2-PMPA (Synonyms: 2-(Phosphonomethyl)pentanedioic acid)
目录号: PL01131 纯度: ≥98%
CAS No. :173039-10-6
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中文名称
2-PMPA
中文别名
2-(膦酰基甲基)戊二酸;2-(PHOSPHONOMETHYL)PENTANEDIOIC ACID
英文名称
2-PMPA
英文别名
2-(Phosphonomethyl)pentanedioic acid;2-(PHOSPHONOMETHYL)PENTANEDIOIC ACID (PMPA);PMPA (NAALADASE INHIBITOR);2-(Phosphonomethyl)-pentandioic acid;2-Phosphonomethyl pentanedioic acid;PMPA;2-PMPA;2-(Phosphonomethyl)pentane-1,5-dioicacid;PMPA(NAALADaseinhibitor);2-(PHOSPHONOMETHYL)-PENTANEDIOIC ACID;2-PMPA(NAALADaseinhibitor);BDBM17659;HMS3267D10;HMS3412K10;HMS3676K10;HMS3749M13;2-Phosphonomethyl-pentanedioic acid;pentanedioic acid analogue, (RS)-1;API0001123;Pentanedioic acid, 2-(phosphonomethyl)-;(R
Cas No.
173039-10-6
分子式
C6H11O7P
分子量
226.12
包装储存
4°C, stored under nitrogen In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)
产品详情
2-PMPA是高效选择性的谷氨酸羧肽酶II (GCPII)抑制剂,IC50值为300 pM。
生物活性
2-PMPA is a potent and selective inhibitor of glutamate carboxypeptidase II (GCPII) with an IC 50 of 300 pM.
性状
Oil
IC50 & Target[1][2]
IC50: 300 pM (GCPII)
体外研究(In Vitro)
2-PMPA is a potent and selective inhibitor of GCPII, an enzyme which catabolizes the abundant neuropeptide N-acetyl-aspartyl-glutamate (NAAG) to N-acetylaspartate (NAA) and glutamate. 2-PMPA demonstrates robust efficacy in numerous animal models of neurological disease. 2-PMPA is a highly polar compound with multiple negative charges causing significant challenges for analysis in biological matrices. 2-PMPA reduces ketamine-induced decrease of cell viability and increase of LDH levels in the mixed cultures but not in the neuronal cultures. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
Intraperitoneal administration of 100 mg/kg 2-PMPA results in maximum concentration in plasma of 275 μg/mL at 0.25 h. The half-life, area under the curve, apparent clearance, and volume of distribution are 0.64 h, 210 μg×h/mL, 7.93 mL/min/kg, and 0.44 L/kg, respectively. 2-PMPA at 250 mg/kg, in an anesthetized mouse, after an initial rise, produces a rapid decline and a striking attenuation in BOLD signals in gray matter. The signature of 2-PMPA on brain T 2 * signals in gray matter at both 167 and 250 mg/kg includes a significant initial rise lasting several minutes. 2-PMPA has neuroprotective activity in an animal model of stroke and anti-allodynic activity in CCI model. Administration of 2-PMPA (50mg/kg) produces a mean peak concentration of 2-PMPA of 29.66±8.1 μM. This concentration is about 100,000 fold more than is needed for inhibition of NAAG peptidase, and
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, stored under nitrogen In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)
参考文献
[1]. Rais R, et al. Bioanalytical method for evaluating the pharmacokinetics of the GCP-II inhibitor 2-phosphonomethyl pentanedioic acid (2-PMPA). J Pharm Biomed Anal. 2014 Jan;88:162-9.
[2]. Zuo D, et al. Existence of glia mitigated ketamine-induced neurotoxicity in neuron-glia mixed cultures of neonatal rat cortex and the glia-mediated protective effect of 2-PMPA. Neurotoxicology. 2014 Sep;44:218-30.
溶解度数据
In Vitro: H2O : ≥ 28 mg/mL (123.83 mM)配制储备液
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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