Lipoic Acid Suppliers USA

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Lipoic acid Lipoic acid ((R)-(+)-α-Lipoic acid) is an antioxidant, which is an essential cofactor of mitochondrial enzyme complexes. (R)-(+)-α-Lipoic acid is more effective than racemic Lipoic acid. Uses: Scientific research. Group: Natural products. Alternative Names: (R)-(+)-α-Lipoic acid; R-(+)-Thioctic acid. CAS No. 1200-22-2. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-18733. MedChemExpress MCE
Lipoic acid, reduced Lipoic acid, reduced. Group: Biochemicals. Alternative Names: (±)-6,8-Dimercaptooctanoic acid; (±)-Dihydrolipoic acid. Grades: Highly Purified. CAS No. 462-20-4. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C8H16O2S2. US Biological Life Sciences. USBiological 7
Worldwide
Lipoic Acid (Thioctic Acid, Alpha Lipoic Acid) Coenzyme in the oxidative decarboxylation reactions of glucose metabolism and the citric acid cycle. Although it is an essential growth factor for various micro-organisms. a-Lipoic acid, is a naturally occuring coenzyme containing a disulfide that has been used to treat polyneuropathies and hepatic disorders. a-Lipoic acid is a potent inhibitor of NFKB activation and HIV-1 tat driven gene expression. Group: Biochemicals. Alternative Names: (+/-)-1,2-Dithiolane-3-pentanoic Acid; (+/-)-1,2-Dithiolane-3-valeric Acid; (+/-)-Thioctic Acid; (RS)-α-Lipoic Acid; DL-Thioctic Acid; Liposan; Lipothion; NSC 628502; NSC 90788; Protogen A; Thioctsan; Tioctacid. Grades: Cell Culture Grade. CAS No. 1077-28-7. Pack Sizes: 10g, 25g, 100g, 500g. Molecular Formula: C8H14O2S2, Molecular Weight: 206.3. US Biological Life Sciences. USBiological 1
Worldwide
(±)-α-Lipoic Acid Methyl Ester-d5 (±)-α-Lipoic Acid Methyl Ester-d5 is an intermediate used in the synthesis of rac α-Lipoic Acid-d5 (L468752), which is a fat-metabolism stimulator. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 500ug, 1mg. Molecular Formula: C9H11D5O2S2, Molecular Weight: 225.38. US Biological Life Sciences. USBiological 3
Worldwide
a-Lipoic acid a-Lipoic acid. Group: Biochemicals. Grades: Highly Purified. CAS No. 62-46-4. Pack Sizes: 25g, 50g, 100g, 250g, 500g. Molecular Formula: C8H14O2S2. US Biological Life Sciences. USBiological 7
Worldwide
(+)-a-Lipoic Acid ((R)-(+)-1,2-Dithiolane-3-pentanoic Acid,) (+)-a-Lipoic Acid ((R)-(+)-1,2-Dithiolane-3-pentanoic Acid,). Group: Biochemicals. Alternative Names: (R)-(+)-1,2-Dithiolane-3-pentanoic Acid. Grades: Highly Purified. Pack Sizes: 5g. US Biological Life Sciences. USBiological 1
Worldwide
a-Lipoic Acid (Thioctic Acid) a-Lipoic Acid (Thioctic Acid). Group: Biochemicals. Alternative Names: Thioctic Acid. Grades: Highly Purified. Pack Sizes: 25g. US Biological Life Sciences. USBiological 1
Worldwide
α-Lipoic Acid α-Lipoic Acid is a metabolic antioxidant that regulates NFκB signal transduction and can protect against oxidative injury. The exogenous compound is reduced intracellularly by enzymes. Its reduced form is involved in radical scavenging, recycling of other antioxidants, accelerating GSH synthesis, and regulating transcription factor activity, specifically NFkappaB. It also acts as a conenzyme that is required for the activity of pyruvate dehydrogenase and glycine decarboxylase, among other enzyme complexes. Studies show that it can prevent a decrease in the renal antioxidant defense system and prevent the increase of lipid peroxidation, platinum content and plasma creatinine concentrations. In other studies, lipoic acid decreased the phagocytosis of myelin by macrophages, acting as a non-specific scavenger of reactive oxygen species (ROS). Applications: A metabolic antioxidant that regulates nf-κb signal transduction. Group: Coenzymes. Synonyms: DL-Thioctic Acid; DL-6,8-Dithiooctanoic acid; 1,2-Dithiolane-3-valeric acid. CAS No. 1077-28-7. Purity: ≥95%. Mole weight: 206.32. Form: Solid. DL-Thioctic Acid; DL-6,8-Dithiooctanoic acid; 1,2-Dithiolane-3-valeric acid; α-Lipoic Acid; 1077-28-7. Cat No: COEC-041. Creative Enzymes
α-Lipoic Acid α-Lipoic Acid (Thioctic acid) is an antioxidant, which is an essential cofactor of mitochondrial enzyme complexes. α-Lipoic Acid inhibits NF-κB -dependent HIV-1 LTR activation [1] [2] [3]. α-Lipoic Acid induces endoplasmic reticulum (ER) stress-mediated apoptosis in hepatoma cells [4]. α-Lipoic Acid can be used with CPUL1 (HY-151802) to construct the self-assembled nanoaggregate CPUL1-LA NA, which has improved antitumor efficacy than CPUL1 [5]. Uses: Scientific research. Group: Natural products. Alternative Names: Thioctic acid; (±)-α-Lipoic acid; DL-α-Lipoic acid. CAS No. 1077-28-7. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-N0492. MedChemExpress MCE
Alphalipoicacid Heterocyclic Organic Compound. Alternative Names: 5-(1,2-Dithiolan-3-yl)pentanoic acid; DL-6,8-Thioctic acid; (±)-α-Lipoic acid; 5-(dithiolan-3-yl)pentanoic acid; (±)-1,2-Dithiolane-3-pentanoic acid; DL-α-Lipoic acid; DL-Thioctic acid; 6,8-Dithiooctanoic acid; 1,2-Dithiolane-3-p. CAS No. 1077-28-5. Molecular formula: C8H14O2S2. Mole weight: 206.326. Appearance: light yellow to yellow powder. Purity: 0.96. IUPACName: DL-Thioctic Acid. Density: 1.218g/cm³. Catalog: ACM1077285. Alfa Chemistry. 4
Alpha Lipoic Acid Alpha Lipoic Acid or ALA, is found in healthy foods such as spinach, chard, collard greens and broccoli, foods often deficient in standard American diets. It is an antioxidant that is found in every human cell. ALA at 5 % has been shown to reduce fine lines caused by sun damage. Uses: Anti-oxidants. Group: Skin Care Active Ingredients. INCI Name: Thioctic Acid. CAS Number: 1077-28-7. Mckinley Resources Inc
United States and all of its trading partners..
α-Lipoic Acid sodium α-Lipoic Acid (Thioctic acid) sodium is an antioxidant, which is an essential cofactor of mitochondrial enzyme complexes. α-Lipoic Acid sodium inhibits NF-κB -dependent HIV-1 LTR activation [1] [2] [3]. α-Lipoic Acid sodium induces endoplasmic reticulum (ER) stress-mediated apoptosis in hepatoma cells [4]. α-Lipoic Acid sodium can be used with CPUL1 (HY-151802) to construct the self-assembled nanoaggregate CPUL1-LA NA, which has improved antitumor efficacy than CPUL1 [5]. Uses: Scientific research. Group: Natural products. Alternative Names: Thioctic acid sodium; (±)-α-Lipoic acid sodium; DL-α-Lipoic acid sodium. CAS No. 2319-84-8. Pack Sizes: 100 mg; 250 mg. Product ID: HY-N0492A. MedChemExpress MCE
α-Lipoic Acid (Standard) α-Lipoic Acid (Standard) is the analytical standard of α-Lipoic Acid. This product is intended for research and analytical applications. α-Lipoic Acid (Thioctic acid) is an antioxidant, which is an essential cofactor of mitochondrial enzyme complexes. α-Lipoic Acid inhibits NF-κB -dependent HIV-1 LTR activation [1] [2] [3]. α-Lipoic Acid induces endoplasmic reticulum (ER) stress-mediated apoptosis in hepatoma cells [4]. α-Lipoic Acid can be used with CPUL1 (HY-151802) to construct the self-assembled nanoaggregate CPUL1-LA NA, which has improved antitumor efficacy than CPUL1 [5]. Uses: Scientific research. Group: Natural products. Alternative Names: Thioctic acid (Standard); (±)-α-Lipoic acid (Standard); DL-α-Lipoic acid (Standard). CAS No. 1077-28-7. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-N0492R. MedChemExpress MCE
Alpha-lipoic Acid USP Alpha-lipoic Acid USP. CAS No. 1077-28-7. Molecular formula: C8H14O2S2. American Molecules LLC
Alpha Lipoic Acid USP Alpha Lipoic Acid USP. Pharma Resources International LLC
CA, FL & NJ
DL-a-Lipoic acid NHS 99+% (NMR) DL-a-Lipoic acid NHS 99+% (NMR). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100mg. US Biological Life Sciences. USBiological 5
Worldwide
DL-alpha-Lipoic acid (DL Thioctic acid) 25g Pack Size. Group: Bioactive Small Molecules, Building Blocks, Chiral Compounds, Flavours and Fragrance Materials. Formula: C8H14O2S2. CAS No. 1077-28-7. Prepack ID 27534819-25g. Molecular Weight 206.33. See USA prepack pricing. Molekula Americas
DL-alpha-Lipoic acid (DL Thioctic acid) 5g Pack Size. Group: Bioactive Small Molecules, Building Blocks, Chiral Compounds, Flavours and Fragrance Materials. Formula: C8H14O2S2. CAS No. 1077-28-7. Prepack ID 27534819-5g. Molecular Weight 206.33. See USA prepack pricing. Molekula Americas
DL-alpha-Lipoic acid NHS DL-alpha-Lipoic acid NHS. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 100mg. US Biological Life Sciences. USBiological 7
Worldwide
γ-Lipoic Acid γ-Lipoic Acid. Group: Biochemicals. Alternative Names: 6,8-Dimercaptooctanoic Acid; (±)-Dihydro-α-lipoic Acid; (±)-Dihydrolipoic Acid; DL-Dihydro-α-lipoic Acid; Dihydrolipoic Acid; Dihydrothioctic Acid; Reduced Lipoic Acid; Reduced Thioctic Acid; Dihydrothioctic Acid; dl-Dihydrolipoic Acid. Grades: Highly Purified. CAS No. 462-20-4. Pack Sizes: 500mg. Molecular Formula: C8H16O2S2, Molecular Weight: 208.34. US Biological Life Sciences. USBiological 4
Worldwide
Homo-a-lipoic acid Homo-a-lipoic acid. Group: Biochemicals. Alternative Names: 1,2-Dithiolane-3-hexanoic acid; 1,2-Dithiolane-3-caproic acid. Grades: Highly Purified. CAS No. 5616-71-7. Pack Sizes: 1mg, 2mg, 5mg, 10mg. Molecular Formula: C9H16O2S2. US Biological Life Sciences. USBiological 7
Worldwide
?-Lipoic acid ?-Lipoic acid. CAS No: 1077-28-7 Sarchem Laboratories
Sarchem Laboratories New Jersey NJ
rac a-lipoic acid rac a-lipoic acid. Group: Biochemicals. Alternative Names: (+/-)-1,2-Dithiolane-3-pentanoic acid; (+/-)-1,2-Dithiolane-3-valeric acid; (+/-)-Thioctic acid. Grades: Highly Purified. CAS No. 1077-28-7. Pack Sizes: 50g, 100g, 250g, 500g, 1kg. Molecular Formula: C8H14O2S2. US Biological Life Sciences. USBiological 8
Worldwide
rac α-Lipoic Acid-d5 A fat-metabolism stimulator. Group: Biochemicals. Alternative Names: (+/-)-1,2-Dithiolane-3-pentanoic Acid-d5; (+/-)-1,2-Dithiolane-3-valeric Acid-d5; (+/-)-Thioctic Acid-d5; (RS)-α-Lipoic Acid-d5;DL-Thioctic Acid-d5; Liposan-d5; Lipothion-d5; NSC 628502-d5; NSC 90788-d5; Protogen A-d5; Thioctsan-d5; Tioctacid-d5. Grades: Highly Purified. CAS No. 1189471-66-6. Pack Sizes: 1mg. US Biological Life Sciences. USBiological 2
Worldwide
rac α-Lipoic Acid-d5 Heterocyclic Organic Compound. Alternative Names: (+/-)-1,2-Dithiolane-3-pentanoic Acid-d5; (+/-)-1,2-Dithiolane-3-valeric Acid-d5; (+/-)-Thioctic Acid-d5; (RS)-α-Lipoic Acid-d5;DL-Thioctic Acid-d5; Liposan-d5; Lipothion-d5; NSC 628502-d5; NSC 90788-d5; Protogen A-d5; Thioctsan-d5; Tioctacid-d5. CAS No. 1189471-66-6. Molecular formula: C8H9D5O2S2. Mole weight: 211.36. Appearance: Pale Yellow Solid. Purity: 0.96. IUPACName: 5,5-dideuterio-5-(3,4,4-trideuteriodithiolan-3-yl)pentanoic acid. Canonical SMILES: C1CSSC1CCCCC(=O)O. Catalog: ACM1189471666. Alfa Chemistry. 2
(R)-(+)-a-Lipoic acid (R)-(+)-a-Lipoic acid. Group: Biochemicals. Alternative Names: (3R)-1,2-Dithiolane-3-pentanoic acid; (R)-(+)-1,2-Dithiolane-3-pentanoic acid; (+)-1,2-Dithiolane-3-valeric acid. Grades: Highly Purified. CAS No. 1200-22-2. Pack Sizes: 10g, 25g, 50g, 100g, 250g. Molecular Formula: C8H14O2S2. US Biological Life Sciences. USBiological 7
Worldwide
(R)-alpha-Lipoic Acid (R)-alpha-Lipoic Acid, a vitamin-like organosulfur compound, is widely used as a dietary supplement and antioxidant. It has been also found to influence the activity of nuclear factor kappa-B (NF-κB). Nutritional supplement in health care products. Uses: Ingredient of health care products. Synonyms: (R)-lipoic acid; (+)-alpha-Lipoic acid; (R)-5-(1,2-Dithiolan-3-yl)pentanoic acid; R-(+)-alpha-Lipoic acid; 5-[(3R)-dithiolan-3-yl]pentanoic acid. Grades: 98%. CAS No. 1200-22-2. Molecular formula: C8H14O2S2. Mole weight: 206.318. BOC Sciences
R-Alpha Lipoic Acid Sodium Salt R-Alpha Lipoic Acid Sodium Salt. CAS No. 176110-81-9. Pharma Resources International LLC
CA, FL & NJ
(S)-(-)-a-Lipoic acid (S)-(-)-a-Lipoic acid. Group: Biochemicals. Alternative Names: (3S)-1,2-Dithiolane-3-pentanoic acid; (S)-(-)-Thioctic acid. Grades: Highly Purified. CAS No. 1077-27-6. Pack Sizes: 500mg, 1g. Molecular Formula: C8H14O2S2. US Biological Life Sciences. USBiological 7
Worldwide
6,8-Dichlorooctanoic Acid Ethyl Ester 6,8-Dichlorooctanoic Acid Ethyl Ester is an industrial toxin as well as an intermediate product of lipoic acid synthesis. Group: Biochemicals. Alternative Names: Ethyl 6,8-Dichlorooctanoate. Grades: Highly Purified. CAS No. 1070-64-0. Pack Sizes: 10g. US Biological Life Sciences. USBiological 2
Worldwide
6-Hydroxy-8-[(phenylmethyl)thio]-octanoic Acid Methyl Ester-d5 Used in the preparation of Lipoic Acid and its derivatives. Group: Biochemicals. Alternative Names: 8-(Benzylthio)-6-hydroxy-octanoic Acid Methyl Ester-d5. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. USBiological 2
Worldwide
8-(Benzylthio)-6-oxo-octanoic Acid Methyl Ester-d4 Used in the preparation of Lipoic Acid and its derivatives. Group: Biochemicals. Alternative Names: 6-Oxo-8-[(phenylmethyl)thio]-octanoic Acid Methyl Ester-d4. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. USBiological 2
Worldwide
8-Chloro-6-oxo-octanoic Acid Ethyl Ester Intermediate in the synthesis of Lipoic Acid and its derivatives. Group: Biochemicals. Grades: Highly Purified. CAS No. 50628-91-6. Pack Sizes: 100mg. US Biological Life Sciences. USBiological 2
Worldwide
8-Methoxy-6-oxo-octanoic Acid Methyl Ester-d4 Used in the synthesis of Lipoic Acid. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. USBiological 2
Worldwide
(+/-)-alpha-Lipoamide (+/-)-alpha-Lipoamide is a coenzyme, which transfer acetyl and hydrogen in Pyruvate deacylation oxidation process. It may be used in treatment of insulin resistance by stimulating mitochondrial biogenesis. It has shown to have a good therapeutic effect on early diabetic nephropathy when used in combination with Alprostadil. Uses: (+/-)-alpha-lipoamide may be used in treatment of insulin resistance by stimulating mitochondrial biogenesis. it has shown to have a good therapeutic effect on early diabetic nephropathy. Synonyms: Lipoamide; Lipoacin; NSC 90787; NSC-90787; NSC90787; Lipoamide;Thioctamide;Thioctic acid amide;Vitamin N;Alpha-Lipoic acid amide;5-(Dithiolan-3-yl)pentanamide;(±)-α-Lipoamide;DL-Lipoamide;DL-6,8-Thioctamide;1,2-Dithiolane-3-pentanamide. Grades: >98 %. CAS No. 940-69-2. Molecular formula: C8H15NOS2. Mole weight: 205.34. BOC Sciences
CAY10506 Peroxisome proliferator-activated receptor gamma (PPARγ), also known as the glitazone receptor, or NR1C3, is a type II nuclear receptor that in humans is encoded by the PPARG gene. CAY10506 is a PPARγ agonist, which is a nuclear transcription factor that controls lipid homeostasis and glucose metabolism. It is a hybrid lipoic acid (anti-diabetic drugs of the thiazolidinedione) TZD derivative that transactivates human PPARγ with an EC50 value of 10 μM. Synonyms: CAY 10506; CAY-10506. Grades: ≥98%. CAS No. 292615-75-9. Molecular formula: C20H26N2O4S3. Mole weight: 454.6. BOC Sciences 10
Devimistat Devimistat (CPI-613) is a mitochondrial metabolism inhibitor. Devimistat is a lipoic acid antagonist that abrogates mitochondrial energy metabolism to induce apoptosis in various cancer cells [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CPI-613. CAS No. 95809-78-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-15453. MedChemExpress MCE
Diaphorase 22 from Recombinant E.coli A flavoprotein (FAD). A component of the multienzyme 2-oxo-acid dehydrogenase complexes. In the pyruvate dehydrogenase complex, it binds to the core of EC 2.3.1.12, dihydrolipoyllysine-residue acetyltransferase, and catalyses oxidation of its dihydrolipoyl groups. It plays a similar role in the oxoglutarate and 3-methyl-2-oxobutanoate dehydrogenase complexes. Another substrate is the dihydrolipoyl group in the H-protein of the glycine-cleavage system (click here for diagram), in which it acts, together with EC 1.4.4.2, glycine dehydrogenase (decarboxylating), and EC 2.1.2.10, aminomethyltransferase, to break down glycine. It can also use free dihydrolipoate, dihydrolipoami...(NADH); lipoamide reductase; lipoamide reductase (NADH); lipoate dehydrogenase; lipoic acid dehydrogenase; lipoyl dehydrogenase; protein-6-N-(dihydrolipoyl)lysine:NAD+ oxidoreductase. Enzyme Commission Number: EC 1.8.1.4. CAS No. 9001-18-7. Diaphorase. Mole weight: ca. 110,000. Activity: >150 U/mg protein. Storage: Store at -20°C. Form: Lyophilized. Source: E. coli. LDP-Glc; LDP-Val; dehydrolipoate dehydrogenase; diaphorase; dihydrolipoamide dehydrogenase; dihydrolipoamide:NAD+ oxidoreductase; dihydrolipoic dehydrogenase; dihydrothioctic dehydrogenase; lipoamide dehydrogenase (NADH); lipoamide oxidoreductase (NADH); lipoamide reductase; lipoamide reductase (NADH); lipoate d Creative Enzymes
Diaphorase from microorganism Diaphorase from microorganism. Better stability and reactivity than dia-187. Group: Enzymes. Synonyms: dehydrolipoate dehydrogenase; diaphorase; dihydrolipoamide dehydrogenase; dihydrolipoamide:NAD+ oxidoreductase; dihydrolipoic dehydrogenase; dihydrothioctic dehydrogenase; lipoamide dehydrogenase (NADH); lipoamide oxidoreductase (NADH); lipoamide reductase; lipoamide reductase (NADH); lipoate dehydrogenase; lipoic acid dehydrogenase; lipoyl dehydrogenase; dihydrolipoyl dehydrogenase; Lipoamide Dehydrogenase. Enzyme Commission Number: EC 1.6.99.-. Diaphorase. Source: Microorganism. dehydrolipoate dehydrogenase; diaphorase; dihydrolipoamide dehydrogenase; dihydrolipoamide:NAD+ oxidoreductase; dihydrolipoic dehydrogenase; dihydrothioctic dehydrogenase; lipoamide dehydrogenase (NADH); lipoamide oxidoreductase (NADH); lipoamide reductase; lipoamide reductase (NADH); lipoate dehydrogenase; lipoic acid dehydrogenase; lipoyl dehydrogenase; dihydrolipoyl dehydrogenase; EC 1.8.1.4; 9001-18-7; Lipoamide Dehydrogenase. Cat No: DIA-275. Creative Enzymes
dihydrolipoyl dehydrogenase A flavoprotein (FAD). A component of the multienzyme 2-oxo-acid dehydrogenase complexes. In the pyruvate dehydrogenase complex, it binds to the core of EC 2.3.1.12, dihydrolipoyllysine-residue acetyltransferase, and catalyses oxidation of its dihydrolipoyl groups. It plays a similar role in the oxoglutarate and 3-methyl-2-oxobutanoate dehydrogenase complexes. Another substrate is the dihydrolipoyl group in the H-protein of the glycine-cleavage system (click here for diagram), in which it acts, together with EC 1.4.4.2, glycine dehydrogenase (decarboxylating), and EC 2.1.2.10, aminomethyltransferase, to break down glycine. It can also use free dihydrolipoate, dihydrolipoamide or...tase (NADH); lipoamide reductase; lipoamide reductase (NADH); lipoate dehydrogenase; lipoic acid dehydrogenase; lipoyl dehydrogenase; protein-6-N-(dihydrolipoyl)lysine:NAD+ oxidoreductase. Enzyme Commission Number: EC 1.8.1.4. CAS No. 9001-18-7. Diaphorase. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1648; dihydrolipoyl dehydrogenase; EC 1.8.1.4; 9001-18-7; LDP-Glc; LDP-Val; dehydrolipoate dehydrogenase; diaphorase; dihydrolipoamide dehydrogenase; dihydrolipoamide:NAD+ oxidoreductase; dihydrolipoic dehydrogenase; dihydrothioctic dehydrogenase; lipoamide dehydrogenase (NADH); lipoamide oxido Creative Enzymes
dihydrolipoyllysine-residue acetyltransferase A multimer (24-mer or 60-mer, depending on the source) of this enzyme forms the core of the pyruvate dehydrogenase multienzyme complex, and binds tightly both EC 1.2.4.1, pyruvate dehydrogenase (acetyl-transferring) and EC 1.8.1.4, dihydrolipoyl dehydrogenase. The lipoyl group of this enzyme is reductively acetylated by EC 1.2.4.1, and the only observed direction catalysed by EC 2.3.1.12 is that where the acetyl group is passed to coenzyme A. Group: Enzymes. Synonyms: acetyl-CoA:dihydrolipoamide S-acetyltransferase; dihydrolipoamide S-acetyltransferase; d. Enzyme Commission Number: EC 2.3.1.12. CAS No. 9032-29-5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2058; dihydrolipoyllysine-residue acetyltransferase; EC 2.3.1.12; 9032-29-5; acetyl-CoA:dihydrolipoamide S-acetyltransferase; dihydrolipoamide S-acetyltransferase; dihydrolipoate acetyltransferase; dihydrolipoic transacetylase; dihydrolipoyl acetyltransferase; lipoate acetyltransferase; lipoate transacetylase; lipoic acetyltransferase; lipoic acid acetyltransferase; lipoic transacetylase; lipoylacetyltransferase; thioltransacetylase A; transacetylase X; enzyme-dihydrolipoyllysine:acetyl-CoA S-acetyltransferase; acetyl-CoA:enzyme 6-N-(dihydrolipoyl)lysine S-acetyltransferase. Cat No: EXWM-2058. Creative Enzymes
DL-Thioctic acid DL-Thioctic acid is a non-specific free radical scavenger and has anti-oxidant properties. It could be used as a fat-metabolism stimulator. Synonyms: Thioctic acid; alpha-Lipoic acid; (+-)-2-dithiolane-3-pentanoic acid; (+-)-2-dithiolane-3-valeric acid; (+/-)-2-dithiolane-3-pentanoic acid; 1,2-Dithiolane-3-pentanoic acid; 1,2-Dithiolane-3-pentanoic acid, (±)-; 1,2-Dithiolane-3-valeric acid, (±)-; (RS)-Lipoic acid; (RS)-α-Lipoic acid; (±)-Lipoic acid; (±)-Thioctic acid; (±)-α-Lipoic acid; 5-(1,2-Dithiolan-3-yl)pentanoic acid; 5-(1,2-Dithiolan-3-yl)valeric acid; 6,8-Thioctic acid; 6-Thioctic acid; DL-6,8-Thioctic acid; DL-6-Thioctic acid; DL-Lipoic acid; DL-α-Lipoic acid; Alipure; Biletan; Byodinoral-R; dl-α-Lipoic acid; Espa-lipon; Liposan; Lipothion; NSC 628502; NSC 90788; Octolipen; Oktolipen; Protogen A; Pyruvate oxidation factor; Thioctic acid; Thioctsan; Tioctidasi; Tioctidasi acetate replacing factor; α-(±)-Lipoic acid; α-lipon 300; α-Liponic acid. Grades: 98%. CAS No. 1077-28-7. Molecular formula: C8H14O2S2. Mole weight: 206.32. BOC Sciences
Lipoamide Lipoamide ((±)-α-Lipoamide) is a monocarboxylic acid derivative of a neutral amide, formed by the condensation of the carboxyl group of lipoic acid and ammonia. Lipoamide protects against oxidative stress-mediated neuronal cell damage and also acts as a coenzyme to transfer acetyl groups and hydrogen during pyruvate deacylation. Lipoamide also stimulates mitochondrial biogenesis in adipocytes through the endothelial NO synthase-cGMP-protein kinase G signaling pathway [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: (±)-α-Lipoamide; DL-Lipoamide; DL-6,8-Thioctamide. CAS No. 940-69-2. Pack Sizes: 100 mg; 500 mg. Product ID: HY-B1142. MedChemExpress MCE
lipoate-protein ligase Requires Mg2+. This enzyme participates in lipoate salvage, and is responsible for lipoylation in the presence of exogenous lipoic acid. The enzyme attaches lipoic acid to the lipoyl domains of certain key enzymes involved in oxidative metabolism, including pyruvate dehydrogenase (E2 domain), 2-oxoglutarate dehydrogenase (E2 domain), the branched-chain 2-oxoacid dehydrogenases and the glycine cleavage system (H protein). Lipoylation is essential for the function of these enzymes. The enzyme can also use octanoate instead of lipoate. Group: Enzymes. Synonyms: lplA (gene name); lplJ (gene name); lipoate protein ligase; lipoate-protein ligase A; LPL; LPL-B. Enzyme Commission Number: EC 6.3.1.20. CAS No. 144114-18-1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-5723; lipoate-protein ligase; EC 6.3.1.20; 144114-18-1; lplA (gene name); lplJ (gene name); lipoate protein ligase; lipoate-protein ligase A; LPL; LPL-B. Cat No: EXWM-5723. Creative Enzymes
lipoyl amidotransferase In the bacterium Listeria monocytogenes the enzyme takes part in a pathway for scavenging of lipoic acid. The enzyme is bound to 2-oxo-acid dehydrogenases such as the pyruvate dehydrogenase complex, where it transfers the lipoyl moiety from lipoyl-[glycine cleavage system H] to the E2 subunits of the complexes. Group: Enzymes. Synonyms: LipL (gene name, ambiguous). Enzyme Commission Number: EC 2.3.1.200. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2145; lipoyl amidotransferase; EC 2.3.1.200; LipL (gene name, ambiguous). Cat No: EXWM-2145. Creative Enzymes
lipoyl synthase This enzyme is a member of the 'AdoMet radical' (radical SAM) family, all members of which produce the 5'-deoxyadenosin-5'-yl radical and methionine from AdoMet [i.e. S-adenosylmethionine, or S-(5'-deoxyadenosin-5'-yl)methionine], by the addition of an electron from an iron-sulfur centre. The radical is converted into 5'-deoxyadenosine when it abstracts a hydrogen atom from C-6 and C-8, leaving reactive radicals at these positions so that they can add sulfur, with inversion of configuration. This enzyme catalyses the final step in the de-novo biosynthesis of the lipoyl cofactor, with the other enzyme involved being EC 2.3.1.181, lipoyl(octanoyl) transferase. Lipoylation is essential ...pathway involves EC 2.7.7.63, lipoate-protein ligase, which can lipoylate apoproteins using exogenous lipoic acid (or its analogues). Group: Enzymes. Synonyms: LS; LipA; lipoate synthase; protein 6-N-(octanoyl)lysine:sulfur sulfurtransferase; protein N6-(octanoyl)lysine:sulfur sulfurtransferase. Enzyme Commission Number: EC 2.8.1.8. CAS No. 189398-80-9. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3366; lipoyl synthase; EC 2.8.1.8; 189398-80-9; LS; LipA; lipoate synthase; protein 6-N-(octanoyl)lysine:sulfur sulfurtransferase; protein N6-(octanoyl)lysine:sulfur sulfurtransferase. Cat No: EXWM-3366. Creative Enzymes
Native Clostridium kluyveri Diaphorase Native Clostridium kluyveri Diaphorase. Applications: Diaphorase from clostridium kluyveri, or lipoyl dehydrogenase, has been used in a study to assess the protein-protein interactions in assembly of lipoic acid on the 2-oxoacid dehydrogenases of aerobic metabolism. lipoyl dehydrogenase has also been used in a study to investigate the redox regulation of tyrosine nitration and 3-nitrotyrosine reduction by antioxidants. Group: Enzymes. Synonyms: dehydrolipoate dehydrogenase; diaphorase; dihydrolipoamide dehydrogenase; dihydrolipoamide:NAD+ oxidoreductase; dihydrolipoic dehydrogenase; dihydrothioctic dehydrogenase; lipoamide dehydrogenase (NADH); lipoamide oxidoreductase (NADH); lipoamide reductase; lipo. Enzyme Commission Number: EC 1.8.1.4. CAS No. 9001-18-7. Diaphorase. Activity: 3.0-20.0 units/mg protein (biuret). Storage: Store at -20°C. Form: Lyophilized powder. Source: Clostridium kluyveri. dehydrolipoate dehydrogenase; diaphorase; dihydrolipoamide dehydrogenase; dihydrolipoamide:NAD+ oxidoreductase; dihydrolipoic dehydrogenase; dihydrothioctic dehydrogenase; lipoamide dehydrogenase (NADH); lipoamide oxidoreductase (NADH); lipoamide reductase; lipoamide reductase (NADH); lipoate dehydrogenase; lipoic acid dehydrogenase; lipoyl dehydrogenase; dihydrolipoyl dehydrogenase; EC 1.8.1.4; 9001-18-7; Lipoamide Dehydrogenase. Cat No: NATE-0875. Creative Enzymes
Native Escherichia coli Thioredoxin Reductase Thioredoxin reductase (TrxR) is an NADPH-dependent oxidoreductase containing one FAD per subunit that reduces the active site disulfide in oxidised thioredoxin (Trx). The molecular weight of the isozymes from mammalian sources vary between 55-67 kDa as compared with 35 kDa in prokaryotes, plants or yeast. The substrate specificity of the mammalian enzyme is much broader than the prokaryotic enzyme reducing both mammalian and E. coli thioredoxins as well as well as non-disulfide substrates such selenite, lipoic acids, lipid hydroperoxides and hydrogen peroxide. Applications: Thioredoxin reductase from escherichia coli can be used in peroxidase-coupled thioredoxin system assay for assessing the peroxidase activitiy of cys-based thiol peroxidases. the product was used for determining the enzymatic activity of his6-ahp1p. Group: Enzymes. Synonyms: NADP-thioredoxi. Enzyme Commission Number: EC 1.8.1.9. CAS No. 9074-14-0. TrxR. Activity: >25 units/mg protein (Bradford). Storage: 2-8°C. Form: ammonium sulfate suspension; Suspension in 3.6 M (NH4)2SO4 containing 30 mM potassium phosphate buffer, pH 7.5, and 2 mM EDTA. Source: Escherichia coli. NADP-thioredoxin reductase; NADPH-thioredoxin reductase; thioredoxin reductase (NADPH); NADPH2:oxidized thioredoxin oxidoreductase; thioredoxin-disulfide reductase; EC 1.8.1.9; TrxR. Cat No: NATE-0718. Creative Enzymes
Native Rat Thioredoxin Reductase Thioredoxin reductase (TrxR) is an NADPH-dependent oxidoreductase containing one FAD per subunit that reduces the active site disulfide in oxidised thioredoxin (Trx). The molecular weight of the isozymes from mammalian sources vary between 55-67 kDa as compared with 35 kDa in prokaryotes, plants or yeast. The substrate specificity of the mammalian enzyme is much broader than the prokaryotic enzyme reducing both mammalian and E. coli thioredoxins as well as well as non-disulfide substrates such selenite, lipoic acids, lipid hydroperoxides and hydrogen peroxide. Applications: Thioredoxin reductase from rat liver can be used for studying the uptake and reduction of a-lipoic acid... NADP-thioredoxin reductase; NADPH-thioredoxin reductase; thioredoxin reductase (NADPH); NADPH2:oxidized thioredoxin oxidoreductase; thioredoxin-disulfide reductase; EC 1.8.1.9; TrxR; 9074-14-0. Enzyme Commission Number: EC 1.8.1.9. CAS No. 9074-14-0. TrxR. Activity: > 100 units/mg protein (Bradford). Storage: -20°C. Form: buffered aqueous glycerol solution; Solution in 50 mM Tris-HCl, pH 7.5, 300 mM NaCl, 1 mM EDTA, and 10% glycerol. Source: Rat liver. Species: Rat. NADP-thioredoxin reductase; NADPH-thioredoxin reductase; thioredoxin reductase (NADPH); NADPH2:oxidized thioredoxin oxidoreductase; thioredoxin-disulfide reductase; EC 1.8.1.9; TrxR; 9074-14-0. Cat No: NATE-0713. Creative Enzymes
(R)-(+)-1,2-Dithiolane-3-pentanoic acid Heterocyclic Organic Compound. Alternative Names: (R)-LIPOIC ACID;R-(+)-ALPHA-LIPOIC ACID;R-ALPHA-LIPOIC ACID;(R)-(+)-1,2-DITHIOLANE-3-PENTANOIC ACID;(R)-(+)-Thioctic Acid ;R-(+)-Alpha-Lipoic Acid 1200-22-2;(3R)-1,2-Dithiolane-3-pentanoic Acid;(R)-(+)-a-Lipoic Acid. CAS No. 1200-22-2. Molecular formula: C8H14O2S2. Mole weight: 206.33. Catalog: ACM1200222. Alfa Chemistry. 3
(R)-(+)-α-Lipoic Amide (R)-(+)-α-Lipoic Amide is amide form of rac α-Lipoic Acid (L468725) and is useful for the prevention of primary hypertension. Group: Biochemicals. Grades: Highly Purified. CAS No. 122999-10-4. Pack Sizes: 10mg, 100mg. Molecular Formula: C8H15NOS2, Molecular Weight: 205.34. US Biological Life Sciences. USBiological 2
Worldwide
Sodium (R)-alpha-lipoate Sodium (R)-alpha-lipoate, a robust antioxidant, is efficaciously exploited to rectify diabetic neuropathy. By enhancing glucose metabolism and curtailing oxidative stress, sodium (R)-alpha-lipoate averts nerve damage. Additionally, research illustrates its prospective role in remedying Alzheimer's disease and multiple sclerosis. Synonyms: Sodium (R)-lipoate; 1,2-Dithiolane-3-pentanoic acid, sodium salt, (R)-; Sodium (R)-5-(1,2-dithiolan-3-yl)pentanoate; 1,2-Dithiolane-3-pentanoic acid, sodium salt, (3R)- (1:1); (R)-lipoic acid sodium salt; R-(+)-alpha-Lipoic acid sodium salt. Grades: ≥95%. CAS No. 176110-81-9. Molecular formula: C8H13NaO2S2. Mole weight: 228.31. BOC Sciences 9
(S)-Thioctic acid (S)-Thioctic acid ((S)-lipoic acid; (S)-5-(1,2-Dithiolan-3-yl)pentanoic acid) is a biochemical reagent that can be used as a biological material or organic compound for life science related research [1]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: (S)-lipoic acid; (S)-5-(1,2-Dithiolan-3-yl)pentanoic acid. CAS No. 1077-27-6. Pack Sizes: 10 mM * 1 mL; 5 g. Product ID: HY-W014590. MedChemExpress MCE
Thioctate trometamol Thioctate trometamol, a derivative of alpha-lipoic acid, displays potent antioxidant effects that aid in the management of diabetic neuropathy, alcoholic liver disease, and associated ailments. By boosting glucose metabolism and mitigating oxidative stress, this pharmaceutical compound facilitates the restoration of metabolic homeostasis. Conventionally available in tablet form for oral administration, Thioctate trometamol boasts excellent patient tolerance. Its striking antioxidant attributes are infinitely promising for disease mitigation in diverse clinical settings. Synonyms: Dexlipotam; Thioctic acid tromethamine; 5-(1,2-Dithiolaln-3-yl)-pentanoic acid tromethamine; Lipoic Acid Tromethamine Salt; 1,2-Dithiolane-3-pentanoic acid, compd. with 2-amino-2-(hydroxymethyl)-1,3-propanediol (1:1). Grades: ≥95%. CAS No. 14358-90-8. Molecular formula: C8H14O2S2.C4H11NO3. Mole weight: 327.46. BOC Sciences 9
Thioctic acid Supplement. CAS No. 1077-28-7. Categories: dl- alpha-lipoic acid, 5-(1,2-dithiolan-3-yl)pentanoic acid, 1. Sostie Inc
US, Austria, Lithuania
Thioctic acid Thioctic acid. Uses: For analytical and research use. Group: Pharma & vet compounds & metabolites; pharma & vet compounds & metabolites; api standards; european pharmacopoeia (ph. eur.); pharmaceutical toxicology; pharmacopoeial standards. Alternative Names: 6,8-Thioctic acid, DL-6,8-Thioctic acid, Espa-lipon, Liposan, 1,2-Dithiolane-3-valeric acid, (+/-)-1,2-Dithiolane-3-pentanoic acid, 6-Thioctic acid, DL-alpha-Lipoic acid, 5-(1,2-Dithiolan-3-yl)valeric acid, DL-Thioctic acid, NSC 628502, Tioctidasi, DL-6-Thioctic acid, Tioctidasi acetate replacing factor, (RS)-alpha-Lipoic acid, Lipothion, NSC 90788, dl-Thioctic acid, Protogen A, (+/-)-1,2-Dithiolane-3-valeric acid, (+/-)-alpha-Lipoic acid, alpha-Liponic acid, Biletan, Tioctacid, Thioctacid,Thioctic Acid, 5-(1,2-Dithiolan-3-yl)pentanoic acid, Pyruvate oxidation factor, dl-Lipoic acid, (RS)-Lipoic acid, (+/-)-Lipoic acid, Thioctsan, Thiotacid, Alipure, 1,2-Dithiolane-3-pentanoic acid, (+/-)-Thioctic acid, Thioctic acid. CAS No. 1077-28-7. IUPAC Name: 5-(dithiolan-3-yl)pentanoic acid. Molecular Formula: C8H14O2S2. Mole Weight: 206.33. Catalog: APS1077287. SMILES: OC(=O)CCCCC1CCSS1. Format: Neat. Alfa Chemistry Analytical Products

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