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New potent and selective human adenosine A3 receptor antagonists
被引:55
作者
:
Baraldi, PG
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Ferrara, Dipartimento Med Clin & Expt, Sez Farmacol, I-44100 Ferrara, Italy
Baraldi, PG
Borea, PA
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Ferrara, Dipartimento Med Clin & Expt, Sez Farmacol, I-44100 Ferrara, Italy
Borea, PA
机构
:
[1]
Univ Ferrara, Dipartimento Med Clin & Expt, Sez Farmacol, I-44100 Ferrara, Italy
[2]
Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
来源
:
TRENDS IN PHARMACOLOGICAL SCIENCES
|
2000年
/ 21卷
/ 12期
关键词
:
D O I
:
10.1016/S0165-6147(00)01581-9
中图分类号
:
R9 [药学];
学科分类号
:
1007 ;
摘要
:
引用
收藏
页码:456 / 459
页数:4
相关论文
共 26 条
[1]
The A3 adenosine receptor mediates cell spreading, reorganization of actin cytoskeleton, and distribution of Bcl-xL:: Studies in human astroglioma cells
[J].
Abbracchio, MP
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Milan, Inst Pharmacol Sci, Milan, Italy
Univ Milan, Inst Pharmacol Sci, Milan, Italy
Abbracchio, MP
;
Rainaldi, G
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Milan, Inst Pharmacol Sci, Milan, Italy
Rainaldi, G
;
Giammarioli, AM
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Milan, Inst Pharmacol Sci, Milan, Italy
Giammarioli, AM
;
Ceruti, S
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Milan, Inst Pharmacol Sci, Milan, Italy
Ceruti, S
;
Brambilla, R
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Milan, Inst Pharmacol Sci, Milan, Italy
Brambilla, R
;
Cattabeni, F
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Milan, Inst Pharmacol Sci, Milan, Italy
Cattabeni, F
;
Barbieri, D
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Milan, Inst Pharmacol Sci, Milan, Italy
Barbieri, D
;
Franceschi, C
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0
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0
h-index:
0
机构:
Univ Milan, Inst Pharmacol Sci, Milan, Italy
Franceschi, C
;
Jacobson, KA
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机构:
Univ Milan, Inst Pharmacol Sci, Milan, Italy
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;
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Univ Milan, Inst Pharmacol Sci, Milan, Italy
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Pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]-pyrimidine derivatives as highly potent and selective human A3 adenosine receptor antagonists
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0
引用数:
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h-index:
0
机构:
Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
Baraldi, PG
;
Cacciari, B
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0
引用数:
0
h-index:
0
机构:
Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
Cacciari, B
;
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机构:
Romagnoli, R
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Spalluto, G
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0
机构:
Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
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;
Klotz, KN
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0
引用数:
0
h-index:
0
机构:
Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
Klotz, KN
;
Leung, E
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0
引用数:
0
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0
机构:
Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
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Varani, K
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Synthesis and biological activity of a new series of N6-arylcarbamoyl, 2-(Ar)alkynyl-N6-arylcarbamoyl, and N6-carboxamido derivatives of adenosine-5′-N-ethyluronamide as A1 and A3 adenosine receptor agonists
[J].
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论文数:
0
引用数:
0
h-index:
0
机构:
Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
Baraldi, PG
;
Cacciari, B
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
Cacciari, B
;
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论文数:
0
引用数:
0
h-index:
0
机构:
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;
论文数:
引用数:
h-index:
机构:
Romagnoli, R
;
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机构:
Spalluto, G
;
Volpini, R
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0
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0
h-index:
0
机构:
Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
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;
Costanzi, S
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
Costanzi, S
;
Vittori, S
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
Vittori, S
;
Cristalli, G
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
Cristalli, G
;
Melman, N
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
Melman, N
;
Park, KS
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0
引用数:
0
h-index:
0
机构:
Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
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;
Ji, XD
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0
引用数:
0
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0
机构:
Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
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;
Jacobson, KA
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0
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0
h-index:
0
机构:
NIDDKD,BIOORGAN CHEM LAB,MOLEC RECOGNIT SECT,NATL INST HLTH,BETHESDA,MD 20892
Baraldi, PG
;
Cacciari, B
论文数:
0
引用数:
0
h-index:
0
机构:
NIDDKD,BIOORGAN CHEM LAB,MOLEC RECOGNIT SECT,NATL INST HLTH,BETHESDA,MD 20892
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;
Spalluto, G
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0
引用数:
0
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0
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NIDDKD,BIOORGAN CHEM LAB,MOLEC RECOGNIT SECT,NATL INST HLTH,BETHESDA,MD 20892
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;
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0
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0
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0
机构:
NIDDKD,BIOORGAN CHEM LAB,MOLEC RECOGNIT SECT,NATL INST HLTH,BETHESDA,MD 20892
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0
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0
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NIDDKD,BIOORGAN CHEM LAB,MOLEC RECOGNIT SECT,NATL INST HLTH,BETHESDA,MD 20892
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;
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论文数:
0
引用数:
0
h-index:
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机构:
NIDDKD,BIOORGAN CHEM LAB,MOLEC RECOGNIT SECT,NATL INST HLTH,BETHESDA,MD 20892
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0
引用数:
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h-index:
0
机构:
NIDDKD,BIOORGAN CHEM LAB,MOLEC RECOGNIT SECT,NATL INST HLTH,BETHESDA,MD 20892
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;
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0
引用数:
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0
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NIDDKD,BIOORGAN CHEM LAB,MOLEC RECOGNIT SECT,NATL INST HLTH,BETHESDA,MD 20892
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0
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0
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Univ Florence, Dipartimento Sci Farmaceut, I-50121 Florence, Italy
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Kuwait Univ, Fac Med, Dept Pharmacol & Toxicol, Safat, Kuwait
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Queens Univ Belfast, Dept Clin Biochem, Belfast BT12 6BJ, Antrim, North Ireland
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共 26 条
[1]
The A3 adenosine receptor mediates cell spreading, reorganization of actin cytoskeleton, and distribution of Bcl-xL:: Studies in human astroglioma cells
[J].
Abbracchio, MP
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Milan, Inst Pharmacol Sci, Milan, Italy
Univ Milan, Inst Pharmacol Sci, Milan, Italy
Abbracchio, MP
;
Rainaldi, G
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Milan, Inst Pharmacol Sci, Milan, Italy
Rainaldi, G
;
Giammarioli, AM
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Milan, Inst Pharmacol Sci, Milan, Italy
Giammarioli, AM
;
Ceruti, S
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Milan, Inst Pharmacol Sci, Milan, Italy
Ceruti, S
;
Brambilla, R
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Milan, Inst Pharmacol Sci, Milan, Italy
Brambilla, R
;
Cattabeni, F
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Milan, Inst Pharmacol Sci, Milan, Italy
Cattabeni, F
;
Barbieri, D
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Milan, Inst Pharmacol Sci, Milan, Italy
Barbieri, D
;
Franceschi, C
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Milan, Inst Pharmacol Sci, Milan, Italy
Franceschi, C
;
Jacobson, KA
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Milan, Inst Pharmacol Sci, Milan, Italy
Jacobson, KA
;
Malorni, W
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0
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0
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0
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Univ Milan, Inst Pharmacol Sci, Milan, Italy
Malorni, W
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241
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Pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]-pyrimidine derivatives as highly potent and selective human A3 adenosine receptor antagonists
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Baraldi, PG
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
Baraldi, PG
;
Cacciari, B
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
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引用数:
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机构:
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0
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0
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0
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0
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0
引用数:
0
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引用数:
h-index:
机构:
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Borea, PA
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0
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0
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42
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-4478
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Synthesis and biological activity of a new series of N6-arylcarbamoyl, 2-(Ar)alkynyl-N6-arylcarbamoyl, and N6-carboxamido derivatives of adenosine-5′-N-ethyluronamide as A1 and A3 adenosine receptor agonists
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Baraldi, PG
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
Baraldi, PG
;
Cacciari, B
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
Cacciari, B
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论文数:
0
引用数:
0
h-index:
0
机构:
Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
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论文数:
引用数:
h-index:
机构:
Romagnoli, R
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论文数:
引用数:
h-index:
机构:
Spalluto, G
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Volpini, R
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
Volpini, R
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Costanzi, S
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
Costanzi, S
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Vittori, S
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
Vittori, S
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Cristalli, G
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
Cristalli, G
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Melman, N
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
Melman, N
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Park, KS
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
Park, KS
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Ji, XD
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
Ji, XD
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Jacobson, KA
论文数:
0
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0
h-index:
0
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Univ Ferrara, Dipartimento Sci Farmaceut, I-44100 Ferrara, Italy
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Baraldi, PG
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0
引用数:
0
h-index:
0
机构:
NIDDKD,BIOORGAN CHEM LAB,MOLEC RECOGNIT SECT,NATL INST HLTH,BETHESDA,MD 20892
Baraldi, PG
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Cacciari, B
论文数:
0
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