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Napelline, a diterpenoid alkaloid found in Aconitum plants like wolfsbane and monkshood, is known for its toxic and medicinal properties. It exhibits significant anti-inflammatory and analgesic effects, positioning it as a promising candidate for the development of innovative pain-relieving medications.

5008-52-6

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5008-52-6 Usage

Uses

Used in Pharmaceutical Industry:
Napelline is used as a potential active ingredient for pain-relief medications due to its notable anti-inflammatory and analgesic properties. Its ability to alleviate pain and reduce inflammation makes it a candidate for the development of new therapeutic agents.
Used in Research and Development:
In the field of medicinal chemistry, NAPELLINE is used as a subject of study for understanding its mechanism of action and potential applications in treating pain and inflammation. This research can lead to the discovery of new drug formulations or the enhancement of existing ones.

Check Digit Verification of cas no

The CAS Registry Mumber 5008-52-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,0 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5008-52:
(6*5)+(5*0)+(4*0)+(3*8)+(2*5)+(1*2)=66
66 % 10 = 6
So 5008-52-6 is a valid CAS Registry Number.
InChI:InChI=1/C22H33NO3/c1-4-23-10-20(3)6-5-17(25)22-15(20)7-13(18(22)23)21-9-12(11(2)19(21)26)14(24)8-16(21)22/h12-19,24-26H,2,4-10H2,1,3H3/t12?,13?,14-,15+,16+,17-,18?,19+,20-,21?,22?/m0/s1

5008-52-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name luciculine

1.2 Other means of identification

Product number -
Other names NAPELLINE

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:5008-52-6 SDS

5008-52-6Relevant academic research and scientific papers

Antiarrhythmic agents based on diterpenoid alkaloids

Yunusov

scheme or table, p. 633 - 638 (2012/02/06)

Diterpenoid alkaloids comprise a large group of natural compounds produced by the plants of the genera Aconitum and Delphinium. Some of these compounds were found to manifest valuable pharmacological properties, including the unique antiarrhythmic activity. Allapinine (derived from the alkaloid lappaconitine) was approved as a drug. The investigation of the structure-activity relationship revealed structural elements responsible for the arrhythmogenic and antiarrhythmic properties.

Five new napelline-type diterpene alkaloids from Aconitum liangshanium

Takayama,Wu,Eda,Oda,Aimi,Sakai

, p. 1644 - 1646 (2007/10/02)

The structures of five new C20-diterpene alkaloids having the napelline skeleton, i.e., 12-epi-lucidusculine (2), 12-epi-19-dehydronapelline (8), 12-epi-19-dehydrolucidusculine (9), liangshanine (3), and liangshanone (11), found from the roots of Aconitum liangshanium, were determined by spectroscopic analysis and chemical reactions.

ALKALOIDS OF THE EPIGEAL PART OF Aconitum karakolicum. THE STRUCTURE OF 12-EPINAPELLINE

Sultankhodzhaev, M. N.,Yunusov, M. S.

, p. 319 - 321 (2007/10/02)

A new alkaloid has been isolated from the eipgeal part of the Aconitum karakolicum Rapaics. and has been called 12-epinapelline.The structure of the new alkaloid has been shown by the preparation of a diacetate and an iso derivative and also by the direct passage from songorine to 12-epinapelline and a study of their spectral characteristics.

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