3-(5-[1,2]Dithiolan-3-yl-pentanoylamino)-propyl-amide, identified by its CAS number 691410-93-2, is a synthetic organic compound characterized by its unique structural features, including a dithiolan moiety and an amide functional group. The presence of the dithiolan ring contributes to its potential reactivity and biological activity, as dithiolanes are known for their ability to participate in redox reactions and interact with various biological targets. The pentanoylamino side chain enhances its solubility and may influence its pharmacokinetic properties. This compound may exhibit properties such as antimicrobial, antioxidant, or anticancer activities, making it of interest in medicinal chemistry and drug development. Its molecular structure suggests potential interactions with biological macromolecules, which could be explored in further research. As with many synthetic compounds, the specific characteristics, including stability, solubility, and reactivity, would depend on the conditions under which it is studied, including pH, temperature, and the presence of other chemical species.

α-
Lipoic acid is a cyclic disulfide antioxidant that interconverts with its reduced dithiol form. It is an essential cofactor for decarboxylation reactions of the citric acid cycle and acts as a general antioxidant.
1
AN-
7 is a more lipophilic analog of α-
lipoic acid with enhanced potency and 1.5-
fold increased maximal capacity to stimulate glucose transport into myocytes.
2
This identifies the analogs of lipoic acid as potential new treatments for diabetes.

3-(5-[1,2]DITHIOLAN-3YL-PENTANOYLAMINO)-PROPYL-AMIDE

691410-93-2: 3-(5-[1,2]Dithiolan-3-yl-pentanoylamino)-propyl-amide, identified by its CAS number 691410-93-2, is a synthetic organic compound characterized by its unique structural features, including a dithiolan moiety and an amide functional group. The presence of the dithiolan ring contributes to its potential reactivity and biological activity, as dithiolanes are known for their ability to participate in redox reactions and interact with various biological targets. The pentanoylamino side chain enhances its solubility and may influence its pharmacokinetic properties. This compound may exhibit properties such as antimicrobial, antioxidant, or anticancer activities, making it of interest in medicinal chemistry and drug development. Its molecular structure suggests potential interactions with biological macromolecules, which could be explored in further research. As with many synthetic compounds, the specific characteristics, including stability, solubility, and reactivity, would depend on the conditions under which it is studied, including pH, temperature, and the presence of other chemical species.

AN-7, a lipophilic α-lipoic acid analog, boosts glucose uptake in cells and has potential as a diabetes treatment.

CAS 691410-93-2

3-(5-[1,2]DITHIOLAN-3YL-PENTANOYLAMINO)-PROPYL-AMIDE

AN-7

Ref: TM-T35628