Investigational Drug Details

Drug ID: D007
Drug Name: Alpha-lipoic acid
Synonyms: (+)-alpha-Lipoic acid; (R)-(+)-Lipoate; (R)-(+)-lipoic acid; (R)-1,2-Dithiolane-3-pentanoic acid; (R)-1,2-dithiolane-3-valeric acid; (R)-6,8-thioctic acid; (R)-lipoic acid; Alpha lipoic acid; alpha-Lipoic acid; D-thioctic acid; Lipoic acid; R-(+)-thioctic acid; R-alpha-lipoic acid; Thioctic acid; Thioctic acid D-form; α-lipoic acid
Type: Chemical drug
DrugBank ID: DB00166
DrugBank Description: A vitamin-like antioxidant.
PubChem ID: 6122
CasNo: 1200-22-2
Repositioning for NAFLD: Yes
SMILES: C(CCCC(=O)O)[C@@H]1CCSS1
Structure:
InChiKey: AGBQKNBQESQNJD-SSDOTTSWSA-N
Molecular Weight: 206.332
DrugBank Targets: Lipoyltransferase 1, mitochondrial; Lipoyl synthase, mitochondrial; Sodium-dependent multivitamin transporter
DrugBank MoA: Lipoic Acid is generally involved in oxidative decarboxylations of keto acids and is presented as a growth factor for some organisms. Lipoic acid exists as two enantiomers, the R-enantiomer and the S-enantiomer. Normally only the R-enantiomer of an amino acid is biologically active, but for lipoic acid the S-enantiomer assists in the reduction of the R-enantiomer when a racemic mixture is given. Some recent studies have suggested that the S-enantiomer in fact has an inhibiting effect on the R-enantiomer, reducing its biological activity substantially and actually adding to oxidative stress rather than reducing it. Furthermore, the S-enantiomer has been found to reduce the expression of GLUT-4s in cells, responsible for glucose uptake, and hence reduce insulin sensitivity.
DrugBank Pharmacology: Lipoic acid (or α-lipoic acid) is able to pass the blood-brain barrier and is putatively used for detoxification of mercury attached to the brain cells. It can mobilise bound mercury into the blood stream as it is a mercaptan (sulfur compound which readily binds to the mercury). In the blood stream, another chelator such as dimercaptosuccinic acid (DMSA) or methylsulfonylmethane (MSM) is used to transfer mercury safely into the urine for excretion. Neither DMSA nor MSM can cross the blood-brain barrier, which is why both lipoic acid and DMSA are used. It is hypothesized that this treatment-along with carnitine, dimethylglycine (DMG), Vitamin B6, folic acid, and magnesium—could be used to treat autism and amalgam poisoning. In this hypothesis, the reason why autism is difficult to treat is that mercury is attached to the brain cells and most medicines and vitamin supplements do not penetrate the blood-brain barrier. However, α-lipoic acid and perhaps vitamin B12 could making it possible for other chelators to remove mercury safely out of the body and could perhaps one day be used as a treatment for autism. Because lipoic acid is related to cellular uptake of glucose and it is both soluble in water and fat, it is being used for treatment in diabetes. It may be helpful for people with Alzheimer's disease or Parkinson's disease.
DrugBank Indication: For nutritional supplementation, also for treating dietary shortage or imbalance.
Targets: LIPT1
Therapeutic Category: Antioxidant drug
Clinical Trial Progress: Phase 4 on-going (NCT04475276)
Latest Progress: Under clinical trials