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Submit ReviewJNJ 1661010
Description: Selective, reversible FAAH inhibitor
Chemical Name: N-Phenyl-4-(3-phenyl-1,2,4-thiadiazol-5-yl)-1-piperazinecarboxamide
Purity: ≥99% (HPLC)
Biological Activity for JNJ 1661010
JNJ 1661010 is a selective, reversible inhibitor of fatty acid amide hydrolase (FAAH) (IC50 = 12 nM). Brain penetrant and active in vivo.
Technical Data for JNJ 1661010
| M. Wt | 365.45 |
| Formula | C19H19N5OS |
| Storage | Store at +4°C |
| Purity | ≥99% (HPLC) |
| CAS Number | 681136-29-8 |
| PubChem ID | 2809273 |
| InChI Key | BHBOSTKQCZEAJM-UHFFFAOYSA-N |
| Smiles | O=C(NC3=CC=CC=C3)N1CCN(C2=NC(C4=CC=CC=C4)=NS2)CC1 |
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Product Datasheets for JNJ 1661010
References for JNJ 1661010
References are publications that support the biological activity of the product.
Keith et al (2008) Thiadiazolopiperazinyl ureas as inhibitors of fatty acid amid hydrolase. Bioorg.Med.Chem.Lett. 18 4838 PMID: 18693015
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Keywords: JNJ 1661010, JNJ 1661010 supplier, Selective, reversible, FAAH, inhibitors, inhibits, Anandamide, Amidase, Fatty, Acid, Amide, Hydrolases, JNJ1661010, Hydrolase, (FAAH), Other, Cannabinoids, 3262, Tocris Bioscience
2 Citations for JNJ 1661010
Citations are publications that use Tocris products. Selected citations for JNJ 1661010 include:
Stone et al (2012) The cytoprotective effects of oleoylethanolamide in Ins-Secr.g cells do not require activation of GPR119. Br J Pharmacol 165 2758 PMID: 22029844
Brown et al (2010) Cannabinoid receptor-dependent and -independent anti-proliferative effects of omega-3 ethanolamides in androgen receptor-positive and -negative prostate cancer cell lines. Carcinogenesis 31 1584 PMID: 20660502
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Literature in this Area
Tocris offers the following scientific literature in this area to showcase our products. We invite you to request* your copy today!
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