KR890003761A - 치료학적 아시클릭 뉴클레오시드 - Google Patents

치료학적 아시클릭 뉴클레오시드 Download PDF

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Publication number
KR890003761A
KR890003761A KR1019880010298A KR880010298A KR890003761A KR 890003761 A KR890003761 A KR 890003761A KR 1019880010298 A KR1019880010298 A KR 1019880010298A KR 880010298 A KR880010298 A KR 880010298A KR 890003761 A KR890003761 A KR 890003761A
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South Korea
Prior art keywords
compound
formula
group
salt
pharmaceutically acceptable
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KR1019880010298A
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English (en)
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KR960002849B1 (ko
Inventor
안토니 크레니트스키 토마스
마리 비이쳄프 리리아
Original Assignee
엠.피.잭슨
더 웰컴 파운데이숀 리미티드
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=26292613&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=KR890003761(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from GB878719367A external-priority patent/GB8719367D0/en
Priority claimed from GB878725939A external-priority patent/GB8725939D0/en
Application filed by 엠.피.잭슨, 더 웰컴 파운데이숀 리미티드 filed Critical 엠.피.잭슨
Publication of KR890003761A publication Critical patent/KR890003761A/ko
Priority to KR1019960000775A priority Critical patent/KR960004940B1/ko
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Publication of KR960002849B1 publication Critical patent/KR960002849B1/ko

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/02Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/18Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 one oxygen and one nitrogen atom, e.g. guanine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/20Antivirals for DNA viruses
    • A61P31/22Antivirals for DNA viruses for herpes viruses

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Virology (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Oncology (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Public Health (AREA)
  • Communicable Diseases (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • Molecular Biology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Saccharide Compounds (AREA)
  • Medicinal Preparation (AREA)

Abstract

내용 없음

Description

치료학적 아시클릭 뉴클레오시드
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (10)

  1. 하기식(Ⅰ)의 화합물 또는 그것의 약학적 허용염.
    (이때 R1은 식 -CH(CH3)2또는 -CH(CH3)CH2CH2의 기를 나타냄)
  2. 2-(2-아미노-1,6-디하이드로-6-옥소-9H-(푸린-9-일)메톡시)에틸L-발리네이트.
  3. 2-(2-아미노-1,6-디하이드로-6-옥소-9H-(푸린-9-일)메톡시)에틸L-이소발리네이트.
  4. 제1항 내지 제3항중 어느 한항에 있어서, 그 염이 산부가염인 식(Ⅰ)화합물의 염.
  5. 제1항 내지 제4항중 어느 한항에 있어서, 그 염이 염산인 식(Ⅰ)화합물의 염.
  6. 제1항에 있어서, 의학적 용도를 위한 화합물.
  7. 제6항에 있어서, 비루스 감염의 치료 또는 예방을 위한 화합물.
  8. 제7항에 있어서, 헤르페스 심플렉스 비루스(Ⅰ)감염의 치료 또는 예방을 위한 화합물.
  9. 식(Ⅰ)의 화합물(제1항의 정의와 같음) 또는 그것의 약학적 허용염의 제조에 있어서, a) 식(Ⅱ)화합물을 임의로 보호된 발린 또는 그것의 기능적인 등가물과 반응시키거나,
    (이때 X는 임의로 보호된 수산기, Y는 임의로 보호된 아미노기임)
    b) 식(Ⅲ)화합물을 식(Ⅰ)화합물 또는 그것의 약학적 허용염으로 전화시키거나
    (이때 R1은 상기와 가고 M은 수산기, G는 아미노기로 치환될 수 있거나 또는 전환될 수 있는 원자 또는 기, 또는 G가 아미노기이며 M은 수산기로 치환되거나 또는 전환될 수 있는 원자 또는 기임)
    c)식(Ⅳ)화합물을 식(Ⅴ)화합물과 반응시킨후
    (상기식에서 X,Y와 R1은 상기와 같고 O와 A는 이탈기 또는 원자 R2는 임의로 보호된 아미노기임)
    i) 보호기 제거 ii) 식(Ⅰ)화합물이 생성되었을때, 이것을 약학적 허용 염으로 전환, iii) 약학적 허용염이 생성되었을때 이것을 모체화합물로 전환시키는 전환 공중들중 하나 이상의 공정을 필요한 순서대로 실시함을 특징으로 하는 방법.
  10. 식(Ⅰ)의 화합물의 활성성분과 그것의 약학적 허용염과 약학적 허용 담체를 함유하는 약학 조성물.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019880010298A 1987-08-15 1988-08-12 아사이클로비르의 발린 에스테르 및 이를 함유하는 약학 조성물 KR960002849B1 (ko)

Priority Applications (1)

Application Number Priority Date Filing Date Title
KR1019960000775A KR960004940B1 (ko) 1987-08-15 1996-01-17 아사이클로비르의 이소로이신 에스테르 및 이를 함유하는 약학 조성물

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
GB8719367 1987-08-15
GB878719367A GB8719367D0 (en) 1987-08-15 1987-08-15 Therapeutic compounds
GB878725939A GB8725939D0 (en) 1987-11-05 1987-11-05 Therapeutic compounds
GB8725939 1987-11-05

Related Child Applications (1)

Application Number Title Priority Date Filing Date
KR1019960000775A Division KR960004940B1 (ko) 1987-08-15 1996-01-17 아사이클로비르의 이소로이신 에스테르 및 이를 함유하는 약학 조성물

Publications (2)

Publication Number Publication Date
KR890003761A true KR890003761A (ko) 1989-04-17
KR960002849B1 KR960002849B1 (ko) 1996-02-27

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ID=26292613

Family Applications (2)

Application Number Title Priority Date Filing Date
KR1019880010298A KR960002849B1 (ko) 1987-08-15 1988-08-12 아사이클로비르의 발린 에스테르 및 이를 함유하는 약학 조성물
KR1019960000775A KR960004940B1 (ko) 1987-08-15 1996-01-17 아사이클로비르의 이소로이신 에스테르 및 이를 함유하는 약학 조성물

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Country Status (30)

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EP (2) EP0596542B1 (ko)
JP (2) JPH0662623B2 (ko)
KR (2) KR960002849B1 (ko)
CN (1) CN1033701C (ko)
AP (2) AP160A (ko)
AT (1) ATE138660T1 (ko)
AU (1) AU612393C (ko)
CS (1) CS276903B6 (ko)
CY (1) CY1833A (ko)
DE (1) DE3855333T2 (ko)
DK (2) DK170045B1 (ko)
ES (1) ES2087639T3 (ko)
FI (1) FI89713C (ko)
GR (1) GR3020372T3 (ko)
HU (1) HU201071B (ko)
IE (1) IE65551B1 (ko)
IL (1) IL87434A (ko)
LU (1) LU88746I2 (ko)
LV (1) LV5264A3 (ko)
MC (1) MC1968A1 (ko)
MX (1) MX9203418A (ko)
MY (1) MY103760A (ko)
NL (1) NL960001I2 (ko)
NO (2) NO167805C (ko)
NZ (1) NZ225809A (ko)
PL (1) PL158285B1 (ko)
PT (1) PT88261B (ko)
SA (1) SA95160244B1 (ko)
SG (1) SG26346G (ko)
SU (1) SU1634138A3 (ko)

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DE69513313T2 (de) * 1994-02-01 2000-07-13 Ajinomoto Kk Verfahren zur Herstellung von Nukleinsäurebasenderivaten
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PE32296A1 (es) * 1994-07-28 1996-08-07 Hoffmann La Roche Ester de l-monovalina derivado de 2-(2-amino-1,6-dihidro-6-oxo-purin-9-il) metoxi-1,3-propandiol y sus sales farmaceuticamente aceptables
GB9501127D0 (en) * 1995-01-20 1995-03-08 Wellcome Found Tablet
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GB9501142D0 (en) * 1995-01-20 1995-03-08 Wellcome Found Compounds for use in medicine
DE19536164A1 (de) * 1995-09-28 1997-04-03 Boehringer Ingelheim Kg Verbessertes Verfahren zur Herstellung von 9-[(2-Hyroxyethoxy)methyl]guanin (Acyclovir)
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CA2332961A1 (en) * 1998-05-21 1999-11-25 Michael Zasloff A method for stimulation of defensin production by exposure to isoleucine
JP5043286B2 (ja) * 2001-09-07 2012-10-10 テバ ファーマシューティカル インダストリーズ リミティド バラシクロビル塩酸塩の結晶型
AU2003240213A1 (en) 2002-06-24 2004-01-06 Ranbaxy Laboratories Limited Process for the preparation of robust formulations of valacyclovir hydrochloride tablets
US20050043329A1 (en) * 2002-09-06 2005-02-24 Shlomit Wizel Crystalline forms of valacyclovir hydrochloride
CN1309732C (zh) * 2002-10-28 2007-04-11 南京长澳医药科技有限公司 6-烷氧基-2’,3’-双脱氧鸟嘌呤核苷的制备方法
EP1638972A2 (en) * 2003-06-02 2006-03-29 Teva Pharmaceutical Industries Limited Novel crystalline forms of valacyclovir hydrochloride
CN1331471C (zh) * 2003-09-22 2007-08-15 陈云芳 盐酸万乃洛韦软胶囊组合物
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WO2006035452A1 (en) * 2004-09-27 2006-04-06 Matrix Laboratories Ltd Novel pseudomorph of valaciclovir hydrochloride
US7846937B2 (en) 2005-05-25 2010-12-07 Eli Lilly And Company Cyclopropanecarboxylate esters of acyclovir
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CN101456859B (zh) * 2009-01-06 2011-07-20 华南理工大学 抗病毒药物缬昔洛韦的制备方法
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CN102850354B (zh) * 2012-10-10 2014-07-23 山东金城医药化工股份有限公司 高纯度cbz-万乃洛韦的制备方法
CN106632335A (zh) * 2016-12-27 2017-05-10 河南康达制药有限公司 一种盐酸伐昔洛韦的制备方法
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HUT47935A (en) 1989-04-28
JPH0662623B2 (ja) 1994-08-17
AU612393C (en) 2006-08-17
AP55A (en) 1989-09-26
NL960001I2 (nl) 1996-11-01
LV5264A3 (lv) 1993-10-10
DK451388A (da) 1989-02-16
NO167805B (no) 1991-09-02
SA95160244B1 (ar) 2006-10-02
DE3855333D1 (de) 1996-07-04
NO1996015I1 (no) 1996-12-17
FI89713C (fi) 1993-11-10
KR960002849B1 (ko) 1996-02-27
CY1833A (en) 1995-12-01
IE65551B1 (en) 1995-11-01
KR960004940B1 (ko) 1996-04-18
LU88746I2 (fr) 1996-10-04
NL960001I1 (nl) 1996-03-01
PT88261B (pt) 1995-03-01
MX9203418A (es) 1992-07-01
EP0308065A2 (en) 1989-03-22
AP8800099A0 (en) 1988-08-01
DK170803B1 (da) 1996-01-22
IL87434A0 (en) 1989-01-31
DK170045B1 (da) 1995-05-08
DK82694A (da) 1994-07-08
PT88261A (pt) 1989-06-30
AP160A (en) 1991-11-18
AU2097888A (en) 1989-02-16
PL274215A1 (en) 1990-02-19
MC1968A1 (fr) 1989-09-29
DK451388D0 (da) 1988-08-12
FI89713B (fi) 1993-07-30
EP0596542A1 (en) 1994-05-11
IE882463L (en) 1989-02-15
IL87434A (en) 1993-06-10
NO883612D0 (no) 1988-08-12
EP0596542B1 (en) 1996-05-29
HU201071B (en) 1990-09-28
ES2087639T3 (es) 1996-07-16
AU612393B2 (en) 1991-07-11
EP0308065A3 (en) 1989-09-27
SG26346G (en) 1995-09-01
JPH07113025B2 (ja) 1995-12-06
EP0308065B1 (en) 1995-01-04
DE3855333T2 (de) 1996-12-05
JPS6468373A (en) 1989-03-14
MY103760A (en) 1993-09-30
CN1032538A (zh) 1989-04-26
FI883757A0 (fi) 1988-08-12
NO167805C (no) 1991-12-11
PL158285B1 (en) 1992-08-31
GR3020372T3 (en) 1996-09-30
JPH03115284A (ja) 1991-05-16
CS8805594A2 (en) 1990-06-13
NO883612L (no) 1989-02-16
FI883757A (fi) 1989-02-16
SU1634138A3 (ru) 1991-03-07
ATE138660T1 (de) 1996-06-15
NZ225809A (en) 1991-07-26
CS276903B6 (en) 1992-09-16
CN1033701C (zh) 1997-01-01

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