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3-(5-[1,2]Dithiolan-3yl-Pentanoylamino)-Propyl-Amide is a complex organic chemical compound characterized by a propyl amide group linked to a pentanoylamino moiety, which is further connected to a dithiolan-3yl ring. This sulfur-containing heterocyclic structure within the compound suggests potential biological activity, making it a promising candidate for pharmaceutical research and development, particularly for drugs targeting specific biological processes or pathways.

691410-93-2

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691410-93-2 Usage

Uses

Used in Pharmaceutical Research:
3-(5-[1,2]Dithiolan-3yl-Pentanoylamino)-Propyl-Amide is used as a research compound for exploring its potential biological activity and therapeutic effects. The presence of the dithiolan-3yl ring indicates that it may interact with biological systems in unique ways, warranting further investigation into its properties and applications.
Used in Drug Development:
In the pharmaceutical industry, 3-(5-[1,2]Dithiolan-3yl-Pentanoylamino)-Propyl-Amide is utilized as a lead compound in the development of new drugs. Its molecular structure and functionality could be optimized to target specific biological pathways or processes, potentially leading to the creation of novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 691410-93-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,1,4,1 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 691410-93:
(8*6)+(7*9)+(6*1)+(5*4)+(4*1)+(3*0)+(2*9)+(1*3)=162
162 % 10 = 2
So 691410-93-2 is a valid CAS Registry Number.

691410-93-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(dithiolan-3-yl)-N-[3-[5-(dithiolan-3-yl)pentanoylamino]propyl]pentanamide

1.2 Other means of identification

Product number -
Other names AN-7

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:691410-93-2 SDS

691410-93-2Downstream Products

691410-93-2Relevant academic research and scientific papers

Synthesis and characterization of new and potent α-lipoic acid derivatives

Gruzman, Arie,Hidmi, Adel,Katzhendler, Jehoshua,Haj-Yehie, Abdalla,Sasson, Shlomo

, p. 1183 - 1190 (2007/10/03)

α-Lipoic acid [5-[1,2]-dithiolan-3-yl-pentanoic acid (LA)] is a natural antioxidant and cofactor of several enzymes. It increases the glucose transport activity in skeletal muscles and adipocytes in a non-insulin dependent manner. Therefore, LA is widely used in Type 2 diabetic patients as an oral auxiliary drug. However, large doses of LA (0.8-1.8 gr/day po) are required due to its unfavorable pharmacokinetic parameters. In order to improve these parameters, we synthesized ester and amide LA derivates. Two of these newly synthesized compounds, 5-[1,2]-dithiolan-3-yl-pentanoic acid 3-(5-[1,2]dithiolan-3yl-pentanoylamino)-propyl]-amide (AN-7) and 5-[1,2]-dithiolan-3-yl-pentanoic acid 3-(5-[1,2]-dithiolan-3yl-pentanoyloxy)- propyl ester (AN-8) augmented the rate glucose transport in myotubes in culture in the absence or presence of insulin. Their potency was 12-fold higher than that of the parent compound; their maximal stimulatory effect was 1.5-fold higher than that of LA. When tested in vivo in streptozotocin-diabetic C57/ Black mice, AN-7 (10 mg/kg/day for 2 weeks, sc) reduced blood glucose level by 39% while a higher dose of LA (50 mg/kg/day for 2 weeks, sc) lowered it by 30%. These results indicate that AN-7 is more potent than LA in augmenting glucose transport in skeletal muscles and reducing blood glucose in diabetic animals.

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