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Home > Products > Sarms Raw Powder > Aicar (Acadesine) CAS 2627-69-2 Sarms Fat Burning Steroids Peptide

Aicar (Acadesine) CAS 2627-69-2 Sarms Fat Burning Steroids Peptide

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Basic Info

Model No.:  2627-69-2

Product Description

Model NO.: 2627-69-2 Customized: Customized Suitable for: Adult Purity: >99% Payment Terms: Western Union, Moneygram, Jp Morgan Chase MW: 258.23 Grade: Pharmaceutical Intermediates Transport Package: Disguised Origin: China Powder: No Certification: GMP, ISO 9001, USP, BP State: Powder CAS: 2627-69-2 Mf: C9h14n4o5 Usage: for The Treatment of Cardiovascular Diseases. Trademark: SENDI Specification: White Powder Aicar (Acadesine) CAS 2627-69-2 Sarms Fat Burning Steroids Peptide

Product Name:  AICAR
Synonyms:  ACADESINE;AICA-RIBOSIDE;AMPK;Z-RIBOSIDE
CAS:    2627-69-2
MF:    C9H14N4O5
MW:    258.23
EINECS:    220-097-5
mp:     214-215 °C
storage temp:     -20°C
solubility   H2O:   >10 mg/mL
Apperance: White or off-white powder. 

Function:

AICAR strongly inhibits the transcription of PPAR&alpha and the coactivation of PPAR&alpha. In adipocyte studies it has been shown to antagonize lipolysis induced by isoprenaline and has been suggested for use in kinase cascade research. Additionally, research indicates that AICAR blocks the differentiation of 3T3-L1 (sc-2243) adipocytes. Studies demonstrate that AICAR can mimic the activity of insulin (sc-211647) by activating AMPK, and affecting the expression of PEPCK-M (PEPCK) and glucose-6-phosphatase (G6Pase).

The 5-aminoimidazole-4-carboxamide ribonucleoside (ZMP) is the monophosphorylated derivative of AICA-Riboside, and it can serve as the substrate for the aminoimidazole carboxamide ribonucleotide transformylase/inosine monophosphate cyclohydrolase (ATIC). AICAR is an inhibitor of Hsp90, mTOR and p70 S6 Kinase.
 
AMP-activated protein kinase (AMPK) functions as a metabolic sensor that regulates lipid and glucose metabolism to maintain cellular energy homeostasis and to protect against metabolic stress.AICAR is a selective activator of AMPK in both hepatocytes and adipocytes. At 0.5 mM it inhibits the synthesis of fatty acids and sterols and inactivates HMG-CoA reductase in rat hepatocytes.

AICAR (0.5 mM) inhibits insulin-stimulated glucose uptake to 62% of controls and reduces GLUT4 translocation 2.5-fold in 3T3-L1 adipocytes. It also blocks the expression of pro-inflammatory cytokines (TNF-α/IL-1β and IL-6), iNOS, COX-2, and MnSOD genes in glial cells and macrophages by inhibiting NFκB and C/EBP pathways.

Usage: pharmaceutical intermediates.For the treatment of cardiovascular diseases.

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