Platelet aggregation inhibitors. 4. N 6 -substituted adenosines.
作者信息
Kikugawa K, Iizuka K, Ichino M
出版信息
J Med Chem. 1973 Apr;16(4):358-64. doi: 10.1021/jm00262a011.
PMID:4716180
Abstract
摘要
相似文献
1
Platelet aggregation inhibitors. 4. N 6 -substituted adenosines.血小板聚集抑制剂。4. N⁶-取代腺苷。
J Med Chem. 1973 Apr;16(4):358-64. doi: 10.1021/jm00262a011.
2
Platelet aggregation inhibitors. 2. Inhibition of platelet aggregation by 5'-, 2-, 6-, and 8-substituted adenosines.
J Med Chem. 1972 Apr;15(4):387-90. doi: 10.1021/jm00274a015.
3
Inhibition of human platelet aggregation by a dibenzazepine compound (GP 44296) and by N-(2,6-dichlorophenyl)-o-aminophenylacetic acid (GP 45840).二苯氮䓬化合物（GP 44296）和N-（2,6-二氯苯基）-邻氨基苯乙酸（GP 45840）对人血小板聚集的抑制作用。
Can J Physiol Pharmacol. 1971 May;49(5):479-81. doi: 10.1139/y71-058.
4
Substituted 3,4-pentadienyldiamines as inhibitors of platelet aggregation.
J Med Chem. 1973 Jun;16(6):688-93. doi: 10.1021/jm00264a024.
5
Platelet aggregation inhibitors. 6. 2-Thioadenosine derivatives.血小板聚集抑制剂。6. 2-硫代腺苷衍生物。
J Med Chem. 1973 Dec;16(12):1381-8. doi: 10.1021/jm00270a014.
6
Aggregation of duck thrombocytes by 5-hydroxytryptamine.5-羟色胺对鸭血小板的聚集作用。
Microvasc Res. 1973 Sep;6(2):229-34. doi: 10.1016/0026-2862(73)90022-8.
7
AMP inhibition of reactions of ADP with washed platelets from humans and rabbits.腺苷一磷酸（AMP）对人及兔洗涤血小板中ADP反应的抑制作用。
Am J Physiol. 1972 Aug;223(2):419-24. doi: 10.1152/ajplegacy.1972.223.2.419.
8
Prostaglandin E 1 inhibition of aggregation of hamster platelets.
Bibl Anat. 1969;10:507-15.
9
The measurement of intravascular aggregation by continuous platelet counting.通过连续血小板计数测量血管内聚集。
Bibl Anat. 1973;12:229-34.
10
Role of cyclic AMP in platelet function.环磷酸腺苷在血小板功能中的作用。
Adv Cyclic Nucleotide Res. 1972;1:231-47.
引用本文的文献
1
A semisynthetic epitope for kinase substrates.一种用于激酶底物的半合成表位。
Nat Methods. 2007 Jun;4(6):511-6. doi: 10.1038/nmeth1048. Epub 2007 May 7.
2
Anticytokinin activity of substituted pyrrolo[2,3-d]pyrimidines.取代吡咯并[2,3 - d]嘧啶的抗细胞分裂素活性。
Proc Natl Acad Sci U S A. 1975 Sep;72(9):3508-12. doi: 10.1073/pnas.72.9.3508.
3
Engineering unnatural nucleotide specificity for Rous sarcoma virus tyrosine kinase to uniquely label its direct substrates.设计针对劳氏肉瘤病毒酪氨酸激酶的非天然核苷酸特异性，以独特地标记其直接底物。
Proc Natl Acad Sci U S A. 1997 Apr 15;94(8):3565-70. doi: 10.1073/pnas.94.8.3565.
4
5'-N-ethylcarboxamidoadenosine: a potent inhibitor of human platelet aggregation.5'-N-乙基羧酰胺腺苷：一种有效的人类血小板聚集抑制剂。
Br J Pharmacol. 1981 Mar;72(3):443-7. doi: 10.1111/j.1476-5381.1981.tb10995.x.
5
Subclasses of adenosine receptors in the central nervous system: interaction with caffeine and related methylxanthines.中枢神经系统中腺苷受体的亚类：与咖啡因及相关甲基黄嘌呤的相互作用。
Cell Mol Neurobiol. 1983 Mar;3(1):69-80. doi: 10.1007/BF00734999.
6
Functionalized congeners of adenosine: preparation of analogues with high affinity for A1-adenosine receptors.腺苷的功能化同系物：对A1 - 腺苷受体具有高亲和力的类似物的制备。
J Med Chem. 1985 Sep;28(9):1341-6. doi: 10.1021/jm00147a039.
7
Inhibition of adenylate cyclase by adenosine analogues in preparations of broken and intact human platelets. Evidence for the unidirectional control of platelet function by cyclic AMP.腺苷类似物对破碎及完整人血小板制剂中腺苷酸环化酶的抑制作用。环磷酸腺苷对血小板功能单向控制的证据。
Biochem J. 1978 Oct 15;176(1):83-95. doi: 10.1042/bj1760083.
Zotero 插件