(22E)-2-methylene-26,27-cyclo-22-dehydro-1α-hydroxy-19-norvitamin D3 derivatives
US-9834512-B2 · Dec 5, 2017 · US
US10494337B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10494337-B2 |
| Application number | US-201615165884-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 26, 2016 |
| Priority date | May 26, 2015 |
| Publication date | Dec 3, 2019 |
| Grant date | Dec 3, 2019 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Disclosed are 1α,25-dihydroxy-24,24-difluoro-2-methylene-19-nor-vitamin D analogs and their pharmaceutical uses. These new vitamin D analogs are 19-nor-vitamin D analogs having two fluorine atom substitutions at the 24 position (C-24) in the side chain and optionally having a 2-methylene substituent.
Opening claim text (preview).
We claim: 1. A compound having the formula: where X 1 , X 2 , and X 3 , which may be the same or different, are each independently selected from hydrogen or a hydroxy-protecting group. 2. The compound of claim 1 wherein X 1 is hydrogen. 3. The compound of claim 1 wherein X 2 is hydrogen. 4. The compound of claim 1 wherein X 1 and X 2 are both t-butyldimethylsilyl. 5. The compound of claim 1 wherein X 3 is hydrogen. 6. The compound of claim 1 wherein X 3 is triethylsilyl. 7. The compound of claim 1 having a formula: 8. A pharmaceutical composition containing an effective amount of the compound of claim 1 or a pharmaceutical salt thereof together with a pharmaceutically acceptable excipient. 9. The pharmaceutical composition of claim 8 wherein said effective amount comprises about 1.0 μg to about 1000.0 μg per gram of the composition.
Related publications grouped by family.
Answers are generated from the same data shown on this page.