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抑制剂 & 化合物

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T79520	HMG-CoA Reductase-IN-1
	HMG-CoA Reductase-IN-1是一种HMG-CoA还原酶抑制剂，显示出高HMGR抑制活性及OATP1B1亲和力，具有pIC50值8.54和pKm值1.98。该化合物适用于高胆固醇血症的研究。
T38249	2-Hydroxy atorvastatin lactone
	2-Hydroxy atorvastatin lactone, a metabolite of Atorvastatin, is an orally active HMG-CoA reductase inhibitor that efficiently reduces blood lipids [1][2].
T81257	Rosuvastatin zinc salt Rosuvastatin zinc
	Rosuvastatin zinc salt (Rosuvastatin zinc)，为Rosuvastatin的含锌盐形态，属于HMG-CoA还原酶抑制剂类药物，常用于动脉粥样硬化的研究领域。
T11572	HMG499	HMG-CoA Reductase	Metabolism
	HMG499是有效，选择性的HMG-CoA 还原酶抑制剂，EC50为 0.41 μM。HMG499可消除他汀类药物诱导的HMGCR 积聚，并且降低血清胆固醇水平，减少动脉粥样硬化。
T61430	S-2E
	S-2E is a compound that functions as an orally active, noncompetitive inhibitor of both HMG-CoA reductase and acetyl-CoA carboxylase. It exhibits an anti-hyperlipidemic action, making it suitable for studying conditions such as familial hypercholesterolemia and mixed hyperlipidemia [1] [2].
T78718	Dim16
	Dim16是一种同时抑制PCSK9和HMG-CoAR的化合物，其对PCSK9的IC50为19 nM，并且能够阻断PCSK9与LDLR的结合，此作用的IC50为0.8 nM。Dim16还能提升HepG2细胞对LDL的吸收。
T36827	Acetoacetyl Coenzyme A (sodium salt hydrate) Acetoacetyl-CoA
	Acetoacetyl-coenzyme A (acetoacetyl-CoA) is a precursor to HMG-CoA in the isoprenoid pathway.[1],[2] It is reversibly converted to acetyl-CoA by acetoacetyl-CoA thiolase in the mitochondria. Acetoacetyl-CoA thiolase (T2) deficiency results in a build-up of ketone bodies leading to intermittent ketoacidosis.[3],[4] Acetoacetyl-CoA is also an intermediate in the microbial biosynthesis of polyhydroxybutyrate.[5]
T36863	Geranylgeranyl Pyrophosphate (ammonium salt) Geranylgeranyl Pyrophosphate (ammonium salt),GGPP
	Geranylgeranyl pyrophosphate is an intermediate in the HMG-CoA reductase pathway derived directly from farnesyl pyrophosphate and used in the biosynthesis of terpenes and terpenoids.[1] It is also serves as a substrate in the prenylation of a variety of critical intracellular proteins including small GTPases.[2] This post-translational modification is necessary for correct localization of proteins to intracellular membranes for proper functionality and has become a focus of anticancer drug disco...
T35718	N-desmethyl Rosuvastatin (sodium salt hydrate)
	N-desmethyl Rosuvastatin is an active metabolite of the HMG-CoA reductase inhibitor rosuvastatin .1,2N-desmethyl Rosuvastatin is formed when rosuvastatin undergoes demethylation, primarily by the cytochrome P450 (CYP) isoform CYP2C9 and to a lesser extent by CYP2C19 and CYP3A4.1 1.Macwan, J.S., Ionita, I.A., and Akhlaghi, F.A simple assay for the simultaneous determination of rosuvastatin acid, rosuvastatin-5S-lactone, and N-desmethyl rosuvastatin in human plasma using liquid chromatography-tand...

化合物

HMG-CoA Reductase-IN-1

Cat.No: T79520

Synonym:

Target:

2-Hydroxy atorvastatin lactone

Cat.No: T38249

Synonym:

Target:

Rosuvastatin zinc salt

Cat.No: T81257

Synonym: Rosuvastatin zinc

Target: HMG-CoA Reductase

Acetoacetyl Coenzyme A (sodium salt hydrate)

Cat.No: T36827

Synonym: Acetoacetyl-CoA

Target:

Geranylgeranyl Pyrophosphate (ammonium salt)

Cat.No: T36863

Synonym: Geranylgeranyl Pyrophosphate (ammonium salt),GGPP

Target:

N-desmethyl Rosuvastatin (sodium salt hydrate)

Cat.No: T35718

Synonym:

Target:

Cat. No.	Product Name	Target	Signaling Pathways
T0683	Mevastatin Compactin,ML236B,美伐他汀	Apoptosis; Antibacterial; Antibiotic; HMG-CoA Reductase; Autophagy; Lipid	Apoptosis; Autophagy; Metabolism; Microbiology/Virology
	Mevastatin (ML236B) 是他汀类 HMG-CoA 还原酶抑制剂。它是一种降脂药，可诱导细胞凋亡，将癌细胞阻滞在 G0/G1期。它还可增加内皮型一氧化氮合酶的 mRNA 和蛋白质水平。它有抗肿瘤活性，用于心血管疾病的研究。
T75626	Ganoderenic acid K
	Ganoderenic acid K，一种从灵芝子实体分离得到的天然产物，对HMG-CoA还原酶(HMGCR)显示出强抑制作用，IC50值为16.5 μM。
T35400	β-Muricholic Acid β-MCA,5β-Cholanic Acid-3α,6β,7β-triol,β-Muricholic Acid
	β-Muricholic acid (β-MCA) is a murine-specific primary bile acid.[1],[2] Dietary administration of β-MCA reduces HMG-CoA reductase activity in liver microsomes from mice fed a high cholesterol and cholic acid diet.[3] Dietary administration of β-MCA also dissolves 100% of gallstones in a gallstone-susceptible mouse model of diet-induced cholesterol gallstones.[4]