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A potent and selective prostaglandin E2 (EP1) antagonist. Displays in vivo analgesic activity in the rat. Does not block PGE1-induced hyperalgesia. Purity: ≥98% (HPLC). Solubility: Soluble in water or DMSO (25mg/ml). Long Term Storage: -20°C.
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Semicarbazide hydrochloride is an orally active urea derivative Semicarbazide hydrochloride binds to copper or iron in cells Semicarbazide hydrochloride inhibits the activity of soluble semicarbazide sensitive amine oxidase (SSAO) Semicarbazide hydrochloride damages cartilage blood vessels ovaries testicles and thyroid follicles[1][2][3][4][5][6][7][8][9]
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