87 Results for "

ACCS

" in MedChemExpress (MCE) Product Catalog:
Products (87)

87 Results for "ACCS" in MCE Product Catalog:

Cat. No.: HY-P10003A
Target:  

Proteasome

Research Areas:  

Others

iso-VQA-ACC TFA is a constitutive proteasome substrate .
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Cat. No.: HY-127128
CAS No.: 88844-73-9
Synonyms: ACC-9089 sulfate
Target:  

Adrenergic Receptor

Research Areas:  

Neurological Disease

Flestolol (ACC-9089) sulfate is a competitive, ultra-short-acting beta-adrenergic blocking agent. Flestolol sulfate shows a half-life of approximately 6.5 minutes. Flestolol sulfate has the potential for the research of chest pain .
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Cat. No.: HY-P10002A
Research Areas:  

Others

EWFW-ACC TFA is a specific immunoproteasome substrate that can be used to study immunoproteasome function .
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Cat. No.: HY-N3055
CAS No.: 31685-80-0
Pinusolide is an AMPK activator and PAF receptor antagonist. Pinusolide activates AMPK, phosphorylates ACC, enhances IRS-1 tyrosine phosphorylation, boosts glucose uptake, and modulates insulin signaling. Pinusolide inhibits caspase-3/7 activation, intracellular calcium elevation, reactive oxygen species overproduction, lipid peroxidation, and tumor cell proliferation. Pinusolide stabilizes superoxide dismutase activity, reduces apoptotic hallmarks, induces mitochondrial pathway apoptosis, and triggers DNA fragmentation. Pinusolide can be used for the research of type 2 diabetes, neurodegenerative diseases, acute lymphoblastic leukemia, acute myeloid leukemia, and Burkitt lymphoma .
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Cat. No.: HY-170931
CAS No.: 2252336-04-0
AMPK activator 16 (compound 6) is a AMP-activated protein kinase (AMPK) inhibitor. AMPK activator 16 shows the most efficient interactions with the key residues of AMPK and demonstrates significant activation of AMPK. AMPK activator 16 increases the expression of phosphorylated AMPK (p-AMPK) and its downstream signaling proteins, such as phosphorylated ACC (Acetyl-CoA Carboxylase) (p-ACC) and phosphorylated raptor (p-raptor), in N2a cells .
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Cat. No.: HY-144701
CAS No.: 690681-65-3
Purity:  99.15%
Target:  

Antibiotic Bacterial

Research Areas:  

Infection Inflammation/Immunology

SABA1 possesses antibacterial properties against Pseudomonas aeruginosa and Escherichia coli, with an IC50 of 4.0 µM against E. coli ACC .
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Cat. No.: HY-169010
CAS No.: 2227423-38-1
Research Areas:  

Infection

Pomalidomide-CO-C5-Br (Compound 6b) is a conjugated compound of the E3 ligand Pomalidomide and linker. It can be used to synthesize highly effective PROTAC molecules targeting ADC (HY-169008) .
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Cat. No.: HY-N0853R
CAS No.: 19885-10-0
Alisol A (Standard) is the analytical standard of Alisol A (HY-N0853). This product is intended for research and analytical applications. Alisol A is an orally active tetracyclic triterpenoid compound of the prototerpane type. Alisol A can be extracted from the rhizome of Alisma orientale. Alisol A activates AMPK/ACC/SREBP-1c, SIRT1, PPARα, inhibits MMP-2/-9, decreases inflammatory cytokine expression (IL-1β, IL-6, IL-8). Alisol A has anti-tumor activity against breast cancer and colorectal cancer. Alisol A has anti-obesity and anti-atherosclerotic activities. Alisol A can be used in the research of hepatitis B, breast cancer, colorectal cancer, atherosclerosis, and obesity .
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Cat. No.: HY-N0772R
CAS No.: 24699-16-9
Isomangiferin (Standard) is the analytical standard of Isomangiferin (HY-N0772). This product is intended for research and analytical applications. Isomangiferin is an orally active xanthone C-glucoside, and its chemical structure is similar to Mangiferin (HY-N0290). Isomangiferin is an effective VEGFR-2 kinase inhibitor, which can induces cell apoptosis, inhibit the growth, metastasis and angiogenesis of breast cancer. Isomangiferin exerts anti-inflammatory effects by inhibiting the HMGB1/NLRP3/NF-κB signaling pathway, thereby improving the renal function indicators of diabetic mice. Isomangiferin exhibits inhibitory effects on various bacteria and herpes simplex virus type 1 (HSV-1). Isomangiferin promotes the migration and osteogenic differentiation of bone marrow mesenchymal stem cells (BMSCs) and reduces cell apoptosis and the production of ROS by activating the AMPK/ACC pathway, thereby facilitating fracture healing.
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Cat. No.: HY-189391
CAS No.: 3027705-65-0
Research Areas:  

Inflammation/Immunology

PF-07905428 is a topical acetyl-CoA carboxylase (ACC) inhibitor designed to minimize systemic exposure. PF-07905428 inhibits ACC, reduces sebaceous lipid production in the skin. PF-07905428 can be used for the research of acne vulgaris .
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Cat. No.: HY-183919
CAS No.: 2237229-78-4
Research Areas:  

Metabolic Disease

ACC2-IN-1 is an orally active, selective inhibitor of acetyl-CoA carboxylase 2 (ACC2), with an IC50 of 1.9 nM against human targets. ACC2-IN-1 acts as a reducing agent to decrease malonyl-CoA levels in skeletal muscle and exhibits a favorable CYP450 inhibition profile. ACC2-IN-1 can be used in the research of type 2 diabetes .
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Cat. No.: HY-137846A
CAS No.: 2334472-62-5
PF-05221304 tromethamine is an orally active, liver-directed and dual ACC1/ACC2 inhibitor with IC50s of 7.5 nM for rat ACC1, 8.2 nM for rat ACC2. PF-05221304 tromethamine is a substrate for organic anion transport polypeptides. PF-05221304 tromethamine directly improves a variety of non-alcoholic fatty liver (NAFL) and non-alcoholic steatohepatitis (NASH) pathogenic factors .
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Cat. No.: HY-107709R
CAS No.: 1039758-22-9
MK-4074 (Standard) is the analytical standard of MK-4074 (HY-107709). This product is intended for research and analytical applications. MK-4074 is a liver-specific inhibitor of acetyl-CoA carboxylase ACC1 and ACC2 with IC50 values of approximately 3 nM.
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Cat. No.: HY-E71732
Research Areas:  

Others

[Acetyl-CoA carboxylase]-phosphatase (EC 3.1.3.44) is a phosphomonoesterase that restores the activity of acetyl-CoA carboxylase (ACC) primarily by removing phosphate groups from the enzyme.
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Cat. No.: HY-KE7017

MCE Fsp I is a restriction enzyme for rapid DNA digestion, including plasmid, genomic DNA as well as PCR products. Isoschizomers: Acc16 I,Nsb I.

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Cat. No.: HY-KE7022

MCE Kpn I is a restriction enzyme for rapid DNA digestion, including plasmid, genomic DNA as well as PCR products. Isoschizomers: Asp718 I, Acc65 I.

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Cat. No.: HY-101842R
CAS No.: 1434639-57-2
Research Areas:  

Cancer

ND-646 (Standard) is the analytical standard of ND-646 (HY-101842). This product is intended for research and analytical applications. ND-646 is an orally bioavailable and steric inhibitor of acetyl-CoA carboxylase (ACC) with IC50s of 3.5 nM and 4.1 nM for recombinant hACC1 and hACC2, respectively.
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Cat. No.: HY-187021
CAS No.: 81017-23-4
Target:  

Fluorescent Dye

Research Areas:  

Infection

3-Carboxyumbelliferyl acetate (compound ACC) is a fluorescent substrate that can be used to detect the activity of the Escherichia coli polysaccharide deacetylase PgaB, with a Km of 1.2 mM. 3-Carboxyumbelliferyl acetate undergoes acetate hydrolysis under the catalysis of E. coli PgaB. 3-Carboxyumbelliferyl acetate can be used in studies related to PgaB enzymatic activity and the mechanism of bacterial biofilm formation .
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Cat. No.: HY-102066R
CAS No.: 1079274-94-4
Synonyms: AZD-7451 (Standard)
Research Areas:  

Cancer

Utatrectinib (Standard) is the analytical standard of Utatrectinib (HY-102066). This product is intended for research and analytical applications. Utatrectinib (AZD-7451) is a potent, selective and orally active Trk inhibitor. Utatrectinib blocks TrkC activation and associated tumorigenic behaviors .
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Cat. No.: HY-184939
CAS No.: 3063509-17-8
THR-β agonist 12 is an orally active, potent, and highly selective thyroid hormone receptor β (THR-β) agonist (EC50 = 36 nM). THR-β agonist 12 shows no significant activity against THRα and exhibits no cardiotoxicity in vivo. THR-β agonist 12 inhibits lipid synthesis by activating the AMPK-ACC-SREBP1 signaling axis. THR-β agonist 12 can be used on research into metabolic dysfunction-associated steatohepatitis (MASH) and related metabolic diseases .
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