37 Results for "

Citrate lyase

" in MedChemExpress (MCE) Product Catalog:
Products (37)

37 Results for "Citrate lyase" in MCE Product Catalog:

Cat. No.: HY-P2843
CAS No.: 9012-83-3
Target:  

Endogenous Metabolite

Research Areas:  

Metabolic Disease

Citrate lyase is an enzyme that converts citrate to oxaloacetate .
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26
26 Publications Verification
Cat. No.: HY-16450
CAS No.: 154566-12-8
Target:  

ATP Citrate Lyase

Research Areas:  

Metabolic Disease

SB 204990 is a potent and specific inhibitor of ATP citrate lyase (ACLY) enzyme.
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23
23 Cited Publications
Cat. No.: HY-12357
CAS No.: 738606-46-7
Purity:  99.97%
Synonyms: ETC-1002; ESP-55016
Target:  

ATP Citrate Lyase AMPK

Research Areas:  

Metabolic Disease

Bempedoic acid (ETC-1002) is an ATP-citrate lyase (ACL) inhibitor . Bempedoic acid (ETC-1002) activates AMPK .
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23
23 Cited Publications
Cat. No.: HY-16107
CAS No.: 943962-47-8
Target:  

ATP Citrate Lyase

Research Areas:  

Metabolic Disease

BMS-303141 is a potent, cell-permeable ATP-citrate lyase (ACL) inhibitor with an IC50 of 0.13 μM.
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2
2 Cited Publications
Cat. No.: HY-127111
CAS No.: 2375840-87-0
Purity:  99.54%
Target:  

ATP Citrate Lyase

Research Areas:  

Cancer

NDI-091143 is a potent and high-affinity human ATP-citrate lyase (ACLY) inhibitor with an IC50 of 2.1 nM (ADP-Glo assay), a Ki of 7.0 nM and a Kd of 2.2 nM. NDI-091143 inhibits ACLY catalysis allosterically, by stabilizing large conformational changes in the citrate domain that indirectly block the binding and recognition of citrate .
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1
1 Cited Publications
Cat. No.: HY-N1437
CAS No.: 6205-14-7
Hydroxycitric acid is an orally active, multi-target, multi-bioactive organic acid. activates Nrf2 and its downstream molecule GPX4, increases glutathione levels, and thereby inhibits ferroptosis. Hydroxycitric acid activates the Nrf2/Keap1 and ACLY/NF-κB signaling pathways, upregulates the activities of antioxidant enzymes such as superoxide dismutase, reduces MDA content, thereby alleviating oxidative stress and renal tubular epithelial cell apoptosis, and improves pulmonary vascular and right ventricular remodeling. Hydroxycitric acid activates both the AMPK and mTORC1/S6K pathways, triggers the unfolded protein response, arrests the cancer cell cycle, and induces DNA fragmentation .
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1
1 Cited Publications
Cat. No.: HY-W338584
CAS No.: 232281-44-6
Tripotassium hydroxycitrate is an orally active, multi-target, multi-bioactive organic acid. Tripotassium hydroxycitrate activates Nrf2 and its downstream molecule GPX4, increases glutathione levels, and thereby inhibits ferroptosis. Tripotassium hydroxycitrate activates the Nrf2/Keap1 and ACLY/NF-κB signaling pathways, upregulates the activities of antioxidant enzymes such as superoxide dismutase, reduces MDA content, thereby alleviating oxidative stress and renal tubular epithelial cell apoptosis, and improves pulmonary vascular and right ventricular remodeling. Tripotassium hydroxycitrate activates both the AMPK and mTORC1/S6K pathways, triggers the unfolded protein response, arrests the cancer cell cycle, and induces DNA fragmentation .
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1
1 Cited Publications
Cat. No.: HY-P72070
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: ACLY; ATP-Citrate (Pro-S-)-lyase; ATP Citrate lyase; Citrate Cleavage Enzyme; ACL; ATP-Citrate Synthase; ATPCL; ATP Citrate Synthase; CLATP
Species:  
Source:  
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Cat. No.: HY-175606
CAS No.: 2588489-03-4
Target:  

ATP Citrate Lyase

Research Areas:  

Cancer

EVT0185 is an orally active ATP citrate lyase (ACLY) inhibitor. EVT0185 is converted to a CoA thioester in the liver by SLC27A2 and interacts with the CoA-binding site of ACLY. EVT0185-CoA inhibits ACLY activity with an IC50 of 2.5 μM. EVT0185 can phenocopy the immune and antitumour effects of genetic ACLY deletion. EVT0185 can increase tumour-infiltrating B cells and chemokine CXCL13 levels. EVT0185 can be used for the research of cancer, such as hepatocellular carcinoma (HCC) .
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Cat. No.: HY-P1123
CAS No.: 87272-20-6
MEDICA16 is an orally active acetyl-CoA carboxylase and ATP-citrate lyase inhibitor. MEDICA16 limits the acetyl-CoA supply for acetyl-CoA carboxylase, inhibits acetyl-CoA carboxylase activity, exerts citrate-competitive inhibitory effects on ATP-citrate lyase, and reduces hepatic AMPK activity. MEDICA16 can be used in research related to insulin resistance, hyperlipidemia, and obesity .
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Cat. No.: HY-N7347
CAS No.: 27750-13-6
Synonyms: Garcinia lactone
(-)-Hydroxycitric acid lactone (Garcinia lactone) is an anti-obesity agent and a popular weight loss food supplement. (-)-Hydroxycitric acid lactone is a potent inhibitor of ATP-citrate lyase. (-)-Hydroxycitric acid lactone catalyzes the extramitochondrial cleavage of citrate to oxaloacetate and acetyl-CoA, limits the availability of acetyl-CoA units required for fatty acid synthesis .
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Cat. No.: HY-136584
CAS No.: 413624-71-2
Purity:  ≥98.0%
ESP15228 is a metabolite of Bempedoic acid (HY-12357). ESP15228 undergoes glucuronidation to form ESP15228-glucuronide. ESP15228 can form excretory ESP15228-taurine conjugate in feces. ESP15228-CoA is a selective hepatic ATP citrate lyase inhibitor. ESP15228 can be used in the research of hypercholesterolemia .
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Cat. No.: HY-17640
CAS No.: 1269181-69-2
Research Areas:  

Metabolic Disease

Nicodicosapent is a fatty acid niacin conjugate that is also an inhibitor of the sterol regulatory element binding protein (SREBP), a key regulator of cholesterol metabolism proteins such as PCSK9, HMG-CoA reductase, ATP citrate lyase, and NPC1L1.
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Cat. No.: HY-172914
CAS No.: 2897695-26-8
ACLY-IN-1 is an orally active ACLY inhibitor. ACLY-IN-1 exhibits potent ACLY inhibitory activity (IC50 = 8.3 nM) and high binding affinity (KD = 72.0 nM) to ACLY. ACLY-IN-1 demonstrates good pharmacokinetic profiles and a potent in vivo hypolipidemic effect .
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Cat. No.: HY-12357S2
CAS No.: 2408131-70-2
Purity:  ≥98.0%
Synonyms: ETC-1002-d4; ESP-55016-d4
Bempedoic acid-d4 is the deuterium labeled Bempedoic acid. Bempedoic acid (ETC-1002) is an ATP-citrate lyase (ACL) inhibitor. Bempedoic acid (ETC-1002) activates AMPK .
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Cat. No.: HY-177136
CAS No.: 3009136-86-8
ACLY-IN-2 (Compound 7) has inhibitory effect against human ATP citrate lyase (hACLY), with an IC50 of less than 1 nM. ACLY-IN-2 can be studied in research on liver-related diseases, type-2 diabetes, autoimmunity, and cancer .
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Cat. No.: HY-12357S
CAS No.: 2408131-71-3
Synonyms: ETC-1002-d5; ESP-55016-d5
Bempedoic acid-d5 is the deuterium labeled Bempedoic acid . Bempedoic acid (ETC-1002) is an ATP-citrate lyase (ACL) inhibitor . Bempedoic acid (ETC-1002) activates AMPK .
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Cat. No.: HY-12357R
CAS No.: 738606-46-7
Synonyms: ETC-1002 (Standard); ESP-55016 (Standard)
Bempedoic acid (Standard) is the analytical standard of Bempedoic acid. This product is intended for research and analytical applications. Bempedoic acid (ETC-1002) is an ATP-citrate lyase (ACL) inhibitor . Bempedoic acid (ETC-1002) activates AMPK .
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Cat. No.: HY-N12336
CAS No.: 308105-06-8
Gnetuhainin I (Compound 5) is a lignin derived from Pouzolzia zeylanica. Gnetuhainin I shows good inhibitory effect on ATP citrate lyase (ACLY) (IC50=2.63 μM) .
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Cat. No.: HY-P2843A
Research Areas:  

Metabolic Disease

Citrate Lyase, Klebsiella pneumoniae (EC 4.1.3.6) catalyzes the first step of Citrate degradation, forming acetate and oxaloacetate. Citrate Lyase, Klebsiella pneumoniae (EC 4.1.3.6) contains 3 polypeptide subunits, α-subunit (a transferase), β-subunit (acyl lyase) and γ-subunit (acyl-carrier protein).
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