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Toxicities of adenosine and 2'-deoxyadrenosine in L cells treated with inhibitors of adenosine deaminase.

作者信息

Lapi L, Cohen S S

出版信息

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

DOI:10.1016/0006-2952(77)90135-6
PMID:299815
Abstract
摘要

相似文献

1
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.
2
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.
3
Increased toxicity of 9-beta-D-arabinofuranosyladenine in the presence of an inhibitor of adenosine deaminase.在腺苷脱氨酶抑制剂存在的情况下,9-β-D-阿拉伯呋喃糖基腺嘌呤的毒性增加。
Ann N Y Acad Sci. 1977 Mar 4;284:91-102. doi: 10.1111/j.1749-6632.1977.tb21939.x.
4
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.
5
Potentiation of cytotoxicity and antitumor activity of adenosine analogs by the adenosine deaminase inhibitor adecypenol.腺苷脱氨酶抑制剂阿德西培诺增强腺苷类似物的细胞毒性和抗肿瘤活性。
J Antibiot (Tokyo). 1989 Nov;42(11):1722-4. doi: 10.7164/antibiotics.42.1722.
6
Effect of adenosine deaminase inhibitors on the apparent rate of phosphorylation of deoxyadenosine.腺苷脱氨酶抑制剂对脱氧腺苷磷酸化表观速率的影响。
Biochem Med. 1981 Jun;25(3):288-97. doi: 10.1016/0006-2944(81)90087-9.
7
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.
8
Two approaches that increase the activity of analogs of adenine nucleosides in animal cells.两种提高腺嘌呤核苷类似物在动物细胞中活性的方法。
Cancer Res. 1975 Jun;35(6):1547-54.
9
Inhibitors of adenosine deaminase and the development of antiviral agents.腺苷脱氨酶抑制剂与抗病毒药物的研发
Ann N Y Acad Sci. 1985;451:204-14. doi: 10.1111/j.1749-6632.1985.tb27111.x.
10
Inhibition of adenosine deaminase to increase the antitumor activity of adenine nucleoside analogues.抑制腺苷脱氨酶以增强腺嘌呤核苷类似物的抗肿瘤活性。
Ann N Y Acad Sci. 1985;451:150-9. doi: 10.1111/j.1749-6632.1985.tb27106.x.

引用本文的文献

1
The Inside Story of Adenosine.腺嘌呤核苷的内幕故事。
Int J Mol Sci. 2018 Mar 9;19(3):784. doi: 10.3390/ijms19030784.
2
The potential of nucleotide analogs as inhibitors of retroviruses and tumors.核苷酸类似物作为逆转录病毒和肿瘤抑制剂的潜力。
Pharm Res. 1984 Jan;1(1):11-8. doi: 10.1023/A:1016370407633.
3
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.
4
Inactivation of liver S-adenosylhomocysteine hydrolase in vitro of rats treated with erythro-9-(2-hydroxynon-3-yl)adenine.用赤藓红-9-(2-羟基壬-3-基)腺嘌呤处理的大鼠肝脏S-腺苷同型半胱氨酸水解酶的体外失活
Biochem J. 1982 Sep 1;205(3):585-92. doi: 10.1042/bj2050585.
5
Erythro-9-(2-hydroxy-3-nonyl) Adenine alone and in combination with 9-beta-D-arabinofuranosyladenine in treatment of systemic herpesvirus infections in mice.单独使用以及与9-β-D-阿拉伯呋喃糖基腺嘌呤联合使用赤藓红-9-(2-羟基-3-壬基)腺嘌呤治疗小鼠全身性疱疹病毒感染。
Antimicrob Agents Chemother. 1980 Oct;18(4):598-603. doi: 10.1128/AAC.18.4.598.
6
Erythro-9-(2-hydroxy-3-nonyl)adenine as a specific inhibitor of herpes simplex virus replication in the presence and absence of adenosine analogues.在有和没有腺苷类似物存在的情况下,9-(2-羟基-3-壬基)腺嘌呤作为单纯疱疹病毒复制的特异性抑制剂。
Proc Natl Acad Sci U S A. 1978 Oct;75(10):4684-8. doi: 10.1073/pnas.75.10.4684.