HEIR
发表于 2025-3-21 18:31:33
书目名称Mechanism of Action of Antieukaryotic and Antiviral Compounds影响因子(影响力)<br> http://figure.impactfactor.cn/if/?ISSN=BK0628642<br><br> <br><br>书目名称Mechanism of Action of Antieukaryotic and Antiviral Compounds影响因子(影响力)学科排名<br> http://figure.impactfactor.cn/ifr/?ISSN=BK0628642<br><br> <br><br>书目名称Mechanism of Action of Antieukaryotic and Antiviral Compounds网络公开度<br> http://figure.impactfactor.cn/at/?ISSN=BK0628642<br><br> <br><br>书目名称Mechanism of Action of Antieukaryotic and Antiviral Compounds网络公开度学科排名<br> http://figure.impactfactor.cn/atr/?ISSN=BK0628642<br><br> <br><br>书目名称Mechanism of Action of Antieukaryotic and Antiviral Compounds被引频次<br> http://figure.impactfactor.cn/tc/?ISSN=BK0628642<br><br> <br><br>书目名称Mechanism of Action of Antieukaryotic and Antiviral Compounds被引频次学科排名<br> http://figure.impactfactor.cn/tcr/?ISSN=BK0628642<br><br> <br><br>书目名称Mechanism of Action of Antieukaryotic and Antiviral Compounds年度引用<br> http://figure.impactfactor.cn/ii/?ISSN=BK0628642<br><br> <br><br>书目名称Mechanism of Action of Antieukaryotic and Antiviral Compounds年度引用学科排名<br> http://figure.impactfactor.cn/iir/?ISSN=BK0628642<br><br> <br><br>书目名称Mechanism of Action of Antieukaryotic and Antiviral Compounds读者反馈<br> http://figure.impactfactor.cn/5y/?ISSN=BK0628642<br><br> <br><br>书目名称Mechanism of Action of Antieukaryotic and Antiviral Compounds读者反馈学科排名<br> http://figure.impactfactor.cn/5yr/?ISSN=BK0628642<br><br> <br><br>
不能仁慈
发表于 2025-3-21 22:18:01
Antitumor Platinum Compounds,ion against Sarcoma 180 and Leukemia L1210 (. et al., 1969; . and . ., 1970), a viral-induced reticulum cell sarcoma in mice (., 1970), the Dunning ascitic leukemia, Walker 256 carcinosarcoma (. et al., 1970),and a DMBA-induced mammary carcinoma (., 1971) in rats.
摇摆
发表于 2025-3-22 02:36:48
,9-β-D-Arabinofuranosyladenine (AraA),d by Parke, Davis and Company (British Patent No. 1,159,290) as an antibiotic produced by .. Chemical synthesis, initially achieved through the conversion of a xylonucleoside to araA (. et al., 1960; . et al., 1962), was subsequently accomplished on a larger scale by the condensation of 2,3,5-tri-O-
熔岩
发表于 2025-3-22 07:19:25
8-Azaguanine,sed this inhibition. In 1949 . and . confirmed these findings when the analog inhibited multiplication of .. Subsequently, several investigators proved 8-azaguanine to be an inhibitor of the chick embryo (. et al., 1950), the Lucerne mosaic virus (., 1952), the . virus (., 1952), human glioblastomas
Myelin
发表于 2025-3-22 09:58:03
Bleomycin,ntineoplastic antibiotic, bleomycin. ., the discoverer of bleomycin (. et al., 1966) has written several reviews dealing primarily with the chemistry, structure, in vitro, and in vivo studies of bleomycin (., 1975, 1976). Other articles dealing more specifically with the extracellular reaction betwe
insomnia
发表于 2025-3-22 15:07:53
Diphtheria Toxin and Exotoxin A from ,,al toxins have been studied in greater depth, and new toxins have been discovered as well. As a result of the expanded interest and efforts there now exists a substantial and rapidly growing body of knowledge about the structures and activities of bacterial toxins from which one can begin to make me
exceptional
发表于 2025-3-22 20:52:09
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漂泊
发表于 2025-3-22 23:54:53
2-Hydroxy-3-Alkyl-1,4-Naphthoquinones,of the antimalarial drug quinine. Faced with entirely inadequate supplies of quinine coupled with the grim prospect of waging tropical warfare in some of the world’s worst malaria-infested regions, the Allied Powers instituted a comprehensive program of research in the chemotherapy of malaria. This
压倒
发表于 2025-3-23 05:27:37
Hydroxystilbamidine,midine, berenil, etc.), it shows strong activity against bacteria, protozoa, and fungi. It is clinically used in systemic mycosis, mainly North American blastomycosis, visceral leishmaniasis, and secondarily in prophylaxis and treatment of African trypanosomiasis, and in cases of malignancy, e.g., m
Endometrium
发表于 2025-3-23 06:36:56
,5-Iodo-2′-Deoxyuridine,e base analogs was initiated by . et al. (1945) and extended by . et al. (1949). The clinical potential of base analogs, whether halogenated or not, has been well recognized in chemotherapy. Furthermore, such compounds have proven to be powerful tools for elucidation of many intricate biochemical ev