37
5
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T8345 |
Carbutamide
|
Others | Others |
Carbutamide 是一代磺酰脲,口服具有活性,具有降血糖作用。 | |||
T21246 |
Metsulfuron-methyl
|
Others | Others |
Metsulfuron-methyl 是一种内吸传导选择性麦田高效磺酰脲类除草剂,主要防治麦田大多数阔叶杂草和禾本科杂草。 | |||
T9222 |
Emlenoflast
MCC7840 |
NOD-like Receptor (NLR); NOD | Immunology/Inflammation; NF-κB |
Emlenoflast (MCC7840) 是一种 NLRP3炎症小体 (NLRP3 inflammasome) 的选择性抑制剂(IC50<100 nM)。它可用于研究炎性疾病。 | |||
T19859 |
Nicosulfuron
Milagro,Accent,Motivell,烟嘧磺隆 |
Others | Others |
Nicosulfuron (Milagro) 是一种磺酰脲类的选择性除草剂,常用作出苗后的除草剂,保护玉米作物免受杂草的侵害。它也能够降低乙酰乳酸合酶的活性。 | |||
T20623 |
Thifensulfuron-methyl
Harmony GT,Refine,Pinnacle,噻吩磺隆 |
Others | Others |
Thifensulfuron-methyl (Pinnacle) 是磺酰脲类除草剂,可用于防治玉米,小麦和大豆田中的阔叶杂草。 | |||
T20804 |
Bensulfuron-methyl
F-5384,DPX 84,F5384,F 5384,苄嘧磺隆 |
Others | Others |
Bensulfuron-methyl (F 5384) 是一种磺酰脲类除草剂,广泛应用于稻田阔叶杂草防治。 | |||
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 。 | |||
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。 | |||
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。 | |||
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。 | |||
T16420 |
P-1075
|
Potassium Channel | Membrane transporter/Ion channel |
P-1075 是磺酰脲受体2相关的 ATP 敏感性的钾通道(SUR2-KIR6)的激活剂,EC50为 45 nM。它在兔子中通过打开线粒体 K (ATP) 通道产生活性氧,产生保护心脏的功效。 | |||
T1634 |
Glibenclamide
格列本脲,Glyburide |
Potassium Channel; Mitochondrial Metabolism; CFTR; P-gp; Autophagy | Autophagy; Membrane transporter/Ion channel; Metabolism; Neuroscience |
Glibenclamide (Glyburide) 是一种具有口服活性的 ATP 敏感的 K+通道抑制剂,可研究糖尿病和肥胖。它抑制 P-糖蛋白,可直接结合并阻断 KATP 的 SUR1亚基并抑制囊性纤维化跨膜传导调节蛋白。它通过诱导膜离子通透性干扰线粒体生物能,可诱导自噬。 | |||
T0371 |
Gliquidone
AR-DF 26,格列喹酮,Glurenorm |
Potassium Channel | Membrane transporter/Ion channel |
Gliquidone (AR-DF 26) 是一种磺酰脲类的抗糖尿病药物,可用于2型糖尿病的研究。 | |||
T1410 |
Torsemide
AC-4464,JDL-464,托拉塞米,Torasemide |
Na-K-Cl cotransporter | Membrane transporter/Ion channel |
Torsemide (AC-4464) 是具有口服活性的亨氏环利尿剂,也具有抗醛固酮和血管舒张活性。它可用于研究心力衰竭、肾脏疾病、肝硬化。 | |||
T1527 |
Gliclazide
格列齐特,S1702,SE1702 |
Potassium Channel | Membrane transporter/Ion channel |
Gliclazide (SE1702) 是一种有效的全细胞的 β 细胞 ATP 敏感型钾流阻断剂,IC50为 184 nM,用作降糖药。 | |||
T31966 |
Glycyclamide
TOLCYCLAMIDE,Tolhexamide,Cyclamide,Glycyclamid,Gliciclamide |
Others | Others |
Glycolamide is a sulfonylurea compound containing cyclohexyl groups. | |||
T27883 |
LY 181984
LY181984,LY-181984,MPCU |
Others | Others |
LY 181984 is an sulfonylurea with antitumor properties. | |||
T13712 |
Glyparamide
|
Others | Others |
Glyparamide is a chlorophenyl-containing sulfonylurea with hypoglycemic activity. | |||
TP2383 |
Glipentide
Staticum,UR661,UR-661,UR 661,Glisentide |
||
Glieptide, a second-generation sulfonylurea, promotes the accumulation of fructose 2, 6-diphosphate in liver cells. | |||
T20722 |
Flucetosulfuron
LGC-42153,LGC 42153,LGC42153 |
Others | Others |
Flucetosulfuron is a sulfonylurea herbicide | |||
T35640 |
trans-carboxy Glimepiride
|
Others | Others |
trans-carboxy Glimepiride is a metabolite of the sulfonylurea glimepiride .1It is formed from glimepiride in a two-step process mediated by the cytochrome P450 (CYP) isoform CYP2C9 and cytosolic enzymes. 1.Noh, K., Kim, E., Jeong, T.C., et al.Simultaneous determination of glimepiride and its metabolites in human plasma by liquid chromatography coupled to a tandem mass spectrometryArch. Pharm. Res.34(12)2073-2078(2011) | |||
T35641 |
trans-hydroxy Glimepiride
|
Others | Others |
trans-hydroxy Glimepiride is an active metabolite of the sulfonylurea glimepiride .1It is formed from glimepiride primarily in the liver by the cytochrome P450 (CYP) isoform CYP2C9. 1.Langtry, H.D., and Balfour, J.A.Glimepiride. A review of its use in the management of type 2 diabetes mellitusDrugs55(4)563-584(1998) | |||
T38456 |
Tribenuron
|
Others | Others |
Tribenuron, a slow acting sulfonylurea herbicide, controls broadleaf weed. | |||
T0371L |
Gliquidone sodium
|
Others | Others |
Gliquidone sodium is a hypoglycemic sulfonylurea which may protect the liver from injury from diabetes. | |||
T84960 |
Nicorandil N-oxide
|
Others | Others |
Nicorandil N-oxide, a metabolite of nicorandil, functions as an activator of the ATP-sensitive potassium channel Kir6.2 (SUR2B/Kir6.2) and is associated with the sulfonylurea receptor 2B (SUR2B), while also serving as a nitric oxide donor. | |||
T9222L |
Emlenoflast sodium
MCC7840 sodium |
NOD | Immunology/Inflammation; NF-κB |
Emlenoflast sodium (MCC7840 sodium)是磺酰脲类化合物,是一种选择性NLRP3炎症小体 (NLRP3 inflammasome) 的抑制剂,对NLRP3炎症小体的IC50值小于 100 nM, 可用于炎性疾病的研究。 | |||
T38615 |
Rimsulfuron
DPX-E9636,Rimsulfuron |
Others | Others |
Rimsulfuron (DPX-E9636) is a sulfonylurea herbicide specifically designed for postemergence application in maize crops. This compound effectively targets and manages grasses as well as certain types of broadleaf weeds. | |||
T61461 |
Anticancer agent 37
|
Others | Others |
Anticancer agent 37 (compound 18) is a sulfonylurea derivative known for its potent anticancer activity. It efficiently inhibits the growth of HePG2 cells, displaying an IC 50 value of 17.2 μg/mL [1]. | |||
T61602 |
Anticancer agent 35
|
Others | Others |
Anticancer agent 35 (compound 10) 是一种磺酰脲类衍生物,一种有效的抗癌剂。Anticancer agent 35 抑制 A549、A431、PACA2 细胞生长,IC50分别为 18.1 μg/mL、4.0 μg/mL、18.9 μg/mL。 | |||
T36740 |
Guanosine 5’-diphosphate (sodium salt hydrate)
|
Others | Others |
Guanosine 5’-diphosphate (GDP) is a purine nucleotide and biosynthetic precursor of guanosine 5’-triphosphate .1It has been used to study the conformations of GTPases.2GDP (100 μM) activates sulfonylurea receptor 2B (SUR2B) linked to the inward-rectifier potassium channel 6.1 (Kir6.1) in HEK293T cells in a patch-clamp assay.3 1.Berg, J.M., Tymoczko, J.L., and Stryer, L.Biochemistry(2002) 2.Vetter, I.R., and Wittinghofer, A.The guanine nucleotide-binding switch in three dimensionsScience294(5545)... | |||
T14040 |
4-Hydroxytolbutamide
Hydroxytolbutamide |
Potassium Channel | Membrane transporter/Ion channel |
4-Hydroxytolbutamide(Hydroxytolbutamide), a metabolite of Tolbutamide, which is metabolized by CYP2C8 and CYP2C9. Tolbutamide is a first generation potassium channel blocker and a sulfonylurea oral antidiabetic[1][2]. | |||
T35635 |
rac-trans-4-hydroxy Glyburide
|
Others | Others |
rac-trans-4-hydroxy Glyburide is an active metabolite of the SUR1/Kir6.2 sulfonylurea inhibitor glyburide .1,2It is formed from glyburide by the cytochrome P450 (CYP) isoforms CYP2C8 and CYP2C9.1rac-trans-4-hydroxy Glyburide inhibits glyburide binding to rat brain synaptosomes at the high and low affinity sites of SUR1/Kir6.2 with IC50values of 0.95 and 100 nM, respectively.2 1.Zharikova, O.L., Fokina, V.M., Nanovskaya, T.N., et al.Identification of the major human hepatic and placental enzymes ... | |||
T62278 |
Anticancer agent 36
|
Others | Others |
Anticancer agent 36 (compound 11) 是一种有效的抗微生物剂和抗癌剂,是一种磺酰脲类衍生物。Anticancer agent 36 对蕈状芽孢杆菌、大肠杆菌和白色念珠菌的微生物生长有抑制作用 (MIC: 0.156 - 0.039 mg/mL)。Anticancer agent 36 能够抑制 A549 细胞 (IC50: 19.7 μg/mL)、PC3 细胞 (IC50: 11.9 μg/mL) 生长。 | |||
T62754 |
Anticancer agent 34
|
Others | Others |
Anticancer agent 34 (compound 9) 是一种磺酰脲类衍生物,也是一种有效的抗微生物剂和抗癌剂。Anticancer agent 34 对蕈状芽孢杆菌、大肠杆菌和白色念珠菌的微生物生长表现出抑制作用 (MIC: 0.039-0.156 mg/ml)。Anticancer agent 34 能够抑制 A549 细胞 (IC50: 8.4 μg/ml)、PC3 细胞 (IC50: 7.8 μg/ml) 的生长。 | |||
T71284 |
Glimepiride urethane
|
Others | Others |
Glimepiride urethane is a third generation sulfonylurea compound, which increases the release of insulin from pancreatic beta cells. In addition, glimepiride increases the activity of intracellular insulin receptors. Glimepiride increases osteoblast proliferation and differentiation, which is thought to be related to its ability to activate the PI3K and Akt pathway. Furthermore, Glimepiride enhances intrinsic peroxisome proliferator-activated receptor γ activity. Glimepiride also increases prote... | |||
T80642 |
Foramsulfuron
|
Others | Others |
Foramsulfuron作为磺酰脲类除草剂,专用于玉米(Zea mays L.)中选择性地防控禾本科以及部分阔叶杂草。该化合物通过抑制关键酶乙酰乳酸合酶(acetolactate synthase, ALS)的活性,从而表现出对杂草的抑制功能,ALS主导支链氨基酸的生物合成途径。 | |||
T79446 |
INF200
|
NOD-like Receptor (NLR) | Immunology/Inflammation |
INF200(compound 5)是一种磺酰脲衍生的抑制剂,既能抑制NLRP3也能抑制NLRP3介导的焦亡(pyroptosis)。在HFD诱导的大鼠模型上,INF200对心脏代谢表现出有益效果,并且在(10 μM)浓度下减少了人巨噬细胞中IL-1β的释放,表现出抗炎特性。它还能改善血糖控制和脂质水平,降低全身炎症和心功能障碍的标志物(尤其是BNP水平)。此外,INF200在血流动力学评估中还可提升心肌损伤后的缺血/再灌注损伤(IRI)恢复。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TMIH-0253 |
Gliclazide-d7
|
||
Gliclazide-d7 是 Gliclazide 的氘代化合物。Gliclazide 的 CAS 号为 21187-98-4。Gliclazide 是一种有效的全细胞的 β 细胞 ATP 敏感型钾流阻断剂,IC50为 184 nM,用作降糖药。 | |||
TMID-0267 |
Glipizide-d11
|
||
Glipizide-d11 是 Glipizide 的氘代化合物。Glipizide 的 CAS 号为 29094-61-9。Glipizide 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 。 | |||
TMIJ-0523 |
Gliquidone-d6
|
||
Gliquidone-d6 是 Gliquidone 的氘代化合物。Gliquidone 的 CAS 号为 33342-05-1。Gliquidone 是一种磺酰脲类的抗糖尿病药物,可用于2型糖尿病的研究。 | |||
T71402 |
Nicorandil-d4
|
||
Nicorandil-d4 is intended for use as an internal standard for the quantification of nicorandil by GC- or LC-MS. Nicorandil is an activator of sulfonylurea receptor 2B (SUR2B) linked to ATP-sensitive potassium channel Kir6.2 (EC50 = ~10 µM) and a nitric oxide (NO) donor. It is selective for SUR2B/Kir6.2 over the SUR2A/Kir6.2 channel (EC50 = >500 µM). Nicorandil activates soluble guanylate cyclase in a cell-free assay and relaxes partially depolarized isolated bovine coronary artery strips (EC50 =... | |||
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... |