Cyclopamine
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Cyclopamine
Cyclopamine (11-deoxojervine) is a naturally-occurring chemical that belongs to the group of steroidal jerveratrum alkaloids. It is a teratogen isolated from the corn lily (Veratrum californicum) that can lead to cyclopia (holoprosencephaly). Cyclopamine was named for one-eyed lambs which were born to sheep which grazed on wild corn lily at a farm in Idaho. In 1957 the US Department of Agriculture started an eleven-year investigation which led to the identification of cyclopamine as the cause of the birth defect.[1]
Physiological effectsCyclopamine inhibits the hedgehog signaling pathway (Hh) by influencing the balance between the active and inactive forms of the Smoothened protein. Medical potentialCyclopamine is currently being investigated as a treatment agent in basal cell carcinoma, medulloblastoma, and rhabdomyosarcoma, tumors that result from excessive Hh activity [2], glioblastoma, and as a treatment agent for multiple myeloma. See alsoPatient trial conducted in Dallas, Texas through APQ research center. Myeloma patient was given 200 mg of cyclopamine daily for two 2 weeks every 3 months for a year, for a total of eight weeks or four times, August 2006-August 2007. M marker was measured and decreased from 1.0 to 0.2 during that time. There is now a new water-soluble version of cyclopamine that will be tested soon. Cyclopamine Tartarate Salt (All Hydroxy Carboxylic Acids) is a white crystaline compound that has been filed for a provisional patent by Logan Natural Products on 2/10/2008. Cyclopamine has been tested on Psoriasis. NotesReferences
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