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Class 552/636 - Unsaturation between the 5- and 6-positions (e.g., dehydroandrosterones, etc.)


Subclass of Class 552 - Organic compounds -- part of the class 532-570 series
Definition: Compounds which contain a double bond between the 5- and
No. of patents: 51
Last issue date: 08/26/2003


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NumberTitleIssue Date
6610866Stereoselective synthesis of 24-hydroxylated compounds useful for the preparation of aminosterols, vitamin D analogs, and other compounds
A method is described for stereoselectively reducing an unsaturated alkyl ketone substituent attached to a fused ring base. In this method, the unsaturated alkyl ketone reacts with a chiral oxazaborolidine reagent. This reaction stereoselectively reduces ...
08/26/2003
6433200Intermediates for preparation of 16-ene-vitamin D derivatives
Intermediates for the preparation of a vitamin D derivative have the following formulas: ##STR1## wherein R9 and R10 may be the same or different and each represents a hydrogen atom or a protecting group, and in Formula (5) the ...
08/13/2002
6369247Process for oxidation of steroidal compounds having allylic groups
The instant invention involves a process for oxidizing compounds containing an allylic group, i.e. those containing an allylic hydrogen or allylic alcohol group, to the corresponding enones, using a ruthenium-based catalyst in the presence of a hydroperox...
04/09/2002
6284750଱-hydroxyacid esters of DHEA useful against skin disorders
Disclosed are compounds of formula II: ##STR1## wherein A is as defined by the specification. Also disclosed are compositions containing the esters and methods for their use in the regulation of skin atrophy and in the treatment of skin disorders such as ...
09/04/2001
6025347Steroid esters useful against skin disorders
Novel steroid esters useful for regulating skin atrophy, and skin maladies, as well as compositions containing the esters and methods for their use are described. A preferred steroid ester is DHEA salicylate. Such types of skin atrophy to be treated inclu...
02/15/2000
5969168Androstanes for inducing hypothalamic effects
The invention relates to novel, androstane steroids which are the ligand semiochemicals which bind to neuroepithelial receptors. The steroids are useful as ligands to neuroepithelial receptors in the human vomeronasal gland to stimulate autonomic and hypo...
10/19/1999
5736537Dehydroep:androsterone sailcylate useful against skin atrophy
Disclosed is the use of dehydroepiandrosterone salicylate in the treatment of skin atrophy. ##STR1## Such types skin atrophy to be treated include the thinning and/or general degradation of the dermis often characterized by a decrease in collagen ...
04/07/1998
5583239Antimicrobial sterol conjugates
The invention discloses steroid conjugates having the following structure: ##STR1## where Y is NHCH2 CH2 CH2 CH2 NH2, NH(CH2)3 NH(CH2)4 NH(CH2)
12/10/1996
5424463Ɗ5-androstenes useful for promoting weight maintenance or weight loss and treatment process
A method for promoting weight control by treating a subject with a therapeutic amount of one of the Ɗ5-androstenes listed below to stimulate weight control without affecting appetite or inducing the synthesis of sex hormones. Ɗ5-Androstenes providing th...
06/13/1995
542430417-aryl-substituted steroidal compounds active on the cardiovascular system
Cardioactive steroidal compounds of the formula I ##STR1## wherein R, R1, R2, R3, R4, R5, R6 and R7 have the meanings shown in the description, and pharmaceutical compositio...
06/13/1995
5387583Compositions containing corticosteroids or analogues thereof and corticosteroid buffering effective amounts of 5-androstene 3B, 17B or 5-androstene 3B, 7B, 17B triol or analogues thereof
3ଲ,17ଲ-androstenediol ("�") and 3ଲ,7ଲ,17ଲ-androstenetriol ("򳊮T") may be used to counteract the antiproliferative and immunosuppressive effects of hydrocortisone and other corticosteroids (i.e., to act as buff...
02/07/1995
5002936Lipophilic complexes of pharmacologically active inorganic mineral acid esters of organic compounds
The present invention provides a composition with the structure (L)m (E)n wherein (L)m and (E)n are bound as a complex, wherein L is a lipophilic compound; wherein E is a nonlipophilic, ionic, inorganic ester of an o...
03/26/1991
4946834Phosphonic acid substituted steroids as steroid 5଱-reductase inhibitors
Invented are substituted acrylate analogues of steroidal synthetic compounds, pharmaceutical compositions containing the compounds, and methods of using these compounds to inhibit steroid 5଱-reductase. Also invented are intermediates used in prepari...
08/07/1990
49258343-methylene-4-androsten-17-ones, process for their production and pharmaceutical preparations containing them
A 3-methylene-4-androsten-17-one of formula I ##STR1## wherein Ra represents a hydrogen atom or a saturated or unsaturated straight-chain or branched-chain, optionally substituted alkyl radical with 1-6 carbon atoms, in which Ra...
05/15/1990
489869417-Hydroxy-steroids
Compounds of the formulae: ##STR1## are useful as anti-cancer, anti-obesity, anti-diabetic, anti-coronary agents, anti-aging agents, anti-hypolipidemic agents and anti-autoimmune agents....
02/06/1990
4780455Lipophilic complexes of pharmacologically active organic compounds
The present invention provides a composition with the structure wherein m and n are each integers, and m and n are different or the same; L is an ampholytic lipid or polymer, or a nonampholytic lipid with hydrophobic properties; E is a nonlipophilic ionic inor...
10/25/1988
4749567Method and product for increasing fertility in sheep using milk protein conjugates
A product and method for increasing fertility in sheep. By "increasing felity" is meant increasing the potential of a flock of sheep to multiply by increasing ovulation in ewes. The product is an immunogenic conjugate of 4-androstene-3, 17-dione and a so...
06/07/1988
470882317 ଱-chloroethynyl pregnane derivatives
Known pregnane derivatives are prepared by esterificiation of known androstane derivatives to give new ester of Formula III ##STR1## wherein in each case symbolizes a single bond or a double bond, n is 1 or 2, R1 is hydrogen or methyl, R
11/24/1987
456700116-Methylene-17଱-hydroxy-progesterones
16-Methylene-17-keto steroids (III) are transformed to the corresponding 16-methylene-17଱-hydroxyprogesterones (VII) which are intermediates useful in the production of betamethasone, diflorasone diacetate and melengesterol acetate....
01/28/1986
4537722Steroid esters preparation
This invention relates to an improved steroid ester synthesis in which carbodiimides and catalytic amounts of 4-(tertiary amino)-pyridines, in combination with acid catalysts, are used as condensing agents, resulting in pure, non discolored compounds in h...
08/27/1985
4502989Aldosterone-antagonistic steroids
Novel spironolactone derivatives characterized by the C11 -C12 double bond which have a potent aldosterone-antagonistic activity without causing potassium loss, used alone in diagnosis and improvement of condition of primary aldoster...
03/05/1985
4452994Process for isolating organic compounds and lithium salt complexes useful in said process
An improved process for isolating organic compounds from crude product or reaction mixtures by dissolving said crude product or reaction mixture in a suitable solvent, contacting the resulting solution with a lithium salt to form a solid metal salt comple...
06/05/1984
445140416ଲ-Methyl steroid process
Ɗ4 -3-keto, Ɗ1,4 -3-keto and 3ଲ-hydroxy 17-keto steroids (I) are transformed into the corresponding 16-ଲ-methyl-17-keto steroids (IV) by first activating the C-16 position, then methylating. By protecting the C-3 positi...
05/29/1984
4443377Isomerization-acylation process
17଱-Hydroxy-6,16-dimethylenepregn-4-ene-3,20-dione simultaneously isomerized and acylated to 17଱-hydroxy-6-methyl-16-methylenepregna-4,6-diene-3,20-dione 17-acetate....
04/17/1984
4416821Process for preparing 16-methylene steroids
A process is disclosed for the production of 17-keto-16-methylene steroids (III) from the corresponding readily available 17-keto steroid (I) via a novel intermediate (II)....
11/22/1983
4383947Introduction of a fluorine atom
Perchloryl fluoride when reacted with the appropriately protected 9଱-hydroxyandrostenedione stereoselectively produces the corresponding 6ଲ-fluoro steroid....
05/17/1983
4360663Steroid hormone-antitumor derivatives
A process for producing a steroid hormone-antitumor derivative which selectively affects to tumor or cancer cells comprises reacting X group of a steroid hormone derivative having the formula ##STR1## wherein ST represents a steroid moiety having a c...
11/23/1982
4357279Preparation of corticoids from 17-keto steroids
A process for the preparation of corticoids (XI) which comprises reacting a protected 17-keto steroid (II) with a metallated 1,2-dihaloethene (III)....
11/02/1982
4346037Base catalyzed acylation with enol esters
This invention relates to processes for base catalyzed acylations using enol esters, for example, isopropenyl acetate. Particularly, the processes are useful for acylating acid sensitive alcohols including hydroxy steroids....
08/24/1982
432241610-Alkynyl steroids
Aromatase inhibitors are provided having the formula ##STR1## wherein represents a single or double bond; R is hydrogen or C1-4 alkyl; R1 is methyl or ethyl; R2 is (H) (OR8) or .dbd.O; R3 is ...
03/30/1982
4311646Process for the preparation of 4,6-dien-3-one steroids
A 4,6-dien-3-one steroid is produced by brominating an enolic ether of a 4-en-3-one steroid in a water-containing organic solvent which is substantially free from acetic acid and sodium acetate to give a 6-bromosteroid and then dehydrobrominating the 6-br...
01/19/1982
4290961Process for catalytically reducing carbonyl compounds
Catalytic reduction of carbonyl compounds by transfer of hydrogen from alcohols to aliphatic, alicyclic, aromatic, homo- and heterocyclic ketones or aldehydes, catalyzed by rhodium or iridium complexes, characterized in that a primary or secondary alcohol...
09/22/1981
428976210-(1,2-Propadienyl) steroids as irreversible aromatase inhibitors
Irreversible aromatase inhibitors are provided having the formulae ##STR1## wherein represents a single or a double bond; R1 is CH3 or C2 H5 ; R2 is (H) (OR8) or O; R3 is H or ...
09/15/1981
4272445Process for preparing active compounds
A process for the preparation of a compound of the formula (A): ##STR1## wherein: R3 is a C1-5 alkyl group, a C3-6 alkenyl group, a C3-6 cycloalkyl group or an alkylphenyl group in which the alkyl moiety co...
06/09/1981
4239681Androst-4-en-19-ols
Derivatives of androst-4-en-19-ol are useful for enhancing libido and related psychic attitudes....
12/16/1980
4203981Novel 17 ଱-aryl-steroids
Novel steroids of the formula ##STR1## wherein R1 is selected from the group consisting of hydrogen and acyl of an organic carboxylic acid of 1 to 18 carbon atoms, R2 is selected from the group consisting of optionally substitut...
05/20/1980
4181669Steroid esters preparation
This invention relates to an improved steroid ester synthesis in which a carbodiimide, in combination with an acid catalyst, is used as condensing agent....
01/01/1980
4180504Method for the preparation of esters
This invention relates to an improved ester synthesis in which a carbodiimide, in combination with an acid catalyst, is used as condensing agent....
12/25/1979
4150044Process for the manufacture of 17଱-hydroxy-21-acetoxy-progesterone
The present invention relates to a process for the manufacture of 17଱ -hydroxy-21-acyloxy-progesterone, in particular of 17଱-hydroxy-21-acetoxy-progesterone (Reichstein's substance S acetate) which is of great importance as a starting material...
04/17/1979
4150126Novel enol esters of steroids, compositions containing such compounds, processes for their preparation and methods of treatment therewith
This invention relates to novel enol esters of steroids having an antitumor activity and to the preparation thereof. The invention is also concerned with pharmaceutical compositions containing the said compounds and methods of treatment therewith....
04/17/1979
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