61
21
15
2
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T1875 |
Atglistatin
|
Lipase | Metabolism |
Atglistatin 是脂肪甘油三酯脂酶的选择性抑制剂(IC50:0.7 μM),在体外具有抑制脂解的功能。 | |||
T10004 |
Palmitodiolein
Triglyceride POO,1,2-Dioleoyl-3-palmitoylglycerol,Glycerol dioleate palmitate |
Others | Others |
Palmitodiolein is a triacylglycerol existed in vegetable oils. | |||
T84385 |
1,2,3-Tri-γ-Linolenoyl Glycerol
γ-Linolenic Acid Triglyceride,γ-Linolenin,Tri-γ-linolenoate |
Others | Others |
1,2,3-Tri-γ-linolenoyl glycerol, a polyunsaturated triacylglycerol featuring γ-linolenoyl side chains at the C-1, C-2, and C-3 positions, occurs in multiple plant species such as blackcurrant, redcurrant, and borage. | |||
T85100 |
1,2,3-Tri-13(E)-Docosenoyl Glycerol
Tridocosenoyl Glycerol,Tribrassidin,Tri-13(E)-Docosenoin,TG(22:1/22:1/22:1),Brassidic Acid Triglyceride,Glycerol Tridocosenoate |
Others | Others |
1,2,3-Tri-13(E)-docosenoyl glycerol, a triacylglycerol featuring 13(E)-docosenoic acid at the \(sn-1\), \(sn-2\), and \(sn-3\) positions, transiently elevates heart triglyceride levels in weanling rats when administered as 15% of a calcium-deficient diet, with levels returning to baseline after 28 days. | |||
T27478 |
GSK3987
|
Liver X Receptor | Metabolism |
GSK3987 是广谱LXRα/β激动剂,EC50分别为 50 nM 和 40 nM。GSK3987增加 ABCA1 和 SREBP-1c 蛋白的表达,诱导细胞甘油三酯的积累和胆固醇流出。 | |||
T10035 |
10,12-Tricosadiynoic acid
TDA,TCDA |
Acyltransferase | Metabolism |
10,12-Tricosadiynoic acid 是一种口服有效的酰基辅酶 A 氧化酶-1 (ACOX1) 抑制剂,具有高特异性,选择性,高亲和力的特点。10,12-Tricosadiynoic acid 可改善线粒体脂质和 ROS 代谢,在高脂饮食或肥胖引起的代谢性疾病中有研究的价值。 | |||
T27719 |
KD-026
SLx 4090,SLx4090,KD026,SLx-4090 |
CETP | Metabolism |
KD-026 (SLx 4090) 是具有口服活性的、肠细胞特异性的微粒体甘油三酯转移蛋白 (MTP)抑制剂,IC50为 8.0 nM。KD-026 (SLx 4090) 在糖尿病2型中有研究的价值。 | |||
TQ0115 |
NB-598
|
Antifungal | Microbiology/Virology |
NB-598 是一种鲨烯环氧化酶竞争性抑制剂,可以阻碍甘油三酯的生物合成。 | |||
T2545 |
Lomitapide Mesylate
甲磺酸洛美他派,BMS-201038 mesylate,AEGR-733 mesylate |
CETP | Metabolism |
Lomitapide Mesylate (BMS-201038 mesylate) 是一种高效MTP 蛋白抑制剂,其体外IC50值为8 nM。 | |||
T0730 |
Triacetin
Glycerol triacetate,三醋酸甘油酯,1,2,3-Triacetoxypropane,Glyceryl triacetate,Glycerin triacetate,三醋精 |
Endogenous Metabolite; Antifungal | Metabolism; Microbiology/Virology |
Triacetin (Glyceryl triacetate) 是是甘油和乙酸的三酯,用作抗真菌剂。 | |||
T24263 |
KLH45
KLH-45,KLH 45 |
Phosphatase | Metabolism |
KLH45 是一种有效的选择性痉挛性截瘫相关甘油三酯水解酶 DDHD2 抑制剂 (IC50 = 1.3 nM)。 | |||
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。 | |||
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。 | |||
T15006 |
Dirlotapide
CP742033,Slentrol |
Others; CETP | Metabolism; Others |
Dirlotapide (CP742033) 是一种肠道选择性微粒体甘油三酯转移蛋白(MTP)抑制剂。它可以减轻糖尿病狗的体重。Dirlotapide 以剂量依赖性方式减少食物摄入量,可能是通过增加 肽YY 释放到循环中。 | |||
T35258 |
YM 16638
YM 638,YM-16638,YM16638 |
LTR | Immunology/Inflammation |
YM 16638 是一种具有口服活性的白三烯(LT)拮抗剂,具有降低甘油三酯和增加过氧化物酶体的作用,可用于研究抗原诱导过敏性绵羊早期和晚期气道反应。 | |||
T9186 |
Ervogastat
PF-06865571 |
Transferase | Metabolism |
Ervogastat (PF-06865571) 是一种有效且耐受性良好的二酰基甘油酰基转移酶 2 抑制剂。 Ervogastat 可降低非酒精性脂肪性肝炎 (NASH) 中的脂肪变性和肝脏甘油三酯水平。 | |||
T31992 |
Granotapide
|
CETP | Metabolism |
Granotapide 是一种微粒体甘油三酯转移蛋白(MTP)抑制剂,治疗和而预防动脉硬化,冠状动脉疾病,代谢综合征,肥胖,糖尿病,糖尿病前期和高血压。 | |||
T6267 |
Lomitapide
AEGR-733,洛美他派,BMS-201038 |
CETP | Metabolism |
Lomitapide (AEGR-733) 是一种高效的微粒体甘油三酯转移蛋白(MTP)抑制剂,体内试验的IC50值为8 nM。 | |||
T11016 |
DGAT-1 inhibitor 2
|
Transferase | Metabolism |
DGAT-1 inhibitor 2是有效的DGAT-1抑制剂,具有减肥功效。 | |||
T73499 |
NG-497
NG497 |
Lipase | Metabolism |
NG-497 是一种具有选择性的小分子人类的脂肪甘油三酯脂肪酶 (ATGL) 抑制剂,可以靶向人类 ATGL 的酶促活性 patatin 样结构域。NG-497在活性位点附近的疏水腔内结合ATGL。NG-497以剂量依赖性和可逆的方式消除人脂肪细胞中的脂肪分解。NG-497 可用于研究癌症。 | |||
T72322 |
R 59-022 hydrochloride
DKGI-I hydrochloride,Diacylglycerol kinase inhibitor I hydrochloride,DKGI-I hydrochloride ; Diacylglycerol kinase inhibitor I hydrochloride |
5-HT Receptor; PKC | Chromatin/Epigenetic; Cytoskeletal Signaling; GPCR/G Protein; Neuroscience |
R 59-022 hydrochloride (DKGI-I hydrochloride) 是一种 5-HT Receptor 拮抗剂,可激活蛋白激酶 C (PKC)。R 59-022 hydrochloride 是一种 DGK 抑制剂 (IC50:2.8 µM),可抑制 OAG 磷酸化为 OAPA。R 59-022 增强血小板中凝血酶诱导的甘油二酯的产生,并抑制嗜中性粒细胞中磷脂酸的产生。 | |||
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。 | |||
T10504 | Implitapide Racemate | Others | Others |
Implitapide Racemate is the racemate of Implitapide. Implitapide is an inhibitor of microsomal triglyceride transfer protein (MTP). | |||
T16158 |
PF-02575799
|
Adenosine Receptor | GPCR/G Protein; Neuroscience |
PF-02575799 is an inhibitor of microsomal triglyceride transfer protein (MTP) (IC50: 0.77±0.29 nM). | |||
T38666 |
CP-346086 dihydrate
|
Others | Others |
CP-346086 dihydrate is a potent and orally active inhibitor of microsomal triglyceride transfer protein (MTP), exhibiting an IC50 value of 2.0 nM for both human and rodent MTP. This compound effectively lowers plasma cholesterol and triglyceride levels in vivo. | |||
T13418 |
CP-319340(free base)
|
Others | Others |
CP-319340 free base is a inhibitor of microsomal triglyceride transfer protein (MTP) . | |||
T24223 |
JTT 130
JTT-130,JTT130 |
Others | Others |
JTT 130 is an agent of hypolipidemic. It inhibits microsomal triglyceride transfer protein. | |||
T26661 |
AS1708727
|
Others | Others |
AS1708727 is a Foxo1 inhibitor, exerting anti-hypertriglyceridemic and anti-diabetic effects by improving triglyceride and blood glucose metabolism at the gene expression level. | |||
T15570 |
Implitapide
英普他派,AEGR 427 |
CETP | Metabolism |
Implitapide is an inhibitor of microsomal triglyceride transfer protein (MTP). | |||
T19105 |
2-γ-Linolenoyl-1,3-dilinoleoyl-sn-glycerol
|
Others | Others |
2-γ-Linolenoyl-1,3-dilinoleoyl-sn-glycerol is a triglyceride. | |||
T85090 |
1,2,3-Tritricosanoyl Glycerol
Tritricosanoin,Glycerol Tritricosanoate,TG(23:0/23:0/23:0) |
Others | Others |
1,2,3-Tritricosanoyl glycerol, a triacylglycerol containing tricosanoic acid at the sn-1, sn-2, and sn-3 positions, serves as an internal standard for the quantification of fatty acids within the triglyceride component of human aortic endothelial cells (HAECs) cultured in media supplemented with stearic and/or oleic acid. | |||
T29448 |
50F10
50 F 10,50-F-10 |
Others | Others |
50F10 is a stabilizer for the active LPL dimer. It can act by preventing angptl4- and heat-induced inactivation of LPL and reducing postprandial triglyceride levels. | |||
T68245 |
PA-082
|
Others | Others |
PA-082 is a Novel partial agonist of peroxisome proliferator-activated receptor-γ (PPARγ), recruiting PPARγ-coactivator-1α, preventing triglyceride accumulation, and potentiating insulin signaling in vitro. | |||
T68588 |
CP-10447
|
Others | Others |
CP-10447 is an inhibitor apolipoprotein B (apoB) and triglyceride secretion in human hepatoma cells (HepG2) by inhibiting MTP activity and stimulating the early ER degradation of apoB. It is useful tool for further study of the mechanisms of apoB secretion and triglyceride-rich lipoprotein assembly. | |||
T27228 |
E-3030 free acid
E-3030,E3030,E 3030 |
Others | Others |
E-3030 free acid is a peroxisome proliferator-activated receptor (PPAR) agonist. E-3030 decreased blood glucose, triglyceride, non-esterified fatty acids, and insulin levels and increased blood adiponectin levels. Triglyceride- and non-high-density lipopr | |||
T35005 |
Usistapide
R-256918,JNJ-16269110,JNJ16269110,R256918,JNJ 16269110,R 256918 |
Others | Others |
UsISpide(JNJ-16269110 R256918) is an inhibitor of microsomal triglyceride transfer protein (MTTP) under development for the treatment of obesity and type 2 diabetes. | |||
T40898 |
DMHCA
|
Others | Others |
DMHCA, a potent, selective LXR agonist, specifically activates the LXR pathway's cholesterol efflux arm, avoiding triglyceride synthesis stimulation. This compound exhibits anti-inflammatory properties and is utilized in researching cholesterol homeostasis and diabetes. | |||
T28196 |
NS-220
LS-191458,NS 220 |
Others | Others |
NS-220, a selective agonist of peroxisome proliferator-activated receptor alpha, potently decreases plasma triglyceride and glucose levels and modifies lipoprotein profiles in KK-Ay mice. | |||
T68375 |
KD026-metabolite
|
Others | Others |
KD026-metabolite, is a metabolite of KD-026. KD026, also known as SLx-4090, is a microsomal triglyceride transfer protein (MTTP) inhibitor potentially for the treatment of type 2 diabetes. | |||
T84645 |
1-Palmitoyl-2-oleoyl-3-linoleoyl-rac-glycerol
POL |
Others | Others |
POL, a prevalent triglyceride component in various seed and vegetable oils such as olive, sesame, soybean, canola, corn, and hazelnut, is standardly utilized in the USP analysis of sesame oil for pharmaceutical applications. | |||
T39303 |
CP-346086
|
Others | Others |
CP-346086 is a highly potent and orally bioavailable inhibitor of microsomal triglyceride transfer protein (MTP), exhibiting an IC50 value of 2.0 nM against both human and rodent MTP. This compound effectively reduces plasma levels of cholesterol and triglycerides when administered in vivo. | |||
T29730 |
AGR-540
AGR540 |
Others | Others |
AGR-540 is a prodrug of AGR-529. AGR-540 has been shown to return plasma triglyceride concentrations to normal levels in mouse models. This effect may be attributed to an interaction of the molecule with A1 purinergic receptors of adipose tissue. | |||
T83275 |
6,9,12,15-Hexadecatetraenoic acid-ethyl ester
|
Others | Others |
6,9,12,15-Hexadecatetraenoic acid-ethyl ester 为口服活性的多不饱和脂肪酸。该化合物摄入后可减少小鼠血浆中甘油三酯含量。 | |||
T85144 |
1,2-Dioleoyl-3-linoleoyl-rac-glycerol
OOL,TG(18:1(9Z)/18:1(9Z)/18:2(9Z,12Z)),TG(18:1/18:1/18:2),TG(54:4) |
Others | Others |
1,2-Dioleoyl-3-linoleoyl-rac-glycerol (OOL) is a triglyceride featuring oleic acid at the sn-1 and sn-2 positions and linoleic acid at the sn-3 position. This compound is prevalent in several seed and vegetable oils, such as those from pumpkin seeds, olives, and sesame. | |||
T85047 |
2-Myristyldipalmitin
TG(16:0/14:0/16:0),1,3-Palmitin-2-Myristin |
Others | Others |
2-Myristyldipalmitin (PMP) 是一种棕榈酸甘油三酯,具有成为威尔逊氏病 (WD) 脂质标记物的潜力。 | |||
T40058 |
IQZ23
IQZ23 |
Others | Others |
IQZ23 is a chemical compound that effectively inhibits adipocyte differentiation by activating the AMPK pathway. It demonstrates high efficacy in reducing triglyceride levels (EC50=0.033 μM) in 3T3-L1 adipocytes. Given its properties, IQZ23 holds potential for research related to obesity and metabolic disorders. | |||
T85229 |
1,3-Dipalmitoyl-2-Docosahexaenoyl Glycerol
TG(16:0/22:6/16:0),1,3-Palmitin-2-Docoahexaenoin,16:0/22:6/16:0-TG |
Others | Others |
1,3-Dipalmitoyl-2-docosahexaenoyl glycerol, a triacylglycerol, features palmitic acid at the sn-1 and sn-3 positions and docosahexaenoic acid at the sn-2 position. Its dietary administration (30 g/kg) has been shown to decrease hepatic triglyceride and cholesterol levels in mice. | |||
T37579 |
GW 1929 hydrochloride
|
Others | Others |
Highly selective orally active peroxisome proliferator-activated receptor (PPAR)γ agonist (pEC50 values are 8.05, < 4 and < 4 for human PPARγ, PPARα and PPARδ receptors respectively). Decreases glucose, fatty acid and triglyceride levels following oral administration in vivo. Brown et al (1999) A novel N-aryl tyrosine activator of peroxisome proliferator-activated receptor-γ reverses the diabetic phenotype of the Zucker diabetic fatty rat. Diabetes 48 1415 PMID:10389847 |Nugent et al (2001) Pote... | |||
T35636 |
SHS4121705
|
Others | Others |
SHS4121705 is an orally bioavailable mitochondrial uncoupler.1It increases oxygen consumption rate in L6 rat myoblast cells with an EC50value of 4.3 μM. SHS4121705 (25 mg/kg per day in the diet) reduces hepatic steatosis, liver triglyceride levels, and plasma alanine aminotransferase (ALT) levels in Stelic animal model (STAM) mice, a model of non-alcoholic steatohepatitis (NASH). 1.Salamoun, J.M., Garcia, C.J., Hargett, S.R., et al.6-Amino[1,2,5]oxadiazolo[3,4-b]pyrazin-5-ol derivatives as effic... | |||
T79764 |
PF-07202954
|
Acyltransferase | Metabolism |
PF-07202954为一种弱碱性DGAT2抑制剂,其对人类DGAT2的IC50值为10 nM。在西方饮食喂养的大鼠模型中,PF-07202954能有效降低肝脏内的甘油三酯含量。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T14862 |
Caprylic/Capric Triglyceride
|
Others | Others |
Caprylic/Capric Triglyceride 是一种从分离的植物油中提取的甘油三酯和酯,以及从椰子油和棕榈仁油中提取的脂肪酸。它具有良好的氧化稳定性,可用作食品添加剂及用于化妆品。 | |||
TWO2727 |
Propane-1,2,3-triyl tripalmitate
Palmitic Triglyceride,Tripalmitin,Tripalmitoylglycerol,Glycerol Tripalmitate,三棕榈酸甘油酯 |
Others; Endogenous Metabolite | Metabolism; Others |
Propane-1,2,3-triyl tripalmitate (Glycerol Tripalmitate) 是内源性代谢产物的一种。 | |||
T19676 |
Tributyrin
NSC661583,NSC 661583,NSC-661583,甘油三丁酸酯 |
Apoptosis | Apoptosis |
Tributyrin (Glyceryl tributyrate) 是一种中性短链脂肪酸甘油三酯,是一种稳定且吸收迅速的丁酸前药。 它通过生物膜扩散并被细胞内脂肪酶代谢,在体内将有效的丁酸直接释放到细胞中,有抗增殖、促凋亡和诱导分化作用。 | |||
T5544 |
2-Furoic acid
Furan-2-carboxylic acid,糠酸 |
Anti-infection; ATP Citrate Lyase; Endogenous Metabolite; Acyltransferase | Metabolism; Microbiology/Virology |
2-Furoic acid (Furan-2-carboxylic acid) 2-Furoic acid 能够降低血清中胆固醇和甘油三酯的水平,具有抗血脂作用。 | |||
T8272 |
Trierucin
|
Others; Endogenous Metabolite | Metabolism; Others |
Trierucin 是一种从种子油中提取的三芥酸甘油三酯。 | |||
TN2197 |
Secoisolariciresinol
|
TNF | Apoptosis |
Secoisolariciresinol 是一种属于苯丙素类的木脂素。 | |||
T3220 |
Euphorbiasteroid
Euphobiasteroid,Euphorbia factor L1,千金子甾醇 |
Others; AMPK | Chromatin/Epigenetic; Others; PI3K/Akt/mTOR signaling |
Euphorbiasteroid (Euphobiasteroid) 是续随子中的一种三环二萜,可抑制酪氨酸酶活性,增强AMPK 的磷酸化。它通过减少细胞内甘油三酯的积累来降低 3T3-L1 细胞的分化,具有抗癌、抗病毒、抗肥胖及多重耐药调节作用。 | |||
T5242 |
Triarachidin
Triarachin,1,2,3-Trieicosanoyl Glycerol,Glycerol Trieicosanoate,三花生精 |
Others; Endogenous Metabolite | Metabolism; Others |
Triarachidin (1,2,3-Trieicosanoyl Glycerol) 是内源性代谢产物的一种。 | |||
T3921 |
Punicalagin
安石榴甙,安石榴苷 |
SARS-CoV; HBV | Microbiology/Virology |
Punicalagin 是一种在石榴中发现的主要鞣花单宁,是可逆且非竞争性的 3CLpro 抑制剂。Punicalagin 具有抗氧化、抗炎和抗肿瘤活性。 | |||
TCS1772 |
Dehydroabietic acid
Dehydroabietate,脱氢松香酸 |
Antifection | Microbiology/Virology |
Dehydroabietic acid (Dehydroabietate) 是 EBV-EA 活化抑制剂。 它是食物衍生化合物,可通过降低血浆葡萄糖、胰岛素水平、血浆甘油三酯 (TG) 和肝 TG 水平来治疗肥胖相关疾病。它的衍生物在动物模型中表现出抗分泌和抗胃蛋白酶作用。 | |||
TN5137 |
Tetramethylkaempferol
|
transporter; PPAR | DNA Damage/DNA Repair; Metabolism |
Tetramethylkaempferol 是一种 PPARγ 激动剂,它可以通过增加脂联素的水平来提高胰岛素敏感性,脂联素是一种与脂肪组织中胰岛素敏感性相关的重要脂肪细胞因子。 它可以浓度依赖性地增强甘油三酯的积累,甘油三酯是脂肪生成的标志物。 | |||
TN3884 |
Dodoviscin I
|
transporter | Metabolism |
Dodoviscin I can promote adipocyte differentiation as characterized by increased triglyceride levels in 3T3L1 cells. | |||
T81013 |
tert-OMe-byakangelicin
|
||
tert-OMe-byakangelicin 是一种香豆素,能够增强肾上腺素诱导的脂肪细胞中的脂肪溶解作用,同时抑制胰岛素在脂肪细胞中刺激的甘油三酯生成。 | |||
TN3885 |
Dodoviscin J
|
transporter | Metabolism |
Dodoviscin J can promote adipocyte differentiation as characterized by increased triglyceride levels in 3T3L1 cells. | |||
TN3883 |
Dodoviscin H
|
transporter | Metabolism |
Dodoviscin H can promote adipocyte differentiation as characterized by increased triglyceride levels in 3T3L1 cells. | |||
T10044 |
13-Oxo-9E,11E-octadecadienoic acid
|
PPAR | DNA Damage/DNA Repair; Metabolism |
13-Oxo-9E,11E-octadecadienoic acid, a potent PPARα activator derived from tomato juice and an isomer of 9-oxo-ODA, exhibits the ability to decrease plasma and hepatic triglyceride levels in obese diabetic mice[1]. | |||
T81222 |
Salvifaricin
|
||
Salvifaricin是一种口服活性的二萜类化合物,可从墨西哥鼠尾草和西班牙鼠尾草中提取。Salvifaricin能显著降低空腹血糖以及血清甘油三酯(TG)水平,表现出抗糖尿病的效果。 | |||
TN3882 |
Dodoviscin A
|
cAMP; Tyrosinase; transporter | GPCR/G Protein; Metabolism; Proteases/Proteasome |
Dodoviscin A may be a new promising pigmentation-altering agent for cosmetic and therapeutic applications, it can inhibit melanin biosynthesis induced by 3-isobutyl-1-methylxanthine and PD98059.Dodoviscin A can promote adipocyte differentiation as charact | |||
T60692 |
Masoprocol
|
Others | Others |
Masoprocol (meso-Nordihydroguaiaretic acid) 是口服有效的脂氧合酶 (lipoxygenase) 抑制剂。Masoprocol 具有出抗高血糖活性,可用于 II 型糖尿病的研究。 Masoprocol 可降低体内肝甘油三酯和葡萄糖浓度。 | |||
TN3112 |
5-Heneicosylresorcinol
|
NADPH-oxidase; Antifection | Immunology/Inflammation; Microbiology/Virology |
5-Heneicosylresorcinol 对 RBL-2H3 细胞中 β-己糖胺酶的释放具有抑制作用,它还可以防止 3T3-L1 细胞中甘油三酯的积累。它对红线虫、秀丽隐杆线虫和松材线虫具有杀线虫活性,ED50 值分别为 80、30 和 180 ug/mL。 | |||
T36563 |
(E)-Guggulsterone
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Others | Others |
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... |
Cat. No. | Product Name | Species | Expression System |
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TMPH-01850 |
PNPLA2 Protein, Human, Recombinant (His & SUMO)
Transport-secretion protein 2,Patatin-like phospholipase dom... |
Human | E. coli |
PNPLA2 Protein, Human, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 71.3 kDa and the accession number is Q96AD5. | |||
TMPH-01612 |
LSR Protein, Human, Recombinant (His)
Lipolysis-stimulated lipoprotein receptor,Angulin-1,LSR |
Human | E. coli |
Probable role in the clearance of triglyceride-rich lipoprotein from blood. Binds chylomicrons, LDL and VLDL in presence of free fatty acids and allows their subsequent uptake in the cells. | |||
TMPH-00491 |
PNLIPRP1 Protein, Canine, Recombinant (His)
Inactive pancreatic lipase-related protein 1,PNLIPRP1 |
Canine | P. pastoris (Yeast) |
May function as inhibitor of dietary triglyceride digestion. Lacks detectable lipase activity towards triglycerides, diglycerides, phosphatidylcholine, galactolipids or cholesterol esters (in vitro). PNLIPRP1 Protein, Canine, Recombinant (His) is expressed in yeast with N-6xHis tag. The predicted molecular weight is 51.7 kDa and the accession number is P06857. | |||
TMPH-00492 |
PNLIPRP1 Protein, Canine, Recombinant (His & SUMO)
Inactive pancreatic lipase-related protein 1,PNLIPRP1 |
Canine | E. coli |
May function as inhibitor of dietary triglyceride digestion. Lacks detectable lipase activity towards triglycerides, diglycerides, phosphatidylcholine, galactolipids or cholesterol esters (in vitro). PNLIPRP1 Protein, Canine, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 65.7 kDa and the accession number is P06857. | |||
TMPH-02509 |
ANGPTL8 Protein, Mouse, Recombinant (E. coli, His)
Angiopoietin-like protein 8,Lipasin,Gm6484,Refeeding-induced... |
Mouse | E. coli |
Hormone that acts as a blood lipid regulator by regulating serum triglyceride levels. May be involved in the metabolic transition between fasting and refeeding: required to direct fatty acids to adipose tissue for storage in the fed state. According to a report, may act by promoting ANGPTL3 cleavage. According to another study, not required for cleavage of ANGPTL3. | |||
TMPK-00764 |
Apolipoprotein A-II/APOA2 Protein, Human, Recombinant (hFc)
Apolipoprotein A-II(1-76),Apolipoprotein A-II,Apo-AII,APOA2,... |
Human | HEK293 Cells |
APOA2 is a protein implicated in triglyceride, fatty acid and glucose metabolism. In pigs, the APOA2 gene is located on pig chromosome 4 (SSC4) in a QTL region affecting fatty acid composition, fatness and growth traits. Apolipoprotein A-II/APOA2 Protein, Human, Recombinant (hFc) is expressed in HEK293 mammalian cells with C-hFc tag. The predicted molecular weight is 36.1 kDa and the accession number is P02652. | |||
TMPK-00795 |
Apolipoprotein A-II/APOA2 Protein, Mouse, Recombinant (hFc)
APOA2,Apolipoprotein A-II(1-76),Apolipoprotein A-II,Apolipop... |
Mouse | HEK293 Cells |
APOA2 is a protein implicated in triglyceride, fatty acid and glucose metabolism. In pigs, the APOA2 gene is located on pig chromosome 4 (SSC4) in a QTL region affecting fatty acid composition, fatness and growth traits. Apolipoprotein A-II/APOA2 Protein, Mouse, Recombinant (hFc) is expressed in HEK293 mammalian cells with C-hFc tag. The predicted molecular weight is 36.2 kDa and the accession number is P09813. | |||
TMPK-01087 |
Apolipoprotein A-V/APOA5 Protein, Mouse, Recombinant (His)
ApoA-V,Apolipoprotein A-V,Rap3,Apoa5,Apo-AV,Apolipoprotein A... |
Mouse | E. coli |
APOA5 is probably the gene with the strongest effect on triglyceride (TG) metabolism. APOA5 is almost exclusively expressed in the liver, and its product apoAV has a very low circulating concentration. New physiological roles of apoAV have been recently elucidated, such as control of chylomicron production in the intestine and TG accumulation in adipose tissue.The key role of APOA5 in TG metabolism has been largely shown through genetic studies in association with either severe or moderate hyper... | |||
TMPJ-01459 |
FGF-21 Protein, Cynomolgus, Recombinant (His)
Fibroblast Growth Factor 21,FGF-21,FGF21 |
Cynomolgus | HEK293 Cells |
Fibroblast Growth Factor 21 (FGF21) is a growth factor that belongs to the FGF family. FGF family proteins play a central role during prenatal development and postnatal growth and regeneration of mamy tissues, by promoting cellular proliferation and differentiation. FGF21 is a potent activator of glucose uptake on adipocytes, protects animal from diet-induced obesity when overexpression in transgenic mice, and lower blood glucose and triglyceride levels when therapeutically adiministered to diab... | |||
TMPH-02510 |
ANGPTL8 Protein, Mouse, Recombinant (His)
Rifl,Refeeding-induced fat and liver protein,Betatrophin,Ang... |
Mouse | P. pastoris (Yeast) |
Hormone that acts as a blood lipid regulator by regulating serum triglyceride levels. May be involved in the metabolic transition between fasting and refeeding: required to direct fatty acids to adipose tissue for storage in the fed state. According to a report, may act by promoting ANGPTL3 cleavage. According to another study, not required for cleavage of ANGPTL3. ANGPTL8 Protein, Mouse, Recombinant (His) is expressed in yeast with N-6xHis tag. The predicted molecular weight is 22.5 kDa and the... | |||
TMPJ-01196 |
ANGPTL8 Protein, Human, Recombinant (hFc)
βtrophin,Angiopoietin-like protein 8,Lipasin,Angptl8,Betatro... |
Human | HEK293 Cells |
The protein specifically promotes pancreatic beta cell proliferation and beta cell mass expansion, thereby improving glucose tolerance. It promotes pancreatic beta cell proliferation without insulin resistance. Also it acts as a blood lipid regulator by regulating serum triglyceride levels and possibly by promoting ANGPTL3 cleavage. It interacts with ANGPTL3. It predominantly expressed in liver and also expressed in adipose tissues. The ability of the protein to induce pancreatic beta cell proli... | |||
TMPJ-00601 |
Apolipoprotein C-II/APOC2 Protein, Human, Recombinant (His)
Apolipoprotein C2,Apolipoprotein C-II,APC2 and APOC2 |
Human | E. coli |
APOC2 activates the lipoprotein lipase in capillaries, which hydrolyzes triglycerides and thus provides free fatty acids for cells. APOC2 is component of the very low density lipoprotein (VLDL) fraction in plasma. It is also an activator of several triacylglycerol lipases. The association of APOC2 with plasma chylomicrons, VLDL, and HDL is reversible, a function of the secretion and catabolism of triglyceride-rich lipoproteins, and changes rapidly. Defects in APOC2 are the cause of hyperlipoprot... | |||
TMPY-03222 |
PNLIP Protein, Human, Recombinant (His)
PL,pancreatic lipase,PTL,PNLIPD |
Human | HEK293 Cells |
PNLIP is an enzyme that belongs to the lipase family. Secreted from the pancreas, PNLIP is the primary lipase that hydrolyzes dietary fat molecules in the human digestive system, converting triglyceride substrates found in ingested oils to monoglycerides and free fatty acids. Bile salts secreted from the liver and stored in gallbladder are released into the duodenum where they coat and emulsify large fat droplets into smaller droplets, thus increasing the overall surface area of the fat, which a... | |||
TMPJ-00286 |
ANGPTL3 Protein, Human, Recombinant (hFc)
ANGPTL3,ANGPT5,Angiopoietin-related protein 3,ANG-5,Angiopoi... |
Human | HEK293 Cells |
Angiopoietin-like 3 (ANGPTL3) is a secreted glycoprotein that is structurally related to the angiopoietins. Mature human ANGPTL3 contains an N-terminal coiled coil domain and a C-terminal fibrinogen-like domain. ANGPTL3 is expressed in the liver from early in development through adulthood. Full length ANGPTL3 circulates in the plasma as do the proteolytically separated N-and C-terminal segments containing the coiled coil domain and fibrinogen-like domains,respectively. ANGPTL3 directly inhibits ... | |||
TMPY-03353 |
CEL Protein, Mouse, Recombinant (His)
1810036E18Rik,carboxyl ester lipase,BAL |
Mouse | Baculovirus Insect Cells |
CEL-maturity onset diabetes of the young (MODY), diabetes with pancreatic lipomatosis and exocrine dysfunction, is due to dominant frameshift mutations in the acinar cell carboxyl ester lipase gene (CEL). Bile-salt activated carboxylic ester lipase (CEL) is a major triglyceride, cholesterol ester and vitamin ester hydrolytic enzyme contained within pancreatic and lactating mammary gland secretions. Carboxyl ester lipase is a digestive pancreatic enzyme encoded by the CEL gene. Mutations in CEL c... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T71306 |
Gemfibrozil-d6
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Gemfibrozil-d6 is intended for use as an internal standard for the quantification of gemfibrozil by GC- or LC-MS. Gemfibrozil is a peroxisome proliferator-activated reporter α and PPARγ agonist. In vivo, gemfibrozil reduces serum total cholesterol, triglyceride, and LDL levels in a rat model of high-cholesterol diet-induced hyperlipidemia. Gemfibrozil reduces atherosclerotic plaque area, superoxide production, and expression of the genes encoding the NF-κB subunit p65 and chemokine (C-C) motif l... | |||
T71305 |
Clofibric Acid-d4
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Clofibric acid-d4 is intended for use as an internal standard for the quantification of clofibric acid by GC- or LC-MS. Clofibric acid is a peroxisome proliferator-activated receptor α (PPARα) agonist (EC50 = 50 µM in a transactivation assay) and the active metabolite of clofibrate. It is formed from clofibrate by tissue and serum esterases. Dietary administration of clofibric acid (0.067-0.22%) reduces serum cholesterol, phospholipid, and triglyceride levels in rats. It decreases glutamate oxal... |