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5
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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
T25276 |
Crilvastatin
PMD387,PMD 387,PMD-387 |
HMG-CoA Reductase | Metabolism |
Crilvastatin (PMD 387) 是一种新型非竞争性羟甲基戊二酰辅酶 A 还原酶抑制剂,具有降胆固醇活性,可抑制遗传性高胆固醇血症大鼠的胆固醇吸收。 | |||
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。 | |||
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。 | |||
T19918 |
Lovastatin hydroxy acid sodium
6-α-Methylcompactin sodium,Lovastatin Na,Lovastatin Sodium,Mevinolin sodium |
||
Lovastatin Sodium is an HMG-CoA reductase inhibitor. | |||
T72101 |
Atorvastatin hemicalcium trihydrate
阿托伐他汀半钙三水合物,阿托他伐汀半钙三水合物 |
||
Atorvastatin hemicalcium trihydrate 是一种具有口服活性的 HMG-CoA 还原酶抑制剂,具有有效降低血脂的能力。Atorvastatin hemicalcium trihydrate 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。 | |||
T40913 |
3α-Hydroxy pravastatin sodium
|
||
3α-Hydroxy pravastatin sodium, the primary metabolite of Pravastatin, is a potent competitive inhibitor of HMG-CoA reductase. | |||
T10402 |
Atorvastatin Epoxy Tetrahydrofuran Impurity
|
Others | Others |
Atorvastatin Epoxy Tetrahydrofuran Impurity is an impurity isolated oxidative degradation products of Atorvastatin. Atorvastatin is an orally active HMG-CoA reductase inhibitor. | |||
T12283 |
O-Methyl Atorvastatin hemicalcium
|
Others | Others |
O-Methyl Atorvastatin is an impurity of Atorvastatin that is an orally active inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase, has the ability to effectively decrease blood lipids. | |||
T10400 |
Atorvastatin acetonide tert-butyl ester
|
Others | Others |
Atorvastatin acetonide tert-butyl ester is a useful pharmaceutical intermediate in the preparation of Atorvastatin salts. Atorvastatin is an HMG-CoA reductase inhibitor. | |||
T10120 |
3-Oxo Atorvastatin
|
Others | Others |
3-Oxo Atorvastatin is an impurity of Atorvastatin. Atorvastatin is an HMG-CoA reductase inhibitor and has the ability to effectively decrease blood lipids. | |||
T71492 |
Atorvastatin strontium
|
||
Atorvastatin strontium is used primarily for lowering blood cholesterol and for prevention of events associated with cardiovascular disease. Like all statins, atorvastatin works by inhibiting HMG-CoA reductase, an enzyme found in liver tissue that plays a key role in production of cholesterol in the body.Atorvastatin is also used for the treatment of dyslipidemia. | |||
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. | |||
T10235 |
Acetyllovastatin
|
Others | Others |
Acetyllovastatin (acetate of Lovastatin) presents a moderate inhibitory effect against the acetylcholinesterase (IC50: 79 μg/mL). Lovastatin displays antifungal activity and suppresses the proliferation of a number of transformed cell lines. | |||
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). | |||
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]. | |||
T15099 |
Desfluoro-atorvastatin
|
Others | Others |
Desfluoro-atorvastatin is an Atorvastatin impurity. Atorvastatin is an orally active inhibitor of HMG-CoA reductase. It has the ability to effectively decrease blood lipids. | |||
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。 | |||
T19551 |
Rosuvastatin D6 Calcium
|
Others | Others |
Rosuvastatin D6 Calcium is deuterium labeled Rosuvastatin, which is a competitive HMG-CoA reductase inhibitor(IC50 of 11 nM). | |||
T11306 |
Fluvastatin D6 sodium
XU 62-320 (D6) |
Others | Others |
Fluvastatin sodium is a first fully synthetic, competitive HMG-CoA reductase inhibitor with an IC50 of 8 nM.Fluvastatin D6 sodium is deuterium labeled Fluvastatin sodium. | |||
T10129 |
(3S,5R)-Fluvastatin sodium
(3S,5R)-XU 62-320 |
Others | Others |
(3S,5R)-Fluvastatin sodium is the (3S,5R)-enantiomer of Fluvastatin. Fluvastatin is a first fully synthetic, competitive HMG-CoA reductase inhibitor (IC50: 8 nM). Fluvastatin protects vascular smooth muscle cells against oxidative stress through the Nrf2- | |||
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. | |||
T69178 |
Rosuvastatin lactone
|
||
Rosuvastatin lactone is the lactone form of the HMG-CoA reductase inhibitor rosuvastatin. It is found in vivo following rosuvastatin administration. Rosuvastatin lactone is an inhibitor of the cytochrome P450 (CYP) isoforms CYP2C9.1 and CYP2C9.3 (IC50s = 8.52 and 4.1 µM, respectively). | |||
T63430 |
Rosuvastatin Sodium
|
||
Rosuvastatin Sodium 是竞争性HMG-CoA 还原酶 (HMGCR) 抑制剂 (IC50: 11 nM),能够有效阻断hERG 电流 (IC50: 195 nM)。Rosuvastatin Sodium 可以有效减少低密度脂蛋白 (LDL) 胆固醇,甘油三酯和 C- 反应蛋白水平。Rosuvastatin Sodium 能够减少成熟 hERG 的表达,并抑制及热休克蛋白 70 (Hsp70) 与 hERG 蛋白的相互作用。 | |||
T38920 |
Atrovastatin-PEG3-FITC
Atrovastatin-PEG3-FITC |
||
Atrovastatin-PEG3-FITC (compound S31) functions as a ligand in fluorescence anisotropy assay. Its primary role is as a KRAS-PDEδ interaction inhibitor. | |||
T71705 |
Glenvastatin
|
||
Glenvastatin 是一种HMG-CoA 还原酶抑制剂,具有吡啶基结构。 | |||
T15127 |
Difluoro atorvastatin
Fluoroatorvastatin |
Others | Others |
Difluoro atorvastatin is an Atorvastatin impurity. Atorvastatin is an orally active HMG-CoA reductase inhibitor and it has the ability to effectively decrease blood lipids. Atorvastatin inhibits human SV-SMC proliferation and invasion (IC50s: 0.39 μM and | |||
TMIH-0242 |
Fluvastatin-d6 Sodium Salt
|
||
Fluvastatin-d6 Sodium Salt 是 Fluvastatin Sodium Salt 的氘代化合物。Fluvastatin Sodium Salt 的 CAS 号为 93957-55-2。Fluvastatin sodium 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。 | |||
T12488 |
Pitavastatin D4
NK-104 D4 |
Others | Others |
Pitavastatin D4 is deuterium labeled Pitavastatin. Pitavastatin is a potent inhibitor of HMG-CoA reductase. | |||
T10127 |
(3R,5S)-Atorvastatin sodium
|
Others | Others |
(3R,5S)-Atorvastatin sodium is an impurity of Atorvastatin. Atorvastatin is an HMG-CoA reductase inhibitor and has the ability to effectively decrease blood lipids. | |||
T71560 |
Atorvastatin magnesium trihydrate
|
||
Atorvastatin magnesium trihydrate is used primarily for lowering blood cholesterol and for prevention of events associated with cardiovascular disease. Like all statins, atorvastatin works by inhibiting HMG-CoA reductase, an enzyme found in liver tissue that plays a key role in production of cholesterol in the body.Atorvastatin is also used for the treatment of dyslipidemia. | |||
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). | |||
T39036 |
(3R,5S)-Fluvastatin
(3R,5S)-Fluvastatin,(3R,5S)-XU 62-320 free acid |
||
(3R,5S)-Fluvastatin, the 3R,5S-isomer of Fluvastatin (XU 62-320 free acid), stands as the inaugural fully synthetic, competitive inhibitor of HMG-CoA reductase, exhibiting an IC50 value of 8 nM. It safeguards vascular smooth muscle cells from oxidative stress by activating the Nrf2-dependent antioxidant pathway. | |||
T10403 |
Atorvastatin ethyl ester
|
Others | Others |
Atorvastatin ethyl ester, a derivative of Atorvastatin, exhibits potent inhibition of 9-cis-RA-induced Gal4 reporter activity. | |||
T7072 |
Pitavastatin
|
||
Pitavastatin (NK-104) 是有效的羟甲基戊二酰-CoA(HMG-CoA)还原酶抑制剂。Pitavastatin 抑制乙酸合成胆固醇,在 HepG2 细胞中的IC50为 5.8 nM。Pitavastatin 是一种高效的肝细胞低密度脂蛋白胆固醇 (LDL-C) 受体诱导剂。Pitavastatin 具有抗动脉粥样硬化、抗哮喘、抗骨关节炎、抗肿瘤、神经保护、肝保护和肾保护等作用。 | |||
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. | |||
T72155 |
(Rac)-3′-Hydroxy simvastatin
|
||
(Rac)-3′-Hydroxy simvastatin 是一种 Simvastatin 代谢物。Simvastatin 是一种竞争性的 HMG-CoA 还原酶抑制剂,Ki 值为 0.2 nM。 | |||
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). |
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。 | |||
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。 | |||
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。 | |||
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。 | |||
T16885 |
Simvastatin acid ammonium
辛伐他汀铵盐,Tenivastatin ammonium |
Others | Others |
Simvastatin ammonium is an active metabolite of simvastatin lactone mediated. Simvastatin ammonium reduces indoxyl sulfate-mediated reactive oxygen species and modulates OATP3A1 expression in cardiomyocytes and HEK293 cells transfected with the OATP3A1 ge |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPJ-00921 |
COL8A1 Protein, Human, Recombinant (His)
Vastatin,Endothelial Collagen,Collagen Alpha-1(VIII... |
Human | HEK293 Cells |
Collagen alpha-1(VIII) chain, also known as endothelial collagen, C3orf7 and COL8A1, can be cleaved into vastatin chain. COL8A1 is a short chain collagen and a major component of the basement membrane of the corneal endothelium. COL8A1 forms homotrimers, or heterotrimers in association with alpha 2(VIII) type collagens. Four homotrimers can form a tetrhedron stabilized by central interacting C-terminal NC1 trimers. COL8A1 contains one C1q domain and is primarily expressed in the subendothelium o... |