(S)-4-Carboxyphenylglycine

Pricing Availability   Qty
说明: Competitive group I mGlu antagonist; also weak group II agonist
别名: (S)-4CPG
纯度: ≥99% (HPLC)
说明书
引用文献 (7)
评论 (1)
文献 (5)

生物活性 for (S)-4-Carboxyphenylglycine

(S)-4-Carboxyphenylglycine is a competitive group I metabotropic glutamate receptor antagonist, with selectivity for mGlu1a/1a over mGlu5a/5b.

技术数据 for (S)-4-Carboxyphenylglycine

分子量 195.17
公式 C9H9NO4
储存 Store at RT
纯度 ≥99% (HPLC)
CAS Number 134052-73-6
PubChem ID 5311459
InChI Key VTMJKPGFERYGJF-ZETCQYMHSA-N
Smiles [H][C@@](N)(C(O)=O)C1=CC=C(C(O)=O)C=C1

上方提供的技术数据仅供参考。批次相关数据请参见分析证书。

Tocris products are intended for laboratory research use only, unless stated otherwise.

溶解性数据 for (S)-4-Carboxyphenylglycine

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
1eq. NaOH 19.52 100 温和加热

制备储备液 for (S)-4-Carboxyphenylglycine

以下数据基于产品分子量 195.17。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

选择批次从而根据批次分子量重新计算:
浓度/溶剂体积/质量 1 mg 5 mg 10 mg
1 mM 5.12 mL 25.62 mL 51.24 mL
5 mM 1.02 mL 5.12 mL 10.25 mL
10 mM 0.51 mL 2.56 mL 5.12 mL
50 mM 0.1 mL 0.51 mL 1.02 mL

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产品说明书 for (S)-4-Carboxyphenylglycine

分析证书/产品说明书
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参考文献 for (S)-4-Carboxyphenylglycine

参考文献是支持产品生物活性的出版物。

Birse et al (1993) Phenylglycine derivatives as new pharmacological tools for investigating the role of metabotropic glutamate receptors in the central nervous system. Neuroscience 52 481 PMID: 7680790

Brabet et al (1995) Phenylglycine derivatives discriminate between mGluR1-and mGluR5-mediated responses. Neuropharmacology 34 895 PMID: 8532171

Doherty et al (1999) Antagonist activity of α-substituted 4-carboxyphenylglycine analogues at group I metabotropic glutamate receptors expressed in CHO cells. Br.J.Pharmacol. 126 205 PMID: 10051137

Eaton et al (1993) Competitive antagonism at metabotropic glutamate receptors by (S)-4-carboxyphenylglycine (CPG) and (RS)-α-methyl-4-carboxyphenylglycine (MCPG). Eur.J.Pharmacol. 244 195 PMID: 8381746


If you know of a relevant reference for (S)-4-Carboxyphenylglycine, please let us know.

关键词: (S)-4-Carboxyphenylglycine, (S)-4-Carboxyphenylglycine supplier, competitive, Group, I, mGlur, antagonists, weak, group, II, agonists, Competitive, Receptors, mGlu2, mGlu3, mGluR2, mGluR3, Glutamate, Metabotropic, mGlu1, mGlu5, mGluR1, mGluR5, (S)-4CPG, (Metabotropic), 0323, Tocris Bioscience

7 篇 (S)-4-Carboxyphenylglycine 的引用文献

引用文献是使用了 Tocris 产品的出版物。 (S)-4-Carboxyphenylglycine 的部分引用包括:

Overocker and Pfau (2012) Cytokine Production Modified by System X(c)- After PM10 and Asbestos Exposure. Proc Natl Acad Sci U S A 23 34 PMID: 23418405

Riz et al (2016) Noncanonical SQSTM1/p62-Nrf2 pathway activation mediates proteasome inhibitor resistance in multiple myeloma cells via redox, metabolic and translational reprogramming. Oncotarget 7 66360 PMID: 27626179

Griffin et al (2015) Repeated cycles of chronic intermittent ethanol exposure increases basal glutamate in the nucleus accumbens of mice without affecting glutamate transport. Front Pharmacol 6 27 PMID: 25755641

Resch et al (2014) Augmented cystine-glutamate exchange by pituitary adenylate cyclase-activating polypeptide signaling via the VPAC1 receptor. Synapse PMID: 25066643


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(S)-4-carboxyphenylglycine (CPG)(0.2 uM).
By Anonymous on 12/11/2019
分析类型: In Vitro
种属: Human
细胞系/组织: LP-1 cell line

Treatment with (S)-4-carboxyphenylglycine (CPG) ensitizes LP-1/Cfz cells. Cellswere treated with the indicated concentrations of carfilzomib for 72 hours in the absence or presence of CPG (0.2 uM)

PMID: 27626179
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