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2-Oxazolidones (Ia→f) were not effective against rat ascites hepatoma AH13 or mouse lymphoid leukemia, L1210. However, among 3-nitroso-2-oxazolidones (IIa→f), compounds IIa, IIb, IIc and IId were active against AH13, and compounds IIa, IIb and IIf were active against L1210. Cyclic N-nitrosocarbamates and N-nitrosoureas showed greater antitumor effects than the corresponding acyclic N-nitroso compounds. Since the reaction of compounds IIa→f with 4-(p-nitrobenzyl) pyridine gave a purple color, their antitumor mechanism presumably involves alkylation ; but there was no correlation between the antitumor activities and the color intensities.
収録刊行物
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- CHEMICAL & PHARMACEUTICAL BULLETIN
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CHEMICAL & PHARMACEUTICAL BULLETIN 29 (8), 2366-2369, 1981
公益社団法人 日本薬学会
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詳細情報 詳細情報について
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- CRID
- 1390001204164304640
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- NII論文ID
- 110003633988
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- NII書誌ID
- AA00602100
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- ISSN
- 13475223
- 00092363
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- PubMed
- 7318043
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- Crossref
- PubMed
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可