AR051958A1 - Derivados heterociclicos utiles como moduladores selectivos del receptor de androgeno (sarms) - Google Patents

Derivados heterociclicos utiles como moduladores selectivos del receptor de androgeno (sarms)

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Publication number
AR051958A1
AR051958A1 ARP050104794A ARP050104794A AR051958A1 AR 051958 A1 AR051958 A1 AR 051958A1 AR P050104794 A ARP050104794 A AR P050104794A AR P050104794 A ARP050104794 A AR P050104794A AR 051958 A1 AR051958 A1 AR 051958A1
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AR
Argentina
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alkyl
group
hydrogen
4alkyl
halogenated
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ARP050104794A
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English (en)
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Janssen Pharmaceutica Nv
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Publication of AR051958A1 publication Critical patent/AR051958A1/es

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/06Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/14Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/08Drugs for disorders of the urinary system of the prostate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • A61P15/08Drugs for genital or sexual disorders; Contraceptives for gonadal disorders or for enhancing fertility, e.g. inducers of ovulation or of spermatogenesis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • A61P15/10Drugs for genital or sexual disorders; Contraceptives for impotence
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • A61P15/16Masculine contraceptives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/10Anti-acne agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/14Drugs for dermatological disorders for baldness or alopecia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D261/00Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/02Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D261/00Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/02Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • C07D261/04Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D263/00Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/04Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D263/06Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by oxygen atoms, attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D263/00Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/08Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D263/16Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D263/00Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/08Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D263/16Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D263/18Oxygen atoms
    • C07D263/20Oxygen atoms attached in position 2
    • C07D263/24Oxygen atoms attached in position 2 with hydrocarbon radicals, substituted by oxygen atoms, attached to other ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/04Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond

Abstract

La presente se refiere a composiciones farmacéuticas que los contienen y a su uso en el tratamiento de desordenes y trastornos modulados por el receptor de androgeno. Reivindicacion 1: Un compuesto de formula (1), en la cual: W está seleccionado del grupo que consiste en O, S y NRF; donde RF está seleccionado del grupo que consiste en hidrogeno, hidroxi, ciano, alquilo C1-4, alcoxi C1-4 y -SO2-alquiloC1-4; R1 está seleccionado del grupo que consiste en alquilo C1-4 y alquilo C1-4 halogenado; R2 está seleccionado del grupo que consiste en hidrogeno, alquilo C1-4, alquilo C1-4 halogenado, -C(O)O-alquiloC1-4, -C(O)-alquiloC1-4 y -C(O)-(alquilo C1-4 halogenado); a es un numero entero de 0 a 1; la formula (2) está seleccionado del grupo que consiste en fenilo, piridilo, pirazinilo, pirimidinilo y piridazinilo; R3 está ausente o está seleccionado del grupo que consiste en hidrogeno, halogeno, alquilo C1-4, alquilo C1-4 halogenado, ciano, nitro, amino, alquilamino C1-4, di(alquilo C1-4)amino, -O-alquiloC1-4, -S(O)0-2-alquiloC1-4, -NRA-C(O)-alquiloC1-4, bencilo, -O-fenilo, -C(O)-fenilo y -S(O)0-2- fenilo; donde RA está seleccionado entre hidrogeno o alquilo C1-4; R4 está ausente o está seleccionado del grupo que consiste en hidrogeno, halogeno, alquilo C1-4, alquilo C1-4 halogenado, ciano, nitro, amino, alquilamino C1-4, di(alquilo C1-4)amino, -O-alquiloC1-4, -S(O)0-2-alquiloC1-4, -NRB-C(O)-alquiloC1-4, bencilo, -O-fenilo y -S(O)0-2-fenilo; donde Rb está seleccionado de hidrogeno o alquilo C1-4; con la condicion de que cuando la formula (2), es fenilo entonces por lo menos uno de R3 o R4 es distinto de hidrogeno; R6 y R7 están cada uno independientemente ausentes, o están seleccionados del grupo que consiste en hidrogeno, halogeno, alquilo C1-4, alquenilo C2-4, alcoxi C1-4, ciano, -C(O)-alquiloC1-4 y -S(O)0-2-alquiloC1-4; con la condicion adicional de que R3 esté ausente cuando un átomo de nitrogeno está presente en la posicion 3 de formula (2); con la condicion adicional de que R4 esté ausente cuando está presente un átomo de nitrogeno en la posicion 4 de formula (2); con la condicion adicional de que R6 esté ausente cuando está presente un átomo de nitrogeno en la posicion 6 de formula (2); con la condicion adicional de que R7 esté ausente cuando está presente un átomo de nitrogeno en la posicion 2 de formula (2); ôel anillo Aö está seleccionado del grupo que consiste en las formulas (3); donde R5' está seleccionado del grupo que consiste en halogeno y alquilo C1-4; y donde R10 y R11 están cada uno independientemente seleccionados de hidrogeno, alquilo C1-4, bencilo o -C(O)-CF3; R5 está seleccionado del grupo que consiste en hidrogeno, carboxi, alquilo, alquilo C1- 4 halogenado, alquilo C1-4 hidroxi sustituido, cicloalquilo, arilo, aralquilo, heteroarilo, heteroaril-alquil-, heterocicloalquilo, heterocicloalquil- alquil-, -C(O)-alquilo, -C(O)-alquiloC1-4 halogenado, -C(O)O-alquiloC1-4, -C(O)O-arilo, -alquiloC1- 4-S(O)0-2-alquiloC1-4, t-butil-dimetil- sililo y trimetilsililo; donde el arilo, cicloalquilo, heteroarilo o heterocicloalquilo, solo o como parte de un grupo sustituyente, está opcionalmente sustituido con uno o más sustituyentes independientemente seleccionados del grupo que consiste en halogeno, hidroxi, alquilo C1-4, alcoxi C1-4, alquilo C1-4 halogenado, alcoxi C1-4 halogenado, ciano, nitro, amino, alquilamino C1-4, di(alquilo C1-4)amino, - NRc-C(O)-alquiloC1-4, NRc-C(O)-alquiloC1-4 halogenado, -C(O)O-alquiloC1-4, -S(O)0-2-alquiloC1-4, -SO2-NRCRD, trimetil-sililo y t-butil- dimetil-sililoxi; donde cada uno de RC y RD están independientemente seleccionados entre hidrogeno o alquilo C1-4; o una sal farmacéuticamente aceptable de los mismos.
ARP050104794A 2004-11-16 2005-11-15 Derivados heterociclicos utiles como moduladores selectivos del receptor de androgeno (sarms) AR051958A1 (es)

Applications Claiming Priority (2)

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US62833704P 2004-11-16 2004-11-16
US11/258,448 US7465809B2 (en) 2004-11-16 2005-10-25 Heterocycle derivatives useful as selective androgen receptor modulators (SARMs)

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AR051958A1 true AR051958A1 (es) 2007-02-21

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US (3) US7465809B2 (es)
EP (1) EP1817292B1 (es)
JP (1) JP4969451B2 (es)
CN (2) CN104803916B (es)
AR (1) AR051958A1 (es)
AU (1) AU2005307003B2 (es)
CA (1) CA2587678C (es)
MY (1) MY142048A (es)
TW (1) TWI483725B (es)
WO (1) WO2006055184A2 (es)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE473741T1 (de) * 2006-02-10 2010-07-15 Janssen Pharmaceutica Nv Neue imidazolopyrazolderivate als selektive androgen-rezeptor-modulatoren
DE102006047617B4 (de) * 2006-10-09 2008-11-27 Clariant International Limited Verfahren zur Herstellung basischer (Meth)acrylamide
ES2488990T3 (es) 2008-02-22 2014-09-01 Radius Health, Inc. Moduladores selectivos del receptor de andrógenos
US8268872B2 (en) 2008-02-22 2012-09-18 Radius Health, Inc. Selective androgen receptor modulators
EP2531029B1 (en) 2010-02-04 2016-10-19 Radius Health, Inc. Selective androgen receptor modulators
WO2011143469A1 (en) 2010-05-12 2011-11-17 Radius Health,Inc Therapeutic regimens
US8642632B2 (en) 2010-07-02 2014-02-04 Radius Health, Inc. Selective androgen receptor modulators
US9290485B2 (en) 2010-08-04 2016-03-22 Novartis Ag N-((6-amino-pyridin-3-yl)methyl)-heteroaryl-carboxamides
WO2012047617A1 (en) 2010-09-28 2012-04-12 Radius Health, Inc. Selective androgen receptor modulators
EP3834824A1 (en) 2014-03-28 2021-06-16 Duke University Method of treating cancer using selective estrogen receptor modulators
US9421264B2 (en) 2014-03-28 2016-08-23 Duke University Method of treating cancer using selective estrogen receptor modulators
WO2017223115A1 (en) 2016-06-22 2017-12-28 Radius Health, Inc. Ar+ breast cancer treatment methods
US11560356B2 (en) * 2016-06-29 2023-01-24 The Regents Of The University Of California Compounds and compositions for the treatment of cancer
CN106748884B (zh) * 2016-12-13 2021-08-20 山西振东制药股份有限公司 一种比卡鲁胺中间体的制备方法
JP7481115B2 (ja) 2017-01-05 2024-05-10 ラジウス ファーマシューティカルズ,インコーポレイテッド Rad1901-2hclの多形性形態
EP3601255A1 (en) 2017-03-21 2020-02-05 AbbVie Deutschland GmbH & Co. KG Proline amide compounds and their azetidine analogues carrying a specifically substituted benzyl radical
SG11202013177WA (en) 2018-07-04 2021-01-28 Radius Pharmaceuticals Inc Polymorphic forms of rad 1901-2hcl
SG11202111402PA (en) 2019-05-14 2021-11-29 Nuvation Bio Inc Anti-cancer nuclear hormone receptor-targeting compounds
US11952349B2 (en) 2019-11-13 2024-04-09 Nuvation Bio Inc. Anti-cancer nuclear hormone receptor-targeting compounds
BR112023019420A2 (pt) 2021-03-23 2023-10-24 Nuvation Bio Inc Compostos de direcionamento ao receptor de hormônio nuclear anticâncer
JP2024516024A (ja) 2021-05-03 2024-04-11 ニューベイション・バイオ・インコーポレイテッド 抗がん核内ホルモン受容体標的化化合物
WO2024010817A2 (en) * 2022-07-07 2024-01-11 University Of Tennessee Research Foundation Selective androgen receptor degrader (sard) o-linked ligands and methods of use thereof

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998022432A1 (fr) * 1996-11-18 1998-05-28 Yamanouchi Pharmaceutical Co., Ltd. Derives d'acylanilide a substitution acylamino ou composition comprenant ces derives
US6339099B1 (en) * 1997-06-20 2002-01-15 Dupont Pharmaceuticals Company Guanidine mimics as factor Xa inhibitors
ES2216579T3 (es) * 1998-10-09 2004-10-16 Janssen Pharmaceutica N.V. Derivados de 4,5-dihidro-isoxazol y su uso farmaceutico.
US6472415B1 (en) * 1998-12-18 2002-10-29 Biophysica, Inc. Androgen receptor suppressors in the therapy and diagnosis of prostate cancer, alopecia and other hyper-androgenic syndromes
WO2002000651A2 (en) 2000-06-27 2002-01-03 Bristol-Myers Squibb Pharma Company Factor xa inhibitors
US7026484B2 (en) * 2001-02-23 2006-04-11 Ligand Pharmaceuticals Incorporated Tricyclic androgen receptor modulator compounds and methods
US6657770B2 (en) * 2001-06-22 2003-12-02 Lucent Technologies Inc. Programmable optical multiplexer/demultiplexer
US6738540B2 (en) * 2001-06-22 2004-05-18 Lucent Technologies Inc. Optical cross-connect switch using programmable multiplexers/demultiplexers
US7030141B2 (en) * 2001-11-29 2006-04-18 Christopher Franklin Bigge Inhibitors of factor Xa and other serine proteases involved in the coagulation cascade
AU2004249697B2 (en) * 2003-06-13 2010-04-22 Janssen Pharmaceutica N.V. Thiazoline derivatives as selective androgen receptor modulators (SARMS)
CN101056862B (zh) * 2004-09-10 2013-03-13 詹森药业有限公司 作为选择性雄激素受体调节剂(sarms)的咪唑烷-2-酮衍生物

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US7781473B2 (en) 2010-08-24
US20090131365A1 (en) 2009-05-21
AU2005307003A1 (en) 2006-05-26
MY142048A (en) 2010-08-30
CN104803916A (zh) 2015-07-29
JP4969451B2 (ja) 2012-07-04
CN101103003A (zh) 2008-01-09
TW200621235A (en) 2006-07-01
CA2587678C (en) 2013-05-21
US20060211756A1 (en) 2006-09-21
AU2005307003B2 (en) 2011-10-13
JP2008520665A (ja) 2008-06-19
WO2006055184A3 (en) 2007-04-05
US8088811B2 (en) 2012-01-03
US7465809B2 (en) 2008-12-16
US20100267670A1 (en) 2010-10-21
TWI483725B (zh) 2015-05-11
EP1817292B1 (en) 2015-04-08
CN104803916B (zh) 2017-08-11
WO2006055184A2 (en) 2006-05-26
CA2587678A1 (en) 2006-05-26
EP1817292A2 (en) 2007-08-15

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