WO2009082720A3 - Substituted 4-{3-[6-amino-9-(3,4-dihydroxy-tetrahydro-furan-2-yl)-9h-purin-2-yl]-prop-2-ynyl}-piperidine-1-carboxylic acid esters as a2ar agonists - Google Patents

Substituted 4-{3-[6-amino-9-(3,4-dihydroxy-tetrahydro-furan-2-yl)-9h-purin-2-yl]-prop-2-ynyl}-piperidine-1-carboxylic acid esters as a2ar agonists Download PDF

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Publication number
WO2009082720A3
WO2009082720A3 PCT/US2008/087875 US2008087875W WO2009082720A3 WO 2009082720 A3 WO2009082720 A3 WO 2009082720A3 US 2008087875 W US2008087875 W US 2008087875W WO 2009082720 A3 WO2009082720 A3 WO 2009082720A3
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WO
WIPO (PCT)
Prior art keywords
purin
ynyl
furan
tetrahydro
dihydroxy
Prior art date
Application number
PCT/US2008/087875
Other languages
French (fr)
Other versions
WO2009082720A2 (en
Inventor
Robert Thompson
Anthony Beauglehole
Frank Schmidtmann
Jayson Rieger
Original Assignee
Pgx Health, Llc
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
Priority to EP08864942A priority Critical patent/EP2234490A4/en
Priority to US12/809,381 priority patent/US8252767B2/en
Priority to JP2010539923A priority patent/JP2011507907A/en
Priority to CN2008801251885A priority patent/CN101938906A/en
Priority to AU2008340186A priority patent/AU2008340186B2/en
Priority to NZ586670A priority patent/NZ586670A/en
Priority to CA2710151A priority patent/CA2710151A1/en
Priority to MX2010006645A priority patent/MX2010006645A/en
Application filed by Pgx Health, Llc filed Critical Pgx Health, Llc
Priority to EA201001031A priority patent/EA019244B1/en
Priority to BRPI0821071-3A priority patent/BRPI0821071A2/en
Publication of WO2009082720A2 publication Critical patent/WO2009082720A2/en
Publication of WO2009082720A3 publication Critical patent/WO2009082720A3/en
Priority to IL206477A priority patent/IL206477A0/en
Priority to ZA2010/04535A priority patent/ZA201004535B/en

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    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H19/00Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
    • C07H19/02Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
    • C07H19/04Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
    • C07H19/16Purine radicals
    • C07H19/167Purine radicals with ribosyl as the saccharide radical
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Abstract

The present invention provides substituted 4-{3-[6-amino-9-(3,4-dihydroxy-tetrahydro-furan-2-yl)-9H-purin-2-yl]-prop-2-ynyl}-piperidine-1-carboxylic acid esters and pharmaceutical compositions containg the same that are selective agonists of A2A adenosine receptors (ARs). These compounds and compositions are useful as pharmaceutical agents.
PCT/US2008/087875 2007-12-20 2008-12-20 Substituted 4-{3-[6-amino-9-(3,4-dihydroxy-tetrahydro-furan-2-yl)-9h-purin-2-yl]-prop-2-ynyl}-piperidine-1-carboxylic acid esters as a2ar agonists WO2009082720A2 (en)

Priority Applications (12)

Application Number Priority Date Filing Date Title
CA2710151A CA2710151A1 (en) 2007-12-20 2008-12-20 Substituted 4-{3-[6-amino-9-(3,4-dihydroxy-tetrahydro-furan-2-yl)-9h-purin-2-yl]-prop-2-ynyl}-piperidine-1-carboxylic acid esters as a2ar agonists
JP2010539923A JP2011507907A (en) 2007-12-20 2008-12-20 Substituted 4- {3- [6-amino-9- (3,4-dihydroxy-tetrahydro-furan-2-yl) -9H-purin-2-yl] -prop-2-ynyl} -piperidine as an A2AR agonist -1-carboxylic acid ester
CN2008801251885A CN101938906A (en) 2007-12-20 2008-12-20 Substituted 4-{3-[6-amino-9-(3, 4-dihydroxy-tetrahydrofuran-2-yl)-9H-purin-2-yl]-propan-2-ynyl}-piperidine-1-carboxylic acid ester as A2AR agonist
AU2008340186A AU2008340186B2 (en) 2007-12-20 2008-12-20 Substituted 4-{3-[6-amino-9-(3,4-dihydroxy-tetrahydro-furan-2-yl)-9H-purin-2-yl]-prop-2-ynyl} -piperidine-1-carboxylic acid esters as A2AR agonists
NZ586670A NZ586670A (en) 2007-12-20 2008-12-20 Substituted 4-{ 3-[6-amino-9-(3,4-dihydroxy-tetrahydro-furan-2-yl)-9h-purin-2-yl]-prop-2-ynyl} -piperidine-1-carboxylic acid esters as a2ar agonists
EP08864942A EP2234490A4 (en) 2007-12-20 2008-12-20 Substituted 4-{3-ý6-amino-9-(3,4-dihydroxy-tetrahydro-furan-2-yl)-9h-purin-2-yl¨-prop-2-ynyl}-piperidine-1-carboxylic acid esters as a2ar agonists
MX2010006645A MX2010006645A (en) 2007-12-20 2008-12-20 Substituted 4-{3-[6-amino-9-(3,4-dihydroxy-tetrahydro-furan-2-yl) -9h-purin-2-yl]-prop-2-ynyl}-piperidine-1-carboxylic acid esters as a2ar agonists.
US12/809,381 US8252767B2 (en) 2007-12-20 2008-12-20 Substituted 4-{3-[6-amino-9-(3, 4-dihydroxy-tetrahydro-furan-2-yl)-9H-purin-2-yl]-prop-2-ynyl}-piperidine-1-carboxylic acid esters as A2AR agonists
EA201001031A EA019244B1 (en) 2007-12-20 2008-12-20 Substituted 4-{3-[6-amino-9-(3,4-dihydroxy-tetrahydro-furan-2-yl)-9h-purin-2-yl]-prop-2-ynyl}piperidine-1-carboxylic acid esters and use thereof
BRPI0821071-3A BRPI0821071A2 (en) 2007-12-20 2008-12-20 Substituted 4- {3- [6-amino-9- (3,4-dihydroxy-tetrahydro-furan-2-yl) -9h-p-urin-2yl] -prop-2-yl} -piperidine-1-carboxylic acid esters as a2ar agonists
IL206477A IL206477A0 (en) 2007-12-20 2010-06-17 Substituted 4-{3-[6-amino-9-(3,4-dihydroxy-tetrahydro-furan-2-yl)-9h-purin-2-yl]-prop-2-ynyl}-piperidine-1-carboxylic acid esters as a2ar agonists
ZA2010/04535A ZA201004535B (en) 2007-12-20 2010-06-25 Substituted 4-{3-[6-amino-9-(3,4-dihydroxy-tetrahydro-furan-2-yl)-9h-purin-2-yl]-prop-2-ynyl}-piperidine-1-carboxylic acid esters as a2ar agonists

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US1530307P 2007-12-20 2007-12-20
US61/015,303 2007-12-20

Publications (2)

Publication Number Publication Date
WO2009082720A2 WO2009082720A2 (en) 2009-07-02
WO2009082720A3 true WO2009082720A3 (en) 2009-08-27

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PCT/US2008/087875 WO2009082720A2 (en) 2007-12-20 2008-12-20 Substituted 4-{3-[6-amino-9-(3,4-dihydroxy-tetrahydro-furan-2-yl)-9h-purin-2-yl]-prop-2-ynyl}-piperidine-1-carboxylic acid esters as a2ar agonists

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US (2) US8293720B2 (en)
EP (1) EP2234490A4 (en)
JP (1) JP2011507907A (en)
KR (1) KR20100103631A (en)
CN (1) CN101938906A (en)
AU (1) AU2008340186B2 (en)
BR (1) BRPI0821071A2 (en)
CA (1) CA2710151A1 (en)
EA (1) EA019244B1 (en)
IL (1) IL206477A0 (en)
MX (1) MX2010006645A (en)
NZ (1) NZ586670A (en)
SG (1) SG186676A1 (en)
UA (1) UA100035C2 (en)
WO (1) WO2009082720A2 (en)
ZA (1) ZA201004535B (en)

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JP5046930B2 (en) * 2004-08-02 2012-10-10 ユニバーシティ オブ バージニア パテント ファウンデーション 2-propynyladenosine analogs with modified 5'-ribose groups having A2A agonist activity
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US9822141B2 (en) 2012-08-01 2017-11-21 Lewis And Clark Pharmaceuticals, Inc. N-alkyl 2-(disubstituted)alkynyladenosine-5-uronamides as A2A agonists
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KR102532198B1 (en) 2012-12-21 2023-05-11 얀센 바이오파마, 인코퍼레이트. Substituted nucleosides, nucleotides and analogs thereof
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BRPI0821071A2 (en) 2015-06-16
US8252767B2 (en) 2012-08-28
ZA201004535B (en) 2012-09-26
EP2234490A4 (en) 2013-03-27
NZ586670A (en) 2012-10-26
UA100035C2 (en) 2012-11-12
AU2008340186A8 (en) 2010-07-29
MX2010006645A (en) 2010-10-05
US20090162292A1 (en) 2009-06-25
AU2008340186B2 (en) 2014-07-10
SG186676A1 (en) 2013-01-30
IL206477A0 (en) 2010-12-30
AU2008340186A1 (en) 2009-07-02
CN101938906A (en) 2011-01-05
KR20100103631A (en) 2010-09-27
WO2009082720A2 (en) 2009-07-02
CA2710151A1 (en) 2009-07-02
US8293720B2 (en) 2012-10-23
EA019244B1 (en) 2014-02-28
EP2234490A2 (en) 2010-10-06
US20110003765A1 (en) 2011-01-06
EA201001031A1 (en) 2011-02-28
JP2011507907A (en) 2011-03-10

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