• 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

Antiallergic agent from natural sources. Structures and inhibitory effect of histamine release of naphthopyrone glycosides from seeds of Cassia obtusifolia L.

作者信息

Kitanaka S, Nakayama T, Shibano T, Ohkoshi E, Takido M

机构信息

College of Pharmacy, Nihon University, Chiba, Japan.

出版信息

Chem Pharm Bull (Tokyo). 1998 Oct;46(10):1650-2. doi: 10.1248/cpb.46.1650.

DOI:10.1248/cpb.46.1650
PMID:9810700
Abstract

Two new naphthopyrones, cassiasides B2 (1) and C2 (2), were isolated from the seeds (Cassiae Semen) of Cassia obtusifolia L. The structures of the two new compounds 1 and 2 were established as rubrofusarin 6-O-beta-D- glucopyranosyl-(1-->6)-O-beta-D-glucopyranosyl-(1-->3)-O-beta-D- glucopyranosyl-(1-->6)-O-beta-D-glucopyranoside and toralactone 9-O-beta-D-glucopyranosyl-(1-->6)-O-beta-D-glucopyranosyl- (1-->3)-O-beta-D-glucopyranosyl-(1-->6)-O-beta-D-glucopyranoside, respectively, on the basis of spectral and chemical evidence. Compound 2 was found to inhibit the histamine release from rat peritoneal exudate mast cells induced by antigen-antibody reaction.

摘要

相似文献

1
Antiallergic agent from natural sources. Structures and inhibitory effect of histamine release of naphthopyrone glycosides from seeds of Cassia obtusifolia L.
Chem Pharm Bull (Tokyo). 1998 Oct;46(10):1650-2. doi: 10.1248/cpb.46.1650.
2
Antiallergic agent from natural sources. 2. Structures and leukotriene release-inhibitory effect of torososide B and torosachrysone 8-O-6"-malonyl beta-gentiobioside from Cassia torosa Cav.天然来源的抗过敏剂。2. 决明属植物决明中托罗皂苷B和托罗大黄素8-O-6''-丙二酰-β-龙胆二糖苷的结构及对白三烯释放的抑制作用
Chem Pharm Bull (Tokyo). 1999 Jul;47(7):915-8. doi: 10.1248/cpb.47.915.
3
Total synthesis of the antiallergic naphtho-alpha-pyrone tetraglucoside, cassiaside C(2), isolated from cassia seeds.从决明子种子中分离得到的抗过敏萘并-α-吡喃酮四糖苷决明子苷C(2)的全合成。
J Org Chem. 2003 Aug 8;68(16):6309-13. doi: 10.1021/jo034223u.
4
Anthraquinone and naphthopyrone glycosides from Cassia obtusifolia seeds mediate hepatoprotection via Nrf2-mediated HO-1 activation and MAPK modulation.决明子种子中的蒽醌和萘并吡喃酮糖苷通过 Nrf2 介导的 HO-1 激活和 MAPK 调节发挥肝保护作用。
Arch Pharm Res. 2018 Jun;41(6):677-689. doi: 10.1007/s12272-018-1040-4. Epub 2018 May 26.
5
Inhibitory activities of major anthraquinones and other constituents from Cassia obtusifolia against β-secretase and cholinesterases.决明子中主要蒽醌类化合物及其他成分对β-分泌酶和胆碱酯酶的抑制活性。
J Ethnopharmacol. 2016 Sep 15;191:152-160. doi: 10.1016/j.jep.2016.06.037. Epub 2016 Jun 15.
6
Bioactive constituents of Chinese natural medicines. II. Rhodiolae radix. (1). Chemical structures and antiallergic activity of rhodiocyanosides A and B from the underground part of Rhodiola quadrifida (Pall.) Fisch. et Mey. (Crassulaceae).
Chem Pharm Bull (Tokyo). 1996 Nov;44(11):2086-91. doi: 10.1248/cpb.44.2086.
7
New antihepatotoxic naphtho-pyrone glycosides from the seeds of Cassia tora.决明种子中的新型抗肝毒性萘并吡喃糖苷。
Planta Med. 1989 Jun;55(3):276-80. doi: 10.1055/s-2006-962003.
8
Two new naphthalenic lactone glycosides from Cassia obtusifolia L. seeds.决明子种子中的两个新萘内酯糖苷。
Arch Pharm Res. 2018 Jul;41(7):737-742. doi: 10.1007/s12272-018-1044-0. Epub 2018 Jun 8.
9
Structure Related Inhibition of Enzyme Systems in Cholinesterases and BACE1 In Vitro by Naturally Occurring Naphthopyrone and Its Glycosides Isolated from Cassia obtusifolia.从决明子中分离得到的天然萘并吡喃酮及其糖苷对胆碱酯酶和 BACE1 体外酶系统的结构相关抑制作用。
Molecules. 2017 Dec 28;23(1):69. doi: 10.3390/molecules23010069.
10
Estrogenic and anti-estrogenic activities of Cassia tora phenolic constituents.决明子酚类成分的雌激素活性和抗雌激素活性。
Chem Pharm Bull (Tokyo). 2007 Oct;55(10):1476-82. doi: 10.1248/cpb.55.1476.

引用本文的文献

1
Aurantio-obtusin exerts an anti-inflammatory effect on acute kidney injury by inhibiting NF-κB pathway.橙黄决明素通过抑制核因子κB(NF-κB)信号通路对急性肾损伤发挥抗炎作用。
Korean J Physiol Pharmacol. 2024 Jan 1;28(1):11-19. doi: 10.4196/kjpp.2024.28.1.11.
2
Phytochemistry, Ethnopharmacological Uses, Biological Activities, and Therapeutic Applications of L.: A Comprehensive Review.植物化学、民族药理学用途、生物学活性和治疗应用的 L.:全面综述。
Molecules. 2021 Oct 15;26(20):6252. doi: 10.3390/molecules26206252.
3
Acetylcholine esterase inhibitory activity of green synthesized nanosilver by naphthopyrones isolated from marine-derived Aspergillus niger.
海洋来源黑曲霉中萘并吡喃酮绿色合成纳米银的乙酰胆碱酯酶抑制活性。
PLoS One. 2021 Sep 10;16(9):e0257071. doi: 10.1371/journal.pone.0257071. eCollection 2021.
4
Dasatinib Inhibits Lyn and Fyn Src-Family Kinases in Mast Cells to Suppress Type I Hypersensitivity in Mice.达沙替尼抑制肥大细胞中的Lyn和Fyn Src家族激酶,以抑制小鼠的I型超敏反应。
Biomol Ther (Seoul). 2020 Sep 1;28(5):456-464. doi: 10.4062/biomolther.2020.013.
5
Water-soluble exudates from seeds of Kochia scoparia exhibit antifungal activity against Colletotrichum graminicola.水飞蓟种子中的水溶性分泌物对禾谷炭疽菌具有抗真菌活性。
PLoS One. 2019 Jun 19;14(6):e0218104. doi: 10.1371/journal.pone.0218104. eCollection 2019.
6
Anti-Inflammatory Effects of Aurantio-Obtusin from Seed of L. through Modulation of the NF-κB Pathway.山茱萸种籽中的橙酮通过调节 NF-κB 通路发挥抗炎作用。
Molecules. 2018 Nov 27;23(12):3093. doi: 10.3390/molecules23123093.
7
Cassiae semen: A review of its phytochemistry and pharmacology (Review).决明子:其植物化学与药理学综述(综述)。
Mol Med Rep. 2017 Sep;16(3):2331-2346. doi: 10.3892/mmr.2017.6880. Epub 2017 Jun 29.
8
A review on herbal antiasthmatics.一篇关于草药抗哮喘药物的综述。
Orient Pharm Exp Med. 2011 Aug;11(2):77-90. doi: 10.1007/s13596-011-0019-1. Epub 2011 Jul 5.
9
New benzophenone and quercetin galloyl glycosides from Psidium guajava L.番石榴叶中新型二苯甲酮和槲皮素酰基化葡萄糖苷
J Nat Med. 2010 Jul;64(3):252-6. doi: 10.1007/s11418-010-0400-2. Epub 2010 Mar 31.
10
GIP2, a putative transcription factor that regulates the aurofusarin biosynthetic gene cluster in Gibberella zeae.GIP2,一种假定的转录因子,可调控玉米赤霉中的金褐霉素生物合成基因簇。
Appl Environ Microbiol. 2006 Feb;72(2):1645-52. doi: 10.1128/AEM.72.2.1645-1652.2006.