Acyltransferase
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DGAT (acyl-CoA: diacylglycerol acyltransferase) is a transmembrane enzyme that acts in the final and committed step of triacylglycerides (TAGs) synthesis, and it has been proposed to be the rate-limiting enzyme in plant storage lipid accumulation. DGAT catalyzes the acylation of sn-1,2-diacylglycerol (DAG) at the sn-3 position using an acyl-CoA substrate. DGAT has been proposed to be the rate-limiting enzyme in plant storage lipid accumulation. DGAT is considered a key enzyme for biotechnological purposes; it might be utilized to increase oil content in oleaginous plant species.
DGAT1 and DGAT2 are two of the enzymes that are responsible for the main part of TAG synthesis in most organisms, and they have been studied in many eukaryotic organisms.
Products Related to Acyltransferase(69)
- GC12391XanthohumolCAS: 6754-58-1Purity: >98.00%
Xanthohumol is the main prenylflavonoid in hops that inhibits diacylglycerol acyltransferase (DGAT) with IC 50 value of 50.3μM.
- GC12604Fumonisin B1CAS: 116355-83-0Purity: >98.00%
Fumonisin B1 is a mycotoxin produced from F. moniliforme, a prevalent fungus of corn and other grains.
- GC15274PF-04620110CAS: 1109276-89-2Purity: >98.00%
PF-04620110 is an orally active, selective diacylglycerol acyltransferase-1 (DGAT1) inhibitor (IC 50 = 19nM).
- GC17342BeauvericinCAS: 26048-05-5Purity: >98.00%
Beauvericin is a cyclic hexadecanopeptide mycotoxin and a potent inhibitor of acyl-CoA:cholesterol acyltransferase 1 (ACAT1), which is involved in multiple tumor-related pathways.
- GC17693Enniatin BCAS: 917-13-5Purity: >98%
ionophore with some capacity to facilitate import of K+ and Na+ across membranes
- GC18959PF-06424439CAS: 1469284-79-4Purity: >98.00%
PF-06424439 is a highly efficient and orally bioavailable selective diacylglycerol acyltransferase 2 (DGAT2) small molecule inhibitor with an IC 50 value of 14nM.
- GC18961Pyripyropene ACAS: 147444-03-9Purity: >95.00%
Acyl-CoA: cholesterol acyltransferase (ACAT) is a key enzyme for cholesteryl ester accumulation in atherogenesis, lipoprotein formation in liver, and cholesterol absorption from intestines, all of which are events that contribute to the atherosclerotic process.
- GC31080GOAT-IN-1CAS: 1452473-54-9Purity: >98.00%
GOAT-IN-1 is an inhibitor of ghrelin O-acyltransferase (GOAT), which could be useful for the prophylaxis or treatment of obesity, diabetes, hyperlipidemia, metabolic, non-alcoholic fatty liver, steatohepatitis, sarcopenia, appetite control, alcohol/narcotic dependence, Alzheimer’s disease, Parkinson’s disease, cerebrovascular dementia, cerebral apoplexy, cerebral infarction, cardic disease, some kind of tumors.
- GC31362MGAT2-IN-1CAS: 1800025-30-2Purity: >99.00%
MGAT2-IN-1 is an orally active inhibitor of monoacylglycerol acyltransferase (MGAT2) with IC50 of 7.8 and 2.4 nM for human and mouse MGAT2, respectively.
- GC31375PF-06471553CAS: 1808094-07-6Purity: >98.00%
PF-06471553 is a potent, selective and orally available monoacylglycerol acyltransferase 3 (MGAT3) inhibitor, with an IC50 of 92 nM.
- GC31548ACAT-IN-1 cis isomerCAS: 145961-79-1Purity: >98%
ACAT-IN-1 cis isomer is a potent ACAT inhibitor with an IC50 of 100 nM.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC14870 | OSMI-1 | 1681056-61-0 | >98.00% | |
OSMI-1 is an O-GlcNAc transferase (OGT) small molecule inhibitor that does not significantly affect other glycosyltransferases. | ||||
| GC10999 | Avasimibe | 166518-60-1 | >98.00% | |
Avasimibe is a selective and oral acyl coenzyme A:cholesterol acyltransferase (ACAT) inhibitor (IC 50 =12μmol/L). | ||||
| GC11036 | LCQ-908 | 956136-95-1 | >98.00% | |
| GC11475 | AZD7687 | 1166827-44-6 | >99.00% | |
| GC12391 | Xanthohumol | 6754-58-1 | >98.00% | |
Xanthohumol is the main prenylflavonoid in hops that inhibits diacylglycerol acyltransferase (DGAT) with IC 50 value of 50.3μM. | ||||
| GC12411 | RHC 80267 | 83654-05-1 | >98.00% | |
RHC 80267 is a potent and selective diacylglycerol lipase (DAGL) inhibitor. RHC 80267 can also inhibit cholinesterase activity (IC₅₀= 4μM), suppress cyclooxygenase (COX) activity, and inhibit phosphatidylcholine hydrolysis. | ||||
| GC12604 | Fumonisin B1 | 116355-83-0 | >98.00% | |
Fumonisin B1 is a mycotoxin produced from F. moniliforme, a prevalent fungus of corn and other grains. | ||||
| GC15274 | PF-04620110 | 1109276-89-2 | >98.00% | |
PF-04620110 is an orally active, selective diacylglycerol acyltransferase-1 (DGAT1) inhibitor (IC 50 = 19nM). | ||||
| GC15614 | A922500 | 959122-11-3 | >98.50% | |
A922500 is a potent, selective, and orally bioavailable diacylglycerol acyltransferase 1 (DGAT-1) inhibitor with IC 50 values of 9 and 22nM against human and mouse DGAT-1, respectively. | ||||
| GC16133 | DGAT-1 inhibitor | 701232-20-4 | >98.00% | |
A DGAT-1 inhibitor | ||||
| GC16257 | AZD 3988 | 892489-52-0 | >98.00% | |
diacylglycerol acyltransferase (DGAT-1) inhibitor | ||||
| GC16823 | Enniatin Complex | 11113-62-5 | >98% | |
ionophore | ||||
| GC17342 | Beauvericin | 26048-05-5 | >98.00% | |
Beauvericin is a cyclic hexadecanopeptide mycotoxin and a potent inhibitor of acyl-CoA:cholesterol acyltransferase 1 (ACAT1), which is involved in multiple tumor-related pathways. | ||||
| GC17693 | Enniatin B | 917-13-5 | >98% | |
ionophore with some capacity to facilitate import of K+ and Na+ across membranes | ||||
| GC18959 | PF-06424439 | 1469284-79-4 | >98.00% | |
PF-06424439 is a highly efficient and orally bioavailable selective diacylglycerol acyltransferase 2 (DGAT2) small molecule inhibitor with an IC 50 value of 14nM. | ||||
| GC18961 | Pyripyropene A | 147444-03-9 | >95.00% | |
Acyl-CoA: cholesterol acyltransferase (ACAT) is a key enzyme for cholesteryl ester accumulation in atherogenesis, lipoprotein formation in liver, and cholesterol absorption from intestines, all of which are events that contribute to the atherosclerotic process. | ||||
| GC30438 | RP 70676 | 136609-26-2 | >99.50% | |
RP 70676 is a potent inhibitor of ACAT, with IC50 of 25 and 44 nM for rat and rabbit ACAT. | ||||
| GC31080 | GOAT-IN-1 | 1452473-54-9 | >98.00% | |
GOAT-IN-1 is an inhibitor of ghrelin O-acyltransferase (GOAT), which could be useful for the prophylaxis or treatment of obesity, diabetes, hyperlipidemia, metabolic, non-alcoholic fatty liver, steatohepatitis, sarcopenia, appetite control, alcohol/narcotic dependence, Alzheimer’s disease, Parkinson’s disease, cerebrovascular dementia, cerebral apoplexy, cerebral infarction, cardic disease, some kind of tumors. | ||||
| GC31362 | MGAT2-IN-1 | 1800025-30-2 | >99.00% | |
MGAT2-IN-1 is an orally active inhibitor of monoacylglycerol acyltransferase (MGAT2) with IC50 of 7.8 and 2.4 nM for human and mouse MGAT2, respectively. | ||||
| GC31375 | PF-06471553 | 1808094-07-6 | >98.00% | |
PF-06471553 is a potent, selective and orally available monoacylglycerol acyltransferase 3 (MGAT3) inhibitor, with an IC50 of 92 nM. | ||||
| GC31384 | FCE 28654 | 169474-77-5 | >98% | |
FCE 28654 is an inhibitor of acylCoA: cholesterol acyltransferase (ACAT), weakly inhibiting ACAT in microsomes from rabbit aorta and intestine, and monkey liver, with IC50s of 2.55, 1.08 and 5.69 μM, respcetively. | ||||
| GC31443 | YM17E | 124900-72-7 | >98% | |
YM17E is an inhibitor of acyl CoA:cholesterol acyltransferase (ACAT), with IC50 of 44 nM in rabbit liver microsomes in vitro. | ||||
| GC31517 | OSMI-4 | 2260791-14-6 | >99.00% | |
OSMI-4 is a potent O-GlcNAc transferase (OGT) inhibitor, with an EC 50 value of 3μM. | ||||
| GC31548 | ACAT-IN-1 cis isomer | 145961-79-1 | >98% | |
ACAT-IN-1 cis isomer is a potent ACAT inhibitor with an IC50 of 100 nM. | ||||
