58
23
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T19367 |
Hypoglycemic agent 1
|
Others | Others |
Hypoglycemic agent 1 has an action for lowering blood sugar. It acts as a therapeutic and/or prophylactic agent for diabetes. | |||
T8345 |
Carbutamide
|
Others | Others |
Carbutamide 是一代磺酰脲,口服具有活性,具有降血糖作用。 | |||
T34532 |
Sari 59-801
Sari-59-801 |
Others | Others |
Sari 59-801 是具有口服活性的降血糖化合物,能够降低几个物种的血糖,且可以提高大鼠和小鼠的血浆中胰岛素水平。 | |||
T15567 |
Imiglitazar
TAK-559 |
PPAR | DNA Damage/DNA Repair; Metabolism |
Imiglitazar (TAK559)是有效的 PPAR-β/δ受体激动剂,具有降血糖作用。 | |||
T0127 |
Glimepiride
Glimperide,HOE-490,格列美脲 |
Potassium Channel | Membrane transporter/Ion channel |
Glimepiride (HOE-490) 是一种中长效的磺酰脲类抗糖尿病化合物,其 ED50=182 μg/k。 | |||
T60715 |
α-Glucosidase-IN-4
|
Glucosidase | Metabolism |
α-Glucosidase-IN-4 是一种有效的α- 葡萄糖苷酶 (α-glucosidase)抑制剂,具有降血压和降糖活性。 | |||
T1333 |
Tolazamide
甲磺氮草脲,妥拉磺脲,U-17835 |
Potassium Channel | Membrane transporter/Ion channel |
Tolazamide (U-17835) 是一种磺脲类降糖药,用于研究 2 型糖尿病,其作用和用途与氯丙酰胺相似。 | |||
T1054 |
Tolbutamide
甲苯磺丁脲,HLS 831 |
Potassium Channel; Autophagy | Autophagy; Membrane transporter/Ion channel |
Tolbutamide (HLS 831) 是一种磺脲类降糖药,作用和用途与氯丙酰胺相似。 | |||
T0150 |
Hydroxyhexamide
乙酸己脲,(±)-Hydroxyhexamid |
Potassium Channel; Drug Metabolite | Membrane transporter/Ion channel; Metabolism |
Hydroxyhexamide ((±)-Hydroxyhexamid) 是Acetohexamide 的活性代谢物, 可用作降血糖药。 | |||
T34973 |
Tyrphostin 8
4-Hydroxybenzylidenemalononitrile |
EGFR; GTPase | Angiogenesis; GPCR/G Protein; JAK/STAT signaling; Tyrosine Kinase/Adaptors |
Tyrphostin 8(4-Hydroxybenzylidenemalononitrile) 是一种有效的 GTP 酶抑制剂,对 EGFR 激酶有抑制作用, IC50 值为 560 μM。Tyrphostin 8 可抑制蛋白丝氨酸/苏氨酸钙调磷酸酶 (IC50=21 μM),增强 Caco-2 细胞中转铁蛋白受体介导的转吞作用,并增加口服胰岛素 - 转铁蛋白的降血糖作用。 | |||
T63166L |
(S, R)-LSN 3318839
(S, R)-LSN 3318839(Isomer-2764704-18-7) |
Glucagon Receptor | GPCR/G Protein |
T26982 |
Cerebrocrast
IOS 11212,IOS-11212,IOS11212 |
Others | Others |
Cerebrocrast (IOS-11212) 是具有抗炎和降血糖活性,促进大鼠肝脏线粒体中 H+ 和 Cl- 的共转运,阻断人血小板活化,可用于研究糖尿病。 | |||
T22683 |
CP-316819
CP 316819,GPi 819 |
Others | Others |
CP-316819 (GPi 819) 是一种高效的糖原磷酸化酶 (GPase) 抑制剂,具有降血糖作用,抑制 huSMGPa 和 huLGPa,可在低血糖期间维持神经元活性,可用于研究高血糖。 | |||
T0191 |
Linagliptin
BI 1356,利格列汀,利拉利汀 |
Ferroptosis; Proteasome; DPP-4; Autophagy | Apoptosis; Autophagy; Proteases/Proteasome; Ubiquitination |
Linagliptin (BI 1356) 是一种有效的、可口服的、基于二氢嘌呤二酮的二肽基肽酶 4 抑制剂,具有降血糖活性。 | |||
T0490 |
Chlorpropamide
Diabinese,氯磺丙脲 |
ATPase; ABC | Membrane transporter/Ion channel |
Chlorpropamide (Diabinese) 是口服降糖剂,可用于研究非胰岛素依赖型糖尿病。 | |||
T62238 |
AMPK activator 4
|
AMPK | Chromatin/Epigenetic; PI3K/Akt/mTOR signaling |
AMPK activator 4 是一种有效且具有选择性的AMPK激活剂,不抑制线粒体复合物 I。AMPK activator 4 选择性地激活肌肉组织中的 AMPK且剂量依赖性地改善正常小鼠的糖耐量,显著降低 db/db 糖尿病小鼠的空腹血糖水平和改善胰岛素抵抗。AMPK activator 4 具有降血糖作用。 | |||
T31976 |
Glymidine sodium
|
Others | Others |
Glymidine sodium 是口服有活性的抗糖尿病药物,也是肝脂肪分解的抑制剂。它通过抑制葡萄糖的形成,也对由于内源性脂质动员抑制而导致的丙酮酸氧化升高具有抑制作用。 | |||
T71812 |
Protonstatin-1
|
||
Protonstatin-1可用作降糖剂和治疗阿尔茨海默病的化合物,可抑制IGFIR 激酶的活性,可用于研究癌症。 | |||
T0334 |
Rosiglitazone
BRL49653,罗格列酮 |
Ferroptosis; TRP/TRPV Channel; PPAR; Autophagy | Apoptosis; Autophagy; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Metabolism |
Rosiglitazone (BRL49653) 是一种 PPARγ 激动剂、TRPC5 激活剂和 TRPM3 抑制剂,具有口服活性。Rosiglitazone 也是一种降糖剂,是噻唑烷二酮类胰岛素增敏剂。 | |||
T1603 |
Glipizide
CP 28720,K 4024,格列吡嗪 |
Potassium Channel; PPAR; ABC | DNA Damage/DNA Repair; Membrane transporter/Ion channel; Metabolism |
Glipizide (CP 28720) 是一种有效的、具有口服活性的磺酰脲类抗糖尿病试剂 (anti-diabetic agent),在 2 型糖尿病的研究中具有价值,但不适用于1 型糖尿病。Glipizide 是通过部分阻断郎格汉斯胰岛细胞中 ATP 敏感钾通道 (KATP)发挥活性 。 | |||
T1112 |
2-(Hydroxymethyl)pyridine
吡啶甲醇,Piconol |
PDE | Metabolism |
2-(Hydroxymethyl)pyridine (Piconol) 可用作有机合成与医药化学中间体,用于刺激性泻药比沙可啶的合成,也可用作具有降血糖活性的吡啶醇。 | |||
T1502 |
Vildagliptin
维达列汀,NVP-LAF 237,维格列汀,LAF237 |
Apoptosis; Ferroptosis; Proteasome; DPP-4 | Apoptosis; Proteases/Proteasome; Ubiquitination |
Vildagliptin (LAF237) 是一种选择性二肽基肽酶IV (DPP-IV) 抑制剂,在人 Caco-2 细胞中抑制 DPP-IV 的IC50为 3.5 nM。它具有出色的口服生物利用度和降血糖活性。 | |||
T8221 |
Insulin (human)
INSULIN,甘精胰岛素,胰岛素,Insulin(human) |
IGF-1R | Tyrosine Kinase/Adaptors |
Insulin (human) 是一种多肽激素,可以促进糖原的合成,调节血液中的葡萄糖水平。Insulin (human) 具有降血糖活性,临床上用于治疗糖尿病患者的高血糖。 | |||
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。 | |||
T0816 |
Acetohexamide
Acetohexamid,醋磺环已脲,Dymelor,醋磺己脲,Gamadiabet |
Potassium Channel; NADPH | Membrane transporter/Ion channel; Metabolism |
Acetohexamide (Acetohexamid) 是磺脲类试剂,可刺激胰腺分泌胰岛素,能够用于 2 型糖尿病的相关研究。 | |||
T1674 |
Nateglinide
那格列奈,A4166,Senaglinide |
Potassium Channel; Proteasome; PPAR | DNA Damage/DNA Repair; Membrane transporter/Ion channel; Metabolism; Proteases/Proteasome; Ubiquitination |
Nateglinide (Senaglinide) 是 D-苯丙氨酸的一种衍生物,是口服有效的、短效促胰岛素释放化合物,也是 DPP IV 抑制剂。 Nateglinide 抑制胰岛 β 细胞中 ATP 敏感的 K+通道。Nateglinide 在 2 型糖尿病中具有研究价值。 | |||
T24270 |
KS370G
KS-370-G,KS 370 G,Caffeic Acid Phenethyl Amide |
||
KS370G (Caffeic Acid Phenethyl Amide) 抑制 UUO 诱导的肾纤维化标志物表达。KS370G 是一种具有口服活性的降糖和心血管保护剂,可减少梗阻肾脏中胶原蛋白的沉积,并显著降低肾脏炎症趋化因子/粘附分子和单核细胞标志物的表达,改善压力过载小鼠心脏左室肥厚和功能。KS370G 可用于研究肾阻塞性肾病。 | |||
T19710 |
Ciglitazone
Ciglitazona,U 63287,ADD3878,ADD-3878,U-63287,ADD 3878 |
Apoptosis; p38 MAPK; PPAR | Apoptosis; DNA Damage/DNA Repair; MAPK; Metabolism |
Ciglitazone (ADD 3878) 是一种强效和选择性的PPARγ激动剂(EC50:3μM)和口服降糖药。Ciglitazone 抑制th17细胞的增殖和分化,降低胰岛素水平、血管内皮生长因子的产生和血压,诱导胃癌细胞的细胞周期停止。Ciglitazone 能诱导负鼠肾上皮细胞的凋亡,激活p38 MAPK 和凋亡诱导因子(AIF)的核转位。 Ciglitazone 在肥胖症和高血糖症的动物模型中表现出降血糖活性。 | |||
T0242 |
Sitagliptin
西他列汀,MK0431,西格列汀 |
Proteasome; DPP-4; Autophagy | Autophagy; Proteases/Proteasome; Ubiquitination |
Sitagliptin (MK0431) 是一种有效的 DPP4抑制剂,在 Caco-2 细胞中,IC50值为 19 nM。它是一种新型口服降糖药,可单独使用或与二甲双胍或噻唑烷二酮联合用于治疗 2 型糖尿病。 | |||
T13712 |
Glyparamide
|
Others | Others |
Glyparamide is a chlorophenyl-containing sulfonylurea with hypoglycemic activity. | |||
T32857 | Lonchocarpene | ||
Lonchocarpene is a hypoglycemic agent From the Amazonian plant Deguelia rufescens var. urucu. | |||
T11431 |
Glycosidase-IN-2
|
Others | Others |
Glycosidase-IN-2 is a glycosidase inhibitor with hypoglycemic activity. | |||
T13711 |
Glyhexamide
Subose,SQ 15860,Serbose |
Others | Others |
Glyhexamide is an effective hypoglycemic compound. | |||
T27415 |
Gliamilide
CP-27,634,CP27,634,CP 27,634 |
||
Gliamilide is a high-potency sulfamylurea hypoglycemic agent. | |||
T34537 | Saudin | ||
Saudin is a naturally occurring hypoglycemic diterpene. | |||
T0371L | Gliquidone sodium | ||
Gliquidone sodium is a hypoglycemic sulfonylurea which may protect the liver from injury from diabetes. | |||
T13478 | β-glycosidase-IN-1 | Integrin | Cytoskeletal Signaling |
β-glycosidase-IN-1 is a piperidine derivative, and is an inhibitor of β-glycosidase. It has hypoglycemic activity. | |||
T69191 |
Pemaglitazar
|
||
Pemaglitazar is a dual peroxisome proliferator-activated receptor (PPAR) alpha and gamma agonist, with hypoglycemic activity. | |||
T63404 | Xelaglifam | ||
Xelaglifam 是 G 蛋白偶联受体 40 (GPR40) 的有效激动剂,表现出降血糖作用。 | |||
T71296 |
4-Aaqb
|
||
4-Aaqb, also known as OB-318, is a natural inhibitor of the autophagy pathway, enhancing immune function, suppressing MAPK and NFκB, showing anti-inflammatory, hypoglycemic, vasorelaxative, and antiproliferative activities. | |||
T68745 |
U 56324
|
||
U-56324 is a hypoglycemic agent derived from nicotinic acid. It was found to inhibit the activity of ATP-sensitive potassium channels in excised patches from mouse pancreatic B-cells. | |||
T11430 |
Glycosidase-IN-1
|
Others | Others |
Glycosidase-IN-1 is a glycosidase inhibitor synthesized from D-mannose with hypoglycemic activity. It can be used to synthesize some immunosuppressive agents and β-glucosidase inhibitors. | |||
T40694 |
4-(3-Methyl-5-oxo-2-pyrazolin-1-yl)benzoic acid
|
||
4-(3-Methyl-5-oxo-2-pyrazolin-1-yl)benzoic acid exhibits hypoglycemic activity and operates through a mechanism dependent on the response to oral glucose overload. | |||
T68196 |
Aminocarnitine
|
||
Aminocarnitine is an inhibitor of fatty acid oxidation that acts as a hypoglycemic and antiketogenic compound. It alters lipidic metabolism by inhibiting carnitine acetyltransferase (CAT) and carnitine palmitoyltransferase (CPT). | |||
T68567 |
AMG-131 besylate
|
||
AMG-131 besylate is a hypoglycemic agent. It is a potent PPARγ partial agonist that displays robust glucose-lowering activity in rodent models of diabetes while exhibiting a reduced side-effects profile compared to marketed TZDs. | |||
T25283 |
Cytochrome P450 2C9
Cyp2C9,Human cytochrome P450 2C9,Cytochrome P 450 2C9,S-Mephenytoin 4-hydroxylase |
||
Cytochrome P450 2C9 is a cytochrome P-450 subtype that possesses specificity for acidic xenobiotics. It oxidizes a wide range of important clinical drugs under the categories of nonsteroidal anti-inflammatory agents, anticoagulants, hypoglycemic agents, a | |||
T35265 |
YM-440
YM440,YM 440 |
||
YM-440 is a novel hypoglycemic agent, an insulin sensitizer, that may be used for the treatment of type 2 diabetes mellitus by reducing glucose 6-phosphatase activity in obese Zucker rats and inhibiting liver glucose output through gluconeogenesis. | |||
T34767 |
TA-1887
TA 1887,TA1887 |
||
TA-1887 is a new type of selective inhibitor of sglt2 for the treatment of type 2 diabetes. It has a significant hypoglycemic effect in KK (HF-KK) mice fed a high-fat diet. TA-1887 has good pharmacokinetic characteristics and significantly increases UGE | |||
T6203L |
Saxagliptin hydrochloride
BMS477118,Saxagliptin,BMS 477118,Saxagliptin HCl,BMS-477118 |
||
Saxagliptin is a new oral hypoglycemic of the new dipeptidyl peptidase-4 (DPP-4) inhibitor class of drugs. Saxagliptin is a competitive DPP4 inhibitor that slows the inactivation of the incretin hormones and reducing fasting and postprandial glucose conce | |||
T68098 |
Midaglizole
(±)-DG5128 free base,DG5128 free base,(±)-DG5128 free base ; DG5128 free base |
||
Midaglizole ((±)-DG5128 free base, DG5128 free base) 是一种有效的α2-adrenoceptor 拮抗剂。Midaglizole 是一种降血糖药。Midaglizole 在具有升高血压并降低血糖水平的作用。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T8319 |
Butyl isobutyl phthalate
ButylIsobutylPhthalate,邻苯二甲酸-1-丁酯-2-异丁酯 |
Glucosidase | Metabolism |
Butyl isobutyl phthalate (ButylIsobutylPhthalate) 是一种非竞争性 α-葡萄糖苷酶抑制剂,IC50=38 μM,可以从海带的根状茎中分离得到。它具有降血糖作用,可用于糖尿病相关的研究。 | |||
T3776 |
Rhapontigenin
丹叶大黄素,Protigenin |
P450; Antibacterial; Antifungal | Metabolism; Microbiology/Virology |
Rhapontigenin (Protigenin) 是一种基于机制的选择性细胞色素 P450 1A1 (IC50: 400 nM) 灭活剂。它是一种芳烃羟化酶,可激活作为致癌物质的多环芳烃。它是白藜芦醇的天然类似物,具有抗癌,抗氧化剂,抗真菌和抗菌活性。 | |||
T2780 |
Catalpol
梓醇,Catalpinoside,Digitalis purpurea L |
Others; HBV | Microbiology/Virology; Others |
Catalpol (Catalpinoside) 是一种在Rehmannia glutinosa 中发现的鸢尾花苷,具有神经保护、降血糖、抗癌、抗痉挛、抗氧化、抗HBV 和抗肝炎病毒作用。 | |||
T38475 |
2,6-Dimethylpyrazine
|
Others | Others |
2,6-Dimethylpyrazine 是食品工业中不可缺少的调味添加剂,也是生产降糖和抗脂解化合物的重要底物。 | |||
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。 | |||
T2889 |
Isoferulic acid
Isoferulate,Hesperetic acid,3-Hydroxy-4-methoxycinnamic acid,Hesperetate,异阿魏酸 |
Influenza Virus; Adrenergic Receptor | GPCR/G Protein; Microbiology/Virology; Neuroscience |
Isoferulic acid (Hesperetate) 是一种肉桂酸衍生物,有抗糖尿病活性和抗流感病毒活性。它能结合并激活 α1-肾上腺素能受体,增强 β-内啡肽的分泌并增加体外葡萄糖的使用。 | |||
TN2326 |
(Z)-Butylidenephthalide
(Z)-3-Butylidenephthalide |
Glucosidase | Metabolism |
(Z)-Butylidenephthalide ((Z)-3-Butylidenephthalide) 具有抗肿瘤和降血糖作用,能有效抑制胶质瘤的肿瘤生长,抑制 R-葡萄糖苷酶活性。 | |||
TN2429 |
Capsiate
|
Antioxidant; TRP/TRPV Channel | Membrane transporter/Ion channel; oxidation-reduction |
Capsiate 是一种具有口服活性的 TRPV1 激动剂,是非刺激性辣椒素类似物,可作为抗过敏剂,具有抗炎、抗氧、降糖和抑制血管生成活性。 | |||
TJS0928 |
Calenduloside E
去葡萄糖竹节参皂苷,Silphioside F |
Others | Others |
Calenduloside E (Silphioside F) 是从辽东楤木中提取的一种五环三萜皂苷。它靶向热休克蛋白90 (Hsp90) ,具有抗凋亡作用。 | |||
TQ0298 |
Fagomine
D-Fagomine |
ROS; glycosidase | Immunology/Inflammation; Metabolism |
Fagomine (D-Fagomine) 是一种温和的糖苷酶 (glycosidase) 抑制剂,是1-脱氧野尻霉素 (DNJ) 的类似物,具有降血糖活性,Fagomine 降低了细胞内活性氧(ROS)的产生和丙二醛(MDA)水平。 | |||
T3665 |
Tectoridin
射干苷,Shekanin |
Estrogen Receptor/ERR; Reductase | Endocrinology/Hormones; Metabolism |
Tectoridin (Shekanin) 是分离自 Maackia amurensis 中的异黄酮,是一种植物雌激素,能够激活雌激素和甲状腺激素受体。它通过 ER 依赖性基因组途径和 GPR30 依赖性非基因组途径发挥雌激素作用。 | |||
T5716 |
4'-Methoxyresveratrol
白藜芦醇-4'-甲醚,4'-O-Methylresveratrol |
advanced glycation end products | Others |
4'-Methoxyresveratrol (4'-O-Methylresveratrol) 是一种多酚类化合物,来源于双翅目植物中,具有抗雄激素、抗真菌和抗炎症作用。它能抑制 RAGE- 介导的 MAPK/NF-κB 信号通路,并激活 NLRP3 炎性体,从而缓解 AGE- 诱导的炎症。 | |||
TN4883 |
Quinine sulfate dihydrate
奎宁树 |
Others | Others |
Quinine sulfate dihydrate 在钾通道阻滞剂中起主要作用。它也被用作抗疟疾、抗胆碱能、抗高血压和降糖药。它抑制线粒体atp 调节的钾通道。它也被用来研究生物结晶血红素,血红素,在疟疾寄生虫的代谢和研究血红素(FP)复合物的毒性。 | |||
T6S1597 |
Mulberroside A
桑皮苷 A,桑皮苷A |
TNF; Tyrosinase; Interleukin | Apoptosis; Immunology/Inflammation; Proteases/Proteasome |
Mulberroside A 是桑中的一种主要活性成分,可降低TNF-α、IL-1β和IL-6的表达,抑制 NALP3、caspase-1 和 NF-κB 的激活以及 ERK、JNK 和 p38 的磷酸化 。它抑制蘑菇酪氨酸酶,具有抗炎和抗细胞凋亡作用。 | |||
T4S0797 |
Berberine
小檗碱,Berberin,Umbellatine,黄连素 |
Reactive Oxygen Species; Topoisomerase; Endogenous Metabolite; Antibacterial; Antibiotic; Autophagy | Autophagy; DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism; Microbiology/Virology; NF-κB |
Berberine (Umbellatine) 是从中草药黄连中分离出来的一种生物碱抗生素。它诱导活性氧生成并抑制 DNA 拓扑异构酶,具有抗肿瘤特性。 | |||
TWS1613 |
Erioside
桑皮苷B,mulberroside B |
Others | Others |
Erioside (mulberroside B) 存在于Lasiosiphon eriocephalus 中,有镇咳、平喘、降血糖、抗肿瘤、治疗痛风的功效。 | |||
TN4793 |
Pinoresinol diacetate
|
Glucokinase | Metabolism |
Pinoresinol diacetate inhibits the enzyme α-glucosidase in vitro and may therefore act as a hypoglycemic agent. | |||
TN1943 |
Momordicoside G
|
Others | Others |
Momordicosides K and L, the main bitter taste triterpene glycosides in Bitter melon; and bitter melon has been reported to have hypoglycemic, anti atherogenic and anti HIV activities. | |||
T81093 | Sterebin F | ||
Sterebin F, 一种甾类化合物,来源于Stevia rebaudiana叶的分离提取,表现出降血糖的活性。 | |||
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. | |||
TN3692 | Conduritol A | TNF | Apoptosis |
Conduritol A has a hypoglycemic effect, can have an effect on regulating the metabolism of blood lipid, free-radical scavenging, enhancing the antioxidant ability, potentiating immune function; it also can markedly prevent the diabetic rats from getting c | |||
T79937 |
Mortatarin F
|
Glucosidase | Metabolism |
Mortatarin F (Compound 1) 是一种具有戊烯基化类黄酮结构的葡萄糖苷酶抑制剂,其IC50值为8.7 μΜ。该化合物可从桑叶中提取,并应用于研究降低血糖效果。 | |||
TN1874 |
Liriodendrin
鹅掌楸苦素 |
ATPase; Potassium Channel; Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation; Membrane transporter/Ion channel |
Liriodendrin 调节肺部炎症、NF-kB (p65) 的磷酸化和血管内皮生长因子 (VEGF) 的表达。Liriodendrin 具有抗炎、镇痛、降血糖活性,在脓毒症引起的急性肺损伤中起保护作用。 |