Zhong et al., 2014 - Google Patents
Discovery of functionalized bisimidazoles bearing cyclic aliphatic-phenyl motifs as HCV NS5A inhibitorsZhong et al., 2014
- Document ID
- 10239553268791020989
- Author
- Zhong M
- Peng E
- Huang N
- Huang Q
- Huq A
- Lau M
- Colonno R
- Li L
- Publication year
- Publication venue
- Bioorganic & Medicinal Chemistry Letters
External Links
Snippet
This Letter describes the discovery of a number of functionalized bisimidazoles bearing a cyclohexylphenyl, piperidylphenyl, or bicyclo [2, 2, 2] octylphenyl motif as HCV NS5A inhibitors. Compounds 2c, 4b and 6 have demonstrated low single-digit nM potency in gt-1a …
- 101800001014 Non-structural protein 5A 0 title abstract description 18
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET 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, rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET 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, rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine, 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
-
- 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 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 C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/19—Cytokines; Lymphokines; Interferons
- A61K38/21—Interferons [IFN]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Zhong et al. | Discovery of functionalized bisimidazoles bearing cyclic aliphatic-phenyl motifs as HCV NS5A inhibitors | |
Lin et al. | Curing a viral infection by targeting the host: the example of cyclophilin inhibitors | |
ES2680550T3 (en) | Hepatitis C virus inhibitor combinations | |
Hwang et al. | Synthesis and anti-viral activity of a series of sesquiterpene lactones and analogues in the subgenomic HCV replicon system | |
Rai et al. | New opportunities in anti-hepatitis C virus drug discovery: targeting NS4B | |
Schmitz et al. | NS5A-from obscurity to new target for HCV therapy | |
Narjes et al. | Discovery of (7 R)-14-cyclohexyl-7-{[2-(dimethylamino) ethyl](methyl) amino}-7, 8-dihydro-6 H-indolo [1, 2-e][1, 5] benzoxazocine-11-carboxylic acid (MK-3281), a potent and orally bioavailable finger-loop inhibitor of the hepatitis C virus NS5B polymerase | |
Huang et al. | Recent development of therapeutics for chronic HCV infection | |
CA2369970A1 (en) | Hepatitis c inhibitor tri-peptides | |
Zhong et al. | Discovery of novel potent HCV NS5B polymerase non-nucleoside inhibitors bearing a fused benzofuran scaffold | |
TW200838529A (en) | Macrocyclic inhibitors of hepatitis C virus | |
Chen et al. | C-6 aryl substituted 4-quinolone-3-carboxylic acids as inhibitors of hepatitis C virus | |
Pawlotsky | What are the pros and cons of the use of host-targeted agents against hepatitis C? | |
Zhong et al. | Discovery of ravidasvir (PPI-668) as a potent pan-genotypic HCV NS5A inhibitor | |
Zoidis et al. | Novel indole–flutimide heterocycles with activity against influenza PA endonuclease and hepatitis C virus | |
Zhang et al. | Discovery and evolution of aloperine derivatives as a new family of HCV inhibitors with novel mechanism | |
Venkatraman et al. | Discovery and structure− activity relationship of P1− P3 ketoamide derived macrocyclic inhibitors of hepatitis C virus NS3 protease | |
Dwyer et al. | Matched and mixed cap derivatives in the tetracyclic indole class of HCV NS5A inhibitors | |
Ruebsam et al. | Pyrrolo [1, 2-b] pyridazin-2-ones as potent inhibitors of HCV NS5B polymerase | |
Zhong et al. | Potent bisimidazole-based HCV NS5A inhibitors bearing annulated tricyclic motifs | |
Chen et al. | The journey to the discovery of boceprevir: an NS3–NS4 HCV protease inhibitor for the treatment of chronic hepatitis C | |
Avolio et al. | Inhibitors of hepatitis C virus NS3/4A: α-Ketoamide based macrocyclic inhibitors | |
US20110064694A1 (en) | Anti-hepatitis c activity of meso-tetrakis-porphyrin analogues | |
Zhong et al. | Structure–activity relationship studies on quinoxalin-2 (1 H)-one derivatives containing thiazol-2-amine against hepatitis C virus leading to the discovery of BH6870 | |
Kang et al. | Synthesis, activity, and pharmacokinetic properties of a series of conformationally-restricted thiourea analogs as novel hepatitis C virus inhibitors |