Pyrazinecarboxylic acid/2-吡嗪羧酸 {[allProObj[0].p_purity_real_show]}

货号:A401180 同义名: 2-甲酸吡嗪

2-Pyrazinecarboxylic acid是通过与天冬氨酸脱羧酶 PanD 结合,抑制分枝杆菌辅酶 A 的合成。

2-Pyrazinecarboxylic acid/2-吡嗪羧酸 化学结构 CAS号:98-97-5
2-Pyrazinecarboxylic acid/2-吡嗪羧酸 化学结构
CAS号:98-97-5
2-Pyrazinecarboxylic acid/2-吡嗪羧酸 3D分子结构
CAS号:98-97-5
2-Pyrazinecarboxylic acid/2-吡嗪羧酸 化学结构 CAS号:98-97-5
2-Pyrazinecarboxylic acid/2-吡嗪羧酸 3D分子结构 CAS号:98-97-5
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2-Pyrazinecarboxylic acid/2-吡嗪羧酸 纯度/质量文件 产品仅供科研

货号:A401180 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 Dehydrogenase 其他靶点 纯度
Trilostane 99+%
AGI-6780 +++

IDH2 R140Q mutant, IC50: 23 nM

99%+
Gimeracil 98%
AGI-5198 ++

R132H-IDH1, IC50: 70 nM

R132C-IDH1, IC50: 0.16 μM

99%+
SW033291 ++++

15-PGDH, Ki: 0.1 nM

15-PGDH, IC50: 1.5 nM

99%+
Mycophenolic acid 99+%
Fomepizole 98%
Leflunomide 98%
3-Nitropropanoic acid 99%+
Isovaleramide 99%
Mycophenolate Mofetil +++

Inosine monophosphate dehydrogenase I, IC50: 39 nM

Inosine monophosphate dehydrogenase II, IC50: 27 nM

98%
MK-8245 ++++

SCD1 (rat), IC50: 3 nM

SCD1 (mouse), IC50: 1 nM

99%+
Vidofludimus ++

Human DHODH, IC50: 134 nM

99%+
Emodin 98%
Ivosidenib 98%
NCT-501 ++

ALDH1A1, IC50: 40 nM

98%
Gossypol 99%+
Devimistat 98%
Disulfiram 98%+
Enasidenib ++++

IDH2, IC50: 12 nM

98%
PluriSIn 1 99%+
ML390 +

DHODH, IC50: 0.56 μM

99%+
Teriflunomide 99%+
Daidzin +++

ALDH-Ⅰ, Ki: 20 nM

98+%
18β-Glycyrrhetinic acid 99%
RRx-001 95%
NCT-503 +

PHGDH, IC50: 2.5 μM

99%+
Vorasidenib 99%+
Ammonium Glycyrrhizinate(x:1) 98+%
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

2-Pyrazinecarboxylic acid/2-吡嗪羧酸 生物活性

描述 Pyrazinecarboxylic acid is an active metabolite of pyrazinamide. Pyrazinamidean is an anti-tubercular agent. In this model for the evaluation of the effects of uricosuric agents, the urinary excretion of pyrazinecarboxylic acid was decreased by probenecid and indicated an inverse correlation between urinary excretion of urate and pyrazinecarboxylic acid. In the in vitro study, the treatment of the vesicles of rat renal brush-border membrane with pyrazinecarboxylic acid produced an increased urate uptake, which was inhibited by uricosuric agents[2]. PZA (pyrazinamide) is converted to pyrazinecarboxylic acid (POA) in plant cells, suppressing the activity of 1-aminocyclopropane-1-carboxylic acid oxidase (ACO), the enzyme catalysing the final step of ethylene formation[3].

2-Pyrazinecarboxylic acid/2-吡嗪羧酸 参考文献

[1]Gopal P, Nartey W, Ragunathan P, Sarathy J, Kaya F, Yee M, Setzer C, Manimekalai MSS, Dartois V, Grüber G, Dick T. Pyrazinoic Acid Inhibits Mycobacterial Coenzyme A Biosynthesis by Binding to Aspartate Decarboxylase PanD. ACS Infect Dis. 2017 Nov 10;3(11):807-819. doi: 10.1021/acsinfecdis.7b00079. Epub 2017 Oct 18. PMID: 28991455; PMCID: PMC5734868.

[2]Taniguchi T, Ashizawa N, Matsumoto K, Iwanaga T. Enhancement of pharmacological effects of uricosuric agents by concomitant treatment with pyrazinamide in rats. Naunyn Schmiedebergs Arch Pharmacol. 2017;390(3):253‐260

[3]Sun X, Li Y, He W, et al. Pyrazinamide and derivatives block ethylene biosynthesis by inhibiting ACC oxidase. Nat Commun. 2017;8:15758. Published 2017 Jun 12

2-Pyrazinecarboxylic acid/2-吡嗪羧酸 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

8.06mL

1.61mL

0.81mL

40.29mL

8.06mL

4.03mL

80.58mL

16.12mL

8.06mL

2-Pyrazinecarboxylic acid/2-吡嗪羧酸 技术信息

CAS号98-97-5
分子式C5H4N2O2
分子量 124.1
SMILES Code C1=NC=CN=C1C(O)=O
MDL No. MFCD00006130
别名 2-甲酸吡嗪
运输蓝冰
InChI Key NIPZZXUFJPQHNH-UHFFFAOYSA-N
Pubchem ID 1047
存储条件

In solvent -20°C:3-6个月-80°C:12个月

Pure form Sealed in dry,2-8°C

溶解方案

DMSO: 50 mg/mL(402.91 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

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