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AR035312A1 - HYDROXAMIC ACID COMPOUNDS CONTAINING ALQUINYL AS MATRIX / TACE METALOPROTEINASE INHIBITORS, PHARMACEUTICAL COMPOSITION THAT INCLUDE THEM AND THE USE OF THE SAME FOR THE MANUFACTURE OF A MEDICINAL PRODUCT - Google Patents

HYDROXAMIC ACID COMPOUNDS CONTAINING ALQUINYL AS MATRIX / TACE METALOPROTEINASE INHIBITORS, PHARMACEUTICAL COMPOSITION THAT INCLUDE THEM AND THE USE OF THE SAME FOR THE MANUFACTURE OF A MEDICINAL PRODUCT

Info

Publication number
AR035312A1
AR035312A1 ARP000100327A ARP000100327A AR035312A1 AR 035312 A1 AR035312 A1 AR 035312A1 AR P000100327 A ARP000100327 A AR P000100327A AR P000100327 A ARP000100327 A AR P000100327A AR 035312 A1 AR035312 A1 AR 035312A1
Authority
AR
Argentina
Prior art keywords
heteroaryl
aryl
alkyl
cycloalkyl
acid compounds
Prior art date
Application number
ARP000100327A
Other languages
Spanish (es)
Original Assignee
Wyeth 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 Wyeth Corp filed Critical Wyeth Corp
Publication of AR035312A1 publication Critical patent/AR035312A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D309/08Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/35Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
    • A61K31/351Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom not condensed with another ring
    • 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
    • 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
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
    • C07D211/60Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
    • C07D211/60Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D211/62Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals attached in position 4
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
    • C07D211/60Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D211/62Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals attached in position 4
    • C07D211/66Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals attached in position 4 having a hetero atom as the second substituent in position 4

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pyrane Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Compuestos de ácido hidroxámico que contienen alquinilo caracterizados porque comprenden un compuesto que tiene la fórmula (1) en la cual R1 es hidrogeno, arilo, heteroarilo, alquilo de C1-8, alquenilo de C2-6, alquinilo de C2-6, cicloalquilo de C3-6, o cicloheteralquilo de C4-8; R2 y R3 son cada uno independientemente hidrógeno, alquilo de C1-6, -CN, o -CCH; R7 es hidrógeno, arilo, aralquilo, heteroarilo, heteroaralquilo, alquilo de C1-6, alquenilo de C2-6, alquinilo de C1-6, cicloalquilo de C3-6, -C(O)-R1, -SO2-R1, -C(O)-NHR1, -C(O)NR5R6, -C(O)R1NR5R6, -C(O)-OR1, -C(NH)-NH2, R8, R9, R10 y R11 son cada uno independientemente, hidrógeno, arilo o heteroarilo, cicloalquilo de C3-6, cicloheteroalquilo C4-8, alquilo de C1-18, alquenilo de C2-18, alquinilo de C2-18, con la condición de que uno de los pares R8, R9, R9 y R10 o R10 y R11 conjuntamente con el átomo o átomos de carbono a los cuales están unidos forman un anillo cicloalquilo de C3-6, o un anillo cicloheteroarilquilo C4-8; R12 es hidrógeno, arilo o heteroarilo, cicloalquilo de C3-6, cicloheteroalquilo C4-8, o alquilo de C1-6; A es O, S, SO, SO2, NR7 o CH2; X es O, S, SO, SO2, NR7 o CH2; Y es arilo o heteroarilo, con la condición de que A y X no están unidos a los átomos adyacentes de Y; y n es 0-2; o una sal farmacéuticamente aceptable del mismo.Alkynyl-containing hydroxamic acid compounds characterized in that they comprise a compound having the formula (1) in which R 1 is hydrogen, aryl, heteroaryl, C 1-8 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, cycloalkyl of C3-6, or C4-8 cycloheteralkyl; R2 and R3 are each independently hydrogen, C1-6 alkyl, -CN, or -CCH; R7 is hydrogen, aryl, aralkyl, heteroaryl, heteroaralkyl, C1-6 alkyl, C2-6 alkenyl, C1-6 alkynyl, C3-6 cycloalkyl, -C (O) -R1, -SO2-R1, - C (O) -NHR1, -C (O) NR5R6, -C (O) R1NR5R6, -C (O) -OR1, -C (NH) -NH2, R8, R9, R10 and R11 are each independently, hydrogen , aryl or heteroaryl, C3-6 cycloalkyl, C4-8 cycloheteroalkyl, C1-18 alkyl, C2-18 alkenyl, C2-18 alkynyl, provided that one of the pairs R8, R9, R9 and R10 or R10 and R11 together with the carbon atom or atoms to which they are attached form a C3-6 cycloalkyl ring, or a C4-8 cycloheteroaryl ring; R12 is hydrogen, aryl or heteroaryl, C3-6 cycloalkyl, C4-8 cycloheteroalkyl, or C1-6 alkyl; A is O, S, SO, SO2, NR7 or CH2; X is O, S, SO, SO2, NR7 or CH2; Y is aryl or heteroaryl, with the proviso that A and X are not attached to the adjacent atoms of Y; and n is 0-2; or a pharmaceutically acceptable salt thereof.

ARP000100327A 1999-01-27 2000-01-26 HYDROXAMIC ACID COMPOUNDS CONTAINING ALQUINYL AS MATRIX / TACE METALOPROTEINASE INHIBITORS, PHARMACEUTICAL COMPOSITION THAT INCLUDE THEM AND THE USE OF THE SAME FOR THE MANUFACTURE OF A MEDICINAL PRODUCT AR035312A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US23803899A 1999-01-27 1999-01-27

Publications (1)

Publication Number Publication Date
AR035312A1 true AR035312A1 (en) 2004-05-12

Family

ID=22896246

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP000100327A AR035312A1 (en) 1999-01-27 2000-01-26 HYDROXAMIC ACID COMPOUNDS CONTAINING ALQUINYL AS MATRIX / TACE METALOPROTEINASE INHIBITORS, PHARMACEUTICAL COMPOSITION THAT INCLUDE THEM AND THE USE OF THE SAME FOR THE MANUFACTURE OF A MEDICINAL PRODUCT

Country Status (13)

Country Link
JP (1) JP2002535390A (en)
KR (1) KR20010101732A (en)
AR (1) AR035312A1 (en)
AT (1) ATE309986T1 (en)
AU (1) AU769418B2 (en)
CA (1) CA2356313A1 (en)
CZ (1) CZ20012711A3 (en)
DE (1) DE60024056D1 (en)
EA (1) EA200100806A1 (en)
HU (1) HUP0200223A3 (en)
IL (1) IL144345A0 (en)
NZ (1) NZ512566A (en)
ZA (1) ZA200105222B (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060058350A1 (en) * 2002-12-26 2006-03-16 Carna Biosciences, Inc. Alkynyl-substituted azasugar derivative and drug containing the same as the active ingredient
AU2007269836A1 (en) * 2006-06-30 2008-01-10 Albany Molecular Research, Inc. Substituted piperidines that increase P53 activity and the uses thereof
KR20110022635A (en) * 2008-06-02 2011-03-07 시플라 리미티드 Synthesis of Levocetirizine and Intermediates for Use therein

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20000075808A (en) * 1997-02-27 2000-12-26 윌리암 에이취 캘넌, 에곤 이 버그 N-Hydroxy-2-(alkyl, aryl, or heteroaryl sulfanyl, sulfinyl or sulfonyl)-3-substituted alkyl, aryl or heteroarylamides as matrix metalloproteinase inhibitors
NZ506184A (en) * 1998-02-19 2003-05-30 American Cyanamid Co N-hydroxy-2-(alkyl, aryl, or heteroaryl sulphanyl, sulphinyl or sulphonyl)-3-substituted-alkyl, aryl or heteroarylamides useful as matrix metalloproteinase inhibitors

Also Published As

Publication number Publication date
HUP0200223A2 (en) 2002-06-29
EA200100806A1 (en) 2002-08-29
AU769418B2 (en) 2004-01-29
ATE309986T1 (en) 2005-12-15
CA2356313A1 (en) 2000-08-03
IL144345A0 (en) 2002-05-23
NZ512566A (en) 2004-02-27
AU2630500A (en) 2000-08-18
KR20010101732A (en) 2001-11-14
HUP0200223A3 (en) 2002-12-28
DE60024056D1 (en) 2005-12-22
ZA200105222B (en) 2002-09-25
CZ20012711A3 (en) 2002-05-15
JP2002535390A (en) 2002-10-22

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AR035312A1 (en) HYDROXAMIC ACID COMPOUNDS CONTAINING ALQUINYL AS MATRIX / TACE METALOPROTEINASE INHIBITORS, PHARMACEUTICAL COMPOSITION THAT INCLUDE THEM AND THE USE OF THE SAME FOR THE MANUFACTURE OF A MEDICINAL PRODUCT

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