AR015241A1 - Antagonistas del receptor de vitronectina composicion farmaceutica que los contiene, procedimiento para su preparacion y su empleo para la fabricacion deun medicamento. - Google Patents

Antagonistas del receptor de vitronectina composicion farmaceutica que los contiene, procedimiento para su preparacion y su empleo para la fabricacion deun medicamento.

Info

Publication number
AR015241A1
AR015241A1 ARP990101019A ARP990101019A AR015241A1 AR 015241 A1 AR015241 A1 AR 015241A1 AR P990101019 A ARP990101019 A AR P990101019A AR P990101019 A ARP990101019 A AR P990101019A AR 015241 A1 AR015241 A1 AR 015241A1
Authority
AR
Argentina
Prior art keywords
alkyl
het
cycloalkyl
co2rg
crg2
Prior art date
Application number
ARP990101019A
Other languages
English (en)
Original Assignee
Smithkline Beecham Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Smithkline Beecham Corp filed Critical Smithkline Beecham Corp
Publication of AR015241A1 publication Critical patent/AR015241A1/es

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D213/72Nitrogen atoms
    • C07D213/74Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
    • 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
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
    • C07D239/32One oxygen, sulfur or nitrogen atom
    • C07D239/42One nitrogen atom
    • 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
    • C07D401/12Heterocyclic 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 linked by a chain containing hetero atoms as chain links
    • 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
    • C07D409/12Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Rheumatology (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pyridine Compounds (AREA)

Abstract

Antagonistas del receptor de vitronectina de formula (I) que son utiles en el tratamiento de osteosporosis: (I) en la que R* es II, X es CRR, NR o S;Y es CRR, NR o S; A es H, halo, ORg, -SRg, -CN, -NRgRk, -NO2, -CF3, -S(O)rCF3, -CO2Rg, -CORg, -CONRg2, -alquilo C1-6, -alquil C0-6-Ar, -alquil C0-6-Het,-alquil C0-6-cicloalquilo C3-6, -S(O)kRg,o CH2N(Rf)2;R1 es-alquil C0-6-Het,-alquil C0-6-Ar, -alquilo C1-6, -H, -CN, -CH=CH2, -C=CH o -S(0)kRg; R2 es III, W es-(CHRg)a-U-(CHRg)b-; U está ausente o esCO, CRg2, C(=CRg2), S(O)k, O, NRg, CRgORg, CR9(ORk)CRg2, CRgCRg(ORk), C(O)CRg2, CRg2C(O), CONRi, NRiCO, OC(O), C(O)O,C(S)O, OC(S), C(S)NRg, NRgC(S), S(O)2NRg, NRgS(O)2, N=N, NRgNRg, NRgNRg2, CRg2CRg, CRg2O, OCRg2, C=C, CRg=CRg, Ar o Het; G es NRe, su o; Rg es H, alquiloC1-6, cilcoalquil C3-7-alquilo C0-6 o Ar-alquilo C0-6; Rk es Rg, -C(O)Rg, o -C(O)ORf; Ri es H, alquilo C1-6, Het-alquilo C0-6, cicloalquil C3-7-alquilo C0-6,Ar-alquil C0-6 o alquilo C1-6 sustituido con uno a tres grupos seleccionados entre halogeno, CN, NRg2, ORg, SRg, CO2Rg y CON(Rg)2; Rf es H, alquilo C1-6 oAr-alquilo C0-6; Re es H, alquilo C1-6, Ar-alquilo C0-6, Het-alquilo C0-6, cicloalquilo C3-7-alquilo C0-6 o (CH2)kCO2Rg; Rb y Rc se seleccionanindependientemente entreH, alquilo C1-6, Ar-alquil C0-6, Het-alquilo C0-6, cicloalquil C3-6-alquilo C0-6, halogeno, CF3, ORf, S(O)kRf, CORf, NO2, N(Rf)2,CO(NRf)2,CH2N(Rf)2,o Rb y Rc están unidos entre sí para formar un anillo carbocíclico o heterocíclico,aromático o no aromático,de 5 o 6 miembros,opcionalmentesustituido hasta con 3 sustituyentes elegidos entre halogeno, CF3, alquilo C1-4, ORf, S(O)kRf, CORf, OH, NO2, N/Rf)2, CON(Rf)2 y CH2N(Rf); o metilendioxi; Q1,Q2, Q3 y Q4 son independientemente N o C-Ry, siempre que no más de uno de Q1,Q2,Q3 y Q4 sea N; R es H, alquilo C1-6, Ar-alquilo C0-6 o cicloalquil C3-6-alquilo C0-6; R es R, -C(O)R o -C(O)OR; Ry es H, halo, -ORg, -SRg, -CN, -NRgRk, -NO2, -CF3,-CF3S(O)r-, -CO2Rg o -CONRg2, o alquilo C1-6 opcionalmentesustituido con halo ORg, SRg,-CN,-NRgR, -NO2,-CF3,RS(O)r-, -CO2Rg, -CORg, o -CONRg2; a es 0, 1 o 2; b es 0, 1 o 2; k es 0, 1 o 2; r es 0, 1 o 2; s es 0, 1 o
ARP990101019A 1998-03-10 1999-03-10 Antagonistas del receptor de vitronectina composicion farmaceutica que los contiene, procedimiento para su preparacion y su empleo para la fabricacion deun medicamento. AR015241A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US7761098P 1998-03-10 1998-03-10
US9606398P 1998-08-11 1998-08-11

Publications (1)

Publication Number Publication Date
AR015241A1 true AR015241A1 (es) 2001-04-18

Family

ID=26759473

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP990101019A AR015241A1 (es) 1998-03-10 1999-03-10 Antagonistas del receptor de vitronectina composicion farmaceutica que los contiene, procedimiento para su preparacion y su empleo para la fabricacion deun medicamento.

Country Status (24)

Country Link
EP (1) EP1061921A4 (es)
JP (1) JP2002506033A (es)
KR (1) KR20010041812A (es)
CN (1) CN1299282A (es)
AP (1) AP2000001898A0 (es)
AR (1) AR015241A1 (es)
AU (1) AU758498B2 (es)
BG (1) BG104824A (es)
BR (1) BR9908636A (es)
CA (1) CA2323208A1 (es)
CO (1) CO5080762A1 (es)
DZ (1) DZ2741A1 (es)
EA (1) EA200000921A1 (es)
HU (1) HUP0101143A3 (es)
ID (1) ID26223A (es)
IL (1) IL138245A0 (es)
NO (1) NO20004503L (es)
OA (1) OA12189A (es)
PE (1) PE20000323A1 (es)
PL (1) PL342881A1 (es)
SK (1) SK13292000A3 (es)
TR (1) TR200002625T2 (es)
UY (2) UY25421A1 (es)
WO (1) WO1999045927A1 (es)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19939980A1 (de) 1999-08-24 2001-03-01 Merck Patent Gmbh Inhibitoren des Integrins alphavbeta¶3¶
DE19939981A1 (de) * 1999-08-24 2001-03-01 Merck Patent Gmbh Neue Inhibitoren des Integrins alphavß3
EG24179A (en) * 1999-09-07 2008-09-28 Smithkline Beecham Corp Vitronectin receptor antagonists
US6881736B1 (en) 1999-09-07 2005-04-19 Smithkline Beecham Corporation Vitronectin receptor antagonists
GB9930570D0 (en) * 1999-12-23 2000-02-16 Pfizer Ltd Therapy
US6448278B2 (en) 1999-12-23 2002-09-10 Pfizer Inc. Procollagen C-proteinase inhibitors
FR2808798A1 (fr) * 2000-05-09 2001-11-16 Hoechst Marion Roussel Inc Nouveaux derives antagonistes du recepteur de la vitronectine
US6900232B2 (en) 2000-06-15 2005-05-31 Pharmacia Corporation Cycloalkyl alkanoic acids as integrin receptor antagonists
US6531494B1 (en) 2001-08-29 2003-03-11 Pharmacia Corporation Gem-substituted αvβ3 antagonists
US6645993B2 (en) 2001-03-30 2003-11-11 Warner-Lambert Company 3-heterocyclylpropanohydroxamic acid PCP inhibitors
US6716842B2 (en) 2002-04-05 2004-04-06 Warner-Lambert Company, Llc Antidiabetic agents
US20070275956A1 (en) * 2003-10-14 2007-11-29 Lohray Braj B Novel Heterocyclic Compounds
JP4853284B2 (ja) * 2004-03-05 2012-01-11 大正製薬株式会社 チアゾール誘導体
UA87854C2 (en) 2004-06-07 2009-08-25 Мерк Энд Ко., Инк. N-(2-benzyl)-2-phenylbutanamides as androgen receptor modulators
KR20080004554A (ko) 2005-04-20 2008-01-09 얀센 파마슈티카 엔.브이. 불소화 피리딘 n―옥사이드 트롬빈 모듈레이터 및 질소를함유하는 헤테로아릴의 n―산화 방법
EP3040329B1 (en) * 2013-08-29 2018-10-10 Kyoto Pharmaceutical Industries, Ltd. Aromatic compound and use thereof in the treatment of disorders associated with bone metabolism
PT3929196T (pt) 2013-09-24 2023-09-11 Fujifilm Corp Composição farmacêutica de um novo composto contendo azoto ou seu sal, ou seu complexo de metal
KR20160147007A (ko) 2014-05-30 2016-12-21 화이자 인코포레이티드 선택적인 안드로겐 수용체 조절제로서의 카보니트릴 유도체
WO2023275715A1 (en) 2021-06-30 2023-01-05 Pfizer Inc. Metabolites of selective androgen receptor modulators

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1209063A (zh) * 1995-12-29 1999-02-24 史密丝克莱恩比彻姆公司 玻连蛋白受体拮抗剂
KR19990076876A (ko) * 1995-12-29 1999-10-25 스티븐 베네티아너 비트로넥틴 수용체 길항제

Also Published As

Publication number Publication date
KR20010041812A (ko) 2001-05-25
AU758498B2 (en) 2003-03-20
CN1299282A (zh) 2001-06-13
UY25519A1 (es) 1999-12-13
CO5080762A1 (es) 2001-09-25
DZ2741A1 (fr) 2003-09-08
JP2002506033A (ja) 2002-02-26
EP1061921A4 (en) 2005-03-30
BR9908636A (pt) 2002-01-08
WO1999045927A1 (en) 1999-09-16
NO20004503D0 (no) 2000-09-08
AP2000001898A0 (en) 2000-09-30
PE20000323A1 (es) 2000-05-24
OA12189A (en) 2006-05-09
HUP0101143A3 (en) 2002-12-28
IL138245A0 (en) 2001-10-31
SK13292000A3 (sk) 2001-06-11
EP1061921A1 (en) 2000-12-27
UY25421A1 (es) 2001-07-31
EA200000921A1 (ru) 2001-04-23
ID26223A (id) 2000-12-07
TR200002625T2 (tr) 2000-12-21
AU2903399A (en) 1999-09-27
NO20004503L (no) 2000-10-10
BG104824A (en) 2001-05-31
CA2323208A1 (en) 1999-09-16
PL342881A1 (en) 2001-07-16
HUP0101143A2 (hu) 2001-08-28

Similar Documents

Publication Publication Date Title
AR015241A1 (es) Antagonistas del receptor de vitronectina composicion farmaceutica que los contiene, procedimiento para su preparacion y su empleo para la fabricacion deun medicamento.
PA8546601A1 (es) Nuevos derivados de indol con afinidad por el receptor 5-ht6
PA8586401A1 (es) 4-piperazinilbencenosulfonilindoles y uso de los mismos
PA8547901A1 (es) Derivados de 4-piperacinilindol con afinidad receptora de 5-ht6
ATE380818T1 (de) Piperazine-substituierte aryl-benzodiazepinen und ihre verwendung als dopaminrezeptor-antagonisten zur behandlung von psychose
PE20040832A1 (es) Derivados de indolil pirazinona
AR038341A1 (es) Compuestos que son agonistas de receptores alfa-1 preferentemente agonistas de receptores alfa-1a/l
PE10499A1 (es) Antagonistas del receptor de vitronectina
PE20061298A1 (es) Compuestos derivados de dihidrobenzofurano como agonistas del receptor de serotonina 5-ht2c
AR050913A1 (es) Compuestos derivados de tiazolpiridina como activadores de glucoquinasa; composiciones farmaceuticas que los contienen y su uso en medicamentos para el tratamiento de la diabetes tipo ii
AR059178A1 (es) Benzotiazoles heteroaril sustituidos, composiciones farmaceuticas que los contienen,y usos terapeuticos, entre ellos, en el tratamiento y/o prevencion de la enfermedad de alzheimer.
RS50290B (sr) Novi derivati 1,3-dihidro-2h-indol-2-ona i njihova upotreba kao liganada za v1b i v1a receptore arginin-vazopresina
RU2007138937A (ru) Производные 1-бензилиндол-2-карбоксамида
HRP20000896B1 (en) Adenosine derivatives
DK1404317T3 (da) 5-Halogentryptaminderivater til anvendelse som ligander af 5-HT6- og/eller 5-HT7-serotoninreceptorer
AR033791A1 (es) Compuestos de acidos oxamicos y derivados como ligandos de receptores tiroideos,su uso. composicion y estuche que lo contiene
CR8505A (es) Derivados de (3-oxo-3,4-dihidroquinoxalin-2-il-amino)-benzamida y compuesto relacionado, como inhibidores de glucogeno fosforilasa para el tratamiento de la diabetes y obesidad
AR004735A1 (es) Quinoleina 4-amido sustituida, un procedimiento para su preparacion, una composicion farmaceutica que los contiene y el uso de los mismos para lapreparacion de un medicamento.
AR065948A1 (es) Antagonistas del receptor de la hormona liberadora de gonadotropina y procedimientos relacionados con los mismos
PE20030610A1 (es) Derivados de 3-azabiciclo[3.1.0]hexano con afinidad a los receptores opioides
AR016433A1 (es) Procedimiento para el tratamiento de la impotencia y composiciones.
AR056103A1 (es) Compuestos de(piran-piperidinil)benzimidazol, composiciones farmaceuticas que los comprenden, proceso de preparacion y usos en el tratamiento de afecciones mediadas por agonistas del receptor muscarinico m1
PE20060632A1 (es) Derivados de arilsulfonilestilbeno como antagonistas de los receptores 5-ht2a
AR048232A1 (es) Piperidinilcarbonil- pirrolidinas y su uso como agonistas de melanocortina cr4
PA8463001A1 (es) Compuestos de eteres ciclicos de piperidinilaminometil trifluorometilo como antagonistas de la sustancia p

Legal Events

Date Code Title Description
FA Abandonment or withdrawal