KR101789430B1 - Smo 저해 활성을 갖는 신규 화합물 및 이를 유효성분으로 포함하는 암 예방 또는 치료용 조성물 - Google Patents

Smo 저해 활성을 갖는 신규 화합물 및 이를 유효성분으로 포함하는 암 예방 또는 치료용 조성물 Download PDF

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KR101789430B1
KR101789430B1 KR1020160081189A KR20160081189A KR101789430B1 KR 101789430 B1 KR101789430 B1 KR 101789430B1 KR 1020160081189 A KR1020160081189 A KR 1020160081189A KR 20160081189 A KR20160081189 A KR 20160081189A KR 101789430 B1 KR101789430 B1 KR 101789430B1
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South Korea
Prior art keywords
cancer
quinazolin
pyridin
compound
dimethylmorpholino
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KR1020160081189A
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English (en)
Korean (ko)
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이경
고혁완
바타라이 디팍
김민경
정주현
이한규
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동국대학교 산학협력단
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Priority to KR1020160081189A priority Critical patent/KR101789430B1/ko
Priority to PCT/KR2017/006692 priority patent/WO2018004213A1/fr
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Publication of KR101789430B1 publication Critical patent/KR101789430B1/ko

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/44Iso-indoles; Hydrogenated iso-indoles
    • C07D209/46Iso-indoles; Hydrogenated iso-indoles with an oxygen atom in position 1
    • 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
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/4035Isoindoles, e.g. phthalimide
    • 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/517Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
    • 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
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • 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
    • C07D239/20Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D239/22Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms directly attached to ring carbon atoms
    • 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
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
KR1020160081189A 2016-06-28 2016-06-28 Smo 저해 활성을 갖는 신규 화합물 및 이를 유효성분으로 포함하는 암 예방 또는 치료용 조성물 KR101789430B1 (ko)

Priority Applications (2)

Application Number Priority Date Filing Date Title
KR1020160081189A KR101789430B1 (ko) 2016-06-28 2016-06-28 Smo 저해 활성을 갖는 신규 화합물 및 이를 유효성분으로 포함하는 암 예방 또는 치료용 조성물
PCT/KR2017/006692 WO2018004213A1 (fr) 2016-06-28 2017-06-26 Nouveau composé ayant une activité inhibitrice de smo et composition comprenant celui-ci en tant qu'ingrédient actif pour prévenir ou traiter le cancer

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR1020160081189A KR101789430B1 (ko) 2016-06-28 2016-06-28 Smo 저해 활성을 갖는 신규 화합물 및 이를 유효성분으로 포함하는 암 예방 또는 치료용 조성물

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KR101789430B1 true KR101789430B1 (ko) 2017-10-25

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KR1020160081189A KR101789430B1 (ko) 2016-06-28 2016-06-28 Smo 저해 활성을 갖는 신규 화합물 및 이를 유효성분으로 포함하는 암 예방 또는 치료용 조성물

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KR (1) KR101789430B1 (fr)
WO (1) WO2018004213A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20220161875A (ko) * 2021-05-31 2022-12-07 주식회사 헤지호그 Gli 활성을 억제하는 피페리딘 유도체 화합물 및 이의 암 치료 용도

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113227089A (zh) 2018-10-31 2021-08-06 吉利德科学公司 作为hpk1抑制剂的取代的6-氮杂苯并咪唑化合物
CA3116347A1 (fr) 2018-10-31 2020-05-07 Gilead Sciences, Inc. Composes 6-azabenzimidazole substitues ayant une activite inhibitrice de hpk1
EP3972695A1 (fr) 2019-05-23 2022-03-30 Gilead Sciences, Inc. Exo-méthylène-oxindoles substitués qui sont des inhibiteurs de hpk1/map4k1
WO2021020363A1 (fr) 2019-07-29 2021-02-04 武田薬品工業株式会社 Composé hétérocyclique
CN114957219B (zh) * 2022-05-10 2023-12-15 苏州大学 一种靶向降解Gli1蛋白的降解剂及其制备方法和应用

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001019800A2 (fr) 1999-09-16 2001-03-22 Curis, Inc. Mediateurs de voies de signalisation hedgehog, preparations et utilisations associees
WO2005021532A1 (fr) 2003-08-25 2005-03-10 Amgen Inc Derives 2,3-dihydro-1h-isoindol-1-one substitues et techniques d'utilisation
WO2005123696A1 (fr) 2004-06-15 2005-12-29 Astrazeneca Ab Quinazolones substitues en tant qu'agents anticancereux
WO2010084050A2 (fr) 2009-01-13 2010-07-29 Novartis Ag Dérivés de quinazolinone utiles comme antagonistes vanilloïdes
WO2012016876A1 (fr) 2010-08-03 2012-02-09 Nerviano Medical Sciences S.R.L. Combinaison thérapeutique comprenant un inhibiteur de parp-1 et un agent antinéoplasique

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07258224A (ja) * 1994-03-24 1995-10-09 Dai Ichi Seiyaku Co Ltd 二環性化合物

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001019800A2 (fr) 1999-09-16 2001-03-22 Curis, Inc. Mediateurs de voies de signalisation hedgehog, preparations et utilisations associees
WO2005021532A1 (fr) 2003-08-25 2005-03-10 Amgen Inc Derives 2,3-dihydro-1h-isoindol-1-one substitues et techniques d'utilisation
WO2005123696A1 (fr) 2004-06-15 2005-12-29 Astrazeneca Ab Quinazolones substitues en tant qu'agents anticancereux
WO2010084050A2 (fr) 2009-01-13 2010-07-29 Novartis Ag Dérivés de quinazolinone utiles comme antagonistes vanilloïdes
WO2012016876A1 (fr) 2010-08-03 2012-02-09 Nerviano Medical Sciences S.R.L. Combinaison thérapeutique comprenant un inhibiteur de parp-1 et un agent antinéoplasique

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20220161875A (ko) * 2021-05-31 2022-12-07 주식회사 헤지호그 Gli 활성을 억제하는 피페리딘 유도체 화합물 및 이의 암 치료 용도
KR102553669B1 (ko) 2021-05-31 2023-07-11 주식회사 헤지호그 Gli 활성을 억제하는 피페리딘 유도체 화합물 및 이의 암 치료 용도

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