WO2013042065A3 - Inhibiteurs de protéines inactivatrices de ribosome de type ii - Google Patents
Inhibiteurs de protéines inactivatrices de ribosome de type ii Download PDFInfo
- Publication number
- WO2013042065A3 WO2013042065A3 PCT/IB2012/054999 IB2012054999W WO2013042065A3 WO 2013042065 A3 WO2013042065 A3 WO 2013042065A3 IB 2012054999 W IB2012054999 W IB 2012054999W WO 2013042065 A3 WO2013042065 A3 WO 2013042065A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- inhibitors
- aromatic
- type
- ribosome inactivating
- inactivating proteins
- Prior art date
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
- A61K31/52—Purines, e.g. adenine
-
- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
- A61K31/7076—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines containing purines, e.g. adenosine, adenylic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P39/00—General protective or antinoxious agents
- A61P39/02—Antidotes
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Toxicology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
L'invention concerne des composés qui sont inhibiteurs de ricine, d'abrine, de Shiga ou de saporine et qui ont une configuration bipartite comprenant une structure hétérocyclique aromatique ressemblant à une fraction adénine en dimension et en forme, connectée à la position C8 d'une structure de cycle cyclique aromatique ou non aromatique ressemblant à une fraction ribose en dimension et en forme. Plus particulièrement, les inhibiteurs ont la formule (I) : (I) où X = -S-, -O-, -CH 2 -, -NH-, -PH-, -O-Y-, -CH 2 -Y-, -NH-Y-, -PH-Y ou -S-Y ; Y = -S-, -O-, -CH 2 -, -NH- ou -PH- ; et W = un cycle cyclique aromatique ou non aromatique à 5 ou 6 chaînons. L'invention concerne également des utilisations de ces composés dans la fabrication d'un médicament et dans le traitement d'un sujet, ainsi qu'un procédé d'identification d'inhibiteurs appropriés.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ZA2011/06840 | 2011-09-20 | ||
ZA201106840 | 2011-09-20 |
Publications (3)
Publication Number | Publication Date |
---|---|
WO2013042065A2 WO2013042065A2 (fr) | 2013-03-28 |
WO2013042065A3 true WO2013042065A3 (fr) | 2013-06-20 |
WO2013042065A4 WO2013042065A4 (fr) | 2013-08-15 |
Family
ID=47116143
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/IB2012/054999 WO2013042065A2 (fr) | 2011-09-20 | 2012-09-20 | Inhibiteurs de protéines inactivatrices de ribosome de type ii |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2013042065A2 (fr) |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998028298A1 (fr) * | 1996-12-24 | 1998-07-02 | Research Development Foundation | Inhibiteurs de ricin et procedes d'utilisation |
WO2001073438A1 (fr) * | 2000-03-24 | 2001-10-04 | Research Development Foundation | Inhibiteurs de ricine et procedes d'utilisation de ces inhibiteurs |
WO2005023203A2 (fr) * | 2003-09-09 | 2005-03-17 | Albert Einstein College Of Medicine Of Yeshiva University | Inhibiteurs d'analogues d'etat de transition de chaine a de toxine de ricin |
WO2006084030A2 (fr) * | 2005-02-01 | 2006-08-10 | Sloan-Kettering Institute For Cancer Research | Petites molecules inhibitrices du hsp90 |
-
2012
- 2012-09-20 WO PCT/IB2012/054999 patent/WO2013042065A2/fr active Application Filing
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998028298A1 (fr) * | 1996-12-24 | 1998-07-02 | Research Development Foundation | Inhibiteurs de ricin et procedes d'utilisation |
WO2001073438A1 (fr) * | 2000-03-24 | 2001-10-04 | Research Development Foundation | Inhibiteurs de ricine et procedes d'utilisation de ces inhibiteurs |
WO2005023203A2 (fr) * | 2003-09-09 | 2005-03-17 | Albert Einstein College Of Medicine Of Yeshiva University | Inhibiteurs d'analogues d'etat de transition de chaine a de toxine de ricin |
WO2006084030A2 (fr) * | 2005-02-01 | 2006-08-10 | Sloan-Kettering Institute For Cancer Research | Petites molecules inhibitrices du hsp90 |
Non-Patent Citations (3)
Title |
---|
BAI Y ET AL: "Identification of new classes of ricin toxin inhibitors by virtual screening", TOXICON, ELMSFORD, NY, US, vol. 56, no. 4, 15 September 2010 (2010-09-15), pages 526 - 534, XP027154311, ISSN: 0041-0101, [retrieved on 20100520] * |
DE S K ET AL: "Discovery of 2-(5-nitrothiazol-2-ylthio)benzo[d]thiazoles as novel c-Jun N-terminal kinase inhibitors", BIOORGANIC & MEDICINAL CHEMISTRY, PERGAMON, GB, vol. 17, no. 7, 1 April 2009 (2009-04-01), pages 2712 - 2717, XP026073620, ISSN: 0968-0896, [retrieved on 20090226], DOI: 10.1016/J.BMC.2009.02.046 * |
HO MENG-CHIAO ET AL: "Transition state analogues in structures of ricin and saporin ribosome-inactivating proteins.", PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 1 DEC 2009, vol. 106, no. 48, 1 December 2009 (2009-12-01), pages 20276 - 20281, XP002693882, ISSN: 1091-6490 * |
Also Published As
Publication number | Publication date |
---|---|
WO2013042065A2 (fr) | 2013-03-28 |
WO2013042065A4 (fr) | 2013-08-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CY1119056T1 (el) | Παραγωγα 2',4',-διφθορο-2'-μεθυλ υποκατεστημενου νουκλεοσιδιου ως αναστολεις αντιγραφης hcv rna | |
EA201201143A1 (ru) | Производные пиразола в качестве ингибиторов jak | |
BR112014008495A2 (pt) | inibidores de proteína quinase | |
CY1118567T1 (el) | Αναστολεις του ιου της ηπατιτιδας c | |
BR112012032234A2 (pt) | "derivados de heteroaril imidazolona como inibidores de jak". | |
EA201200938A1 (ru) | Производные имидазопиридина в качестве ингибиторов jak | |
EA201000100A1 (ru) | Гетероциклические соединения, полезные в качестве ингибиторов mk2 | |
MY159958A (en) | 5,5-fused arylene or heteroarylene hepatitis c virus inhibitors | |
CY1114356T1 (el) | Αναστολεις του ιου της ηπατιτιδας c | |
BR112013003101A2 (pt) | inibidores do vírus da hepatite c | |
BR112013023876A2 (pt) | derivados de pirroltriazinona como inibidores de pi3k | |
PE20151448A1 (es) | Compuestos de tiazolcarboxamidas y piridinacarboxamida utiles como inhibidores de quinasa pim | |
UA108221C2 (uk) | Похідні тіофен-2-карбонової кислоти як інгібітори вірусів flaviviridae | |
BR112014001801A2 (pt) | indazóis | |
EA200970805A1 (ru) | Ингибиторы серинпротеаз для лечения hcv инфекций | |
EA201491180A1 (ru) | 4'-азидо,3'-фторзамещенные производные нуклеозидов в качестве ингибиторов репликации рнк вируса гепатита с | |
BR112014033080A2 (pt) | inibidores do vírus da hepatite c | |
NI201100062A (es) | Inhibidores de las enzimas de proteína cinasa activadas por mitógeno p38. | |
EA201490596A1 (ru) | Новые производные дигидрохинолин-2-она | |
BR112013020042A2 (pt) | inibidores de vírus da hepatite c | |
CY1116775T1 (el) | Παραγωγα πυριμιδονης ως αναστολεις της ιστικης τρανσγλουταμινασης | |
BR112013002729A2 (pt) | inibidores de vírus de hepatite c | |
EA201270535A1 (ru) | Пуриновые производные, применимые в качестве ингибиторов hsp90 | |
BR112014003693A2 (pt) | amino quinazolinas como inibidores de quinase | |
EA201390156A1 (ru) | ПРОИЗВОДСТВО ИНТЕР-АЛЬФА-ИНГИБИТОРНЫХ БЕЛКОВ (IaIp) ИЗ ПЛАЗМЫ |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 12780544 Country of ref document: EP Kind code of ref document: A2 |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 12780544 Country of ref document: EP Kind code of ref document: A2 |