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WO/2008/034796A2 |
This invention relates to novel estratrien-triazoles of general formula (I) useful in therapy, especially for use in the treatment and/or prevention of a steroid hormone dependent disorder, preferably a steroid hormone dependent disease ...
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WO/2007/140380A2 |
In various aspects, the present teachings provide labeling reagents and sets of labeling reagents containing one or more heavy atom isotopes for the relative quantitation, absolute quantitation, or both, of hydroxylated compounds includi...
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WO/2007/118830A1 |
Compounds of formula (I) wherein: the groups are as defined in the description, are useful for the preparation of medicaments for the treatment of cardiovascular disorders, in particular heart failure and hypertension. The compounds are ...
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WO/2007/118832A2 |
Compounds of formula (I) wherein: the groups are as defined in the description, are useful for the preparation of medicaments for the treatment of cardiovascular disorders, in particular heart failure and hypertension. The compounds are ...
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WO/2007/081835A2 |
The invention features compounds of formulas I or II: and pharmaceutically acceptable salts and prodrugs thereof, as well methods for modulating the effects of local and systemic hypoxic events using the compounds.
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WO/2007/073424A1 |
The invention encompasses substantially pure rocuronium bromide.
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WO/2007/033348A2 |
The invention encompasses processes for synthesizing l-[17β-acetyloxy-3α- hydroxy-2β-(4-morpholmyl)-5α-androstan-16β-yl]-l-(2-prope
nyl)pyrrolidinium bromide (rocuronium bromide) and intermediates thereof.
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WO/2007/031833A2 |
The present invention provides a novel series of imidazolyl substituted steroidal and indan-1-one derivatives and salts thereof having the following general structural formulae (A and B)
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WO/2007/025632A2 |
The invention relates to new steroids nitrooxyderivatives, to topical pharmaceutical formulations thereof, and their use for treating skin or mucosal membrane diseases or disorders. These new steroids nitrooxyderivatives have an improved...
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WO/2007/024338A2 |
The present invention is a prodrug derivative of ethinyl estradiol according to Formula I: Formula I
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WO/2007/008474A2 |
The present invention is a prodrug derivative of estradiol according to Formula I:
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WO/2006/125800A1 |
The present invention relates to novel substituted steroid derivatives which represent selectiv inhibitors of the 17β-hydroxysteroid dehydrogenase type I (17β-HSD1) and, in addition, which may represent inhibitors of the steroid sulpha...
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WO/2006/093993A1 |
Described are steroidal C- 17 benzoazoles, pyrimidinoazoles (azabenzoazoles) and diazines. Methods for their synthesis are also described, which include methods having a step of nucleophilic vinylic 'addition-elimination' substitution re...
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WO/2006/055009A1 |
Compounds that function as lamprey attractants and methods.
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WO/2006/046123A2 |
The present invention relates to new compounds represented by Formula I: wherein M represents a macrolide subunit of the substructure VIII: L represents the chain of the substructure IX or XIII: Z represents the steroid or nonsteroidal s...
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WO/2006/038047A1 |
The invention relates to a new, environment-friend process for the synthesis of the known 4,4'-[3α,17β-bis(acetoxy)-5α-androstane-2β,l6β-diyl]-bi
s(l,l-dimethyl-ρiρerazinium) dibromide of formula (I) (from now on pipecuronium brom...
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WO/2006/032885A2 |
The present invention provides a compound comprising a steroidal ring system and an optional group R1 selected from any one of -OH, a sulphamate group, a phosphonate group, a thiophosphonate group, a sulphonate group or a sulphonamide gr...
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WO/2006/021776A1 |
A salt of a compound of formula (I) may be made with methanesulfonic acid. The salt and salts with other acids may be prepared by recovering from methyl tert-butyl ether (MTBE).
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WO/2006/021777A1 |
A compound of formula (I) or a pharmaceutically-acceptable salt thereof, may be made by a process including a triflating step by which a ketone of formula (II) is converted into a triflate of formula (III) in the presence of a base compr...
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WO/2005/118612A1 |
Cholesterol-modified anti-cancer therapeutic drug compounds, bile-acid-modified anti-cancer therapeutic drug compounds, and bile-acid-derivative-modified anti-cancer therapeutic drug compounds; emulsion, microemulsion, and micelle formul...
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WO/2005/105822A2 |
The invention relates to a novel multi step process of making compounds of Formula (I), wherein R1 is an alkoxy group and R2 is an optionally substituted, N-attached heteroaryl. The hydrogen at the 5-position can be &agr or β isomer, pr...
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WO/2005/092912A1 |
The subject invention provides a compound according to Formula I, wherein Formula (1) is O, NOH, NO(1-4C)alkyl, NO(1-4C)acyl; Al-A5 are C, substituted with RI, or N, provided that at least one and not more than three of Al-A5 are N; or o...
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WO/2005/068487A2 |
A novel process for preparing (2beta,3alpha,5alpha,16alpha,17beta)-17-acetoxy-3-hydroxy-2-
(4-morpholinyl)-16-(1-pyrrolidinyl) androstane, a known intermediate in the synthesis of the skeletal muscle relaxant rocuronium bromide, is discl...
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WO/2005/014613A1 |
The present invention relates to thiomorpholino steroid compounds of general formula (I), which may advantageously be employed to stimulate meiosis in human oocytes, the steroid being specifically characterized by a thiomorpholino moiety...
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WO/2005/007670A1 |
A method for preparing a 1-androstene derivative which comprises reacting a 2-iodo-androstane derivative with an oxidizing agent while maintaining the pH of the reaction mixture at a specific range gives the 1-androstene derivative with ...
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WO/2004/101595A1 |
Compounds and methods for modulating mesenchymal cell function, for instance smooth muscle and fibroblast proliferation or cytokine expression, and for treating conditions associated with mesenchymal cell function, for instance airway hy...
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WO/2004/098538A2 |
The invention describes novel nitrosated and/or nitrosylated compounds of the invention, and pharmaceutically acceptable salts thereof, and novel compositions comprising at least one nitrosated and/or nitrosylated compound of the inventi...
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WO/2004/096829A2 |
The invention relates to a method of preparing compounds having general formula (I), wherein: R1, R2, R3, n and X are as defined in the description. The invention also relates to the intermediate compounds used to implement said method.
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WO/2004/096830A1 |
The present invention relates to the chemical synthesis of solanum glycosides, in particular to the synthesis of solasonine as well as to novel β-monosaccharide intermediate compounds, of Formula (II), where each R1 is the same or diffe...
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WO/2004/085459A1 |
The present invention provides a compound comprising a steroidal ring system and an optional group R1 selected from any one of -OH, a sulphamate group, a phosphonate group, a thiophosphonate group, a sulphonate group or a sulphonamide gr...
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WO/2004/066920A2 |
The present invention encompasses compounds of Formula (I) or ph armaceutically acceptable salts or hydrates thereof, which are useful as selective glucocorticoid receptor ligands for treating a variety of autoimmune and inflammatory dis...
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WO/2004/045536A2 |
A method for modifying at least one non-ester-containing parent compound, and the compounds produced using such method, which compounds are deployed to temporarily incapacitate at least one subject are disclosed. The modified compounds a...
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WO/2004/045533A2 |
A method and compositions for treating persistent pulmonary hypertension in human newborns that deploys an intravenous infusion of a modified drug formed by adding one or more of a predetermined chemical arrangement to an efficacious par...
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WO/2004/043986A1 |
This invention relates to processes for the preparation of novel , substituted steroid compounds of Formula 1, wherein R1 is H or. COR2; R2 is C1-C6 alkyl or Ct-C6 alkoxy; Z1 is CH2, or wherein OR3 is in the &agr configuration; R3 is H o...
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WO/2004/037843A2 |
The present invention relates to multifunctional steroid compounds combining a steroid component with SOD mimic component and optionally also with NO donor component, and to their use in treating and preventing disorders associated with ...
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WO/2004/005310A2 |
The present invention relates (a) to new compounds represented by Formula (I): wherein M represents a macrolide subunit (macrolide moiety) derived from macrolide possessing the property of accumulation in inflammatory cells, S represents...
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WO/2004/005313A2 |
The present invention relates (a) to new compounds represented by Formula I wherein M represents a macrocode subunit (macrolide moiety) derived from macrolide possessing the property of accumulation in inflammatory cells, V represents an...
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WO/2004/000802A2 |
Disclosed are scaffolded maleimide clusters, methods of making said clusters and use of said clusters as templates for multivalent peptide assembly. Multiple maleimide functionalities were introduced onto a scaffold molecule by the react...
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WO/2003/089449A2 |
The invention relates to sterol derivatives of formula (I) and to a method for the production of said compounds, a medicament using one of said compounds and a pharmaceutical composition comprising said medicament.
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WO/2003/072555A1 |
The invention relates to substituted 3-phenyl-5-alkoxy-1,3,4-oxadiazol-2-ones, of general formula (I), wherein R1 represents C7-C22 alkyl, C2-C4 alkyl that is substituted by C4-C20 alkoxy, C6-C10 aryl, C6-C10 aryloxy or C4-C12-alkoxy-C2-...
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WO/2003/070194A2 |
Amino acid corticosteroid esters which may function as pro-drugs, and formulations of the amino acid corticosteroid esters with a second active ingredient such as formoterol are disclosed. Composition of the invention include amino acid ...
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WO/2003/064443A2 |
Nitrooxy derivatives of steroidal compounds of general formula (I) B− X1 − NO2 or esters or salts thereof, wherein: B is a steroidal radical, X1 is a bivalent linking group comprising an aromatic or heterocyclic ring.
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WO/2003/053360A2 |
A method and composition for the treatment, prevention and&sol or prophylaxis of a host, and in particular, a human, infected with Epstein−Barr virus (EBV), is provided that includes administering an effective amount of a 5−substitut...
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WO/2003/045972A1 |
The invention relates to 17$g(a)-alkyl-17$g(b)-oxy-estra-1,3,5(10)-trienes having an anti-oestrogen action, of general formula (I). The invention also relates to 17-oxo-estra-1,3,5(10)-trienes and 17$g(b)-hydroxy-estra-1,3,5(10)-trienes ...
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WO/2003/035668A2 |
Novel Anti-inflammatory Androstane DerivativesThere are provided compounds of formula (I) wherein R1 represents O, S or NH;R2 represents -C(&equals O)-aryl or -C(&equals O)-heteroaryl;R3 represents hydrogen, methyl (which may be in eithe...
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WO/2003/026568A2 |
Compounds of structural formula (I) as herein defined are disclosed as useful in a method for modulating a function of the androgen receptor in a tissue selective manner in a patient in need of such modulation, as well as in a method of ...
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WO/2003/024940A1 |
The invention concerns a ligand comprising (I) wherein n is an integer from 1 to 5 Y is CO2H or PO3H2T represents −X or −phenyl−X, wherein X represents NO2, NH2, NCS, NHCOCH2−Z, NHCO−W−COCNHS, −NH−Q, −NHCS−Q, −NHCOC...
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WO/2003/009853A1 |
This invention generally pertains to the field of psychiatry. In particular, this invention pertains to the discovery that agents capable of inhibiting the binding of cortisol to its receptors can be used in methods for preventing antips...
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WO/2002/100879A1 |
There are provided compounds of formula (I) wherein R¿1? represents C¿1-6? alkyl or C¿1-6? haloalkyl; R¿2? represents a 4-7 membered non-aromatic ring containing 1-3 heteroatoms selected from O, N and S optionally substituted with on...
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WO2001042273A9 |
This invention relates to methods for treating asthma or allergy in a mammal by administering a 3-aminosteroid compound to a mammal in need thereof. The 3-aminosteroid compound being capable of down regulating the IL-9 pathway and allevi...
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