HUE025723T2 - Dialkoxikinazolin-származékok mint KDR inhibitorok - Google Patents

Dialkoxikinazolin-származékok mint KDR inhibitorok Download PDF

Info

Publication number
HUE025723T2
HUE025723T2 HUE09743783A HUE09743783A HUE025723T2 HU E025723 T2 HUE025723 T2 HU E025723T2 HU E09743783 A HUE09743783 A HU E09743783A HU E09743783 A HUE09743783 A HU E09743783A HU E025723 T2 HUE025723 T2 HU E025723T2
Authority
HU
Hungary
Prior art keywords
alkyl
compound
aryl
heteroaryl
rti
Prior art date
Application number
HUE09743783A
Other languages
English (en)
Inventor
Wei-Guo Su
Weihan Zhang
Xiaoqiang Yan
Yumin Cui
Yongxin Ren
Jifeng Duan
Original Assignee
Hutchison Medipharma Entpr 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 Hutchison Medipharma Entpr Ltd filed Critical Hutchison Medipharma Entpr Ltd
Publication of HUE025723T2 publication Critical patent/HUE025723T2/hu

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/14Vasoprotectives; Antihaemorrhoidals; Drugs for varicose therapy; Capillary stabilisers

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Diabetes (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Rheumatology (AREA)
  • Vascular Medicine (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Epidemiology (AREA)
  • Pain & Pain Management (AREA)
  • Endocrinology (AREA)
  • Emergency Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Dermatology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Obesity (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Claims (3)

  1. Szabadalmi igénypontok L ügy alább; képied vegyidet:
    * a képletben Rj.. M.2? %, íip R* és Räe mfodegvskértek jelentése egymástól függetlenül 11, halogén, nitro, amine, ciano, hklroxik l-IO szénatomot tartalmazó alkil, 2-10 szénatomot tartabnaml síken 11, 2-1Ö szénatomot tartalmazó alkmtl, 6 szénatomot tartalmazó monocMusos, 10 szénatomot tartalmazó bicikfosos vágj·· 34 szénatomot tartalmazó trieik Insos árit, .1-12 szénatomot tartalmazó cikloaikil, 3-S-lagú moaodkíosos, k- i 2~tagé btcíkittsos vagy 11'14-tsgó trieiklusos· heierodkloalklh Jt-S-tagiV monoeikhtsos, 8- )2-tsg{j. bictklusos vagy 11 *i4*tagó trt-elklusos heteroaril, aikoxi, afkiltto, alktikarbonii, karboxi, aikoxikarbontf, ammokarbonri or aminoszulfom!; Il ï 6s R, mindegyikének jelentése alkod;, kijelentése alkil; jelentése rtSlOJNI’y^, ahol RB és % mindegyikének jelentése egymástól foggetforfoi H,; alkil, a&eml, alklnll, adt, dkfoaidl, heleroeskloalksl vagy hetmtaril, vagy Rs és együtt 3 - S-tagn, 1-3 hétéro-atomot tartalmazó gyűrűt képeznek azzal a. oíRogtfoaíonnnah amelyhez kapcsolódnak; X jelentése O, és Z jelentése· X: ahol az alkil, álként!, síkból, dkloalkll, heteróeikloaÉíi, aril, heteroaril és alkod csoportok- mindegyike magába .foglal helveítesltetlee vagy hehettedioit csoportokat, és a. helyettesítők, a következük közül vannak megválásává· halogén, htátoxtl, amino, ctano, -mrro, merkapto, alkoxikarborsii, amidé, ksrboxt,afkánsad&all, alkilkarbonil. karban) tdo, karbamlt, karhoz ti, ttonretéo,· tsociaPáixt, szalfonamido, alkil, alkenti, alklnil slkoxs, aril, heteroaril, cikloalkH és betetodkloslkil,
  2. 2, Az 1 igénypont szerinti vegytllet, áltól az alkil, atkeoll, aikmii, dktóalfell. heteroelklfodkil, aril, hetentaril és alkoxi «sopoaek. mindegyike helyetted teilen, .3. Áz 1, igénypont .szerinti· vegyitlei, ahol Rfi jelentése nreíth 4 Az I, Igénypert szerinti vegytlet, ahol Ra és % mindegyikének jelentése egymástól riggeíienill fi, alkil vagy clkloalkE 5. A 4. igénypont szerinti vegyüld, ahol Rg jelentése H ás Rä, jelentése metik é, A 4. Igénypont szerinti vegyidét, -aholR.^ és :R4 mindegyikének jelentése metoxt. 7. ,½ ?. igánypordsaemá yegy öletek kWf a» sláfeEiak valamelyike:
    képletn vegySkt.
  3. 9. Gyógyászati készítmény amely magába foglal egy í. igénypont szmtät vegyületsí és egy győgyásza- tilag: s-ífogiAalö :'í:>íd->aóai!yag;>t i(í< Egy L igénypont: szerinti vsgyülst érkèpxÔdëssei {mgh^sésk} kapcsolatos; rendellenesség: kezelésére való alkalmazásra, íl.> A 3Ö. igénypont szerinti vegyidet, a&amp;ol az érképzédésset (agglogesézis) kapcsolatos rendellenesség rák, MSs korra! Összetlíggő macnla-degenerácio vagy krónikás gyniladlisos feeíegság;,
HUE09743783A 2008-05-09 2009-05-08 Dialkoxikinazolin-származékok mint KDR inhibitorok HUE025723T2 (hu)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US12/118,019 US7829574B2 (en) 2008-05-09 2008-05-09 Substituted quinazoline compounds and their use in treating angiogenesis-related diseases

Publications (1)

Publication Number Publication Date
HUE025723T2 true HUE025723T2 (hu) 2016-04-28

Family

ID=41265455

Family Applications (1)

Application Number Title Priority Date Filing Date
HUE09743783A HUE025723T2 (hu) 2008-05-09 2009-05-08 Dialkoxikinazolin-származékok mint KDR inhibitorok

Country Status (21)

Country Link
US (3) US7829574B2 (hu)
EP (1) EP2297115B1 (hu)
JP (2) JP5856842B2 (hu)
KR (2) KR20160045925A (hu)
AU (1) AU2009244130B2 (hu)
BR (1) BRPI0908675B1 (hu)
CA (1) CA2723148C (hu)
CY (1) CY1117222T1 (hu)
DK (1) DK2297115T3 (hu)
ES (1) ES2550245T3 (hu)
HR (1) HRP20150954T1 (hu)
HU (1) HUE025723T2 (hu)
MX (2) MX2010012168A (hu)
MY (1) MY155566A (hu)
NZ (1) NZ588900A (hu)
PL (1) PL2297115T3 (hu)
PT (1) PT2297115E (hu)
RU (1) RU2506261C2 (hu)
SI (1) SI2297115T1 (hu)
TW (1) TWI458724B (hu)
WO (1) WO2009137797A2 (hu)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7829574B2 (en) 2008-05-09 2010-11-09 Hutchison Medipharma Enterprises Limited Substituted quinazoline compounds and their use in treating angiogenesis-related diseases
NZ595087A (en) * 2009-02-11 2013-03-28 Merck Patent Gmbh Novel amino azaheterocyclic carboxamides
SI3575288T1 (sl) 2009-09-03 2022-01-31 Bristol-Myers Squibb Company Kinazolini kot ionski kanalni inhibitorji kalija
CN105461702A (zh) * 2014-09-10 2016-04-06 和记黄埔医药(上海)有限公司 6-(6,7-二甲氧基喹唑啉-4-基氧基)-n,2-二甲基苯并呋喃-3-甲酰胺晶型
JP6740354B2 (ja) 2015-10-05 2020-08-12 ザ トラスティーズ オブ コロンビア ユニバーシティー イン ザ シティー オブ ニューヨーク オートファジーの流れ及びホスホリパーゼd及びタウを含むタンパク質凝集体のクリアランスの活性化剤ならびにタンパク質症の治療方法
US11016085B2 (en) 2016-04-25 2021-05-25 The Johns Hopkins University ZNT8 assays for drug development and pharmaceutical compositions
CN111316099A (zh) 2017-07-12 2020-06-19 约翰霍普金斯大学 用于1型糖尿病诊断的基于脂蛋白体的znt8自身抗原
WO2019183916A1 (zh) * 2018-03-30 2019-10-03 杭州领业医药科技有限公司 呋喹替尼的共晶、其制备方法、组合物和用途
CN113166241A (zh) 2018-08-16 2021-07-23 约翰霍普金斯大学 人类znt8抗体
CN111184698A (zh) * 2018-11-15 2020-05-22 和记黄埔医药(上海)有限公司 呋喹替尼制剂及其应用
CN110898065A (zh) * 2019-11-25 2020-03-24 南通大学 呋喹替尼或其盐在制备治疗脉络膜新生血管药物中的用途
TW202309022A (zh) 2021-04-13 2023-03-01 美商努法倫特公司 用於治療具egfr突變之癌症之胺基取代雜環

Family Cites Families (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9300059D0 (en) 1992-01-20 1993-03-03 Zeneca Ltd Quinazoline derivatives
HRP970371A2 (en) 1996-07-13 1998-08-31 Kathryn Jane Smith Heterocyclic compounds
US6235741B1 (en) 1997-05-30 2001-05-22 Merck & Co., Inc. Angiogenesis inhibitors
RU2262935C2 (ru) 1999-02-10 2005-10-27 Астразенека Аб Производные хиназолина в качестве ингибиторов ангиогенеза
US6943161B2 (en) 1999-12-28 2005-09-13 Pharmacopela Drug Discovery, Inc. Pyrimidine and triazine kinase inhibitors
DE10009267A1 (de) * 2000-02-26 2001-08-30 Goedecke Ag Verfahren zur einfachen Herstellung von (3-Chlor-4-fluor-phenyl)-[7-(3-morpholin-4-yl-propoxy)-6-nitro-quinazolin-4-yl]-amin bzw. (3-Chlor-4-fluor-phenyl)-[7-(3-morpholin-4-yl-propoxy)-6-amino-quinazolin-4-yl]-amin
AR035851A1 (es) * 2000-03-28 2004-07-21 Wyeth Corp 3-cianoquinolinas, 3-ciano-1,6-naftiridinas y 3-ciano-1,7-naftiridinas como inhibidoras de proteina quinasas
UA73993C2 (uk) * 2000-06-06 2005-10-17 Астразенека Аб Хіназолінові похідні для лікування пухлин та фармацевтична композиція
EP1326859A1 (en) * 2000-10-13 2003-07-16 AstraZeneca AB Quinazoline derivatives with anti-tumour activity
US6939866B2 (en) * 2000-10-13 2005-09-06 Astrazeneca Ab Quinazoline derivatives
US20040092750A1 (en) 2001-03-01 2004-05-13 Tomoyuki Hasegawa 2-methylindole-4-acetic acid, process for producing the same, and process for producing intermediate therefor
AU2002347336A1 (en) * 2001-12-05 2003-06-17 Astrazeneca Ab Quinoline derivatives
TWI329105B (en) 2002-02-01 2010-08-21 Rigel Pharmaceuticals Inc 2,4-pyrimidinediamine compounds and their uses
GB0206215D0 (en) 2002-03-15 2002-05-01 Novartis Ag Organic compounds
UA77303C2 (en) * 2002-06-14 2006-11-15 Pfizer Derivatives of thienopyridines substituted by benzocondensed heteroarylamide useful as therapeutic agents, pharmaceutical compositions and methods for their use
CN1678321A (zh) 2002-07-29 2005-10-05 里格尔药品股份有限公司 用2,4-嘧啶二胺化合物治疗或者预防自体免疫性疾病的方法
JP2009513502A (ja) * 2003-07-02 2009-04-02 エフ.ホフマン−ラ ロシュ アーゲー アリールアミン置換キナゾリノン化合物
US7442698B2 (en) 2003-07-24 2008-10-28 Amgen Inc. Substituted heterocyclic compounds and methods of use
GB0318423D0 (en) 2003-08-06 2003-09-10 Astrazeneca Ab Chemical compounds
GB0321710D0 (en) 2003-09-16 2003-10-15 Novartis Ag Organic compounds
GEP20084572B (en) * 2003-12-23 2008-12-25 Pfizer Novel quinoline derivatives
WO2005097137A2 (en) * 2004-03-31 2005-10-20 The Scripps Research Institute Advanced quinazoline based protein kinase inhibitors
WO2005114219A2 (en) * 2004-05-20 2005-12-01 Wyeth Assays to identify irreversibly binding inhibitors of receptor tyrosine kinases
WO2005115145A2 (en) 2004-05-20 2005-12-08 Wyeth Quinone substituted quinazoline and quinoline kinase inhibitors
WO2006071079A1 (en) 2004-12-29 2006-07-06 Hanmi Pharm. Co., Ltd. Quinazoline derivatives for inhibiting cancer cell growth and method for the preparation thereof
KR100735639B1 (ko) 2004-12-29 2007-07-04 한미약품 주식회사 암세포 성장 억제 효과를 갖는 퀴나졸린 유도체 및 이의제조방법
WO2006138304A2 (en) 2005-06-14 2006-12-28 Taigen Biotechnology Pyrimidine compounds
WO2007066181A2 (en) 2005-12-05 2007-06-14 Pfizer Products Inc. Methods of preparing a vegf-r inhibitor
US7601844B2 (en) * 2006-01-27 2009-10-13 Bristol-Myers Squibb Company Piperidinyl derivatives as modulators of chemokine receptor activity
GB0604937D0 (en) * 2006-03-10 2006-04-19 Novartis Ag Organic compounds
AU2007249762A1 (en) * 2006-05-15 2007-11-22 Senex Biotechnology, Inc Identification of CDKI pathway inhibitors
TW200922590A (en) * 2007-09-10 2009-06-01 Curis Inc VEGFR inhibitors containing a zinc binding moiety
US7829574B2 (en) * 2008-05-09 2010-11-09 Hutchison Medipharma Enterprises Limited Substituted quinazoline compounds and their use in treating angiogenesis-related diseases

Also Published As

Publication number Publication date
NZ588900A (en) 2012-12-21
TWI458724B (zh) 2014-11-01
MX2014001023A (es) 2014-05-22
BRPI0908675B1 (pt) 2022-01-25
WO2009137797A3 (en) 2010-02-25
PT2297115E (pt) 2015-10-26
US8497372B2 (en) 2013-07-30
MX2010012168A (es) 2011-02-18
US20110015213A1 (en) 2011-01-20
CA2723148C (en) 2015-01-20
MX340021B (es) 2016-06-22
MY155566A (en) 2015-10-30
CY1117222T1 (el) 2017-04-05
AU2009244130A1 (en) 2009-11-12
EP2297115A4 (en) 2012-03-14
TW201002694A (en) 2010-01-16
US20090281130A1 (en) 2009-11-12
US7829574B2 (en) 2010-11-09
EP2297115B1 (en) 2015-07-22
AU2009244130B2 (en) 2012-11-01
PL2297115T3 (pl) 2015-12-31
WO2009137797A2 (en) 2009-11-12
SI2297115T1 (sl) 2015-10-30
US8212033B2 (en) 2012-07-03
JP2014177499A (ja) 2014-09-25
KR20110013381A (ko) 2011-02-09
DK2297115T3 (en) 2015-08-10
ES2550245T3 (es) 2015-11-05
JP2011519956A (ja) 2011-07-14
BRPI0908675A2 (pt) 2015-08-04
EP2297115A2 (en) 2011-03-23
CA2723148A1 (en) 2009-11-12
RU2010150345A (ru) 2012-06-20
RU2506261C2 (ru) 2014-02-10
US20120238572A1 (en) 2012-09-20
JP5856842B2 (ja) 2016-02-10
HRP20150954T1 (hr) 2015-10-09
KR20160045925A (ko) 2016-04-27
KR101686679B1 (ko) 2016-12-14

Similar Documents

Publication Publication Date Title
DK2297115T3 (en) DIALCOXYQUINAZOLINE DERIVATIVES AS KDR INHIBITORS
TWI484960B (zh) 嘧啶衍生物
TWI642667B (zh) 吡啶並嘧啶類衍生物、其製備方法及其在醫藥上的應用
EP2318378B1 (en) Quinazoline derivatives
BRPI0805826B1 (pt) compostos espiro-substituídos, composição farmacêutica e uso
CN106478502B (zh) 1,2,3,4-四氢异喹啉衍生物、其制备方法和应用
DE68919475T2 (de) Bivalente liganden, wirksam für die blockierung des enzyms acat.
WO2010025138A2 (en) Pyrimidine compounds
US20060110467A1 (en) Cancer chemotherapy
JPS63264580A (ja) 3−(2−ハロアルキル)−1,4−オキサチインおよび2−(2−ハロアルキル)−1,4−ジチイン
AU2008240084B2 (en) Pyrimidine derivatives
JP5561648B2 (ja) ロダシアニン誘導体及びリーシュマニア感染症治療用医薬組成物
KR100621192B1 (ko) 무스카린 수용체 작용물질로서 작용하는1,2,3,4-테트라하이드로피리미디닐-1,2,4-옥사다이아졸유도체와 이의 제조방법