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26000-17-9

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26000-17-9 Usage

General Description

Lycoctonine is a chemical compound found in various plant species, including the Lycopodium family of mosses and certain members of the Papaveraceae family of flowering plants. It is a type of alkaloid and has been found to possess strong anti-inflammatory and analgesic properties. Additionally, lycoctonine has shown potential as a natural remedy for treating various ailments, including arthritis, rheumatism, and other inflammatory conditions. Its biological activity and potential medicinal uses have attracted considerable interest from researchers and scientists. Further studies on lycoctonine may lead to the development of new pharmaceuticals and natural remedies for treating inflammation-related diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 26000-17-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,0,0 and 0 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 26000-17:
(7*2)+(6*6)+(5*0)+(4*0)+(3*0)+(2*1)+(1*7)=59
59 % 10 = 9
So 26000-17-9 is a valid CAS Registry Number.
InChI:InChI=1/C25H41NO7/c1-6-26-11-22(12-27)8-7-16(31-3)24-14-9-13-15(30-2)10-23(28,17(14)18(13)32-4)25(29,21(24)26)20(33-5)19(22)24/h13-21,27-29H,6-12H2,1-5H3/t13-,14-,15+,16+,17-,18+,19-,20+,21?,22+,23-,24+,25-/m1/s1

26000-17-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name LYCOCTONINE

1.2 Other means of identification

Product number -
Other names Chasmanin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:26000-17-9 SDS

26000-17-9Relevant articles and documents

REACTIONS OF LYCOCTONINE ALKALOIDS WITH ACETIC ANHYDRIDE AND p-TOLUENESULFONIC ACID

Narzullaev, A. S.,Yunusov, M. C.

, p. 475 - 477 (1991)

The reactions of alkaloids having a 7,8-diol system - lycoctonine, browniine, and dihydromonticoline - with acetic anhydride and p-toluenesulfonic acid have been studied.The optimum conditions for this reaction, leading to anhydro compounds, have been found.

Covalent attachment of antagonists to the α7 nicotinic acetylcholine receptor: Synthesis and reactivity of substituted maleimides

Ambrus, Joseph I.,Halliday, Jill I.,Kanizaj, Nicholas,Absalom, Nathan,Harpsoe, Kasper,Balle, Thomas,Chebib, Mary,McLeod, Malcolm D.

supporting information; experimental part, p. 6699 - 6701 (2012/08/14)

The 3-methylmaleimide congeners of the natural product methyllycaconitine (MLA) and an analogue covalently attach to functional cysteine mutants of the α7 nicotinic acetylcholine receptor (nAChR).

Rapid and Efficient Isolation of the Nicotinic Receptor Antagonist Methyllycaconitine from Delphinium: Assignment of the Methylsuccinimide Absolute Stereochemistry as S

Coates, Philippa A.,Blagbrough, Ian S.,Hardick, David J.,Rowan, Michael G.,Wonnacott, Susan,Potter, Barry V. L.

, p. 8701 - 8704 (2007/10/02)

Methyllycaconitine (MLA) has been isolated from Garden Hybrid Delphinium and purified by vacuum liquid chromatography. 13C NMR and optical rotation has been used to characterize the absolute configuration of the methylsuccinimide moiety as S.Ligand binding assays confirmed the potency of MLA and its selectivity for α-bungarotoxin-sensitive neuronal nicotinic acetylcholine receptors.

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