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Capsazepine

ALX-550-145

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Capsaicin antagonist

Analog of capsaicin (Prod. No. BML-EI125-0200) that acts as a capsaicin antagonist. Inhibits resiniferatoxin and capsaicin-induced contractions of guinea pig trachea. Inhibits C-fiber-smooth muscle contractions induced by capsaicin, bradykinin and neurokinin A. Increases intracellular Ca²⁺ levels.

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Product Details

Alternative Name	N-[2-(4-Chlorophenyl)ethyl]-1,3,4,5-tetrahydro-7,8-dihydroxy-2H-2-benzazepine-2-carbothioamide
Appearance	White to off-white powder.
CAS	138977-28-3
Formula	C₁₉H₂₁ClN₂O₂S
MW	376.9
Purity	≥97% (HPLC, TLC)
Solubility	Soluble in methanol, 100% ethanol (25mg/ml) or DMSO (25mg/ml).
Source	Synthetic.

Handling & Storage

Use/Stability	As indicated on product label or CoA when stored as recommended.
Long Term Storage	+4°C
Shipping	Ambient Temperature

Regulatory Status	RUO – Research Use Only

Pharmacological Properties of Propiverine Contribute to Improving Lower Urinary Tract Dysfunctions in Rats with Spinal Cord Injuries: F. Sakakibara, et al.; Drug Res. (Stuttg.) 66, 464 (2016), Application(s): Drugs and treatmnet of rats, Abstract — Full Text
Glucose concentration in culture medium affects mRNA expression of TRPV1 and CB1 receptors and changes capsaicin toxicity in PC12 cells: Mohammadi-Farani, A., Ghazi-Khansari, M., et al.; Iran J. Basic. Med. Sci. 17, 673 (2014), Abstract
Piperine, a dietary phytochemical, inhibits angiogenesis: Doucette, C. D., Hilchie, A. L., et al.; J. Nutr. Biochem. 24, 231 (2013), Abstract
Effect of capsazepine on cytosolic Ca(2+) levels and proliferation of human prostate cancer cells: J.K. Huang, et al.; Toxicol. In Vitro 20, 567 (2006), Abstract
Capsazepine is a novel activator of the delta subunit of the human epithelial Na+ channel: H. Yamamura, et al.; J. Biol. Chem. 279, 44483 (2004), Abstract
Characterization of the human HCN1 channel and its inhibition by capsazepine: C.H. Gill, et al.; Br. J. Pharmacol. 143, 411 (2004), Abstract
Capsazepine protects against neuronal injury caused by oxygen glucose deprivation by inhibiting I(h): A.M. Ray, et al.; J. Neurosci. 23, 10146 (2003), Abstract
Halogenation of a capsaicin analogue leads to novel vanilloid TRPV1 receptor antagonists: Appendino, G., Harrison, S., et al.; Br. J. Pharmacol. 139, 1417 (2003), Abstract
The discovery of capsazepine, the first competitive antagonist of the sensory neuron excitants capsaicin and resiniferatoxin: C.S. Walpole, et al.; J. Med. Chem. 37, 1942 (1994), Abstract
Inhibition by capsazepine of resiniferatoxin- and capsaicin-induced contractions of guinea pig trachea: J.L. Ellis & B.J. Undem; J. Pharmacol. Exp. Ther. 268, 85 (1994), Abstract

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Capsazepine

ALX-550-145

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