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Search Results for " glucose uptake "

38

抑制剂 & 化合物

14

天然产物

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Cat. No.	Product Name	Target	Signaling Pathways
T14327	AS1949490	Phosphatase	Metabolism
	AS1949490 是选择性SHIP-2抑制剂，其IC50=620 nM。它能够通过上调L6肌管GLUT1基因激活葡萄糖代谢。
T4534	BMS-309403	FABP	Metabolism
	BMS309403 是有效的、选择性脂肪细胞脂肪酸结合蛋白 aFABP 抑制剂。它可改善载脂蛋白 E 缺乏症小鼠和培养的人内皮细胞的内皮功能。它能够与蛋白质内部的脂肪酸结合口袋相互作用，竞争性地抑制内源性脂肪酸的结合。
T22276	Bis(maltolato)oxovanadium(IV) 双(麦芽醇)氧钒(IV),BMOV,Bis maltolato oxovanadium,Bis(maltolato)oxovanadium (IV),bis maltolato oxo vanadium,Bis(maltolato)oxovanadium (IV)	Phosphatase; Others	Metabolism; Others
	Bis(maltolato)oxovanadium(IV) (BMOV) 是一种有效的胰岛素增敏剂，也是一种有效的、竞争性的、可逆的、口服具有活性的光谱蛋白酪氨酸磷酸酶 (PTP) 抑制剂。它抑制HCPTPA，PTP1B，HPTPβ和SHP2的IC50分别为 126 nM，109 nM，26 nM 和 201 nM。
T36665	Dehydro Nifedipine BAY-b 4759
	Dehydro Nifedipine (BAY-b 4759) 是人血浆中硝苯地平的主要代谢物。Dehydro Nifedipine 抑制PC-12细胞葡萄糖摄取，IC50值为130 μM，硝苯地平是一种钙通道阻滞剂，用于治疗高血压和心绞痛。当硝苯地平被细胞色素P450 (CYP)异构体CYP3A4和CYP3A5代谢时形成脱氢硝苯地平。
T14017	2-NBDG 2-(N-7-硝基-2,1,3-苯并恶二唑-4-氨基)-2-脱氧-D-葡萄糖	Others	Others
	2-NBDG 是一种荧光指示剂 (λex=467 nm，λem=542 nm)，是一种荧光 D-葡萄糖类似物，可用于监测活细胞中的葡萄糖吸收。
T33412	MitoPQ MitoParaquat	Glucokinase; transporter	Metabolism
	MitoPQ (MitoParaquat) 是一个线粒体靶向的小分子化合物。MitoPQ 选择性加强线粒体超氧化物和过氧化氢的含量，抑制胰岛素刺激的葡萄糖摄取和葡萄糖转运蛋白 4 (GLUT4）向脂肪细胞和肌管中质膜的易位。MitoPQ 可用于研究线粒体氧化应激与调节的 GLUT4 转运。
T20029	Buformin hydrochloride NSC528218,NSC-528218,盐酸丁双胍,NSC 528218	AMPK	Chromatin/Epigenetic; PI3K/Akt/mTOR signaling
	Buformin hydrochloride (NSC-528218) 是一种有效的 AMPK 激活剂，是一种双胍类的口服抗糖尿病药物。Buformin 延缓胃肠道对葡萄糖的吸收，增加胰岛素敏感性和葡萄糖对细胞的吸收，并抑制肝脏对葡萄糖的合成。Buformin 也具有抗癌活性，可用于各种癌症研究。
T67893	PTP1B-IN-22	Phosphatase	Metabolism
	PTP1B-IN-22是一种蛋白酪氨酸磷酸酶1B (PTP1B)抑制剂，可抑制骨骼肌 L6肌管的葡萄糖摄取。
T24793	SIRT6-IN-5 SIRT6 inhibitor5,SIRT6 IN 5,SIRT6 inhibitor-5,SIRT6 inhibitor 5	Sirtuin	Chromatin/Epigenetic; DNA Damage/DNA Repair
	SIRT6-IN-5（SIRT6 inhibitor 5）是一种具有有效性和选择性的 SIRT6 抑制剂，IC50 值为 34 μM。SIRT6-IN-5 具有免疫抑制和化疗增敏作用，可增加 H3K9 的乙酰化并增加培养细胞中的葡萄糖摄取，减少 T 细胞增殖。
T8526	Metformin 甲福明,二甲双胍,1,1-Dimethylbiguanide	Mitophagy; AMPK; Autophagy	Autophagy; Chromatin/Epigenetic; PI3K/Akt/mTOR signaling
	Metformin (1,1-Dimethylbiguanide) 是一种 AMPK 激活剂，具有血脑屏障渗透性。Metformin 可通过提高胰岛素敏感性和减少肠道对葡萄糖的吸收来改善血糖控制，常用于 2 型糖尿病的研究。
T69146	Suksdorfin	PPAR	DNA Damage/DNA Repair; Metabolism
	Suksdorfin 具有降血糖作用，可促进脂肪细胞分化并增强脂联素的产生，可激活过氧化物酶体增殖物激活受体 γ （PPARγ），可促进脂肪细胞对胰岛素依赖性葡萄糖的摄取，可用于肥胖相关研究。
T8773	MID-1	Others; IGF-1R	Others; Tyrosine Kinase/Adaptors
	MID-1 是 MG53-IRS-1 相互作用的抑制剂，能够破坏 MG53 与 IRS-1 的分子缔合，并消除 MG53 诱导的 IRS-1 泛素化和骨骼肌降解，升高 IRS-1 表达水平，增加胰岛素信号传导和葡萄糖摄取。
T12853	SBI-477	Others	Others
	SBI-477 是化学探针，能够使转录因子MondoA 失活，刺激胰岛素信号传导，使胰岛素途径抑制剂硫氧还蛋白相互作用蛋白和抑制蛋白结构域 4 的表达降低。它能够协调地抑制三酰基甘油酯合成，促进人骨骼肌细胞中的基础葡萄糖摄取。
T40413	SW157765	transporter	Metabolism
	SW157765 是一种选择性葡萄糖转运体 GLUT8（SLC2A8）抑制剂，是很多化合物的前药，以剂量依赖性方式选择性地抑制SW157765敏感细胞中荧光 2-脱氧葡萄糖（2DG）的摄取，可用于研究肺癌。
T22223	3PO	Glucokinase; Autophagy	Autophagy; Metabolism
	3PO 是一种 PFKFB3 的小分子抑制剂，IC50值为22.9 μM。它抑制几种人类恶性造血和腺癌细胞系的增殖，IC50在1.4到24 μM 之间。它抑制葡萄糖摄取，并降低 Fru-2,6-BP、乳酸、ATP、NAD+ 和 NADH 的细胞内浓度。
TP2312	MOTS-c(Human) Acetate（1627580-64-6 free）	Others; AMPK	Chromatin/Epigenetic; Others; PI3K/Akt/mTOR signaling
	MOTS-c(Human) Acetate（1627580-64-6 free）是一种线粒体衍生肽。它诱导 AMP 类似物 AICAR 的积累，增加 AMPK 的激活和其下游 GLUT4 的表达。它可诱导葡萄糖摄取并提高胰岛素敏感性。它对调节肥胖、糖尿病、运动和长寿有重要意义。
T21399	Luseogliflozin TS71,TS-071,TS 71,TS071,TS-71,TS 071
	Luseogliflozin, a potent and competitive inhibitor of sodium-dependent glucose cotransporter 2 (SGLT2), competitively inhibits human SGLT2-mediated glucose uptake with a Ki value of 1.10 nM.
T70862	AMPK Activator SC4
	SC4 is a potent, direct AMPK activator. SC4 preferentially activates α2 complexes and stimulates skeletal muscle glucose uptake.
T25111	AS1938909 AS 1938909,AS-1938909
	AS1938909 is a SHIP2 inhibitor that works by increasing Akt phosphorylation, glucose consumption, and glucose uptake in L6 myotubes, specifically upregulating the GLUT1 gene.
T30261	AZD6482 (S-isomer) AZD-6482,AZD 6482,AZD6482 (S),AZD6482
	AZD6482 (S-isomer) is a potent, selective, ATP-competitive PI3Kβ inhibitor (IC(50) 0.01 μm), which can inhibit insulin-induced in vitro glucose uptake by human adipocytes (IC(50) is 4.4 μm).
T26395	6-Benzylthioinosine 6-BT,6Benzylthioinosine,6-Bn-thioinosine
	6-Benzylthioinosine, a broad-spectrum metabolic inhibitor, inhibits glucose uptake, decreases glycolysis and ATP concentration with minimal changes in ROS and mitochondrial respiration.
T23837	Buformin 丁双胍,W37,W 37,H 224,W-37
	Buformin (1-butylbiguanide) is an oral antidiabetic drug of the biguanide class. It also inhibits the synthesis of glucose by the liver. Buformin delays absorption of glucose from the gastrointestinal tract increases insulin sensitivity and glucose uptake
T62409	PI3K-IN-23
	PI3K-IN-23 是一种 (E)-9-oxooctadec-10-en-12-ynoic acid 类似物，能够促进葡萄糖摄取 (EC50: 7.00 μM)。
T81935	L-Glutamic γ-monohydroxamate
	L-Glutamic γ-monohydroxamate是一种特异性抗肿瘤试剂，能够抑制癌细胞的增殖，并针对性地阻止微血管内皮细胞摄取L-组氨酸。作为钒配体，该化合物还能激活脂肪细胞对葡萄糖的摄取和代谢，进而有效降低血糖水平。
T61804	GSK-3β inhibitor 6
	GSK-3β inhibitor 6 is a highly potent inhibitor of GSK-3β, with an IC50 value of 24.4 μM. It demonstrates significant enhancement of hepatocyte glucose uptake (38%). This compound holds great potential for studying various diseases including diabetes, inflammation, cancer, Alzheimer's disease, and bipolar disorder [1].
T64361	6-NBDG	Others	Others
	6-NBDG 是一种荧光葡萄糖类似物，可用作荧光探针。6-NBDG 可用于监测葡萄糖转运和摄取。6-NBDG 可用于检测富含巨噬细胞的动脉粥样硬化斑块。
TP1233	Amylin (8-37), rat Amylin (8-37) (mouse, rat)
	Amylin (8-37), rat is a truncated analog of native Amylin that selectively inhibits insulin-related glucose uptake and glycogen deposition in muscle tissue. Amylin is also known as islet amyloid precursor peptide (IAPP) and is co-secreted with insulin fro
T79644	Antidiabetic agent 2	Glucosidase	Metabolism
	Antidiabetic agent 2 (Compound 56) 作为一种葡萄糖摄取促进剂，能有效地抑制DPP-4, PTP-1B, α-淀粉酶和α-葡萄糖苷酶，其IC50s分别达到0.036、0.042、0.241、0.185 μM，表现出显著的降血糖作用。
T83374	2-Quinizarincarboxylic acid
	2-Quinizarinfascia（Compound 15）作为葡萄糖摄取抑制剂，在50 μM 浓度下显示了24.9%的抑制效率。
T71981	Gliclazide-d4
	Gliclazide-d4 is intended for use as an internal standard for the quantification of gliclazide by GC- or LC-MS. Gliclazide is a sulfonylurea and an inhibitor of pancreatic β-cell ATP-sensitive potassium (KATP) channels. It is selective for pancreatic β-cell over cardiac and arterial smooth muscle cell KATP channels. Gliclazide (5 μM) increases insulin-induced glucose uptake and glucose transporter 4 (GLUT4) translocation to the plasma membrane in a differentiated 3T3L1 adipocyte model of insulin...
T69380	Cinnamic acid, hydrazide
	Cinnamic acid, hydrazide is an unsaturated carboxylic acid and precursor to aspartame via enzyme-catalysed amination to phenylalanine. Cinnamic acid may be useful in prevention or treatment of Diabetes through various mechanism of actions including stimulation of insulin secretion, improvement of pancreatic β-cell functionality, inhibition of hepatic gluconeogenesis, enhanced glucose uptake, increased insulin signaling pathway, delay of carbohydrate digestion and glucose absorption, and inhibiti...
T78184	MMV009085
	MMV009085是一种针对恶性疟原虫己糖转运体PfHT1的特异性抑制剂，具有潜在的抗疟效果。它同时抑制人葡萄糖转运蛋白，强效抑制葡萄糖吸收（IC50：2.6 μM）及恶性疟原虫3D7株的生长（EC50：1.23±0.04 μM）。
T60858	MOPIPP
	MOPIPP 是新型的吲哚基查尔酮，可以透过血脑屏障。MOPIPP 对胶质母瘤细胞的肿瘤进展有抑制作用。MOPIPP 诱导细胞空泡化并增加自噬体数量。MOPIPP 还会触发细胞巨泡式死亡，并且中断葡萄糖摄取和糖酵解代谢。
T76039	MOTS-c(human) acetate
	MOTS-c(human) acetate 是一种线粒体衍生的肽，可诱导 AMP 类似物AICAR 的积累，增加AMPK 的激活及其下游GLUT4的表达。MOTS-c(human) acetate 可诱导葡萄糖摄取并改善胰岛素敏感性，对肥胖，糖尿病，运动和长寿的调节具有影响。
T78703	PTP1B/AKR1B1-IN-2	Phosphatase	Metabolism
	PTP1B/AKR1B1-IN-2（化合物7f）是一种双重PTP1B/AKR1B1抑制剂，具有IC50：3.2和2.1 μM，Ki：4.0和0.9μM。该化合物作为胰岛素模拟剂，能够改善小鼠C2C12肌母细胞的葡萄糖摄取，并可用于2型糖尿病（T2DM）的研究。
T37787	10-Nitrolinoleic acid
	10-Nitrolinoleate is the product of nitration of linoleate by NO-derived reactive species. Other nitrolinoleates detected in human plasma and urine include 9-, 12-, and 13-nitrolinoleate. Nitrolinoleates activate peroxisome proliferator-activated receptor γ (PPARγ; Ki = 133 nM), inducing CD36 expression in macrophages, adipocyte differentiation, and glucose uptake. Nitrolinoleates can also be metabolized by smooth muscle cells to produce nitrite derivatives which in turn form NO, leading to incr...
T63866	GSK-3β inhibitor 7
	GSK-3β inhibitor 7 是一种 GSK-3β 抑制剂 (IC50: 5.25 μM)。GSK-3β inhibitor 7 通过插入 GSK-3β 的 ATP-binding binding 口袋并形成氢键发挥作用。GSK-3β inhibitor 7 具有较高的肝细胞葡萄糖摄取率 (83.5%)，能够用于研究癌症、糖尿病、炎症、阿尔茨海默病和双相情感障碍等多种疾病。
T37579	GW 1929 hydrochloride
	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...

化合物

Cat.No: T14327

Target: Phosphatase

Cat.No: T4534

Target: FABP

Bis(maltolato)oxovanadium(IV)

Cat.No: T22276

Synonym: 双(麦芽醇)氧钒(IV),BMOV,Bis maltolato oxovanadium,Bis(maltolato)oxovanadium (IV),bis maltolato oxo vanadium,Bis(maltolato)oxovanadium (IV)

Target: Phosphatase, Others

Dehydro Nifedipine

Cat.No: T36665

Synonym: BAY-b 4759

Cat.No: T14017

Synonym: 2-(N-7-硝基-2,1,3-苯并恶二唑-4-氨基)-2-脱氧-D-葡萄糖

Target: Others

Cat.No: T33412

Synonym: MitoParaquat

Target: Glucokinase, transporter

Buformin hydrochloride

Cat.No: T20029

Synonym: NSC528218,NSC-528218,盐酸丁双胍,NSC 528218

Target: AMPK

Cat.No: T67893

Target: Phosphatase

Cat.No: T24793

Synonym: SIRT6 inhibitor5,SIRT6 IN 5,SIRT6 inhibitor-5,SIRT6 inhibitor 5

Target: Sirtuin

Cat.No: T8526

Synonym: 甲福明,二甲双胍,1,1-Dimethylbiguanide

Target: Mitophagy, AMPK, Autophagy

Cat.No: T69146

Target: PPAR

Cat.No: T8773

Target: Others, IGF-1R

Cat.No: T12853

Target: Others

Cat.No: T40413

Target: transporter

Cat.No: T22223

Target: Glucokinase, Autophagy

MOTS-c(Human) Acetate（1627580-64-6 free）

Cat.No: TP2312

Target: Others, AMPK

Cat.No: T21399

Synonym: TS71,TS-071,TS 71,TS071,TS-71,TS 071

AMPK Activator SC4

Cat.No: T70862

Cat.No: T25111

Synonym: AS 1938909,AS-1938909

AZD6482 (S-isomer)

Cat.No: T30261

Synonym: AZD-6482,AZD 6482,AZD6482 (S),AZD6482

6-Benzylthioinosine

Cat.No: T26395

Synonym: 6-BT,6Benzylthioinosine,6-Bn-thioinosine

Cat.No: T23837

Synonym: 丁双胍,W37,W 37,H 224,W-37

Cat.No: T62409

L-Glutamic γ-monohydroxamate

Cat.No: T81935

GSK-3β inhibitor 6

Cat.No: T61804

Cat.No: T64361

Target: Others

Amylin (8-37), rat

Cat.No: TP1233

Synonym: Amylin (8-37) (mouse, rat)

Antidiabetic agent 2

Cat.No: T79644

Target: Glucosidase

2-Quinizarincarboxylic acid

Cat.No: T83374

Cat.No: T71981

Cinnamic acid, hydrazide

Cat.No: T69380

Cat.No: T78184

Cat.No: T60858

MOTS-c(human) acetate

Cat.No: T76039

PTP1B/AKR1B1-IN-2

Cat.No: T78703

Target: Phosphatase

10-Nitrolinoleic acid

Cat.No: T37787

GSK-3β inhibitor 7

Cat.No: T63866

GW 1929 hydrochloride

Cat.No: T37579

Cat. No.	Product Name	Target	Signaling Pathways
TL0006	Cichoric Acid 菊苣酸,Dicaffeoyltartaric acid,Chicoric Acid	Reactive Oxygen Species; HIV Protease	Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB; Proteases/Proteasome
	Cichoric Acid (Dicaffeoyltartaric acid) 是一种天然化合物，具有抗氧化作用。
T9352	hydrocotarnine	Others	Others
	hydrocotarnine 是 Cbl 的抑制剂。
T8771	Pongamol	Others	Others
	Pongamol 是一种从 Pongamia pinnata 果实中鉴定出的铅分子，对骨骼肌细胞的葡萄糖摄取和 GLUT4 易位。
TN1740	Homoeriodictyol 高胜草酚,高圣草酚	5-HT Receptor; transporter; Sodium Channel; Drug Metabolite	GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Neuroscience
	Homoeriodictyol 是 Eriocitrin 的代谢物，属于黄酮类。Eriocitrin 是强效抗氧化剂。
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。
T6S0232	Eriodictyol 圣草酚,Huazhongilexone	Influenza Virus; DNA/RNA Synthesis; Nrf2; Endogenous Metabolite	Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism; Microbiology/Virology
	Eriodictyol (Huazhongilexone) 是从中草药中得到的一种黄酮类天然产物，具有抗氧化、抗炎和抗糖尿病作用。它还是一种流感依赖 RNA 的RNA 聚合酶抑制剂，IC50为 18 nM。它可诱导Nrf2信号通路。
T2P2923	Stearic acid 硬脂酸,Isostearic acid,Octadecanoic acid,Cetylacetic acid	Phosphatase; Endogenous Metabolite	Metabolism
	Stearic acid (Cetylacetic acid) 是长链饱和脂肪酸，存在于许多动植物油脂中。
TN1013	Cucurbitacin D	Apoptosis	Apoptosis
	Cucurbitacin D 是一种从 Ecballium elaterium （L.）分离出来的三萜类化合物，具有抗癌抗肿瘤活性，抑制转移性 PrC 中的葡萄糖摄取和乳酸产生，诱导独立于 ERK1/2 激活的炎症小体激活。 Cucurbitacin D 是巨噬细胞中的一种新的炎症小体激活剂，通过调节 JAK/STAT3、PI3K/Akt/mTOR 和 MAPK 信号通路抑制 HepG2 细胞增殖并诱导细胞凋亡，可用于研究宫颈癌、白血病和前列腺癌。
T5S1172	Tiliroside 银椴甙,Tribuloside,银椴苷；椴树苷	Antioxidant	oxidation-reduction
	Tiliroside (Tribuloside) 是糖苷类黄酮，是 α-淀粉酶的非竞争性抑制剂(Ki:84.2 μM)。它抑制胃肠道中碳水化合物的消化和葡萄糖的吸收，具有抗糖尿病作用。
T39613	11-epi-mogroside V
	11-epi-mogroside V, a compound found in the fruit of Siraitia grosvenori, possesses significant bioactivity by enhancing glucose uptake in vitro, specifically in human HepG2 cells.
TN1368	Alisol C	Others	Others
	Alisol C can improve glucose uptake in Hep G2 cells, it may be one of the therapeutic material basis in hypoglycemic activities in A. orientalis. Alisol C,16,23-oxido-alisol B and alisol O in Zexie may cause nephrotoxicity.
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.
TN4691	Octadecyl caffeate	Others	Others
	z-Octadecyl caffeate may have pain-relieving activity. Octadecyl caffeate and coptisonine can stimulate glucose uptake at 25 and 50 ug/mL. Octadecyl caffeate and octadecyl coumarate applied to the surface of susceptible varieties in laboratory bioassays r
TN4997	Serpentine	IGF-1R	Tyrosine Kinase/Adaptors
	Serpentine 是一种玫瑰花根中的生物碱，可用作胰岛素增敏剂，以协助胰岛素降低血糖。Serpentine 可激活 AMPK 磷酸化，从而刺激C2C12细胞对葡萄糖的摄取。Serpentine 可增加了肌肉组织中GSK-3β mRNA的表达，从而增强葡萄糖摄取。Serpentine 显著增加胰高血糖素分泌和肝糖异生。在高脂肪饮食/链脲佐菌素（HFD/STZ）诱导的糖尿病小鼠中，Serpentine 显著延长了胰岛素的降血糖时间，显著降低了外源性胰岛素的使用，抑制了内源性胰岛素的分泌。

天然产物

Cat.No: TL0006

Synonym: 菊苣酸,Dicaffeoyltartaric acid,Chicoric Acid

Target: Reactive Oxygen Species, HIV Protease

Cat.No: T9352

Target: Others

Cat.No: T8771

Target: Others

Homoeriodictyol

Cat.No: TN1740

Synonym: 高胜草酚,高圣草酚

Target: 5-HT Receptor, transporter, Sodium Channel, Drug Metabolite

Cat.No: TN2111

Synonym: Naringenin 7-0-glucoside,柚皮素-7-O-葡萄糖苷

Target: Phosphatase, Anti-infection, Virus Protease

Cat.No: T6S0232

Synonym: 圣草酚,Huazhongilexone

Target: Influenza Virus, DNA/RNA Synthesis, Nrf2, Endogenous Metabolite

Cat.No: T2P2923

Synonym: 硬脂酸,Isostearic acid,Octadecanoic acid,Cetylacetic acid

Target: Phosphatase, Endogenous Metabolite

Cat.No: TN1013

Target: Apoptosis

Cat.No: T5S1172

Synonym: 银椴甙,Tribuloside,银椴苷；椴树苷

Target: Antioxidant

11-epi-mogroside V

Cat.No: T39613

Cat.No: TN1368

Target: Others

Cat.No: TN1462

Synonym: 2',4',5-三羟基-7-甲氧基异黄酮,木豆异黄酮

Target: ERK, MEK, Akt

Octadecyl caffeate

Cat.No: TN4691

Target: Others

Cat.No: TN4997

Target: IGF-1R

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