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Piperlotine A Sale

目录号 : GC38565

Piperlotine A 是从罗洛胡椒中分离得到的生物碱,具有抗血小板聚集的作用。

Piperlotine A Chemical Structure

Cas No.:389572-70-7

规格 价格 库存 购买数量
1mg
¥1,206.00
现货
5mg
¥3,627.00
现货
10mg
¥6,174.00
现货

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Sample solution is provided at 25 µL, 10mM.

产品文档

Quality Control & SDS

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产品描述

Piperlotine A is an alkaloid isolated from Piper lolot, with potent antiplatelet aggregation activity[1].

[1]. Li CY, et al. Isolation and identification of antiplatelet aggregatory principles from the leaves of Piper lolot. J Agric Food Chem. 2007 Nov 14;55(23):9436-42.

Chemical Properties

Cas No. 389572-70-7 SDF
Canonical SMILES COC(C=C1)=CC=C1/C=C/C(N2CCCC2)=O
分子式 C14H17NO2 分子量 231.29
溶解度 Soluble in DMSO 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 4.3236 mL 21.6179 mL 43.2358 mL
5 mM 0.8647 mL 4.3236 mL 8.6472 mL
10 mM 0.4324 mL 2.1618 mL 4.3236 mL
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Research Update

Cyrene: a bio-based solvent for the Mizoroki-Heck reaction of aryl iodides

Org Biomol Chem 2023 Jan 4;21(2):351-358.PMID:36503937DOI:10.1039/d2ob02012b.

The development of greener and more sustainable methods, as well as the adaptation of already existing protocols to more environmentally friendly procedures, has become crucial for organic synthesis. The introduction and utilization of greener solvents is a very promising alternative, especially when they can replace toxic organic solvents in the known and widely used organic reactions. Cyrene has appeared to be an excellent alternative solvent for a number of organic reactions. In this work, the development of a new, greener and more economical protocol for the Mizoroki-Heck reaction is described, using Cyrene as the green solvent and Pd/C as the palladium catalyst source. A wide substrate scope for the coupling of aryl iodides with acrylamides, acrylates, acrylic acid, acrylonitrile and styrene was demonstrated. The recyclability of Cyrene and the leaching of palladium in the final product were examined in order to enhance the industrial applicability of this protocol. Furthermore, the synthesis of the natural product Piperlotine A is reported.

Isolation and identification of antiplatelet aggregatory principles from the leaves of Piper lolot

J Agric Food Chem 2007 Nov 14;55(23):9436-42.PMID:17941696DOI:10.1021/jf071963l.

The methanolic extract of Piper lolot, having shown potent inhibitory activity on platelet aggregation induced by arachidonic acid (AA) and platelet activating factor (PAF), was subjected to activity-guided isolation to yield twelve new amide alkaloids, piperlotine A-L (1-12), along with twenty-nine known compounds. Their structures were elucidated on the basis of spectroscopic analysis. The isolated compounds were tested for their inhibitory activity on the rabbit platelet aggregation. The compounds Piperlotine A (1), piperlotine C (3), piperlotine D (4), piperlotine E (5), 3-phenyl-1-(2,4,6-trihydroxyphenyl)propan-1-one (21), 3-(4-methoxyphenyl)-1-(2,4,6-trihydroxyphenyl)propan-1-one (22), 1-trans-cinnamoylpyrrolidine (24), sarmentine (26), pellitorine (27), methyl 3-phenylpropionate (32), and (10S)-10-hydroxypheophorbide a methyl ester (40) showed potent antiplatelet aggregation activity.