WO2006138118A2 - Anti-viral compositions comprising heterocyclic substituted phenyl furans and related compounds - Google Patents
Anti-viral compositions comprising heterocyclic substituted phenyl furans and related compounds Download PDFInfo
- Publication number
- WO2006138118A2 WO2006138118A2 PCT/US2006/021993 US2006021993W WO2006138118A2 WO 2006138118 A2 WO2006138118 A2 WO 2006138118A2 US 2006021993 W US2006021993 W US 2006021993W WO 2006138118 A2 WO2006138118 A2 WO 2006138118A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- composition
- hiv
- alkyl
- group
- acid
- Prior art date
- Legal status (The legal status 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 status listed.)
- Ceased
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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- 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
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
-
- 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
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/501—Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
-
- 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
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
-
- 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
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Definitions
- the group heterocyclic stands for optionally substituted saturated, partially saturated, aromatic cyclics, which contain one or more heteroatoms selected from nitrogen, oxygen and sulfur and can also be benz-fused to an optionally substituted aromatic cyclic or heterocyles.
- Substituents for aryl and heterocyclyl can be selected from those mentioned for alkyl .
- This invention provides an antiviral pharmaceutical composition
- an antiviral pharmaceutical composition comprising an effective amount of a compound with formula I, or a pharmaceutically acceptable salt, and a pharmaceutically acceptable carrier.
- NB-206 and its analogs have potent inhibitory activity on infection by laboratory-adapted and primary HIV-I strains
- T-20 targets the viral envelope glycoprotein gp41 (14,38,41,42).
- T-20 like other peptides derived from the HIV-I gp41 CHR region, such as SJ-2176 (11,43) and C34 (17) , inhibits HIV-I fusion and entry. It has shown great promise against HIV replication in clinical trials (14,44). However, it has two major limitations: lack of oral availability (delivered by subcutaneous injection) and high cost of production (40) . Thus, development of small molecule HIV-I fusion inhibitors is urgently needed.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Virology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA002608821A CA2608821A1 (en) | 2005-06-15 | 2006-06-06 | Anti-viral compositions comprising heterocyclic substituted phenyl furans and related compounds |
| JP2008516935A JP2008543836A (ja) | 2005-06-15 | 2006-06-06 | 複素環置換フェニルフランおよび関連化合物を含む抗ウイルス組成物 |
| EP06772346A EP1896033A4 (en) | 2005-06-15 | 2006-06-06 | ANTIVIRAL COMPOSITIONS WITH HETEROCYCLIC SUBSTITUTED PHENYLFURANES AND RELATED COMPOUNDS |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US69112005P | 2005-06-15 | 2005-06-15 | |
| US60/691,120 | 2005-06-15 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| WO2006138118A2 true WO2006138118A2 (en) | 2006-12-28 |
| WO2006138118A3 WO2006138118A3 (en) | 2007-07-26 |
| WO2006138118B1 WO2006138118B1 (en) | 2007-09-20 |
Family
ID=37570970
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US2006/021993 Ceased WO2006138118A2 (en) | 2005-06-15 | 2006-06-06 | Anti-viral compositions comprising heterocyclic substituted phenyl furans and related compounds |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US20060287319A1 (enExample) |
| EP (1) | EP1896033A4 (enExample) |
| JP (1) | JP2008543836A (enExample) |
| CA (1) | CA2608821A1 (enExample) |
| WO (1) | WO2006138118A2 (enExample) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011502998A (ja) * | 2007-11-01 | 2011-01-27 | ザ ユーエイビー リサーチ ファウンデイション | ウイルス感染の治療および予防 |
| US8455516B2 (en) | 2010-01-15 | 2013-06-04 | Touro University | HIV-1 fusion inhibitors and methods |
| CN103402516A (zh) * | 2010-06-17 | 2013-11-20 | 富津世生物技术有限公司 | 用作抗病毒药物的化合物、组合物及使用方法 |
| WO2024260445A1 (zh) * | 2023-06-21 | 2024-12-26 | 上海科技大学 | 一种噻唑烷二酮类化合物、其药物组合物和其用途 |
| US12421626B2 (en) | 2018-06-29 | 2025-09-23 | Fred Hutchinson Cancer Center | Cell-stored barcoded deep mutational scanning libraries and uses of the same |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7728013B2 (en) | 2005-05-10 | 2010-06-01 | Intermune, Inc. | Method of modulating stress-activated protein kinase system |
| US20070099970A1 (en) * | 2005-08-19 | 2007-05-03 | Mackerell Alexander | Immunomodulatory compounds that target and inhibit the pY'binding site of tyrosene kinase p56 LCK SH2 domain |
| US8304413B2 (en) | 2008-06-03 | 2012-11-06 | Intermune, Inc. | Compounds and methods for treating inflammatory and fibrotic disorders |
| AR081930A1 (es) | 2010-06-16 | 2012-10-31 | Ardea Biosciences Inc | Compuestos de tioacetato |
| US9023876B2 (en) * | 2010-07-08 | 2015-05-05 | Adhaere Pharmaceuticals, Inc. | Compounds and methods for regulating integrins |
| ES2766751T3 (es) | 2012-04-20 | 2020-06-15 | Gb006 Inc | Composiciones para la regulación de integrinas |
| AR092742A1 (es) | 2012-10-02 | 2015-04-29 | Intermune Inc | Piridinonas antifibroticas |
| CN103724337A (zh) * | 2012-10-15 | 2014-04-16 | 南京大学 | 一类含萘环和噻唑啉酮结构的吡唑啉类衍生物及其制法 |
| WO2015153683A1 (en) | 2014-04-02 | 2015-10-08 | Intermune, Inc. | Anti-fibrotic pyridinones |
| CN111747944B (zh) * | 2020-07-13 | 2022-09-30 | 复旦大学 | 广谱抗包膜病毒化合物、组合物及其应用 |
| WO2022225572A1 (en) * | 2021-04-22 | 2022-10-27 | New York Blood Center, Inc. | Respiratory virus inhibitors |
| CN115444846A (zh) * | 2022-09-01 | 2022-12-09 | 中国人民解放军军事科学院军事医学研究院 | HIV-1Tat蛋白抑制剂及其应用 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR9913157A (pt) * | 1998-08-21 | 2001-05-15 | Viropharma Inc | Processos para tratar ou previnir infecção causada por pelo menos um vìrus das flaviviridae e doenças associadas com a referida infecção e infecção causada por pelo menos um vìrus do gênero hepacivìrus da flaviviridade e doenças associadas com a referida infecção, composição farmacêutica para tratar ou previnir infecções virais, e, composto |
| US20050042674A9 (en) * | 2002-02-21 | 2005-02-24 | Lin Yu | Common ligand mimics: thiazolidinediones and rhodanines |
| US20040002526A1 (en) * | 2002-04-03 | 2004-01-01 | Cell Therapeutics, Inc. | Phospholipase D inhibitors and uses thereof |
| AU2003294275A1 (en) * | 2002-11-21 | 2004-06-18 | New York Blood Center | Compounds for inhibition of hiv infection by blocking hiv entry |
| EP1651226B1 (en) * | 2003-07-11 | 2010-02-24 | Proteologics, Inc. | Ubiquitin ligase inhibitors and methods related thereto |
| EP1654380A4 (en) * | 2003-08-14 | 2009-09-09 | Insight Biopharmaceuticals Ltd | METHODS AND PHARMACEUTICAL COMPOSITIONS FOR MODULATING HEPARANASE ACTIVATION AND USES THEREOF |
| US7566732B2 (en) * | 2003-10-28 | 2009-07-28 | Rigel Pharmaceuticals, Inc. | Rhodanine compositions for use as antiviral agents |
-
2006
- 2006-06-06 US US11/448,439 patent/US20060287319A1/en not_active Abandoned
- 2006-06-06 JP JP2008516935A patent/JP2008543836A/ja not_active Withdrawn
- 2006-06-06 CA CA002608821A patent/CA2608821A1/en not_active Abandoned
- 2006-06-06 WO PCT/US2006/021993 patent/WO2006138118A2/en not_active Ceased
- 2006-06-06 EP EP06772346A patent/EP1896033A4/en not_active Withdrawn
Non-Patent Citations (1)
| Title |
|---|
| See references of EP1896033A4 * |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011502998A (ja) * | 2007-11-01 | 2011-01-27 | ザ ユーエイビー リサーチ ファウンデイション | ウイルス感染の治療および予防 |
| US8455516B2 (en) | 2010-01-15 | 2013-06-04 | Touro University | HIV-1 fusion inhibitors and methods |
| CN103402516A (zh) * | 2010-06-17 | 2013-11-20 | 富津世生物技术有限公司 | 用作抗病毒药物的化合物、组合物及使用方法 |
| US12421626B2 (en) | 2018-06-29 | 2025-09-23 | Fred Hutchinson Cancer Center | Cell-stored barcoded deep mutational scanning libraries and uses of the same |
| WO2024260445A1 (zh) * | 2023-06-21 | 2024-12-26 | 上海科技大学 | 一种噻唑烷二酮类化合物、其药物组合物和其用途 |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2006138118B1 (en) | 2007-09-20 |
| CA2608821A1 (en) | 2006-12-28 |
| EP1896033A2 (en) | 2008-03-12 |
| EP1896033A4 (en) | 2010-12-22 |
| US20060287319A1 (en) | 2006-12-21 |
| WO2006138118A3 (en) | 2007-07-26 |
| JP2008543836A (ja) | 2008-12-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Jiang et al. | N-substituted pyrrole derivatives as novel human immunodeficiency virus type 1 entry inhibitors that interfere with the gp41 six-helix bundle formation and block virus fusion | |
| Zhao et al. | Identification of N-phenyl-N′-(2, 2, 6, 6-tetramethyl-piperidin-4-yl)-oxalamides as a new class of HIV-1 entry inhibitors that prevent gp120 binding to CD4 | |
| WO2006138118A2 (en) | Anti-viral compositions comprising heterocyclic substituted phenyl furans and related compounds | |
| Lu et al. | Development of small-molecule HIV entry inhibitors specifically targeting gp120 or gp41 | |
| Jiang et al. | A screening assay for antiviral compounds targeted to the HIV-1 gp41 core structure using a conformation-specific monoclonal antibody | |
| US20070232684A1 (en) | Compounds for inhibition of HIV infection by blocking HIV entry | |
| Liu et al. | Different from the HIV fusion inhibitor C34, the anti-HIV drug Fuzeon (T-20) inhibits HIV-1 entry by targeting multiple sites in gp41 and gp120 | |
| Liu et al. | Theaflavin derivatives in black tea and catechin derivatives in green tea inhibit HIV-1 entry by targeting gp41 | |
| Schmidt et al. | Small-molecule inhibitors of dengue-virus entry | |
| O’Keefe et al. | Analysis of the interaction between the HIV-inactivating protein cyanovirin-N and soluble forms of the envelope glycoproteins gp120 and gp41 | |
| US20090176776A1 (en) | Small molecule inhibitors of hiv-1 capsid assembly | |
| An et al. | Amino acid derivatives of the (−) enantiomer of gossypol are effective fusion inhibitors of human immunodeficiency virus type 1 | |
| EP1161564A1 (en) | SCREENING OF ANTIVIRAL COMPOUNDS TARGETED TO THE HIV-1 gp41 CORE STRUCTURE | |
| He et al. | Conserved salt bridge between the N-and C-terminal heptad repeat regions of the human immunodeficiency virus type 1 gp41 core structure is critical for virus entry and inhibition | |
| Urvashi et al. | Development of azaindole-based frameworks as potential antiviral agents and their future perspectives | |
| Zhao et al. | XTT formazan widely used to detect cell viability inhibits HIV type 1 infection in vitro by targeting gp41 | |
| Zhang et al. | Identification of an HIV-1 replication inhibitor which rescues host restriction factor APOBEC3G in Vif–APOBEC3G complex | |
| Pan et al. | Combinations of the first and next generations of human immunodeficiency virus (HIV) fusion inhibitors exhibit a highly potent synergistic effect against enfuvirtide-sensitive and-resistant HIV type 1 strains | |
| Cale et al. | Antigenic analysis of the HIV-1 envelope trimer implies small differences between structural states 1 and 2 | |
| TW200409629A (en) | 2,4-disubstituted-pyridine N-oxides useful as HIV reverse transcriptase inhibitors | |
| US10300080B2 (en) | Methods and compounds to inhibit enveloped virus release | |
| Garg et al. | Mechanism of feline immunodeficiency virus envelope glycoprotein-mediated fusion | |
| Pu et al. | Rational design of a novel small-molecule HIV-1 inactivator targeting both gp120 and gp41 of HIV-1 | |
| Yu et al. | Identification of a novel small-molecule inhibitor of the HIV-1 reverse transcriptase activity with a non-nucleoside mode of action | |
| US20220348569A1 (en) | Respiratory virus inhibitors |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
| ENP | Entry into the national phase |
Ref document number: 2608821 Country of ref document: CA |
|
| WWE | Wipo information: entry into national phase |
Ref document number: 2006772346 Country of ref document: EP |
|
| ENP | Entry into the national phase |
Ref document number: 2008516935 Country of ref document: JP Kind code of ref document: A |
|
| NENP | Non-entry into the national phase |
Ref country code: DE |