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55290-63-6

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55290-63-6 Usage

Description

Atractylodin, a bioactive compound derived from the Atractylodes plant, is a colorless needle crystal with a melting point ranging from 50.5 to 53 degrees Celsius. It is known for its diverse range of pharmacological properties, making it a valuable component in various applications.

Uses

Used in Pharmaceutical Industry:
Atractylodin is used as a therapeutic agent for its hepatoprotective effects, aiding in the protection and regeneration of liver cells. It is particularly useful in treating liver diseases and conditions caused by toxins or viral infections.
Atractylodin is also used as a hypoglycemic agent, helping to lower blood sugar levels and providing relief for individuals with diabetes.
Furthermore, Atractylodin serves as an anti-inflammatory agent, reducing inflammation and alleviating pain associated with various conditions.
In the realm of oncology, Atractylodin is used as an anti-tumor agent, exhibiting potential in inhibiting tumor growth and progression.
Additionally, Atractylodin possesses antibacterial and antiviral properties, making it a useful component in the development of treatments for bacterial and viral infections.
Used in Research and Development:
Atractylodin is utilized in content determination, identification, and pharmacological experiments due to its distinctive chemical properties and diverse range of biological activities. This makes it a valuable tool for scientists and researchers in the field of drug discovery and development.

Pharmacology

Atractylodes is a substance extracted from the dried rhizomes of Atractylodes japonica or Atractylodes japonica. Volatile oil is the main active ingredient in Atractylodes Rhizoma, among which the highest content is Atractylodes Rhizoma, which has pharmacological activities such as lowering blood sugar, diuresis, promoting gastric emptying, anti-inflammatory and anti-tumor.

Check Digit Verification of cas no

The CAS Registry Mumber 55290-63-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,2,9 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 55290-63:
(7*5)+(6*5)+(5*2)+(4*9)+(3*0)+(2*6)+(1*3)=126
126 % 10 = 6
So 55290-63-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H10O/c1-2-3-4-5-6-7-8-10-13-11-9-12-14-13/h2-3,8-12H,1H3/b3-2+,10-8+

55290-63-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(1E,7E)-nona-1,7-dien-3,5-diynyl]furan

1.2 Other means of identification

Product number -
Other names Atractylodin

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:55290-63-6 SDS

55290-63-6Relevant articles and documents

METHOD FOR PRODUCING ATRACTYLODIN AND COBALT COMPLEX COMPOUND

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Paragraph 0038, (2017/02/24)

PROBLEM TO BE SOLVED: To provide a method for producing atractylodin using a cobalt complex compound of atractylodin where the storage of atractylodin having an unstable chemical structure is made possible for a long period, and the cobalt complex compound. SOLUTION: Provided is a cobalt complex compound represented by formula (I). Also provided is a method for producing atractylodin provided with a step where the cobalt complex compound and a deprotection agent are reacted (A respectively independently denotes CO, P(RA)3 or NO; RA denotes a 1 to 4C straight chain or branched chain alkyl group, phenyl group, aldehyde group, carboxyl group or ester group substituted or unsubstituted with a hydroxyl group, an aldehyde group, a carboxyl group or an ester group; in the case the RA is 2 or more, respectively, independent;and R1 denotes H, a methyl group, a hydroxymethyl group, an aldehyde group or a carboxyl group). SELECTED DRAWING: None COPYRIGHT: (C)2016,JPOandINPIT

Synthesis of naturally occurring acetylenes via an alkylidene carbenoid rearrangement

Shi Shun, Annabelle L. K.,Tykwinski, Rik R.

, p. 6810 - 6813 (2007/10/03)

Naturally occurring mosquito larvicidal acetylenes 1 and 2, and analogues 3 and 4, each containing either a 1,3-butadiynyl or a 1,3,5-hexatriynyl moiety, are synthesized via a Fritsch - Buttenberg - Wiechell rearrangement. The alkylidene carbenoid interme

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