Invention Grant
- Patent Title: (20R)-2α-methyl-19,26,2-trinor-vitamin D analogs
- Patent Title (中): (20R)-2α-甲基-19,26,2-三 - 维生素D类似物
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Application No.: US12171085Application Date: 2008-07-10
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Publication No.: US08193169B2Publication Date: 2012-06-05
- Inventor: Hector F. DeLuca , Pawel Grzywacz , Lori A. Plum , Margaret Clagett-Dame
- Applicant: Hector F. DeLuca , Pawel Grzywacz , Lori A. Plum , Margaret Clagett-Dame
- Applicant Address: US WI Madison
- Assignee: Wisconsin Alumni Research Foundation
- Current Assignee: Wisconsin Alumni Research Foundation
- Current Assignee Address: US WI Madison
- Agency: Andrus, Sceales, Starke & Sawall, LLP
- Main IPC: A61K31/59
- IPC: A61K31/59 ; C07C401/00 ; C07C35/17 ; A61P17/00

Abstract:
This invention discloses (20R)-2α-methyl-19,26,27-trinor-vitamin D analogs, and specifically (20R)-2α-methyl-19,26,27-trinor-1α,25-dihydroxyvitamin D3, and pharmaceutical uses therefor. This compound exhibits transcription activity as well as pronounced activity in arresting the proliferation of undifferentiated cells and inducing their differentiation to the monocyte thus evidencing use as an anti-cancer agent and for the treatment of skin diseases such as psoriasis as well as skin conditions such as wrinkles, slack skin, dry skin and insufficient sebum secretion. This compound also shows very low activity in vivo on bone calcium mobilization and intestinal calcium transport activity compared to the native hormone 1α,25-dihydroxyvitamin D3, and therefore may be used to treat autoimmune disorders or inflammatory diseases in humans as well as renal osteodystrophy. This compound may also be used for the treatment or prevention of obesity.
Public/Granted literature
- US20080300223A1 (20R)-2a-Methyl-19,26,27-Trinor-Vitamin D Analogs Public/Granted day:2008-12-04
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