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Submit ReviewSA 47 is a selective inhibitor of fatty acid amide hydrolase (FAAH). Exhibits greater selectivity for FAAH than URB 597 against multiple carboxylesterases.
分子量 | 334.41 |
公式 | C17H26N4O3 |
储存 | Store at -20°C |
纯度 | ≥99% (HPLC) |
CAS Number | 792236-07-8 |
PubChem ID | 9840648 |
InChI Key | HSYCMGWPPRTNKH-UHFFFAOYSA-N |
Smiles | CC1=CC=CC(N2CCC(CCNC(OCC(NC)=O)=O)CC2)=N1 |
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.
参考文献是支持产品生物活性的出版物。
Zhang et al (2007) Fatty acid amide hydrolase inhibitors display broad selectivity and inhibit multiple carboxylesterases as off-targets. Neuropharmacology 52 1095 PMID: 17217969
Ahn et al (2009) Fatty acid amide hydrolase as a potential therapeutic target for the treatment of pain and CNS disorders. Expert Opin.Drug Discov. 4 763 PMID: 20544003
关键词: SA 47, SA 47 supplier, SA47, FAAH, fatty, acid, amide, hydrolase, inhibitors, inhibits, selective, Fatty, Acid, Amide, Hydrolase, (FAAH), Other, Cannabinoids, 4785, Tocris Bioscience
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Tocris offers the following scientific literature in this area to showcase our products. We invite you to request* your copy today!
*请注意,Tocris 仅会向正规科研企业/机构地址发送文献。
The key feature of drug addiction is the inability to stop using a drug despite clear evidence of harm. This poster describes the brain circuits associated with addiction, and provides an overview of the main classes of addictive drugs and the neurotransmitter systems that they target.