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1
Effect of 781094, a new selective alpha-adrenoceptor antagonist, on the aggregatory responses of human blood platelets and on binding of [3H]-dihydroergocryptine to these cells.新型选择性α-肾上腺素受体拮抗剂781094对人血小板聚集反应及[3H]-二氢麦角隐亭与这些细胞结合的影响。
Br J Pharmacol. 1983 Jun;79(2):401-7. doi: 10.1111/j.1476-5381.1983.tb11012.x.
2
Interaction of selective alpha-adrenoceptor agonists and antagonists with human and rabbit blood platelets.选择性α-肾上腺素能受体激动剂与拮抗剂与人及兔血小板的相互作用。
Br J Pharmacol. 1980;71(1):121-34. doi: 10.1111/j.1476-5381.1980.tb10917.x.
3
Studies of alpha 2-adrenergic receptors of intact and functional washed human platelets by binding of 3H-dihydroergocryptine and 3H-yohimbine--correlation of 3H-yohimbine binding with the potentiation by adrenaline of ADP-induced aggregation.通过3H-二氢麦角隐亭和3H-育亨宾结合对完整且功能正常的洗涤人血小板的α2-肾上腺素能受体的研究——3H-育亨宾结合与肾上腺素对ADP诱导聚集的增强作用之间的相关性。
Thromb Haemost. 1985 Aug 30;54(2):402-8.
4
Effects of imidazoline and non-imidazoline α-adrenergic agents on rabbit platelet aggregation.咪唑啉和非咪唑啉 α-肾上腺素能药物对兔血小板聚集的影响。
Pharmacology. 2013;91(3-4):135-44. doi: 10.1159/000346269. Epub 2013 Jan 25.
5
Identification of human platelet alpha 2-adrenoceptors with a new antagonist [3H]-RX821002, a 2-methoxy derivative of idazoxan.用新型拮抗剂[3H]-RX821002(咪唑克生的2-甲氧基衍生物)鉴定人血小板α2-肾上腺素能受体。
Br J Pharmacol. 1990 Aug;100(4):862-6. doi: 10.1111/j.1476-5381.1990.tb14105.x.
6
The use of ex vivo platelet aggregation to confirm the in vivo alpha 2-adrenoreceptor antagonist effect of idazoxan in man.
J Pharmacol Methods. 1987 Sep;18(2):95-102. doi: 10.1016/0160-5402(87)90001-5.
7
Identification of alpha-adrenergic receptors in human platelets by [3H]dihydroergocryptine binding.通过[3H]二氢麦角隐亭结合鉴定人血小板中的α-肾上腺素能受体。
J Clin Invest. 1978 Feb;61(2):395-402. doi: 10.1172/JCI108950.
8
Effects of imidazoline and non-imidazoline alpha-adrenergic agents on canine platelet aggregation.咪唑啉和非咪唑啉α-肾上腺素能药物对犬血小板聚集的影响。
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Differential labeling of platelet alpha 2 adrenoceptors by 3H dihydroergocryptine and 3H yohimbine in patients with myeloproliferative disorders.
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10
Studies on RX 781094: a selective, potent and specific antagonist of alpha 2-adrenoceptors.RX 781094的研究:一种α2肾上腺素能受体的选择性、强效且特异性拮抗剂。
Br J Pharmacol. 1983 Mar;78(3):489-505. doi: 10.1111/j.1476-5381.1983.tb08809.x.

本文引用的文献

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PLATELET SEQUESTRATION IN MAN. I. METHODS.人体中的血小板隔离。一、方法。
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Some quantitative uses of drug antagonists.药物拮抗剂的一些定量应用。
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Direct evidence for a role for Ca2+ in amine storage granule secretion by human platelets.钙离子在人血小板胺储存颗粒分泌中起作用的直接证据。
Thromb Res. 1980 Nov 15;20(4):437-46. doi: 10.1016/0049-3848(80)90282-0.
4
UK-14,304, a potent and selective alpha2-agonist for the characterisation of alpha-adrenoceptor subtypes.UK-14,304,一种用于鉴定α-肾上腺素能受体亚型的强效选择性α2-激动剂。
Eur J Pharmacol. 1981 Jul 10;72(4):413-5. doi: 10.1016/0014-2999(81)90588-4.
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Interaction of selective alpha-adrenoceptor agonists and antagonists with human and rabbit blood platelets.选择性α-肾上腺素能受体激动剂与拮抗剂与人及兔血小板的相互作用。
Br J Pharmacol. 1980;71(1):121-34. doi: 10.1111/j.1476-5381.1980.tb10917.x.
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A biphasic response of platelets to serotonin.血小板对血清素的双相反应。
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Influence of lysolecithin on platelet aggregation initiated by 5-hydroxytryptamine.
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8
Relationship between the inhibition constant (K1) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reaction.抑制常数(K1)与导致酶促反应50%抑制率(I50)的抑制剂浓度之间的关系。
Biochem Pharmacol. 1973 Dec 1;22(23):3099-108. doi: 10.1016/0006-2952(73)90196-2.
9
Simultaneous radioenzymatic determination of plasma and tissue adrenaline, noradrenaline and dopamine within the femtomole range.飞摩尔范围内血浆和组织中肾上腺素、去甲肾上腺素及多巴胺的同步放射酶法测定
Life Sci. 1976 Oct 15;19(8):1161-74. doi: 10.1016/0024-3205(76)90251-4.
10
Interaction of human blood platelets with the 2',3'-dialdehyde and 2',3'-dialcohol derivatives of adenosine 5'-diphosphate and adenosine 5'-triphosphate.人血小板与5'-二磷酸腺苷和5'-三磷酸腺苷的2',3'-二醛及2',3'-二醇衍生物的相互作用。
Eur J Biochem. 1978 Aug 1;88(2):543-54. doi: 10.1111/j.1432-1033.1978.tb12480.x.

新型选择性α-肾上腺素受体拮抗剂781094对人血小板聚集反应及[3H]-二氢麦角隐亭与这些细胞结合的影响。

Effect of 781094, a new selective alpha-adrenoceptor antagonist, on the aggregatory responses of human blood platelets and on binding of [3H]-dihydroergocryptine to these cells.

作者信息

Kerry R, Scrutton M C

出版信息

Br J Pharmacol. 1983 Jun;79(2):401-7. doi: 10.1111/j.1476-5381.1983.tb11012.x.

DOI:10.1111/j.1476-5381.1983.tb11012.x
PMID:6140040
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2044865/
Abstract

781094 (2-(2(1, 4-benzodioxanyl))-2-imidazoline hydrochloride) is a potent competitive inhibitor of the aggregatory responses of human platelets induced by adrenaline (pA2 = 7.3) and UK-14304. 781094 is a more potent inhibitor of the pro-aggregatory response to clonidine than of that to methoxamine. The alpha 2/alpha 1-adrenoceptor selectivity ratio is 11.4. 781094 is a potent inhibitor of the binding of [3H]-dihydroergocryptine to platelet lysates. 781094 has no effect on the aggregatory responses of human platelets induced by adenosine-5'-pyrophosphate (ADP), 5-hydroxytryptamine, thrombin, U-46619, or arginine-vasopressin provided that the platelet-rich plasma does not exhibit enhanced responsiveness. In some instances high concentrations of 781094 potentiate the aggregatory response to collagen. In platelet-rich plasma which exhibits enhanced responsiveness, 781094 causes partial inhibition of the aggregatory responses to 5-hydroxytryptamine, ADP and vasopressin at concentrations similar to those required to inhibit the response to adrenaline. 781094 acts as a specific antagonist for the responses mediated by human platelet alpha-adrenoceptors and exhibits moderate selectivity for the alpha 2-adrenoceptors on this cell.

摘要

781094(2-(2(1,4-苯并二氧杂环己基))-2-咪唑啉盐酸盐)是一种强效竞争性抑制剂,可抑制肾上腺素(pA2 = 7.3)和UK-14304诱导的人血小板聚集反应。781094对可乐定促聚集反应的抑制作用比对甲氧明的更强。α2/α1肾上腺素能受体选择性比值为11.4。781094是[3H]-二氢麦角隐亭与血小板裂解物结合的强效抑制剂。只要富血小板血浆没有表现出增强的反应性,781094对腺苷-5'-焦磷酸(ADP)、5-羟色胺、凝血酶、U-46619或精氨酸加压素诱导的人血小板聚集反应没有影响。在某些情况下,高浓度的781094会增强对胶原蛋白的聚集反应。在反应性增强的富血小板血浆中,781094在抑制肾上腺素反应所需的类似浓度下,会部分抑制对5-羟色胺、ADP和加压素的聚集反应。781094作为人血小板α-肾上腺素能受体介导反应的特异性拮抗剂,对该细胞上的α2-肾上腺素能受体表现出中等选择性。