• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Low mitogenic activity of synthetic lipid A analog, 2,3-acyloxyacylgalactosamine-4-phosphate, in cultured murine splenocytes.

作者信息

Shimizu T, Masuzawa T, Iwamoto Y, Yanagihara Y, Sano K, Ikeda K, Achiwa K

机构信息

University of Shizuoka, School of Pharmaceutical Sciences, Japan.

出版信息

Biol Pharm Bull. 1993 Feb;16(2):201-2. doi: 10.1248/bpb.16.201.

DOI:10.1248/bpb.16.201
PMID:8364456
Abstract

The mitogenicity of chemically synthesized lipid A analogs, 2,3-acyloxyacylglucosamine-4-phosphate (A-103) and 2,3-acyloxyacylgalactosamine-4-phosphate (A-113), was compared. Synthetic lipid A analogs of the disaccharide-type (506), the monosaccharide-type (A-103) suspended in RPMI-1640 medium supplemented with triethylamine, and Salmonella typhimurium LT-2 lipopolysaccharide (LPS) were capable of increasing the incorporation of [3H]thymidine into splenocytes of C57BL/6 mice at various doses ranging from 1.0 to 100 micrograms/ml. However, the mitogenic activity of A-113 at these doses was markedly weaker than the activity of the above materials. When the A-103 and A-113 were suspended in RPMI-1640 medium supplemented with ethanol, the mitogenic activity of A-113 also showed lower activity than that of A-103 in the splenocytes of C57BL/6 mice. These findings indicate that the mitogenic activity of synthetic lipid A of the monosaccharide-type is affected by a kind of composed sugar.

摘要

相似文献

1
Low mitogenic activity of synthetic lipid A analog, 2,3-acyloxyacylgalactosamine-4-phosphate, in cultured murine splenocytes.
Biol Pharm Bull. 1993 Feb;16(2):201-2. doi: 10.1248/bpb.16.201.
2
Biological activities of chemically synthesized N-acetylneuraminic acid-(alpha 2----6)-monosaccharide analogs of lipid A.化学合成的脂多糖A的N-乙酰神经氨酸-(α2→6)-单糖类似物的生物活性。
FEBS Lett. 1988 Feb 8;228(1):99-101. doi: 10.1016/0014-5793(88)80593-3.
3
Biological activities of chemically synthesized derivatives of lipid A: tetraacetyl-monosaccharides linked to 2,3-acyloxyacylglucosamine-4-phosphate.脂质A化学合成衍生物的生物活性:与2,3-酰氧基酰基葡糖胺-4-磷酸连接的四乙酰单糖。
Chem Pharm Bull (Tokyo). 1989 Sep;37(9):2535-6. doi: 10.1248/cpb.37.2535.
4
Mitogenic activity and lethal toxicity of lipid A analogs, glucosamine-phosphate carrying aromatic alkyl groups, in mice.携带芳香烷基的磷酸葡糖胺脂质A类似物在小鼠体内的促有丝分裂活性和致死毒性。
Biol Pharm Bull. 1993 Sep;16(9):932-4. doi: 10.1248/bpb.16.932.
5
Succinylated lipid A is a potent and specific inhibitor of endotoxin mitogenicity.琥珀酰化脂多糖是一种有效的内毒素促有丝分裂活性特异性抑制剂。
J Gen Microbiol. 1992 Dec;138(12):2503-8. doi: 10.1099/00221287-138-12-2503.
6
Antitumor activity against Meth A fibrosarcoma and biologic activities of synthetic monosaccharide analogs of lipid A in mice.合成脂质A单糖类似物对小鼠Meth A纤维肉瘤的抗肿瘤活性及生物学活性
Mol Biother. 1990 Jun;2(2):110-4.
7
Biological activities of chemically synthesized N-acylated serine-linked lipid A analog in mice.化学合成的N-酰化丝氨酸连接脂质A类似物在小鼠体内的生物学活性
Int J Immunopharmacol. 1994 Aug;16(8):659-65. doi: 10.1016/0192-0561(94)90139-2.
8
Mitogenic activities of synthetic lipid A analogs and suppression of mitogenicity of lipid A.合成脂多糖A类似物的促有丝分裂活性及脂多糖A促有丝分裂活性的抑制
Infect Immun. 1984 May;44(2):427-33. doi: 10.1128/iai.44.2.427-433.1984.
9
Biological activity of chemically synthesized core sugar linked lipid A analog, heptose-(alpha 1----5)-2-keto-3-deoxyoctonic acid-(alpha 2----6)-2,3-diacyloxyacylglucosamine-4-phosphate.化学合成的核心糖连接脂质A类似物,庚糖-(α1----5)-2-酮-3-脱氧辛酸-(α2----6)-2,3-二酰氧基酰基葡糖胺-4-磷酸的生物活性。
Int J Immunopharmacol. 1992 Feb;14(2):221-6. doi: 10.1016/0192-0561(92)90034-i.
10
Antitumor activity, mitogenicity, and lethal toxicity of chemically synthesized monosaccharide analogs of lipid A.脂多糖A化学合成单糖类似物的抗肿瘤活性、促有丝分裂活性和致死毒性。
J Pharmacobiodyn. 1988 Jul;11(7):512-8. doi: 10.1248/bpb1978.11.512.