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62320

DL-α-Liponsäure

≥98.0% (HPLC), solid

Synonym(e):

(±)-1,2-Dithiolan-3-valeriansäure, 6,8-Dithiooctansäure, DL-6,8-Thioctsäure, Lip(S2)

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€ 111,00

25 G

€ 282,00

€ 111,00


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Über diesen Artikel

Empirische Formel (Hill-System):
C8H14O2S2
CAS-Nummer:
Molekulargewicht:
206.33
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21
EC Number:
214-071-2
MDL number:
Beilstein/REAXYS Number:
81853
Assay:
≥98.0% (HPLC), ≥98.0%
Form:
solid

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Unterstützung erhalten

Produktname

DL-α-Liponsäure, ≥98.0%

Quality Level

assay

≥98.0% (HPLC), ≥98.0%

form

solid

ign. residue

≤0.1%

loss

≤0.2% loss on drying

bp

>286 °C/1.013 hPa

mp

60-62 °C

solubility

water: 0.87 g/L at 22 °C

density

1.4 g/cm3 at 23 °C

functional group

carboxylic acid, disulfide

storage temp.

2-8°C

SMILES string

[OC(=O)CCCCC1CCSS1], OC(=O)CCCCC1CCSS1

InChI

[1S/C8H14O2S2/c9-8(10)4-2-1-3-7-5-6-11-12-7/h7H,1-6H2,(H,9,10)], 1S/C8H14O2S2/c9-8(10)4-2-1-3-7-5-6-11-12-7/h7H,1-6H2,(H,9,10)

InChI key

[AGBQKNBQESQNJD-UHFFFAOYSA-N], AGBQKNBQESQNJD-UHFFFAOYSA-N

Gene Information

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General description

α-lipoic acid (ALA, thioctic acid) is a natural organosulfur compound produced in plants, animals and humans. It is a powerful antioxidant and plays a role in the forming nucleic acids, building blocks of DNA.

This product is a racemic mixture.

Application

(±)-α-Lipoic acid has been used:

  • In in vitro lipoylation studies and in the pyruvate dehydrogenase complex (PDC)-pyruvate dehydrogenase kinase (PDHK) functional assay.
  • To investigate its antioxidative effect on developing cerebellum of rats exposed to arsenic during postnatal period.

Biochem/physiol Actions

Antioxidant and coenzyme needed for the activity of enzyme complexes such as pyruvate dehydrogenase and glycine decarboxylase.
Antioxidant and coenzyme needed for the activity of enzyme complexes such as those of pyruvate dehydrogenase and glycine decarboxylase. Exogenous thioctic acid is reduced intracellularly by two or more enzymes. The reduced form then influences a number of cell processes by direct radical scavenging, recycling of other antioxidants, increasing glutathione synthesis, and modulating transcription factor activity particularly that of NF-κB. Decreases the phagocytosis of myelin by macrophages.
(±)-α-Lipoic acid exhibits direct free radical scavenging property and reduces the increased oxidative stress. In addition, it might also exhibit prooxidant activity. α-Lipoic acid functions as an important prosthetic group in α-keto acid dehydrogenase complexes of the mitochondria. It acts as a potential therapeutic for diabetic patients with distal symmetric polyneuropathy (DSP). α-Lipoic acid is also used in the treatment of energy-impaired and redox unbalanced diseases.

pictograms

Exclamation markEnvironment

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

Lagerklasse

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Die Dokumentenbibliothek aufrufen

Oral treatment with alpha-lipoic acid improves symptomatic diabetic polyneuropathy: the SYDNEY 2 trial
Ziegler D, et al.
Diabetes Care, 29(11), 2365-2370 (2006)
Catherine Grogan et al.
Sensors (Basel, Switzerland), 20(3) (2020-02-12)
The high sensitivity of silicon microcantilever sensors has expanded their use in areas ranging from gas sensing to bio-medical applications. Photochromic molecules also represent promising candidates for a large variety of sensing applications. In this work, the operating principles of
Antioxidant and prooxidant activities of alpha-lipoic acid and dihydrolipoic acid
Moini H, et al.
Toxicology and Applied Pharmacology, 182(1), 84-90 (2002)
Insights on the Use of ?-Lipoic Acid for Therapeutic Purposes
Salehi B., et. al.
Biomolecules, 9(8), 356-356 (2019)
Ameliorative role of antioxidant supplementation on sodium-arsenite induced adverse effects on the developing rat cerebellum
Kaushal P, et al.
Journal of Ayurveda and integrative medicine (2019)

Artikel

Antioxidants protect biological systems from oxidative damage produced by oxygen-containing free radicals and from redoxactive transition metal ions such as iron, copper, and cadmium.

Global Trade Item Number

SKUGTIN
62320-5G-F04061832705774
62320-25G-F04061832705477

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