Citrate Lyase Suppliers USA
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Product | Description | |
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BMS 303141 (ATP Citrate Lyase Inhibitor, Orally Bioavailable, 3,5-Dichloro-2-hydroxy-N-(4-methoxy[1,1'-biphenyl]-3-yl)-benzenesulfonamide) Quick inquiry Where to buy Suppliers range | ATP citrate lyase (ACL) inhibitor (IC50 = 0.13um for human recombinant ACL); blocks lipid synthesis (IC50 = 8um in HepG2 cells). Displays no cytotoxicity up to a concentration of 50um. Lowers plasma glucose and triglycerides in a mouse model of hyperlipidemia. Orally bioavailable. Group: Biochemicals. Grades: Highly Purified. CAS No. 943962-47-8. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
Antimycin A1 Quick inquiry Where to buy Suppliers range | Antimycin A is a macrolide antibiotic produced by Streptomyces kitasawaensis, Str. griseus and Str. antibioticus. Antimycin A1 can inhibit atp-citrate lyase activity. Synonyms: dihydrosamidin. Grades: >98% by HPLC. CAS No. 642-15-9. Molecular formula: C28H40N2O9. Mole weight: 548.62. | |
Antimycin A2 Quick inquiry Where to buy Suppliers range | Antimycin A is a macrolide antibiotic produced by Streptomyces kitasawaensis, Str. griseus and Str. antibioticus. Antimycin A2 can inhibit atp-citrate lyase activity. Synonyms: 3-(3-Formamidosalicylamido)-8-hexyl-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl butyrate. Grades: 90%. CAS No. 27220-57-1. Molecular formula: C27H38N2O9. Mole weight: 534.60. | |
Antimycin A3 Quick inquiry Where to buy Suppliers range | Antimycin A is a macrolide antibiotic produced by Streptomyces kitasawaensis, Str. griseus and Str. antibioticus. Antimycin A3 can inhibit atp-citrate lyase activity. Synonyms: Blastomycin. Grades: >98% by HPLC. CAS No. 522-70-3. Molecular formula: C26H36N2O9. Mole weight: 520.57. | |
Antimycin A4 Quick inquiry Where to buy Suppliers range | Antimycin A is a macrolide antibiotic produced by Streptomyces kitasawaensis, Str. griseus and Str. antibioticus. Antimycin A4 can inhibit atp-citrate lyase activity. Synonyms: 8-Butyl-3-(3-formamido-2-hydroxybenzamido)-2,6-dimethyl-4,9-dioxo-1,5-dioxonan-7-yl butyrate. Grades: >98% by HPLC. CAS No. 27220-59-3. Molecular formula: C25H34N2O9. Mole weight: 506.54. | |
ETC-1002 Quick inquiry Where to buy Suppliers range | ETC-1002 is a novel, first-in-class, orally available, once-daily LDL-C lowering small molecule and is activator of hepatic AMP-activated protein kinase (AMPK). It also has potent inhibitory activity against hepatic ATP-citrate lyase. Synonyms: ESP-55016; ESP55016; ESP 55016; ETC-1002; ETC 1002; ETC1002; Bempedoate; Bempedoic acid. Grades: >98%. CAS No. 738606-46-7. Molecular formula: C19H36O5. Mole weight: 344.49. | |
(-)-Hydroxycitric acid Quick inquiry Where to buy Suppliers range | (-)-Hydroxycitrate is a potent competitive inhibitor of ATP citrate lyase, which inhibits fatty acid synthesis, lipogenesis, food intake and induced weight loss. Synonyms: Garcinia acid. Grades: 95%. CAS No. 27750-10-3. Molecular formula: C6H8O8. Mole weight: 208.12. | |
Hydroxycitric acid Quick inquiry Where to buy Suppliers range | Hydroxycitric acid is a natural compound found in the fruits of Garcinia atroviridis. Hydroxycitric acid acts as an inhibitor of the enzyme ATP-citrate lyase. Nutritional supplement in health care products. Uses: Ingredient of health care products. Synonyms: Hydroxycitrate; (-)-Hydroxycitric acid; Hydroxycitricacid; 1,2-Dihydroxy-1,2,3-propanetricarboxylic acid. Grades: 60%. CAS No. 6205-14-7. Molecular formula: C6H8O8. Mole weight: 208.122. | |
MEDICA 16 Quick inquiry Where to buy Suppliers range | MEDICA 16 is a selective free fatty acid 1 receptor agonist. It is also an ATP citrate lyase inhibitor. MEDICA 16 shows hypolipidemic and antidiabetogenic effects in the rat. Synonyms: MEDICA 16; MEDICA16; MEDICA-16; 3,3,14,14-Tetramethylhexadecanedioic acid. Grades: ≥98% by HPLC. CAS No. 87272-20-6. Molecular formula: C20H38O4. Mole weight: 342.51. | |
Radicicol Quick inquiry Where to buy Suppliers range | Antibiotic. Protein tyrosine kinase inhibitor. Has antifungal, antimalarial, antiangiogenic (in vivo), anti-inflammatory and antiviral activity. Cyclooxygenase-2 (COX-2) expression inhibitor without affecting COX-1 expression in LPS-stimulated macrophages. Induces the differentiation of HL-60 cells into macrophages. Potent HSP90 inhibitor. Anticancer compound. In vivo Rad/Raf interaction inhibitor. Inhibitor of AP-1-, NF-kappaB- and serum response factor (SRF)-mediated transcription. Suppresses expression of iNOS (NOS II). Non-competitive inhibitor of ATP citrate lyase. DNA topoisomerase VI and type II DNA topoisomerase inhibitor. Protects against LPS/IFN-gamma-induced neuronal cell death. Apoptosis inducer. Group: Biochemicals. Grades: Highly Purified. CAS No. 12772-57-5. Pack Sizes: 1mg, 5mg. Molecular Formula: C18H17ClO6. US Biological Life Sciences. | Worldwide |
SB 204990 Quick inquiry Where to buy Suppliers range | SB 204990 is a prodrug of SB 201076, which is an ATP citrate lyase (ACLY) inhibitor. SB 204990 inhibits cholesterol and fatty acid synthesis in a dose-dependent manner in HepG2 cells. SB 204990 was shown to decrease plasma levels of the lipoproteins VLDL, LDL, and HDL in dogs. Synonyms: SB-204990; SB 204990; SB204990; (3R,5S)-rel-5-[6-(2,4-Dichlorophenyl)hexyl]tetrahydro-3-hydroxy-2-oxo-3-furanacetic acid. Grades: ≥98% by HPLC. CAS No. 154566-12-8. Molecular formula: C18H22Cl2O5. Mole weight: 389.27. |