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18
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T14933 |
Cetaben
|
Others | Others |
Cetaben 是不依赖 PPARα 的过氧化物酶体增殖物。它可有效降低胆固醇和甘油三酸酯的浓度,是一种非纤维化降血脂药。 | |||
T3941 |
Choline Fenofibrate
Trilipix,ABT-335,非诺贝特胆碱 |
P450; COX; PPAR | DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism; Neuroscience |
Choline Fenofibrate (Trilipix) 是 Fenofibric acid 的胆碱盐,在胃肠道中释放游离的 Fenofibric acid。Fenofibric acid 是一种合成的苯氧基异丁酸衍生物和具有抗高血脂活性的前药。 | |||
T5123 |
Pirozadil
|
Others | Others |
Pirozadil 是降血脂药。 | |||
T15471 |
Hepronicate
Megrin |
Others | Others |
Hepronicate(Megrin) 是一种具有降血脂和血管扩张活性的小分子化合物。 | |||
T19864 |
Xenalipin
BW 207U |
Others | Others |
Xenalipin (BW 207U) 具有降血脂作用。它可以降低大鼠的血液胆固醇和甘油三酯。 | |||
T31083 |
CP-868388 free base
CP868388,CP 868388,(-)-CP-868388,UNII-999KY5ZIGB,CP-868388 |
PPAR | DNA Damage/DNA Repair; Metabolism |
CP-868388 free base (CP-868388) 是一种具有口服活性、有效性和选择性的 PPARα 激动剂,具有降血脂和抗炎活性,可用于研究血脂异常。 | |||
T30506 |
BMS-212122
UNII-0Z473OO6GB,BMS212122,BMS 212122 |
CETP | Metabolism |
BMS-212122 (UNII-0Z473OO6GB) 是一种有效的微粒体甘油三酯转移蛋白(MTP )抑制剂,在动物实验中显示出降血脂作用。BMS-212122 显著减少动脉粥样硬化斑块中的脂质含量和单核细胞衍生(CD68+)细胞。 | |||
T27832 |
Lifibrol
U 83860,K-12148,K-12.148,U-83860,K12148 |
Lipid | Metabolism |
Lifibrol (U-83860) 是一种胆固醇合成抑制剂。Lifibrol 具有抗胆固醇和降血脂的作用,可促进高胆固醇血症和混合型高脂血症患者体内低密度脂蛋白载脂蛋白 B-100 的转化。 | |||
T1162 |
Acipimox
Olbemox,K-9321,阿西莫司,阿昔莫司 |
Others | Others |
Acipimox (K-9321) 是烟酸类似物,能够急性抑制脂解作用,抑制全身游离脂肪水平,改善胰岛素敏感性。 | |||
T67974 |
Berberine ursodeoxycholate
HTD1801,BUDCA |
||
Berberine ursodeoxycholate (HTD1801) 是一种口服有效的降血脂剂 ,是 Berberine 和 Ursodeoxycholic acid 的一种离子盐。Berberine ursodeoxycholate 具有广泛的代谢活性,可显著降低肝脏脂肪含量。Berberine ursodeoxycholate 可用于研究高脂血症、非酒精性脂肪性肝炎 (NASH) 和糖尿病。 | |||
T1415 |
Gemfibrozil
吉非罗齐,CI-719,Jezil,Decrelip,Lopid |
P450; Adrenergic Receptor; PPAR | DNA Damage/DNA Repair; GPCR/G Protein; Metabolism; Neuroscience |
Gemfibrozil (CI-719) 是一种PPAR-α激活剂,可作为降脂药。它也是P450非选择性抑制剂,对 CYP2C9、2C19、2C8 和 1A2 的Ki 值分别为 5.8、24、69 和 82 μM。 | |||
T34872 |
Tiadenol
LL 1558,NSC66316,LL-1558,LL1558 NSC 66316,NSC-66316 |
||
Tiadenol is a Hypolipidemic Agent. | |||
T13821 |
Pirinixil
BR-931,匹立昔尔 |
Others | Others |
Pirinixil is a hypolipidemic low toxicity agent. | |||
T30238 |
Axitirome
CGS-26214,CGS 26214,CGS26214 |
||
Axitirome, also known as CGS 26214, is a hypolipidemic agent. | |||
T13909 | TA-1801 | Others | Others |
TA-1801 is an agent of hypolipidemic. | |||
T34552 |
SC 33459
SC-33459,SC33459 |
||
SC 33459 is a hypolipidemic agent. | |||
T24223 |
JTT 130
JTT-130,JTT130 |
||
JTT 130 is an agent of hypolipidemic. It inhibits microsomal triglyceride transfer protein. | |||
T15256 |
Etofylline clofibrate
|
Others | Others |
Etofylline clofibrate has a hypolipidemic and antithrombotic effect and it also has an agonistic interaction with intimal PGI2. | |||
T13972 |
Y-9738
|
ROCK | Cell Cycle/Checkpoint; Cytoskeletal Signaling; Stem Cells |
Y-9738 is an agent of hypolipidemic. | |||
T30977 |
Clofibride
|
||
Clofibrin is a kind of hypolipidemic drug, which can reduce Hypertriglyceride and hypercholesterolemia. | |||
T82853 |
BM 15766 sulfate
|
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BM 15766 sulfate是一种7-脱氢胆固醇δ7-还原酶的抑制剂,具有降低血浆胆固醇水平的作用,属于降血脂剂类药物。 | |||
T35448 |
10-Thiastearic Acid
|
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Heteroatom-substituted fatty acids have been observed to modulate the extension and desaturating of fatty acids, and to influence their distribution within phospholipids pools. 10-Thiastearic acid inhibits desaturation of radiolabeled stearate to oleate in rat hepatocytes and hepatoma cells by more than 80% at a concentration of 25 μM. This activity is associated with a hypolipidemic effect, making this 10-thiastearic acid a useful tool for evaluating new anti-obesity therapeutics. | |||
T64171 | LXR antagonist 2 | ||
LXR antagonist 2 (compound 10rr) 是一种有效的 LXR (肝 X 受体) 反向激动剂,能够作用于 LXRβ (IC50: 0.36 μM) 和 LXRα (IC50: 2.25 μM)。 LXR antagonist 2 是一种脂肪生成抑制剂,能够下调 LXR 靶基因 SREBP-1c、ACC、FAS 和 SCD-1。LXR antagonist 2 对 Triton WR-1339 诱导的高脂血症小鼠表现出降脂活性。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3S0175 |
Gardenia yellow
alpha-Crocin,Crocin I,Crocine,西红花苷 I,西红花苷I,藏红花 |
Sirtuin | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Gardenia yellow (Crocin I) 是藏红花素家族的一员,作为可口服的抗抑郁剂,能增强 SIRT3的 mRNA 的表达,具有抗动脉粥样硬化和降血脂作用。 | |||
T2756 |
Swertiamarin
獐牙菜苦苷,獐牙菜苦甙,Swertiamaroside |
Others | Others |
Swertiamarin (Swertiamaroside) 是一种裂环烯醚萜苷,在 Enicostemma Species 属植物中发现,具有降血糖和降血脂作用。 | |||
T5707 |
3-O-Methylgalangin
3-Methylgalangin,GALANGIN-3-METHYLETHER,高良姜素 3-O-甲醚,高良姜素-3-甲醚 |
Antibacterial | Microbiology/Virology |
3-O-Methylgalangin (GALANGIN-3-METHYLETHER) 是一种来源于高良姜根茎的天然黄酮,具有抗菌活性,抑制胰腺脂肪酶。 | |||
T2840 |
Phloracetophenone
2,4,6-三羟基苯乙酮,2,4,6-trihydroxyacetophenone,1-(2,4,6-Trihydroxyphenyl)ethanone |
Others; P450; Antibacterial; Antibiotic | Metabolism; Microbiology/Virology; Others |
Phloracetophenone (1-(2,4,6-Trihydroxyphenyl)ethanone) 是多叶姜黄中苯乙酮糖苷的糖苷配基部分,具有抗肥胖,降血脂和降低胆固醇作用,能够增强胆固醇 7α-羟化酶的活性。 | |||
T5690 |
7,4'-Di-O-methylapigenin
芹菜素二甲醚,4',7-DIMETHOXY-5-HYDROXYFLAVONE |
Amylase | Metabolism |
7,4'-Di-O-methylapigenin (4',7-DIMETHOXY-5-HYDROXYFLAVONE) 可能具有抗真菌c.zeyheri 的作用,是一种潜在的抗真菌药物。它还能抑制药物流出泵(IC50 = 51.64μg /毫升)。 | |||
T3884 |
Neoandrographolide
Neoandrographiside,新穿心莲内酯 |
NOS; COX | Immunology/Inflammation; Neuroscience |
Neoandrographolide (Neoandrographiside) 是一种二萜类化合物,从穿心莲中分离得到。 | |||
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。 | |||
T5431 |
[10]-Shogaol
10-姜烯酚,10-Shogaol |
Antioxidant; COX | Immunology/Inflammation; Neuroscience; oxidation-reduction |
[10]-Shogaol (10-Shogaol) 是一种从生姜中提取的抗氧化剂,用于皮肤细胞增殖和迁移增强剂。它抑制 COX-2,IC50值为 7.5 μM,可能有降血脂和胰岛素增敏作用。 | |||
T5311 |
Crocin (Gardenia Fruits Extract)
藏红花,西红花苷 |
Others | Others |
Crocin (Gardenia Fruits Extract)(42553-65-1)是藏红花(Crocus sativus L.)的水溶性类胡萝卜素色素。藏红花素具有抗炎、抗氧化、抗凋亡、抗哮喘、抗癌、降血脂等作用。 | |||
T8189 |
Dihydroberberine
|
Potassium Channel; HSP; HER | Angiogenesis; Cytoskeletal Signaling; JAK/STAT signaling; Membrane transporter/Ion channel; Metabolism; Tyrosine Kinase/Adaptors |
Dihydroberberine 可抑制人类 ether-a-go-go 相关基因 (hERG) 通道并显着降低 Hsp90 表达及其与 hERG 的相互作用,具有抗动脉粥样硬化、抗炎、降血脂和抗肿瘤活性。 | |||
T4749 |
Squalene
角鲨烯,Nikko Squalane EX,Super Squalene,AddaVax,all-trans-Squalene,trans-Squalene,Spinacene |
Reactive Oxygen Species; Endogenous Metabolite; Antifungal | Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB |
Squalene (AddaVax) 是胆固醇合成的中间产物,具有降血脂、保肝、心脏保护、抗氧化和抗毒活性等多种药理特性。它还具有抗真菌活性,可用于毛癣菌治疗的相关研究。 | |||
TN1868 | Ligupurpuroside A | LDL; AMPK | Chromatin/Epigenetic; Metabolism; PI3K/Akt/mTOR signaling |
Ligupurpuroside A has antioxidant,and hypolipidemic effects, it can significantly inhibit lipid accumulation in HepG2 cell at the concentration of 50 μMol/L. | |||
TN4138 | Globularin | Others | Others |
Globularin has hypoglycaemic and hypolipidemic activities in normal and streptozotocin-induced diabetic rats. | |||
TN1462 |
Cajanin
2',4',5-三羟基-7-甲氧基异黄酮,木豆异黄酮 |
ERK; MEK; Akt | Cytoskeletal Signaling; MAPK; PI3K/Akt/mTOR signaling |
Cajanin has potential hypolipidemic effects,possibly via up-regulating the ABCA1 protein expression,subsequently resulting in increased macrophage cholesterol efflux and RCT, it can significantly improve basal glucose uptake in HepG2 cells, its improving effect is concentration dependent, it exhibits effects stronger than that of rosiglitazone, which has been used as an antidiabetic drug. | |||
T11202 |
Enniatin complex
|
Others | Others |
Enniatin complex, a mixture of cyclohexadepsipeptides predominantly derived from various Fusarium species of fungi, exhibits inhibitory effects on enzymes such as acyl-CoA: cholesterol acyl transferase. Furthermore, it has demonstrated the ability to induce apoptosis in multiple cancer cell lines. In addition to these activities, the Enniatin complex possesses ionophoric, antibiotic, and in vitro hypolipidemic properties. | |||
TN6613 | Delphinidin-3-O-galactoside chloride | ||
Delphinidin-3-O-galactoside chloride has anti-obesity and hypolipidemic effects. Delphinidin-3-O-galactoside (D3G) is a water-soluble anthocyanin with antioxidant activity. D3G is capable of masking the EGCG-induced cytotoxicity and ER stress, presumably | |||
TN5431 |
Icariside E4
|
Antioxidant; AMPK; Liver X Receptor; Lipid; Fatty Acid Synthase | Chromatin/Epigenetic; Metabolism; oxidation-reduction; PI3K/Akt/mTOR signaling |
Icariside E4是一种从小叶榆中提取得到天然化合物, 通过AMPK 磷酸化和抑制HepG1细胞中MID1IP2的低脂化作用。Icariside E4具有抗伤害,抗氧化,抗阿尔茨海默氏症和抗炎作用,抑制了SREBP-1c,肝脏X 受体-α(LXR)和FASN 在HepG2细胞中从头脂肪生成的表达。Icariside E4是治疗脂肪肝疾病的有效候选药物,在HepG1细胞中具有低脂化潜力。 | |||
T36563 |
(E)-Guggulsterone
|
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Bile acids are essential for solubilization and transport of dietary lipids, are the major products of cholesterol catabolism, and are physiological ligands for farnesoid X receptor (FXR), a nuclear receptor that regulates genes involved in lipid metabolism.1They are also inherently cytotoxic, as physiological imbalance contributes to increased oxidative stress.2,3Bile acid-controlled signaling pathways are promising novel targets to treat such metabolic diseases as obesity, type II diabetes, hy... |