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Picfeltarraenin IB Sale

(Synonyms: 苦玄参苷 IB) 目录号 : GC36915

Picfeltarraenin IB, a cucurbitacin glycoside isolated from Picriafel-terrae, is an inhibitor of acetylcholinesterase (AChE). Picfeltarraenin IB can be used for the treatment of herpes infections, cancer and inflammation.

Picfeltarraenin IB Chemical Structure

Cas No.:97230-46-1

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产品描述

Picfeltarraenin IB, a cucurbitacin glycoside isolated from Picriafel-terrae, is an inhibitor of acetylcholinesterase (AChE). Picfeltarraenin IB can be used for the treatment of herpes infections, cancer and inflammation.

[1] Lu Wen, et al. Pharmacogn Mag. 2013 Oct;9(Suppl 1):S25-31. [2] Y Huang, et al. J Nat Prod. 1998 Jun 26;61(6):757-61.

Chemical Properties

Cas No. 97230-46-1 SDF
别名 苦玄参苷 IB
Canonical SMILES C[C@]([C@]([C@]1(OC(C(C)C)=CC1=O)C)([H])[C@H](O)C2)(CC3=O)[C@@]2([C@@](CC=C4[C@@]5([H])CC[C@@H](O[C@@](O[C@H](CO)[C@@H](O)[C@@H]6O)([H])[C@@H]6O[C@@](O[C@@H](C)[C@H](O)[C@H]7O)([H])[C@@H]7O)C4(C)C)([H])[C@@]35C)C
分子式 C42H64O14 分子量 792.95
溶解度 DMSO : 250 mg/mL (315.28 mM; Need ultrasonic) 储存条件 4°C, protect from light
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1 mM 1.2611 mL 6.3056 mL 12.6111 mL
5 mM 0.2522 mL 1.2611 mL 2.5222 mL
10 mM 0.1261 mL 0.6306 mL 1.2611 mL
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Research Update

Simultaneous quantification of picfeltarraenins IA and IB in rat plasma by UPLC-MS/MS: Application to a pharmacokinetic study

J Pharm Biomed Anal 2016 Feb 20;120:32-7.PMID:26690256DOI:10.1016/j.jpba.2015.11.031.

A simple and rapid quantitative UPLC-MS/MS method for simultaneous determination of picfeltarraenins IA and IB in rat plasma was developed and validated in accordance with the US FDA Bioanalytical Guidance (2001). Analytes were extracted from rat plasma by using methanol and separated on Agilent ZORBAX SB-C18 (50mm×2.1mm, 1.8μm) column by using a mobile phase composed of methanol and water (70:30, v/v). Eluents were monitored by ESI tandem mass spectrometry detection with SRM mode using ion transitions m/z 785.4→639.5, m/z 815.5→669.5, and m/z 763.5→455.3 for picfeltarraenin IA, Picfeltarraenin IB, and internal standard, respectively. The method was validated over the linear range of 11.5-1150ng/mL and 13.0-1300ng/mL. The developed analytical method was applied to support a pharmacokinetic study on simultaneous estimation of picfeltarraenins IA and IB in rats.

Bioassay- and liquid chromatography/mass spectrometry-guided acetylcholinesterase inhibitors from Picriafel-terrae

Pharmacogn Mag 2013 Oct;9(Suppl 1):S25-31.PMID:24143041DOI:10.4103/0973-1296.117857.

Background: Picria fel-terrae is a traditional Chinese medicine. Materials and methods: A new approach to the search for acetylcholinesterase (AChE) inhibitors from Picria fel-terrae is presented. Results: Bioassay- and LC-MS-guided fractionation of the ethyl acetate extract was from traditional Chinese medicine P.fel-terrae. Following primary extraction, the ethyl acetate extracts fraction of P.fel-terrae showed strong AChE inhibitory activities. So the sample was separated using highperformance liquid chromatography (HPLC). The effluent was split towards two identical 96-well fraction collectors, and the presence of the biologically interesting portion and chromatographic fractions could be readily detected by analyzing selected ion chromatograms through an electrophoresis-electrospray ionization mass spectrometry (ESIMS) system for accurate mass measurement. One 96-well plate was used for a bioassay (AChE-inhibitory assay) and detected the bioactivity and position of the relevant peak in the chromatogram. The positive well in the second 96-well plate was used for identification by LC-(+) ESIMS. Conclusion: As abovementioned, the AChE inhibitory constituents from P.fel-terrae by LC-bioassay-ESIMS were rapid identified. Liquid chromatography/ mass spectrometry (LC-MS) screening detected the presence of six active compounds, identified as picfeltarraenin IA (1), Picfeltarraenin IB (2), picfeltarraenin IV (3), picfeltarraenin X (4), picfeltarraenin XI (5), and one unknown compound. The structures were further determined by 13C NMR. The six compounds expressed stronger AChE inhibition than the known AChE inhibitorTacrine. Above all, the value of this LC-bioassay-ESIMS methodology is highlighted by the finding and structure elucidation of the active constituents from many other structural families of natural products.

Complement-inhibiting cucurbitacin glycosides from Picria fel-terrae

J Nat Prod 1998 Jun 26;61(6):757-61.PMID:9644059DOI:10.1021/np9705773.

Four cucurbitacin glycosides were isolated from Picriafel-terrae and identified by MS and NMR spectroscopy as picfeltarraenin IA (1), Picfeltarraenin IB (2), picfeltarraenin IV (4), and a new compound picfeltarraenin VI (3) (picfeltarraegenin I 3-O-beta-D-xylopyranoside). All four compounds acted as inhibitors on both the classical and alternative pathways of the complement system, with compound 3 exhibiting the highest inhibitory activity (IC50 29 +/- 2 microM and 21 +/- 1 microM, respectively). Compounds 1-4 showed no antiviral, antibacterial, or antifungal activities. Picfeltarraenin IA and IB were tested in an in vitro human tumor cell line panel, but displayed no cytotoxic activity.

A new cucurbitacin from Picria fel-terrae

J Asian Nat Prod Res 2006 Jun;8(4):367-71.PMID:16864449DOI:10.1080/10286020500034998.

A new cucurbitacin, picfeltarraenone II (1) as well as four known cucurbitacins, picfeltarraegenin I (2), picfeltarraenin IA (3), Picfeltarraenin IB (4), and picfeltarraenin IV (5), have been isolated and characterized from the whole plant of Picria fel-terrae. The purity of picfeltarraenin IA has been determined by TLC and HPLC.