86
12
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T14342 |
Atorvastatin lactone
|
HMG-CoA Reductase | Metabolism |
Atorvastatin lactone 是一种 Atorvastatin 的前药。其中 Atorvastatin 是口服具有活力的 3- 羟基 -3- 甲基戊二酰辅酶 A 还原酶抑制剂。 | |||
T1487 |
Fluvastatin sodium
XU 62320 sodium,XU-62-320,氟伐他汀钠,Fluvastatin sodium salt |
Ferroptosis; HMG-CoA Reductase; Autophagy | Apoptosis; Autophagy; Metabolism |
Fluvastatin sodium (Fluvastatin sodium salt) salt 是羟甲基戊二酰辅酶 A 还原酶的竞争性抑制剂,IC50为 8 nM。它通过依赖 Nrf2 的抗氧化通路保护血管平滑肌细胞免受氧化应激,是一种常用的降胆固醇剂。 | |||
T6450 |
Clinofibrate
克利贝特,S-8527,Lipoclin |
HMG-CoA Reductase; Autophagy | Autophagy; Metabolism |
Clinofibrate (Lipoclin) 是一种降脂剂,可抑制羟甲基戊二酰辅酶 A 还原酶。它用于控制血液中的高胆固醇和甘油三酯水平。 | |||
T6994 |
SR12813
SR-12813,SR 12813,GW 485801 |
HMG-CoA Reductase; Autophagy | Autophagy; Metabolism |
SR12813 (GW 485801) 是一种人孕烷X 受体激动剂,还是一种 3-羟基-3-甲基-戊二酰辅酶 A 还原酶抑制剂,IC50值为 0.85 μM。 | |||
T12092 |
Monacolin J
Antibiotic MB 530A,Lovastatin diol lactone,辛伐他汀内酯二醇 |
HMG-CoA Reductase; Autophagy | Autophagy; Metabolism |
Monacolin J (Antibiotic MB 530A) 是一种胆固醇生物合成抑制剂,抑制 HMG-CoA 还原酶的活性。 | |||
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。 | |||
T3116 |
Atorvastatin hemicalcium salt
Lipitor,Atorvastatin hemicalcium,Atorvastatin Calcium,CI-981,阿托伐他汀钙,Sortis |
Ferroptosis; HMG-CoA Reductase; Autophagy | Apoptosis; Autophagy; Metabolism |
Atorvastatin hemicalcium salt (Atorvastatin Calcium) 是一种口服有效的 HMG-CoA 还原酶抑制剂 ,可用作降低胆固醇的药物。它抑制人 SV-SMC 增殖和侵袭,IC50分别为 0.39 μM 和 2.39 μM。 | |||
T1676 |
Rosuvastatin
罗伐他汀,ZD 4522,瑞舒伐他汀 |
Potassium Channel; HMG-CoA Reductase; Autophagy | Autophagy; Membrane transporter/Ion channel; Metabolism |
Rosuvastatin (ZD 4522) 是一种抗血脂药,可竞争性抑制羟甲基戊二酰辅酶 A 还原酶,用于降低血浆胆固醇水平和预防心血管疾病。它降低低密度脂蛋白胆固醇、甘油三酯和 C-反应蛋白水平。它阻断人类醚-a-go-go 相关基因电流,IC50为 195 nM,延迟心脏复极化,延长动作电位持续时间和校正 QT 间期间隔。 | |||
T2534 |
Pitavastatin calcium
P-872441,nisvastatin,itavastatin,Pitavastatin hemicalcium,匹伐他汀钙,NK-104 |
Apoptosis; Mitophagy; Endogenous Metabolite; HMG-CoA Reductase; Autophagy | Apoptosis; Autophagy; Metabolism |
Pitavastatin calcium (NK-104) 是一种羟甲基戊二酰-CoA 还原酶抑制剂。它在 HepG2 细胞中抑制乙酸合成胆固醇的IC50为 5.8 nM。它是高效的肝细胞低密度脂蛋白胆固醇受体诱导剂。具有抗癌活性。 | |||
T1510 |
Rosuvastatin calcium
ZD 4522 Calcium,ZD4522,Rosuvastatin hemicalcium,瑞舒伐他汀钙 |
Potassium Channel; HMG-CoA Reductase; Autophagy | Autophagy; Membrane transporter/Ion channel; Metabolism |
Rosuvastatin calcium (ZD4522) 是肝羟甲基戊二酰辅酶 A 还原酶的选择性和竞争性抑制剂,具有抗血脂活性。它降低成熟 hERG 的表达以及热休克蛋白 70 与 hERG 蛋白的相互作用,还降低低密度脂蛋白胆固醇、甘油三酯和 C-反应蛋白水平。它阻断人类醚-a-go-go 相关基因电流,延迟心脏复极化,来延长动作电位持续时间和校正 QT 间期间隔。 | |||
T20765 |
Atorvastatin
阿托伐他汀,阿伐他汀 |
HMG-CoA Reductase; Autophagy | Autophagy; Metabolism |
Atorvastatin 是一种具有口服活性的 HMG-CoA 还原酶抑制剂,通过激活肝细胞色素p450加快代谢,具有有效降低血脂的能力。Atorvastatin 以 IC50 值分别为 0.39 μM 和 2.39 μM 来抑制人 SV-SMC 细胞的增殖和侵袭。Atorvastatin 与氯吡格雷同时服用两种可能会导致患者血栓事件增加。 | |||
T21405 |
Fluvastatin
Canef,XU-62320,Vastin,Cranoc,Lescol |
HMG-CoA Reductase | Metabolism |
Fluvastatin (XU-62320) 是一种具有高效性和竞争性的 HMG-CoA 还原酶抑制剂(IC50 :8 nM),可通过依赖 Nrf2 通路抑制血管平滑肌细胞免受氧化应激,用于降低血浆胆固醇水平和预防心血管疾病。 | |||
T13131 |
Tert-Buthyl Pitavastatin
|
HMG-CoA Reductase | Metabolism |
tert-Buthyl Pitavastatin 是 Pitavastatin 的代谢产物。其中Pitavastatin 是HMG-CoA 还原酶抑制剂。 | |||
T25285 |
Dalvastatin
RG-12561,RG 12561,RG12561 |
HMG-CoA Reductase | Metabolism |
Dalvastatin (RG-12561) 是一种可口服的 HMG-CoA 还原酶和降胆固醇合成的抑制剂。Dalvastatin 竞争性地抑制大鼠肝脏HMG-CoA还原酶,IC50值为3.4 nmol / l。 Dalvastatin 在在大鼠实验中,抑制肝切片中的胆固醇生物合成,ED50值为0.9。 | |||
T10324 |
Anhydrosimvastatin
Dehydro simvastatin,脱水辛伐他汀 |
HMG-CoA Reductase | Metabolism |
Anhydrosimvastatin (Dehydro simvastatin) 是 Simvastatin 的一种杂质。其中Simvastatin 是竞争性的 HMG-CoA 还原酶抑制剂。 | |||
T24865 |
Tenivastatin
L-654969,L654969,Simvastatin acid,L 654969,Simvastatin hydroxy acid |
ROS; HMG-CoA Reductase | Immunology/Inflammation; Metabolism |
Tenivastatin (Simvastatin acid) 是一种抗高脂血症的 HMG-CoA 还原酶抑制剂,抑制活性氧 (ROS) 产生,可用于研究原发性高脂血症。 | |||
TQ0045 |
2-Hydroxy atorvastatin calcium salt
|
Drug Metabolite | Metabolism |
2-Hydroxy atorvastatin calcium salt 是 Atorvastatin 钙盐的羟基代谢物,Atorvastatin 是一种有效的 HMG-CoA 还原酶抑制剂 (IC50 = 8 nM)。 | |||
T12652 |
(Rac)-5-Keto Fluvastatin
5-Ketofluvastatin,3-Hydroxy-5-Keto Fluvastatin,rac 5-Keto Fluvastatin |
Others | Others |
(Rac)-5-Keto Fluvastatin (rac 5-Keto Fluvastatin) 是 Fluvastatin 的杂质,Fluvastatin 是一种 HMG-CoA 还原酶的抑制剂。 | |||
T12490 |
Pitavastatin lactone
|
Others | Others |
Pitavastatin lactone 是 Pitavastatin 在人体中的主要代谢产物。Pitavastatin 是 HMG-CoA 还原酶竞争性抑制剂。 | |||
T20887 |
Atorvastatin Sodium
Lipitor |
LDL; Aquaporin; HMG-CoA Reductase | Membrane transporter/Ion channel; Metabolism |
Atorvastatin Sodium (Lipitor) 是一种HMG-CoA 还原酶的竞争性抑制剂,增加肝细胞上低密度脂蛋白(LDL)受体的表达。Atorvastatin sodium 处理抑制水汽蛋白4来减轻缺血性脑水肿。 | |||
T26644 |
Apomine
SK&F-99085,APB-231-A2,APB-231-A-2,SR-9223i,SK&F-99085,SR-45023A |
HMG-CoA Reductase | Metabolism |
Apomine (SR-9223i) 是一种 HMG-CoA-还原酶抑制剂,可在体外促进骨髓瘤细胞的凋亡,并与体内骨髓瘤的调节有关。 Apomine 加速 3-羟基-3-甲基戊二酰-CoA 还原酶的降解并刺激低密度脂蛋白受体活性。 Apomine 通过下调 3-羟基-3-甲基戊二酰-CoA 还原酶来增强洛伐他汀对骨髓瘤细胞的抗肿瘤作用。 | |||
T19918 |
Lovastatin hydroxy acid sodium
6-α-Methylcompactin sodium,Lovastatin Na,Lovastatin Sodium,Mevinolin sodium |
||
Lovastatin Sodium is an HMG-CoA reductase inhibitor. | |||
T14931 | Cerivastatin | Others | Others |
Cerivastatin is a highly potent, well-tolerated, and orally active HMG-CoA reductase inhibitor (Ki: 1.3 nM/L). Cerivastatin also inhibits proliferation and invasiveness of MDA-MB-231 cells, mainly by RhoA inhibition with anti-cancer effect. Cerivastatin r | |||
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。 | |||
T24323 |
L 669262
L-669,262,L 669,262,L669,262,L-669262,L669262 |
||
L 669262 is a potent inhibitor of HMG-CoA reductase. | |||
T70633 |
GR-92549
|
||
GR-92549 is an HMG-CoA reductase inhibitor. | |||
T10070 |
2'-Ethyl Simvastatin
|
HMG-CoA Reductase | Metabolism |
2'-Ethyl Simvastatin is a Mevinolin analog with HMG-CoA reductase inhibition. | |||
T21080 |
(3S,5S)-Atorvastatin
ent-Atorvastatin,3S,5S-Atorvastatin,(3S,5S)-阿托伐他汀 |
||
ent-Atorvastatin is a selective and competitive inhibitor of HMGCR (HMG-CoA reductase). | |||
T26044 |
Rawsonol
|
||
Rawsonol is a HMG-CoA reductase inhibitor from the tropical green alga Avrainvillea rawsoni. | |||
T71040 |
GR-95030X
|
||
GR-95030X is a a novel HMG-CoA reductase inhibitor. | |||
T28440 |
PPD 10558
PPD-10558,RBx10558,RBx-10558,PPD10558,RBx 10558 |
||
PPD 10558, a HMG-CoA reductase inhibitor, is used potentially for treatment of primary hypercholesterolemia. | |||
T13380 |
(Z)-Pitavastatin calcium
|
Others | Others |
(Z)-Pitavastatin calcium is the Z-Isomer of Pitavastatin hemicacium. Pitavastatin calcium is a potent of hydroxymethylglutaryl-CoA (HMG-CoA) reductase. | |||
T22405 | Pravastatin | Others | Others |
Pravastatin is a lipoprotein-lowering drug via reversibly inhibiting hydroxymethylglutaryl-CoA (HMG-CoA) reductase and the synthesis of very-low-density lipoproteins. | |||
T69006 |
Atorvastatin lysine
|
||
Atorvastatin lysine is a selective and competitive HMGCR (HMG-CoA reductase) inhibitor. | |||
T10132 | (3S,5S)-Pitavastatin calcium | Others | Others |
(3S,5S)-Pitavastatin calcium is the 3-epimer of Pitavastatin which is a potent HMG-CoA reductase inhibitor. | |||
T10136 | 4-Acetylsimvastatin | Others | Others |
4-Acetylsimvastatin is acetylated simvastatin. Simvastatin is a competitive inhibitor of HMG-CoA reductase (Ki: 0.2 nM). | |||
T21042 | Fluvastatin Methyl Ester | ||
Fluvastatin Methyl Ester is a precursor of Fluvastatin, a blocker of the enzyme HMG-CoA reductase in liver. | |||
T10130 |
(3S,5R)-Pitavastatin calcium
|
Others | Others |
(3S,5R)-Pitavastatin calcium is the enantiomer of Pitavastatin which is a potent HMG-CoA reductase inhibitor. | |||
T10131 |
(3S,5R)-Rosuvastatin
|
Others | Others |
(3S,5R)-Rosuvastatin is the (3R,5R)-enantiomer of Rosuvastatin. Rosuvastatin is a competitive HMG-CoA reductase inhibitor (IC50: 11 nM). | |||
T10126 | (3R,5R)-Rosuvastatin | Others | Others |
(3R,5R)-Rosuvastatin is the (3R,5R)-enantiomer of Rosuvastatin. Rosuvastatin is a competitive HMG-CoA reductase inhibitor (IC50: 11 nM). | |||
T24461 |
Mevinolinic acid
L 154819,L-154819,MK 819,MSD 803 acid,Monacolinic K acid |
||
Mevinolinic acid is an active metabolite of Lovastatin. Lovastatin is an HMG-CoA reductase inhibitor. | |||
T21363 |
Atorvastatin calcium trihydrate
CI-981,atorvastatin, calcium salt,CI981,Atorvastatin,CI 981 |
||
Atorvastatin is used to inhibits HMG-CoA reductase for lowering blood cholesterol and for prevention of events associated with cardiovascular disease. | |||
T68566 |
Pitavastatin methyl ester
|
||
Pitavastatin methyl ester is the methyl ester derivative of Pitavastatin -- a competitive inhibitor of HMG-CoA reductase and an anti-lipemic agent. | |||
T40913 |
3α-Hydroxy pravastatin sodium
|
||
3α-Hydroxy pravastatin sodium, the primary metabolite of Pravastatin, is a potent competitive inhibitor of HMG-CoA reductase. | |||
T70419 | Cerivastatin lactone | ||
Cerivastatin lactone is a metabolite of a competitive inhibitor of HMG-CoA reductase, Cerivastatin. Cerivastatin lactone shows inhibitory effects on CYP3A4/5 activity. | |||
T71705 |
Glenvastatin
|
||
Glenvastatin 是一种HMG-CoA 还原酶抑制剂,具有吡啶基结构。 | |||
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]. | |||
T10401 |
Atorvastatin acetonide
|
Others | Others |
Atorvastatin acetonide is an impurity of Atorvastatin. Atorvastatin is an HMG-CoA reductase inhibitor and has the ability to effectively decrease blood lipids. | |||
T40557 |
Simvastatin Acyl-β-D-glucuronide
|
||
Simvastatin Acyl-β-D-glucuronide, a metabolite formed from Simvastatin, acts as a competitive inhibitor of HMG-CoA reductase, showcasing a potent Ki of 0.2 nM. | |||
T10767 | Cerivastatin sodium | HMG-CoA Reductase | Metabolism |
Cerivastatin sodium is a synthetic lipid-lowering agent and a highly potent and orally active HMG-CoA reductase inhibitor (Ki: 1.3 nM). It also inhibits the proliferation and invasiveness of MDA-MB-231 cells, mainly by RhoA inhibition. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN1733 |
Hesperetin 7-O-glucoside
|
Anti-infection; Antibacterial; HMG-CoA Reductase | Metabolism; Microbiology/Virology |
Hesperetin 7-O-glucoside 是通过 Hesperidin 的酶促转化产生的一种人 HMG-CoA 还原酶抑制剂,具有降压作用,可抑制幽门螺杆菌的生长。 | |||
TN1438 |
beta-Amyrin acetate
beta-香树脂醇乙酸酯 |
Antioxidant; HMG-CoA Reductase; Epoxide Hydrolase; Antifungal | Metabolism; Microbiology/Virology; oxidation-reduction |
beta-Amyrin acetate 抑制 HMG-CoA 还原酶 (HMGCR) 和 sEH 活性,IC50 为 3.4 μM。 beta-Amyrin acetate 具有抗炎、抗真菌、抗氧化和抗高血脂活性。 | |||
T1207 |
Lovastatin
MK-803,洛伐他汀,Mevinolin |
Ferroptosis; HMG-CoA Reductase; Autophagy | Apoptosis; Autophagy; Metabolism |
Lovastatin (MK-803) 是一种 HMG-CoA 还原酶抑制剂,用于降低胆固醇。 | |||
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。 | |||
T1664 |
Meglutol
Dicrotalic acid,3-Hydroxy-3-methylglutaric acid,美格鲁托 |
Endogenous Metabolite; HMG-CoA Reductase; Autophagy | Autophagy; Metabolism |
Meglutol (3-Hydroxy-3-methylglutaric acid) 是一种抗血脂剂,可降低胆固醇、甘油三酯、血清 β-脂蛋白和磷脂。它抑制胆固醇生物合成中的限速酶羟甲基戊二酰辅酶 A 还原酶的活性。 | |||
T0672 |
Pravastatin sodium
CS-514 Sodium,普伐他汀钠,CS-514 (sodium) |
Ferroptosis; HMG-CoA Reductase; Autophagy | Apoptosis; Autophagy; Metabolism |
Pravastatin sodium (CS-514 (sodium)) 是一种 HMG-CoA 还原酶抑制剂,抑制甾醇合成,IC50 为 5.6 μM。 | |||
T0687 |
Simvastatin
辛伐他汀,MK-0733,MK 733 |
Apoptosis; Mitophagy; Ferroptosis; HMG-CoA Reductase; Autophagy | Apoptosis; Autophagy; Metabolism |
Simvastatin (MK 733) 是一种 HMG-CoA 还原酶抑制剂 (Ki=0.2 nM),具有口服活性。Simvastatin 具有降血脂活性,可以抑制肝脏产生胆固醇,还可以用于预防心血管疾病。 | |||
TN6715 |
7-Ketocholesterol
|
Others | Others |
7-Ketocholesterol 是胆固醇的代谢物。 | |||
T4717 |
25-Hydroxycholesterol
25-羟基胆固醇,25-羟基胆甾醇 |
Others; Endogenous Metabolite; HMG-CoA Reductase | Metabolism; Others |
25-Hydroxycholesterol 是胆固醇的代谢产物,由巨噬细胞响应 Toll 样受体激活而分泌。它有效抑制 B 细胞产生 IgA,EC50约为 65 nM。 | |||
TN2111 |
Prunin
Naringenin 7-0-glucoside,柚皮素-7-O-葡萄糖苷 |
Phosphatase; Anti-infection; Virus Protease | Metabolism; Microbiology/Virology |
Prunin (Naringenin 7-0-glucoside) 是一种人肠道病毒 A71 抑制剂。它抑制蛋白酪氨酸磷酸酶 1B,IC50值为 5.5 μM。 | |||
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] |