2'-脱氧助间型霉素和赤藓红-9-(2-羟基-3-壬基)腺嘌呤对脑腺苷脱氨酶的抑制作用 - Suppr

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超能文献

Inhibition of brain adenosine deaminase by 2'-deoxycoformycin and erythro-9-(2-hydroxy-3-nonyl) adenine.

作者信息

Skolnick P, Nimitkitpaisan Y, Stalvey L, Daly J W

出版信息

J Neurochem. 1978 Jun;30(6):1479-82. doi: 10.1111/j.1471-4159.1978.tb10496.x.

DOI:10.1111/j.1471-4159.1978.tb10496.x

PMID:670988

Abstract

摘要

相似文献

Inhibition of brain adenosine deaminase by 2'-deoxycoformycin and erythro-9-(2-hydroxy-3-nonyl) adenine.2'-脱氧助间型霉素和赤藓红-9-(2-羟基-3-壬基)腺嘌呤对脑腺苷脱氨酶的抑制作用

J Neurochem. 1978 Jun;30(6):1479-82. doi: 10.1111/j.1471-4159.1978.tb10496.x.

Effects of 2'-deoxycoformycin and erythro-9-(2-hydroxy-3-nornyl)adenine on plasma levels and urinary excretion of 9-beta-D-arabinofuranosyladenine in the mouse 1,2,3.

Cancer Treat Rep. 1978 Mar;62(3):369-73.

Toxicities of adenosine and 2'-deoxyadrenosine in L cells treated with inhibitors of adenosine deaminase.用腺苷脱氨酶抑制剂处理的L细胞中腺苷和2'-脱氧腺苷的毒性。

Biochem Pharmacol. 1977 Jan 1;26(1):71-6. doi: 10.1016/0006-2952(77)90135-6.

Inhibition of PHA and NaI04 mitogenesis by the adenosine deaminase inhibitors erythro-9-(2-hydroxy-3-nonyl) adenine (EHNA) and 2-deoxycoformycin (2-dCF).

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Effect of chirality in erythro-9-(2-hydroxy-3-nonyl) adenine (EHNA) on adenosine deaminase inhibition.赤型-9-(2-羟基-3-壬基)腺嘌呤（EHNA）的手性对腺苷脱氨酶抑制作用的影响。

Biochem Pharmacol. 1982 Mar 1;31(5):879-82. doi: 10.1016/0006-2952(82)90479-8.

Enhancement of the biological activity of adenosine analogs by the adenosine deaminase inhibitor 2'-deoxycoformycin.腺苷脱氨酶抑制剂2'-脱氧助间型霉素增强腺苷类似物的生物活性

Pharmacology. 1977;15(1):84-9. doi: 10.1159/000136666.

Comparison of the activity of 2'-deoxycoformycin and erythro-9-(2-hydroxy-3-nonyl)adenine in vivo.体内2'-脱氧助间型霉素与赤型-9-(2-羟基-3-壬基)腺嘌呤活性的比较。

Biochem Pharmacol. 1979;28(2):201-6. doi: 10.1016/0006-2952(79)90504-5.

Inhibition of human T-cell rosette formation by the adenosine deaminase inhibitor erythro-9-(2-hydroxy-3-nonyl) adenine hydrochloride (EHNA).腺苷脱氨酶抑制剂盐酸erythro-9-(2-羟基-3-壬基)腺嘌呤（EHNA）对人T细胞玫瑰花结形成的抑制作用。

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Adenosine deaminase inhibitors. Conversion of a single chiral synthon into erythro- and threo-9-(2-hydroxy-3-nonyl)adenines.腺苷脱氨酶抑制剂。将单一手性合成子转化为赤藓型和苏阿糖型-9-(2-羟基-3-壬基)腺嘌呤。

J Med Chem. 1981 Dec;24(12):1383-5. doi: 10.1021/jm00144a002.

Sedative and electroencephalographic actions of erythro-9-(2-hydroxy-3-nonyl)-adenine (EHNA): relationship to inhibition of brain adenosine deaminase.赤藓红-9-(2-羟基-3-壬基)-腺嘌呤（EHNA）的镇静和脑电图作用：与脑腺苷脱氨酶抑制作用的关系。

Psychopharmacology (Berl). 1983;79(2-3):126-9. doi: 10.1007/BF00427798.

引用本文的文献

Adenosine deaminase inhibitors: their role in chemotherapy and immunosuppression.腺苷脱氨酶抑制剂：它们在化疗和免疫抑制中的作用。

Cancer Chemother Pharmacol. 1980;4(4):227-35. doi: 10.1007/BF00255266.

Deoxycoformycin: neurological toxicity.脱氧助间型霉素：神经毒性。

Cancer Chemother Pharmacol. 1981;5(3):193-6. doi: 10.1007/BF00258479.

Psychopharmacology (Berl). 1983;79(2-3):126-9. doi: 10.1007/BF00427798.

Endogenous adenosine as a modulator of hippocampal acetylcholine release.内源性腺苷作为海马乙酰胆碱释放的调节剂。

Naunyn Schmiedebergs Arch Pharmacol. 1984 Oct;327(4):319-25. doi: 10.1007/BF00506243.

Effects of adenosine uptake blockers and adenosine on evoked potentials of guinea-pig olfactory cortex.腺苷摄取阻滞剂和腺苷对豚鼠嗅觉皮质诱发电位的影响。

Pflugers Arch. 1986 Jan;406(1):25-30. doi: 10.1007/BF00582948.

Activation of A1 adenosine receptors decreases the release of serotonin in the rabbit hippocampus, but not in the caudate nucleus.A1 腺苷受体的激活会减少家兔海马体中血清素的释放，但在尾状核中则不会。

Naunyn Schmiedebergs Arch Pharmacol. 1988 Dec;338(6):664-70. doi: 10.1007/BF00165632.

Adenosine deaminase and adenosine uptake inhibitions facilitate ventilation in rats.腺苷脱氨酶和腺苷摄取抑制作用可促进大鼠的通气。

Naunyn Schmiedebergs Arch Pharmacol. 1989 Aug;340(2):230-8. doi: 10.1007/BF00168974.

Further studies of the mechanism(s) of polyunsaturated-fatty-acid-mediated increases in intracellular cAMP formation in N1E-115 neuroblastoma cells.对多不饱和脂肪酸介导N1E - 115神经母细胞瘤细胞内cAMP生成增加的机制的进一步研究。

Neurochem Res. 1992 Nov;17(11):1069-77. doi: 10.1007/BF00967283.

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