CO5700801A2 - Tratamiento del transtorno por deficit de atencion con hiper actividad - Google Patents

Tratamiento del transtorno por deficit de atencion con hiper actividad

Info

Publication number
CO5700801A2
CO5700801A2 CO05056569A CO05056569A CO5700801A2 CO 5700801 A2 CO5700801 A2 CO 5700801A2 CO 05056569 A CO05056569 A CO 05056569A CO 05056569 A CO05056569 A CO 05056569A CO 5700801 A2 CO5700801 A2 CO 5700801A2
Authority
CO
Colombia
Prior art keywords
alkyl
substituted
effective amount
haloalkyl
cycloalkyl
Prior art date
Application number
CO05056569A
Other languages
English (en)
Inventor
Vincent Edward Groppi Jr
Eric Jon Jacobsen
Piotr Karpinski
Original Assignee
Pharmacia & Upjohn Co Llc
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 Pharmacia & Upjohn Co Llc filed Critical Pharmacia & Upjohn Co Llc
Publication of CO5700801A2 publication Critical patent/CO5700801A2/es

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • 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
    • A61K31/468-Azabicyclo [3.2.1] octane; Derivatives thereof, e.g. atropine, cocaine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system

Landscapes

  • Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical & Material Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Emergency Medicine (AREA)
  • Neurosurgery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biomedical Technology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Neurology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Mechanical Treatment Of Semiconductor (AREA)
  • Developing Agents For Electrophotography (AREA)
  • Liquid Crystal Substances (AREA)

Abstract

1.- Una composición que comprende una cantidad eficaz de un agonista completo de nAChR a7 y una cantidad eficaz de un inhibidor de la recaptación de monoamina, una cantidad eficaz de un psicoestimulante, o una cantidad eficaz de un inhibidor de la recaptación de monoamina y una cantidad eficaz de un psicoestimulante.2.- La composición de la reivindicación 1, en la que el agonista es un compuesto de Fórmula I: Azabiciclo-N(R1)-C(=X)-W Fórmula I en la que azabiciclo es donde X es O o S;R0 es H, alquilo inferior, alquilo inferior sustituido o haloalquilo inferior;Cada R1 es H, alquilo, cicloalquilo, haloalquilo, fenilo sustituido o naftilo sustituido;Cada R2 es independientemente F, CI, Br, I, alquilo, alquilo sustituido, haloalquilo, cicloalquilo, arilo, o R2 está ausente con la condición de que k1-2, k1-6, k2, k5, k6 o k7 es 0;k1-2 es 0 ó 1;k1-6 es 0 ó 1, con la condición de que la suma de k1-2 y k1-6 sea uno;k2 es 0 ó 1;k5 es 0, 1, ó 2;k6 es 0, 1 ó 2;k7 es 0 ó 1;R2-3 es H, F, CI, Br, I, alquilo, haloalquilo, alquilo sustituido, cicloalquilo, o arilo;Cada R3 es independientemente H, alquilo o alquilo sustituido;R4 es H, alquilo, un grupo protector amino o un grupo alquilo que tiene 1-3 sustituyentes seleccionados entre F, CI, Br, I, -OH, -CN, -NH2, -NH(alquilo) o -N(alquilo)2; ...
CO05056569A 2002-12-11 2005-06-10 Tratamiento del transtorno por deficit de atencion con hiper actividad CO5700801A2 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US43258602P 2002-12-11 2002-12-11

Publications (1)

Publication Number Publication Date
CO5700801A2 true CO5700801A2 (es) 2006-11-30

Family

ID=32507968

Family Applications (1)

Application Number Title Priority Date Filing Date
CO05056569A CO5700801A2 (es) 2002-12-11 2005-06-10 Tratamiento del transtorno por deficit de atencion con hiper actividad

Country Status (23)

Country Link
US (1) US20050107425A1 (es)
EP (1) EP1572300A1 (es)
JP (1) JP2006510663A (es)
KR (1) KR20050085538A (es)
CN (1) CN1735441A (es)
AP (1) AP2005003336A0 (es)
AU (1) AU2003283656A1 (es)
BR (1) BR0317229A (es)
CA (1) CA2509142A1 (es)
CO (1) CO5700801A2 (es)
CR (1) CR7868A (es)
EA (1) EA200500783A1 (es)
EC (1) ECSP055852A (es)
HR (1) HRP20050522A2 (es)
IS (1) IS7858A (es)
MA (1) MA27606A1 (es)
MX (1) MXPA05006336A (es)
NO (1) NO20053185L (es)
OA (1) OA12969A (es)
PL (1) PL377552A1 (es)
TN (1) TNSN05158A1 (es)
WO (1) WO2004052461A1 (es)
ZA (1) ZA200504338B (es)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10164139A1 (de) 2001-12-27 2003-07-10 Bayer Ag 2-Heteroarylcarbonsäureamide
GB0310867D0 (en) * 2003-05-12 2003-06-18 Novartis Ag Organic compounds
KR101176670B1 (ko) 2004-03-25 2012-08-23 메모리 파마슈티칼스 코포레이션 인다졸, 벤조티아졸, 벤조이소티아졸, 벤즈이속사졸, 및그의 제조법 및 용도
GB0424564D0 (en) * 2004-11-05 2004-12-08 Novartis Ag Organic compounds
WO2008083442A1 (en) * 2007-01-10 2008-07-17 Brc Operations Pty Limited Method for formulating combination medications for adhd
CA2681934A1 (en) * 2007-03-28 2008-10-02 High Point Pharmaceuticals, Llc 11beta-hsd1 active compounds
SA08290475B1 (ar) 2007-08-02 2013-06-22 Targacept Inc (2s، 3r)-n-(2-((3-بيردينيل)ميثيل)-1-آزا بيسيكلو[2، 2، 2]أوكت-3-يل)بنزو فيوران-2-كربوكساميد، وصور أملاحه الجديدة وطرق استخدامه
MX2010009110A (es) * 2008-02-19 2010-11-30 Adolor Corp Beloxepina, sus enantiomeros, y analogos de la misma para el tratamiento de dolor.
US8927549B2 (en) 2008-11-21 2015-01-06 High Point Pharmaceuticals, Llc Adamantyl benzamide derivatives
TW201031664A (en) 2009-01-26 2010-09-01 Targacept Inc Preparation and therapeutic applications of (2S,3R)-N-2-((3-pyridinyl)methyl)-1-azabicyclo[2.2.2]oct-3-yl)-3,5-difluorobenzamide
EP2571874B1 (en) 2010-05-17 2016-03-30 Forum Pharmaceuticals Inc. A crystalline form of (r)-7-chloro-n-(quinuclidin-3-yl)benzo[b]thiophene-2-carboxamide hydrochloride monohydrate
WO2012015715A1 (en) 2010-07-27 2012-02-02 High Point Pharmaceuticals, Llc Substituted thiazol-2-ylamine derivatives, pharmaceutical compositions, and methods of use as 11-beta hsd1 modulators
AU2013259871A1 (en) 2012-05-08 2014-11-20 Forum Pharmaceuticals Inc. Methods of maintaining, treating or improving cognitive function
CA2891122C (en) 2012-11-14 2021-07-20 The Johns Hopkins University Methods and compositions for treating schizophrenia
WO2023022256A1 (ko) 2021-08-19 2023-02-23 단국대학교 천안캠퍼스 산학협력단 Kds2010을 유효성분으로 포함하는 주의력결핍 과잉행동장애의 예방 또는 치료용 약학적 조성물
KR20230027862A (ko) 2021-08-20 2023-02-28 단국대학교 천안캠퍼스 산학협력단 주의력결핍 과잉행동장애의 진단을 위한 gat-3의 용도
KR102597711B1 (ko) 2021-08-20 2023-11-06 단국대학교 천안캠퍼스 산학협력단 Snap5114을 유효성분으로 포함하는 주의력결핍 과잉행동장애의 예방 또는 치료용 약학적 조성물
WO2023022269A1 (ko) 2021-08-20 2023-02-23 단국대학교 천안캠퍼스 산학협력단 주의력결핍 과잉행동장애의 예방 또는 치료용 약학적 조성물

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020016334A1 (en) * 2000-07-31 2002-02-07 Coe Jotham Wadsworth Pharmaceutical composition for the treatment of attention deficit hyperactivity disorder (ADHD)
US20030236287A1 (en) * 2002-05-03 2003-12-25 Piotrowski David W. Positive allosteric modulators of the nicotinic acetylcholine receptor

Also Published As

Publication number Publication date
CR7868A (es) 2005-07-08
BR0317229A (pt) 2005-11-01
KR20050085538A (ko) 2005-08-29
EA200500783A1 (ru) 2005-12-29
PL377552A1 (pl) 2006-02-06
ZA200504338B (en) 2006-07-26
ECSP055852A (es) 2005-09-20
EP1572300A1 (en) 2005-09-14
OA12969A (en) 2006-10-13
US20050107425A1 (en) 2005-05-19
WO2004052461A1 (en) 2004-06-24
AU2003283656A1 (en) 2004-06-30
CA2509142A1 (en) 2004-06-24
TNSN05158A1 (fr) 2007-05-14
MA27606A1 (fr) 2005-11-01
NO20053185D0 (no) 2005-06-29
JP2006510663A (ja) 2006-03-30
CN1735441A (zh) 2006-02-15
IS7858A (is) 2005-05-23
AP2005003336A0 (en) 2005-06-30
NO20053185L (no) 2005-08-17
MXPA05006336A (es) 2005-08-26
HRP20050522A2 (en) 2005-12-31

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