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- 详细信息
- 技术资料
- 保存条件:
Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year
- 保质期:
Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year
- 英文名:
Sarcosine
- 库存:
现询
- 供应商:
北京索莱宝科技有限公司
- CAS号:
107-97-1
- 规格:
500mg/100mg/50mg/20mg
| 规格: | 500mg | 产品价格: | ¥790.0 |
|---|---|---|---|
| 规格: | 100mg | 产品价格: | ¥490.0 |
| 规格: | 50mg | 产品价格: | ¥350.0 |
| 规格: | 20mg | 产品价格: | ¥260.0 |
是I型甘氨酸转运蛋白(GlyT1)和N-甲基-D-天冬氨酸受体(NMDAR)共激动剂的竞争性抑制剂。
| 基本信息 | |
| CAS | No.107-97-1 |
| 中文名称 | 肌氨酸 |
| 英文名称 | Sarcosine |
| 别名 | 肌氨酸;N-甲基甘氨酸;甲氨基乙酸;肉素;肉氨基酸; |
| 分子式 | C3H7NO2 |
| 分子量 | 89.09 |
| 溶解性 | Soluble in Water |
| 纯度 | HPLC≥98% |
| 外观(性状) | White to yellow Solid |
| 储存条件 | Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year |
| EC | EINECS 203-538-6 |
| MDL | MFCD00004279 |
| SMILES | O=C(O)CNC |
| InChIKey | FSYKKLYZXJSNPZ-UHFFFAOYSA-N |
| InChI | InChI=1S/C3H7NO2/c1-4-2-3(5)6/h4H,2H2,1H3,(H,5,6) |
| PubChem CID | 1088 |
| 靶点 | GlyT;NMDAR |
| 通路 | Membrane Transporter&Ion Channel;Neuronal Signaling |
| 背景说明 | 是I型甘氨酸转运蛋白(GlyT1)和N-甲基-D-天冬氨酸受体(NMDAR)共激动剂的竞争性抑制剂。 |
| 生物活性 | Sarcosine, a natural amino acid found in muscles and other body tissues, is an endogenous glycine transporter type 1 inhibitor that increases the glycine concentration, resulting in an indirect potentiation of the N-methyl-D-aspartate (NMDA) subtype of glutamate receptors. Sarcosine, similar to other NMDA receptor-activating agents, is an effective adjuvant in the treatment of schizophrenia.Sarcosine, a glycine transporter type 1 inhibitor and an N-methyl-D-aspartate (NMDA) receptor co-agonist at the glycine binding site, potentiates NMDA Receptor function. [1-2]. |
| In Vitro | Sarcosine acts as a full agonist, yet DMG is a partial agonist at glycine binding site of NMDA receptors. The molecular docking analysis indicated that the interactions of glycine, sarcosine, and DMG to NMDA receptors are highly similar, supporting that the glycine binding site of NMDA receptors is a critical target site for sarcosine and DMG.[2] |
| 细胞实验 | In the iv PTZ test, sarcosine did not exert a significant effect on the seizure threshold at any of the doses tested (100, 200, 400 and 800 mg/kg, IP). However, at doses of 400 and 800 mg/kg, sarcosine significantly raised the threshold for electroconvulsions (p < 0.01).[1] |
| 动物实验 | Animal Model: Albino Swiss mice weighing (25-30 g);Dosage: 100 mg/kg, 200 mg/kg, 400 mg/kg, 800 mg/kg;Administration: Intraperitoneal injection[2] |
| 数据来源文献 | [1]. Katarzyna Soca?a, et al. Effects of sarcosine, a glycine transporter type 1 inhibitor, in two mouse seizure models. Pharmacol Rep. Mar-Apr 2010;62(2):392-7. [2]. Mei-Yi Lee, et al. Effects of sarcosine and N, N-dimethylglycine on NMDA receptor-mediated excitatory field potentials. J Biomed Sci. 2017; 24: 18. |
| 单位 | 瓶 |
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IS0850 肌氨酸 氨基酸及其衍生物 索莱宝
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