Homma et al., 1992 - Google Patents
Nucleosides and nucleotides. 112. 2-(1-Hexyn-1-yl) adenosine-5'-uronamides: a new entry of selective A2 adenosine receptor agonists with potent antihypertensive …Homma et al., 1992
- Document ID
- 12266999144120172856
- Author
- Homma H
- Watanabe Y
- Abiru T
- Murayama T
- Nomura Y
- Matsuda A
- Publication year
- Publication venue
- Journal of medicinal chemistry
External Links
Snippet
Chemical modificationsof the potent A2 adenosine receptor agonist 2-(l-hexyn-l-yl) adenosine (7, 2-HA) at the S'-position have been carried out to find more potent andselective A2 agonists. These analogues were evaluated for adenosine and A2 receptor …
- 230000003389 potentiating 0 title abstract description 21
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/16—Purine radicals
- C07H19/20—Purine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/06—Pyrimidine radicals
- C07H19/10—Pyrimidine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids
-
- 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
- A61K31/70—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
- A61K31/7068—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 having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
- A61K31/7072—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 having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid having two oxo groups directly attached to the pyrimidine ring, e.g. uridine, uridylic acid, thymidine, zidovudine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C335/00—Thioureas, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C335/04—Derivatives of thiourea
- C07C335/16—Derivatives of thiourea having nitrogen atoms of thiourea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Homma et al. | Nucleosides and nucleotides. 112. 2-(1-Hexyn-1-yl) adenosine-5'-uronamides: a new entry of selective A2 adenosine receptor agonists with potent antihypertensive activity | |
FI93217B (en) | Process for the preparation of esters and amides of therapeutically active nucleoside derivatives | |
Matsuda et al. | Nucleosides and nucleotides. 103. 2-Alkynyladenosines: a novel class of selective adenosine A2 receptor agonists with potent antihypertensive effects | |
ES2201552T3 (en) | ADENOSINE RECEIVER A1 AGONISTS. | |
DK170893B1 (en) | New 5'-deoxy-5-fluorocytidine derivatives, a process for the preparation thereof, pharmaceutical agents containing such derivatives and the use of the derivatives to prepare an antitumor agent | |
Watanabe et al. | Synthesis and anti-HIV-1 activity of 2'-" up"-fluoro analogs of active anti-AIDS nucleosides 3'-azido-3'-deoxythymidine (AZT) and 2', 3'-dideoxycytidine (DDC) | |
WO2003062256A1 (en) | 2'-beta-modified-6-substituted adenosine analogs and their use as antiviral agents | |
CA2685748A1 (en) | Azido purine nucleosides for treatment of viral infections | |
FI81587B (en) | FOERFARANDE FOER FRAMSTAELLNING AV FARMACEUTISKT ANVAENDBARA N6-SUBSTITUERADE DEOXIRIBOSANALOGER AV ADENOSINER. | |
CA3085337A1 (en) | Cyclic dinucleotides as sting agonists | |
WO2011005595A2 (en) | 2-5a analogs and their methods of use | |
US20020150936A1 (en) | Methods for synthesizing nucleosides, nucleoside derivatives and non-nucleoside derivatives | |
WO2010068708A2 (en) | 3'-azido purine nucleotide prodrugs for treatment of viral infections | |
FI77666B (en) | FOERFARANDE FOER FRAMSTAELLNING AV PHARMACEUTISKT ANVAENDBARA N6-SUBSTITUERADE ADENOSINER. | |
Gawin et al. | Synthesis and antiviral evaluation of acyclic azanucleosides developed from sulfanilamide as a lead structure | |
CN102285969B (en) | N-1-substituted piperidin-4-arylamine derivatives and preparation method and use thereof | |
US5229505A (en) | N6 -[3-(1-substituted)indolylethyl] adenosine 5'-carboxamides and their pharmaceutical compositions | |
WO2003053989A1 (en) | Masked phosphate containing nucleoside derivatives and their use as antivirals | |
AU616914B2 (en) | Therapeutic necleosides | |
DE68918036T2 (en) | Nucleoside derivatives. | |
Zhang et al. | Synthesis of neplanocin F analogues as potential antiviral agents | |
CA1262898A (en) | 2,n.sup.6-substituted adenosines derivatives and methods of use | |
Narayanasamy et al. | Synthesis and anti-HIV activity of (−)-β-d-(2R, 4R)-1, 3-dioxolane-2, 6-diamino purine (DAPD)(amdoxovir) and (−)-β-d-(2R, 4R)-1, 3-dioxolane guanosine (DXG) prodrugs | |
Wang et al. | Synthesis and in vitro anti-hepatitis B virus activity of six-membered azanucleoside analogues | |
JPH0692986A (en) | Substituted nucleoside derivative, its production and medicinal composition containing it |