NZ744884A - Tlr7 agonist crystalline form a, preparation method and use thereof - Google Patents

Tlr7 agonist crystalline form a, preparation method and use thereof

Info

Publication number
NZ744884A
NZ744884A NZ744884A NZ74488417A NZ744884A NZ 744884 A NZ744884 A NZ 744884A NZ 744884 A NZ744884 A NZ 744884A NZ 74488417 A NZ74488417 A NZ 74488417A NZ 744884 A NZ744884 A NZ 744884A
Authority
NZ
New Zealand
Prior art keywords
crystalline form
preparation
tlr7 agonist
tlr7
agonist
Prior art date
Application number
NZ744884A
Other languages
English (en)
Inventor
Zhaozhong Ding
Ling Yang
Fei Sun
Yinghu Hu
Yilong Zhou
Zheng Wang
Rui Zhao
Original Assignee
Chia Tai Tianqing Pharmaceutical Group Co 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 Chia Tai Tianqing Pharmaceutical Group Co Ltd filed Critical Chia Tai Tianqing Pharmaceutical Group Co Ltd
Publication of NZ744884A publication Critical patent/NZ744884A/en

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic 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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13—Crystalline forms, e.g. polymorphs

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Virology (AREA)
  • Communicable Diseases (AREA)
  • Epidemiology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
NZ744884A 2016-02-05 2017-02-04 Tlr7 agonist crystalline form a, preparation method and use thereof NZ744884A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CN201610082029.8A CN107043379A (zh) 2016-02-05 2016-02-05 一种tlr7激动剂的晶型a、其制备方法和医药用途
PCT/CN2017/072891 WO2017133684A1 (zh) 2016-02-05 2017-02-04 一种tlr7激动剂的晶型a、其制备方法和用途

Publications (1)

Publication Number Publication Date
NZ744884A true NZ744884A (en) 2022-09-30

Family

ID=59499348

Family Applications (1)

Application Number Title Priority Date Filing Date
NZ744884A NZ744884A (en) 2016-02-05 2017-02-04 Tlr7 agonist crystalline form a, preparation method and use thereof

Country Status (27)

Country Link
US (2) US10442811B2 (enExample)
EP (1) EP3412672B1 (enExample)
JP (1) JP6889171B2 (enExample)
KR (1) KR102393280B1 (enExample)
CN (2) CN107043379A (enExample)
AR (1) AR107548A1 (enExample)
AU (1) AU2017215801B2 (enExample)
CA (1) CA3013518C (enExample)
CL (1) CL2018002092A1 (enExample)
DK (1) DK3412672T3 (enExample)
EA (1) EA035951B1 (enExample)
ES (1) ES2830443T3 (enExample)
HR (1) HRP20201644T1 (enExample)
HU (1) HUE051399T2 (enExample)
IL (1) IL260968B (enExample)
LT (1) LT3412672T (enExample)
MX (1) MX374297B (enExample)
NZ (1) NZ744884A (enExample)
PH (1) PH12018501643A1 (enExample)
PL (1) PL3412672T3 (enExample)
PT (1) PT3412672T (enExample)
SG (1) SG11201806683UA (enExample)
SI (1) SI3412672T1 (enExample)
TW (1) TWI754629B (enExample)
UA (1) UA121161C2 (enExample)
WO (1) WO2017133684A1 (enExample)
ZA (1) ZA201805186B (enExample)

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CR20180229A (es) 2015-10-29 2018-08-24 Novartis Ag Conjugados de anticuerpos que comprenden un agonista del receptor tipo toll
CN107043378A (zh) * 2016-02-05 2017-08-15 正大天晴药业集团股份有限公司 一种吡咯并[3,2-d]嘧啶类化合物的制备方法及其中间体
CN107043379A (zh) * 2016-02-05 2017-08-15 正大天晴药业集团股份有限公司 一种tlr7激动剂的晶型a、其制备方法和医药用途
CN107043380A (zh) * 2016-02-05 2017-08-15 正大天晴药业集团股份有限公司 一种tlr7激动剂的马来酸盐、其晶型c、晶型d、晶型e、制备方法和用途
CN112105620B (zh) * 2018-05-25 2026-02-24 正大天晴药业集团股份有限公司 用于治疗肺癌的tlr7激动剂及其药物组合
BR112021015577A2 (pt) 2019-02-08 2021-10-05 Research & Business Foundation Sungkyunkwan University Complexo-colesterol agonista do receptor toll-like 7 ou 8 e uso do mesmo
ES3070986T3 (en) 2019-03-15 2026-06-18 Chia Tai Tianqing Pharmaceutical Group Co Ltd Toll-like receptor agonists for use in the treatment of hepatitis b
SG11202111488YA (en) * 2019-04-23 2021-11-29 Chia Tai Tianqing Pharmaceutical Group Co Ltd Solid pharmaceutical composition comprising tlr7 agonist
CN115666637A (zh) 2020-03-02 2023-01-31 蛋白科技先锋 基于病原体细胞壁骨架的模拟活病原体的纳米粒子及其制备方法
EP4194008A4 (en) 2020-08-04 2025-01-08 Progeneer Inc. Kinetically acting adjuvant ensemble
US20230277525A1 (en) 2020-08-04 2023-09-07 Progeneer Inc Conjugate of functional drug and toll-like receptor 7 or 8 agonist of which active site is temporarily inactivated and use thereof
WO2022031021A1 (ko) 2020-08-04 2022-02-10 성균관대학교산학협력단 동력학적 제어가 가능한 아주번트를 포함하는 mrna 백신
CN119431359A (zh) * 2023-07-28 2025-02-14 苏州申拓医药科技有限公司 一种tlr7/8激动剂的可药用盐、晶型及其制备方法、药物组合物和用途
WO2025110816A1 (ko) 2023-11-23 2025-05-30 프로지니어 주식회사 암의 치료를 위한 활성화 부위가 일시적으로 비활성화된 톨-유사 수용체 7 또는 8 작용자와 항암 치료의 병용요법

Family Cites Families (14)

* Cited by examiner, † Cited by third party
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JP3376479B2 (ja) * 1991-08-12 2003-02-10 武田薬品工業株式会社 縮合ピリミジン誘導体、その製造法および用途
CA2620182A1 (en) * 2005-08-22 2007-03-01 Dennis A. Carson Tlr agonists
UY32306A (es) 2008-12-09 2010-07-30 Gilead Sciences Inc Derivados de pteridinona y pirimidinodiazepinona y composiciones farmacéuticas que modulan en forma selectiva los receptores tipo toll, métodos y usos
JP5813785B2 (ja) 2011-02-04 2015-11-17 デュケイン ユニバーシティー オブ ザ ホリー スピリット 抗チューブリン活性を有する二環式および三環式のピリミジンチロシンキナーゼ阻害剤ならびに患者の処置方法
WO2013103967A1 (en) 2012-01-05 2013-07-11 Northeastern University Allosteric modulators of cb1 cannabinoid receptors
MX386924B (es) * 2012-10-10 2025-03-19 Janssen Sciences Ireland Uc Derivados pirrolo[3,2-d]pirimidínicos para el tratamiento de infecciones víricas y otras enfermedades.
JP6216387B2 (ja) 2012-11-20 2017-10-18 グラクソスミスクライン・リミテッド・ライアビリティ・カンパニーGlaxoSmithKline LLC 新規化合物
KR20150085081A (ko) * 2012-11-20 2015-07-22 글락소스미스클라인 엘엘씨 신규 화합물
SMT201700378T1 (it) * 2012-11-20 2017-09-07 Glaxosmithkline Llc Nuovi composti
WO2015168269A1 (en) 2014-05-01 2015-11-05 Novartis Ag Compounds and compositions as toll-like receptor 7 agonists
CN105367576A (zh) 2014-08-15 2016-03-02 正大天晴药业集团股份有限公司 作为tlr7激动剂的吡咯并嘧啶化合物
CN112898308B (zh) * 2014-08-15 2026-08-07 正大天晴药业集团股份有限公司 作为tlr7激动剂的吡咯并嘧啶化合物
CN107043380A (zh) 2016-02-05 2017-08-15 正大天晴药业集团股份有限公司 一种tlr7激动剂的马来酸盐、其晶型c、晶型d、晶型e、制备方法和用途
CN107043379A (zh) * 2016-02-05 2017-08-15 正大天晴药业集团股份有限公司 一种tlr7激动剂的晶型a、其制备方法和医药用途

Also Published As

Publication number Publication date
MX374297B (es) 2025-03-06
HUE051399T2 (hu) 2021-03-01
PT3412672T (pt) 2020-11-11
JP2019505533A (ja) 2019-02-28
US10947245B2 (en) 2021-03-16
KR102393280B1 (ko) 2022-05-02
CA3013518C (en) 2022-07-19
TWI754629B (zh) 2022-02-11
EA035951B1 (ru) 2020-09-04
HK1259170A1 (zh) 2019-11-29
CN108602831B9 (zh) 2020-12-04
AR107548A1 (es) 2018-05-09
AU2017215801A1 (en) 2018-08-23
DK3412672T3 (da) 2020-10-19
SI3412672T1 (sl) 2021-02-26
KR20180104117A (ko) 2018-09-19
IL260968B (en) 2022-05-01
EP3412672B1 (en) 2020-07-15
SG11201806683UA (en) 2018-09-27
PH12018501643A1 (en) 2019-06-03
US10442811B2 (en) 2019-10-15
HRP20201644T1 (hr) 2020-12-25
AU2017215801B2 (en) 2020-09-10
LT3412672T (lt) 2020-11-10
EA201891768A1 (ru) 2019-01-31
ES2830443T3 (es) 2021-06-03
CA3013518A1 (en) 2017-08-10
CL2018002092A1 (es) 2018-12-07
WO2017133684A1 (zh) 2017-08-10
ZA201805186B (en) 2024-08-28
US20190040071A1 (en) 2019-02-07
CN108602831B (zh) 2020-11-03
EP3412672A1 (en) 2018-12-12
US20200039988A1 (en) 2020-02-06
CN107043379A (zh) 2017-08-15
MX2018009501A (es) 2018-12-11
EP3412672A4 (en) 2019-07-17
TW201728589A (zh) 2017-08-16
PL3412672T3 (pl) 2021-01-25
JP6889171B2 (ja) 2021-06-18
CN108602831A (zh) 2018-09-28
UA121161C2 (uk) 2020-04-10
BR112018015880A2 (pt) 2018-12-26

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