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Class 540/101 - The hetero ring and acyclic chalcogen are both bonded directly at the 17 position of the cyclopentanohydrophenanthrene ring system


Subclass of Class 540 - Organic compounds -- part of the class 532-570 series
Definition: Compounds wherein both the hetero ring and acyclic chalcogen
No. of patents: 9
Last issue date: 07/17/2001


NumberTitleIssue Date
626204217ଲ-amino and hydroxylamino-11ଲ-arylsteroids and their derivatives having agonist or antagonist hormonal properties
The invention is directed to a novel class of steroids which exhibit potent antiprogestational activity....
07/17/2001
5792859Intermediates for 20-oxo-17଱,21-diol steroids
Novel intermediate compounds of formula IV, V, VI, VII and VIII which are useful for the preparation of steroids of the formula ##STR1## wherein the substituents are defined in the specification....
08/11/1998
5723638Process for 20-oxo-17଱,21-diol steroids
The invention is drawn to a process for the preparation of a steroid of the formula ##STR1## wherein R1 is hydrogen or alkyl of 1 to 4 carbon atoms, R2 is alkyl of 1 to 4 carbon atoms and theo A, B, C, and D ring system has at ...
03/03/1998
572122717-aryl and 17-heterocyclyl-14ଲ-5଱-androstane, androstene and androstadiene derivatives active on the cardiovascular system, processes for their preparation and pharmaceutical compositions containing same
17-Aryl -5଱,14ଲ-androstane, androstene and androstadiene derivatives of formula (I): ##STR1## wherein the symbol --- represents a single or a double bond; when the double bond is not present in the 4 or 5 position, the hydrogen in po...
02/24/1998
510899619-nor-3-keto steroids
A compound selected from the group consisting of a compound of the formula ##STR1## wherein R2 and R'2 are individually hydrogen or methyl, R11 is an organo of 1 to 18 carbon atoms optionally containing at least one h...
04/28/1992
4511511Prednisolone derivatives
Novel prednisolone derivatives modified at C-17,C-20 and/or C-21 positions. Many of the compounds are anti-inflammatory agents which do not significantly suppress the pituitary-adrenal axis....
04/16/1985
4340538Process for producing 6଱-fluoro-Ɗ1,4 -3-keto steroids
Two processes are disclosed (one-pot and two-pot) for the transformation of a 6ଲ-fluoro-Ɗ1,4 -3-keto steroid (IV) to a 6଱-fluoro-Ɗ1,4 -3-keto steroid (VI). These processes permit the introduction of a fluorine atom at t...
07/20/1982
4192871Chemical compounds
Pregnanes and androstanes are described which essentially possess a 3଱-hydroxy group, a 5଱-hydrogen atom or a 4.5- or 5,6-double bond, a 17଱-hydrogen atom and an 11ଲ-aminoester group. Other optional substituents or double bonds may...
03/11/1980
4089852Process for the preparation of 21-hydroxy-16-pregnen-20-one derivatives
Ɗ16 -21-HYDROXY-20-KETO STEROIDS OF THE PREGNANE SERIES HAVING AN OTHERWISE UNSUBSTITUTED D-ring and a 13-methyl or -ethyl group, and 21-ethers and -esters thereof, are produced by reaction of a corresponding D-ring saturated 17-keto steroid w...
05/16/1978
 
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