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Clerodendrin

目录号 : GC67859

Clerodendrin 是一种可从 Lobelia chinensis 中分离得到的天然产物。Clerodendrin 是一种有效的双重白介素-4 (IL-4) 抑制剂和 β-己糖氨基苷酶 (Hex) 抑制剂。

Clerodendrin Chemical Structure

Cas No.:119738-57-7

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10mg
¥3,600.00
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产品文档

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产品描述

Clerodendrin is a nature product could be isolated from Lobelia chinensis. Clerodendrin is a potent dual Interleukin-4 (IL-4) inhibitor and β-hexosaminidase (Hex) inhibitor[1].

Clerodendrin (10 μM; 1 and 3 h) inhibits IL-4 mRNA expression and the release of β-hexosaminidase in Propidium Iodide -induced RBL-2H3 cells[1].

[1]. Young KT, et, al. Inhibition of Interleukin-4 and β-Hexosaminidase Release in RBL-2H3 Cells by Compounds Isolated from Lobelia chinensis. 2021,27(4):251-6.

Chemical Properties

Cas No. 119738-57-7 SDF Download SDF
分子式 C27H26O17 分子量 622.49
溶解度 DMSO : 50 mg/mL (80.32 mM; Need ultrasonic) 储存条件 Store at -20°C
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溶解性数据

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1 mg 5 mg 10 mg
1 mM 1.6065 mL 8.0323 mL 16.0645 mL
5 mM 0.3213 mL 1.6065 mL 3.2129 mL
10 mM 0.1606 mL 0.8032 mL 1.6065 mL
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Research Update

Clerodendrin I, a New Neoclerodane Diterpenoid from Clerodendron trichotomum

Biosci Biotechnol Biochem 1999;63(10):1795-7.PMID:26300171DOI:10.1271/bbb.63.1795.

A new neoclerodane diterpenoid, Clerodendrin I, was isolated from leaves of Clerodendron trichotomum as a feeding stimulant of the turnip sawfly, Athalia rosae ruficornis, and characterized as a threo epimer of Clerodendrin F in the 2,3-diacetoxy-2-methylbutanoyloxy moiety at the C-3β position.

Comprehensive review of Clerodendrum phlomidis: a traditionally used bitter

Zhong Xi Yi Jie He Xue Bao 2010 Jun;8(6):510-24.PMID:20550872DOI:10.3736/jcim20100602.

Clerodendrum phlomidis Linn. f., (syn. Clerodendrum multiflorum (Burm.f) O. Kuntze, Volkameria multiflorum Burm. f.) (Lamiaceae) is an important and well known medicinal plant extensively used in Ayurveda and Siddha system of medicine for treatment of various ailments. The popular therapies include on inflammation, diabetes, nervous disorder, asthma, rheumatism, digestive disorders, and urinary disorders as well as a bitter tonic. It was reported that pectolinaringenin, scutellarein, clerodin, Clerodendrin, clerosterol, 24beta-ethylcholesta-5,22E,25-triene-3beta-ol, lup-20(29)-en-3-triacontanoate, 4,2',4'-trihydroxy-6'-methoxychalcone-4,4'alpha-D-diglucoside, 7-hydroxyflavone, 7-hydroxyflavanone-7-O-glucoside and alpha-L-rhamnopyranosyl-(1-2)alpha-D-glucopyranosyl-7-O-naringin-4'-O-alpha-D-glucopyranoside-5-methyl ether had been isolated from this plant. The alcoholic and aqueous extracts were reported active as analgesic, antidiarrhoeal, antiplasmodial, hypoglycemic, minor tranquilizers, anti-asthmatic, antifungal, nematicidal, anti-amnestic and anti-arthritic. There are coincidences between some of the traditional usages of this plant and experimentally observed effects of the extracts but very few biological studies available on bioactive fractions and/or pure compounds. This review is an attempt to compile the exhaustive literature on Clerodendrum phlomidis, to highlight, analyze and critically assess the pharmaceutical potential of this underestimated plant in a systematic way.

Antifeedant and growth inhibitory effects of some neo-clerodane diterpenoids isolated from Clerodendron species (Verbenaceae) on Earias vitella and Spodoptera litura

J Agric Food Chem 2003 Mar 12;51(6):1555-9.PMID:12617583DOI:10.1021/jf025920a.

Antifeedant and growth inhibitory effects of various neo-clerodane diterpenoids having a furofuran moiety, isolated from Clerodendron spp., were studied using Earias vitella and Spodoptera litura. The compounds Clerodendrin B, 3-epicaryoptin, 15-hydroxyepicaryoptin, and clerodin were effective antifeedants at 10 microg/cm(3) (30 microg/g) of diet against E. vitella and at 10 microg/cm(2) of leaf against S. litura. All of the tested compounds, namely, Clerodendrin B, 3-epicaryoptin, Clerodendrin C, 15-hydroxyepicaryoptin, Clerodendrin B acetate, and clerodin, showed good insect growth inhibitory activity even at lower concentrations.