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Submit ReviewPotent competitive vanilloid TRPV1 (VR1) receptor antagonist (IC50 = 10 nM). Inhibits capsaicin-induced [Ca2+]i increase in rat DRG neurons, and guinea pig bladder and trachea contractions in vitro.
分子量 | 419.3 |
公式 | C17H26INO3 |
储存 | Store at RT |
纯度 | ≥99% (HPLC) |
CAS Number | 859171-97-4 |
PubChem ID | 5149140 |
InChI Key | AAORACFZMYMFCG-UHFFFAOYSA-N |
Smiles | CCCCCCCCC(=O)NCC1=CC(OC)=C(O)C=C1I |
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。
Appendino et al (2003) Halogenation of a capsaicin analogue leads to novel vanilloid TRPV1 receptor antagonists. Br.J.Pharmacol. 139 1417 PMID: 12922928
关键词: 6-Iodonordihydrocapsaicin, 6-Iodonordihydrocapsaicin supplier, Potent, competitive, vanilloids, receptors, antagonists, VR1, TRPV, Channels, Transient, Receptor, Potential, 1975, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。 6-Iodonordihydrocapsaicin 的部分引用包括:
Kaji et al (2011) Effects of luminal thymol on epithelial transport in human and rat colon. Am J Physiol Gastrointest Liver Physiol 300 G1132 PMID: 21372164
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