MA38540A1 - Dérivés de naphtyridine utiles comme antagonistes de l'intégrine alpha-v-bêta-6 - Google Patents

Dérivés de naphtyridine utiles comme antagonistes de l'intégrine alpha-v-bêta-6

Info

Publication number
MA38540A1
MA38540A1 MA38540A MA38540A MA38540A1 MA 38540 A1 MA38540 A1 MA 38540A1 MA 38540 A MA38540 A MA 38540A MA 38540 A MA38540 A MA 38540A MA 38540 A1 MA38540 A1 MA 38540A1
Authority
MA
Morocco
Prior art keywords
beta
alpha
derivatives useful
integrin antagonists
naphthyridine derivatives
Prior art date
Application number
MA38540A
Other languages
English (en)
Other versions
MA38540B1 (fr
Inventor
Niall Andrew Anderson
Brendan John Fallon
John Martin Pritchard
Original Assignee
Glaxosmithkline Ip Dev Ltd
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 Glaxosmithkline Ip Dev Ltd filed Critical Glaxosmithkline Ip Dev Ltd
Publication of MA38540A1 publication Critical patent/MA38540A1/fr
Publication of MA38540B1 publication Critical patent/MA38540B1/fr

Links

Classifications

    • 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
    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4151,2-Diazoles
    • A61K31/41551,2-Diazoles non condensed and containing further heterocyclic rings
    • 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
    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4375Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
    • 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
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • 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
    • C07D401/14Heterocyclic 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 three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings

Abstract

L'invention porte sur un composé de formule (i) ou un sel de celle-ci (i), dans laquelle r1 représente un atome d'hydrogène, un groupe méthyle ou un groupe éthyle, r2 représente un atome d'hydrogène ou un atome de fluor et r3 représente un atome d'hydrogène, un groupe méthyle ou un groupe éthyle.
MA38540A 2013-03-28 2014-03-26 Dérivés de naphtyridine utiles comme antagonistes de l'intégrine alpha-v-bêta-6 MA38540B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB1305668.4A GB201305668D0 (en) 2013-03-28 2013-03-28 Avs6 Integrin Antagonists
PCT/EP2014/056013 WO2014154725A1 (fr) 2013-03-28 2014-03-26 Dérivés de naphtyridine utiles comme antagonistes de l'intégrine alpha-v-bêta-6

Publications (2)

Publication Number Publication Date
MA38540A1 true MA38540A1 (fr) 2017-02-28
MA38540B1 MA38540B1 (fr) 2017-10-31

Family

ID=48444909

Family Applications (1)

Application Number Title Priority Date Filing Date
MA38540A MA38540B1 (fr) 2013-03-28 2014-03-26 Dérivés de naphtyridine utiles comme antagonistes de l'intégrine alpha-v-bêta-6

Country Status (38)

Country Link
US (2) US10023568B2 (fr)
EP (2) EP2989100B1 (fr)
JP (1) JP6095847B2 (fr)
KR (2) KR101775085B1 (fr)
CN (1) CN105189499B (fr)
AR (1) AR095768A1 (fr)
AU (1) AU2014243068C1 (fr)
BR (1) BR112015024530A8 (fr)
CA (1) CA2903358A1 (fr)
CL (1) CL2015002860A1 (fr)
CR (1) CR20150509A (fr)
CY (1) CY1120188T1 (fr)
DK (1) DK2989100T3 (fr)
DO (1) DOP2015000251A (fr)
EA (1) EA027305B1 (fr)
ES (1) ES2665597T3 (fr)
GB (1) GB201305668D0 (fr)
HK (1) HK1214262A1 (fr)
HR (1) HRP20180528T1 (fr)
HU (1) HUE036750T2 (fr)
IL (1) IL241184A0 (fr)
LT (1) LT2989100T (fr)
MA (1) MA38540B1 (fr)
ME (1) ME02987B (fr)
MX (1) MX363288B (fr)
NO (1) NO2989100T3 (fr)
NZ (1) NZ629025A (fr)
PE (1) PE20151606A1 (fr)
PH (1) PH12015502232A1 (fr)
PL (1) PL2989100T3 (fr)
PT (1) PT2989100T (fr)
RS (1) RS57220B1 (fr)
SG (1) SG11201506813QA (fr)
SI (1) SI2989100T1 (fr)
TW (1) TWI632143B (fr)
UA (1) UA114952C2 (fr)
UY (1) UY35505A (fr)
WO (1) WO2014154725A1 (fr)

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GB201417002D0 (en) * 2014-09-26 2014-11-12 Glaxosmithkline Ip Dev Ltd Novel compound
GB201417011D0 (en) * 2014-09-26 2014-11-12 Glaxosmithkline Ip Dev Ltd Novel compounds
GB201417018D0 (en) * 2014-09-26 2014-11-12 Glaxosmithkline Ip Dev Ltd Novel compounds
GB201417094D0 (en) * 2014-09-26 2014-11-12 Glaxosmithkline Ip Dev Ltd Novel compounds
BR112017019412A2 (pt) 2015-03-11 2018-05-02 Glaxosmithkline Ip Dev Ltd proteínas ligadoras de tslp
GB201615588D0 (en) 2016-09-14 2016-10-26 Glaxosmithkline Ip Dev Ltd TSLP Binding Proteins
GB201604589D0 (en) * 2016-03-18 2016-05-04 Glaxosmithkline Ip Dev Ltd Chemical compound
GB201604680D0 (en) 2016-03-21 2016-05-04 Glaxosmithkline Ip Dev Ltd Chemical Compounds
GB201604681D0 (en) 2016-03-21 2016-05-04 Glaxosmithkline Ip Dev Ltd Chemical Compounds
CA3042684A1 (fr) 2016-11-08 2018-05-17 Bristol-Myers Squibb Company Amides d'azole et amines en tant qu'inhibiteurs d'integrine .alpha.v
EP3538526B1 (fr) 2016-11-08 2024-04-10 Bristol-Myers Squibb Company Composés mono et spirocycliques contenant du cyclobutane et de l'azétidine en tant qu'inhibiteurs de l'intégrine alpha v
LT3538525T (lt) 2016-11-08 2022-09-26 Bristol-Myers Squibb Company Propiono rūgštys, pakeistos 3 padėtyje, kaip alfa v integrino inhibitoriai
AU2017359027A1 (en) 2016-11-08 2019-06-20 Bristol-Myers Squibb Company Indazole derivatives as αV integrin antagonists
US10717736B2 (en) * 2016-11-08 2020-07-21 Bristol-Myers Squibb Company Pyrrole amides as alpha V integrin inhibitors
US10696672B2 (en) 2016-12-23 2020-06-30 Pliant Therapeutics, Inc. Amino acid compounds and methods of use
US11046685B2 (en) 2017-02-28 2021-06-29 Morphic Therapeutic, Inc. Inhibitors of (α-v)(β-6) integrin
US20180244648A1 (en) 2017-02-28 2018-08-30 Lazuli, Inc. Inhibitors of (alpha-v)(beta-6) integrin
JP7291696B2 (ja) 2017-11-07 2023-06-15 ブリストル-マイヤーズ スクイブ カンパニー アルファvインテグリン阻害剤としてのピロロピラジン誘導体
WO2019173653A1 (fr) 2018-03-07 2019-09-12 Pliant Therapeutics, Inc. Composés d'acides aminés et leurs procédés d'utilisation
EA202190134A1 (ru) 2018-06-27 2021-03-26 Плайэнт Терапьютикс, Инк. Соединения аминокислот с неразветвленными линкерами и способы их применения
EP3843728A4 (fr) * 2018-08-29 2022-05-25 Morphic Therapeutic, Inc. Inhibiteurs de l'intégrine (alpha-v)(bêta -6)
CR20210109A (es) 2018-08-29 2021-06-24 Morphic Therapeutic Inc INHIBICIÓN DE LA INTEGRINA av ß6
WO2020047208A1 (fr) * 2018-08-29 2020-03-05 Morphic Therapeutic, Inc. Inhibiteurs de l'intégrine (alpha-v)(bêta-6)
GB202010626D0 (en) 2020-07-10 2020-08-26 Univ Nottingham Compound
WO2022183360A1 (fr) * 2021-03-02 2022-09-09 Tsao Yeou Ping Peptides synthétiques courts et leurs utilisations pour le traitement de la sécheresse oculaire

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Also Published As

Publication number Publication date
PH12015502232B1 (en) 2016-02-01
EA027305B1 (ru) 2017-07-31
NO2989100T3 (fr) 2018-07-28
AU2014243068A1 (en) 2015-10-08
EP2989100A1 (fr) 2016-03-02
AU2014243068B2 (en) 2017-01-05
UY35505A (es) 2014-10-31
HRP20180528T1 (hr) 2018-05-04
CN105189499B (zh) 2016-09-28
CR20150509A (es) 2016-03-04
JP6095847B2 (ja) 2017-03-15
CY1120188T1 (el) 2018-12-12
PT2989100T (pt) 2018-05-18
MX2015013742A (es) 2016-02-29
EA201591503A1 (ru) 2016-04-29
SI2989100T1 (en) 2018-06-29
AU2014243068C1 (en) 2017-05-25
US20160280705A1 (en) 2016-09-29
DK2989100T3 (en) 2018-04-23
RS57220B1 (sr) 2018-07-31
UA114952C2 (uk) 2017-08-28
EP2989100B1 (fr) 2018-02-28
PL2989100T3 (pl) 2018-07-31
GB201305668D0 (en) 2013-05-15
PE20151606A1 (es) 2015-11-24
TWI632143B (zh) 2018-08-11
CA2903358A1 (fr) 2014-10-02
ME02987B (fr) 2018-10-20
US20180291022A1 (en) 2018-10-11
ES2665597T3 (es) 2018-04-26
SG11201506813QA (en) 2015-10-29
MA38540B1 (fr) 2017-10-31
HUE036750T2 (hu) 2018-07-30
WO2014154725A1 (fr) 2014-10-02
EP3360876A1 (fr) 2018-08-15
JP2016515557A (ja) 2016-05-30
KR101775085B1 (ko) 2017-09-05
AR095768A1 (es) 2015-11-11
KR20170103033A (ko) 2017-09-12
KR20150135790A (ko) 2015-12-03
NZ629025A (en) 2017-05-26
CL2015002860A1 (es) 2016-03-28
TW201533042A (zh) 2015-09-01
CN105189499A (zh) 2015-12-23
BR112015024530A2 (pt) 2017-07-18
US10450312B2 (en) 2019-10-22
PH12015502232A1 (en) 2016-02-01
KR102042141B1 (ko) 2019-11-07
US10023568B2 (en) 2018-07-17
LT2989100T (lt) 2018-05-25
HK1214262A1 (zh) 2016-07-22
DOP2015000251A (es) 2016-02-29
MX363288B (es) 2019-03-19
BR112015024530A8 (pt) 2019-12-10
IL241184A0 (en) 2015-11-30

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