31
7
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
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。 | |||
T7714 |
Temocapil
|
Tyrosinase | Proteases/Proteasome |
Temocapil 是一种酪氨酸激酶抑制剂。 | |||
T1615 |
Irbesartan
厄贝沙坦,SR-47436,BMS-186295 |
Apoptosis; RAAS | Apoptosis; Endocrinology/Hormones |
Irbesartan (SR-47436) 是一种 1 型血管紧张素 II 受体拮抗剂,IC50为1.3 nM。 | |||
TQ0157 |
EIPA
L593754,MH 12-43 |
Sodium Channel; TRP/TRPV Channel | Membrane transporter/Ion channel |
EIPA (L593754) 是一种有效的TRPP3 channel 抑制剂,IC50为 10.5 μM。EIPA 对Na+/H+交换 (NHE) 和巨噬细胞也有抑制作用。 | |||
T6698 |
Temocapril hydrochloride
CS-622 HCl,Acecol,Temocapril HCl,CS-622,盐酸替莫普利 |
RAAS | Endocrinology/Hormones |
Temocapril hydrochloride (CS-622 HCl) 是血管紧张素转化酶 (ACE) 抑制剂。Temocapril HCl 能够用于充血性心力衰竭、急性心肌梗死、高血压、胰岛素抵抗和肾脏疾病的研究。 | |||
T1182 |
Levocarnitine propionate hydrochloride
Propionyl-L-carnitine hydrochloride,L-Propionylcarnitine chloride,丙酰左旋肉碱盐酸盐,ST-261,丙酰肉碱盐酸盐 |
Histamine Receptor | GPCR/G Protein; Immunology/Inflammation; Neuroscience |
Levocarnitine propionate hydrochloride (ST-261) 可用于肾功能恶化,充血性心脏衰竭,间歇性跛行等疾病的研究。 | |||
T22882 |
JP1302
|
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
JP1302 是一种具有选择性的 α2C 肾上腺受体拮抗剂,其对人类 α2C 受体的 Kb 值为 16 nM,Ki 为 28 nM。JP1302 具有抗抑郁活性,可破坏 FACT 复合物并降解组蛋白H1,可用于研究神经精神障碍、急性肾功能衰竭和肾损伤。 | |||
TQ0200 |
Paricalcitol
|
||
Paricalcitol 是一种 vitamin D receptor 激活剂,是一种 vitamin D 类似物,用于研究继发性甲状旁腺功能亢进,该疾病与慢性肾功能衰竭有关。 | |||
T16782 |
Rolofylline
KW-3902,MK-7418,KF-15372 |
Adenosine Receptor | GPCR/G Protein; Neuroscience |
Rolofylline (KW-3902) 是一种具有选择性腺苷 A1 受体拮抗剂,可用于研究急性充血性心力衰竭和肾功能障碍,可用与研究神经退行性疾病。 | |||
T61383 |
Diaziquone
NSC 182986 |
||
Diaziquone (NSC-182986)是一种水溶性的合成的氮杂环苯醌,可增强对血脑屏障的渗透,具有抗肿瘤活性,可用于治疗极性肾功能衰竭。 | |||
T17284 |
Zardaverine
BY 290,B 84290 |
PDE | Metabolism |
Zardaverine (BY 290) 是一种可口服且具有选择性和有效性的 PDE3/4 抑制剂 ,具有支气管扩张活性和抗肝癌活性。Zardaverine 在血小板中的作用是通过PDE III同工酶介导,可用于研究急性肾衰竭呵呵慢性气流阻塞。 | |||
T28222 |
5-Hydroxy-1-methylhydantoin
HD-003,HD003,5-羟基-1-甲基咪唑啉-2,4-二酮,NZ419,NZ-419,HD 003,NZ 419 |
Bradykinin Receptor | GPCR/G Protein |
5-Hydroxy-1-methylhydantoin (HD-003) 是一种可能用于治疗肾衰竭的抗氧化剂。它是肌酐代谢物,是一种羟基自由基清除剂,此前已显示通过抑制大鼠慢性肾病的进展来提供肾脏保护。 它是一种新型抗氧化药物,可完全抑制 B2-激肽受体(B2KR) 对 VSMC 中高葡萄糖 (25 mM) 刺激的反应,并且还显示可减弱 BK 对 VSMC 重塑的影响。它抑制 BK 诱导的 MAPK 磷酸化增加并减弱 VSMC 中结缔组织生长因子 (CTGF) 蛋白水平的增加。这些研究结果表明,它可能通过其抗氧化特性赋予血管保护免受高葡萄糖浓度和 BK 刺激以改善血管损伤和重塑。 | |||
T31594 |
EA-230
EA 230,NMPF-46,NMPF46,NMPF 46 |
||
Ea-230 is an immunomodulator that may be used in the treatment of renal failure. | |||
T33856 |
PA 21
PA21 |
||
PA 21 is an iron-based noncalcium phosphate binder that prevents vascular calcification in chronic renal failure rats. | |||
T33600 |
Naxifylline
CVT 124,CVT-124,CVT124,BG9719 |
||
Naxifylline is an A1 adenosine receptor antagonist that promotes urine volume to prevent the decline in renal function observed during diuretic therapy for the treatment of edema associated with congestive heart failure. | |||
T70480 |
FPL-65447 hydrochloride
|
||
FPL-65447 hydrochloride is a selective D1 receptor agonist that has potential for the acute treatment of renal and cardiac failure and of sepsis and septic shock. | |||
T80891 |
Urodilatin
|
||
Urodilatin为ANF-(99-126)的同类物,属于利尿钠调节肽。该化合物主要应用于急性肾功能衰竭、充血性心力衰竭、支气管哮喘等疾病的研究领域。 | |||
T12363 |
Paricalcitol-D6
|
Others | Others |
Paricalcitol-D6 is the deuterated form of Paricalcitol, which is used for the prevention and treatment of secondary hyperparathyroidism (excessive secretion of parathyroid hormone) associated with chronic renal failure. | |||
T1400L |
Demeclocycline
Ledermycin,Bioterciclin,Deteclo,Declostatin,Deganol |
Antibacterial | Microbiology/Virology |
Demeclocycline (Declostatin) 是一种四环素类抗生素,产自金霉素链霉菌(Streptomyces aureofaciens)菌株。Demeclocycline 具有抗菌活性,能抑制血管加压素对肾小管的作用,从而导致利尿。Demeclocycline 可用诱导尿崩症和急性肾衰竭。 | |||
T76125 |
Creatininase
CAH,Creatinine amidohydrolase |
Endogenous Metabolite | Metabolism |
Creatininase (CAH) 是一种从 Pseudomonas putida 中发现的同六聚体酶,可用于研究肌酐检测的生物传感器和慢性肾功能衰竭。 | |||
T75272 | Paricalcitol-d | ||
Paricalcitol-d6,是一种Paricalcitol的氘代物,主要用于治疗与慢性肾衰竭相关的继发性甲状旁腺机能亢进。 | |||
T71065 |
Quinapril-d5
|
||
Quinapril-d5 is intended for use as an internal standard for the quantification of quinapril by GC- or LC-MS. Quinapril is a prodrug form of the angiotensin converting enzyme (ACE) inhibitor quinaprilat. In vivo, quinapril reduces mean arterial pressure in renal hypertensive and spontaneously hypertensive rats. It inhibits angiotensin I-induced pressor responses in normotensive rats and dogs. Quinapril prevents left ventricular heart failure in CHF 14.6 cardiomyopathic hamsters. Formulations con... | |||
T82941 |
Atriopeptin III (rat)
ANP 127-150 (rat) |
||
Atriopeptin III (ANP 127-150) (rat)是包含24个氨基酸的心房肽,作用为有效的血管舒张剂及利尿剂。在输尿管梗阻大鼠模型中,Atriopeptin III (rat)能够改善肾功能并降低血压,同时适用于慢性肾功能衰竭研究。 | |||
T39063 |
Azilsartan mepixetil
|
||
Azilsartan mepixetil is a potent angiotensin II receptor antagonist with enhanced efficacy and prolonged duration of action. It exhibits more prominent and sustained effects in lowering blood pressure and heart rate, while maintaining a high level of safety. Furthermore, Azilsartan mepixetil demonstrates optimal protective efficacy for cardiovascular and renal functions. Hence, it holds promise for the research and treatment of hypertension, chronic heart failure, and diabetic nephropathy. | |||
T61983 |
Trichlormethiazide sodium
|
||
Trichlormethiazide sodium 是口服有效的噻嗪类利尿剂,显示降压活性。在急性肾功能衰竭大鼠中,Trichlormethiazide sodium 可增加尿量、Na 和 K 排泄,并有改善肌酐清除率 (CCRE)。 | |||
T33851 |
Ozolinone
W 3282,W3282,W-3282 |
||
Ozolinone is an active metabolite of etozoline which acts as a loop diuretic --- a diuretic that acts at the ascending limb of the loop of Henle in the kidney. Loop diuretics are primarily used in medicine to treat hypertension and edema often due to cong | |||
T62909 | SGC agonist 2 | ||
SGC agonist 2 是一种有效的可溶性鸟苷酸环化酶 (SGC) 激动剂。其中可溶性鸟苷酸环化酶是 NO-sGC-cGMP 信号通路中的关键信号转导酶。SGC agonist 2 具有潜力进行心血管疾病 (心力衰竭、心绞痛、肺动脉高压、心肌梗塞) 和纤维化疾病 (肾纤维化、系统性硬化症) 的研究。 | |||
T76762 | Tabalumab | ||
Tabalumab (LY2127399) 是一种人源化的抗BAFF(B 细胞激活因子) 单克隆抗体 (IgG4 型),对膜结合和可溶性BAFF 具有中和活性。Tabalumab 可用于自身免疫性疾病,如类风湿性关节炎、肾衰竭和系统性红斑狼疮的研究。 | |||
T62134 | A1/A3 AR antagonist 1 | ||
A1/A3 AR antagonist 1 (compound 10) 是一种有效的、双重腺苷酸 1 (A1)和腺苷酸 3 (A3)受体拮抗剂,能够作用于人 A1 (Ki: 37.6 nM)、人 A3 (Ki: 25.4 nM) 和大鼠 A1 (Ki: 1.47 nM)。A1/A3 AR antagonist 1 能够用于研究肾衰竭、炎症性肺部疾病和阿尔茨海默症。 | |||
T70990 |
ADMA-d6
|
||
NG,NG-dimethyl-L-arginine-d6 (ADMA-d6) (hydrochloride) is intended for use as an internal standard for the quantification of NG,NG-dimethyl-L-arginine by GC- or LC-MS. ADMA is an endogenous inhibitor of nitric oxide synthase (NOS). It is formed from arginine by protein arginine methyltransferases (PRMTs) and degraded by dimethylarginine dimethylaminohydrolases (DDAHs) and alanine-glyoxylate aminotransferase 2 (AGXT2). ADMA levels are increased concomitant with an increase in blood pressure in Da... | |||
T70313 | Indoxyl Sulfate-d5 potassium salt | ||
Indoxyl sulfate-d5 is intended for use as an internal standard for the quantification of indoxyl sulfate by GC- or LC-MS. Indoxyl sulfate is a uremic toxin and a metabolite of tryptophan. It is formed via sulfation of indole, an intermediate generated from tryptophan by intestinal bacteria, by the sulfotransferase (SULT) isoform 1A1 variant 2 (SULT1A1*2) in the liver. Indoxyl sulfate activates the aryl hydrocarbon receptor (AhR) in HepG2 40/6 hepatoma cells (EC50 = 12.1 nM in a reporter assay). ... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3999 |
D(+)-Galactosamine hydrochloride
D-半乳糖胺盐酸盐,D-氨基半乳糖盐酸盐,D-Galactosamine HCl |
Others | Others |
D(+)-Galactosamine hydrochloride (D-Galactosamine HCl) 是一种被证实的实验毒素,它能够产生自由基及UTP 核苷酸的消耗导致肝损伤,中毒剂量会造成肾功能不全,而肾功能衰竭通常和终末期肝损伤有关。脂多糖/D-Galactosamine 诱导的急性肝损伤是一种已知的暴发性肝衰竭动物模型。 | |||
T8150 |
Nudifloramide
1-Methyl-6-oxo-1,6-dihydropyridine-3-carboxamide,1-甲基-6-氧代吡啶-3-甲酰胺 |
PARP; Endogenous Metabolite | Chromatin/Epigenetic; DNA Damage/DNA Repair; Metabolism |
Nudifloramide (1-Methyl-6-oxo-1,6-dihydropyridine-3-carboxamide) 是烟酰胺-腺嘌呤二核苷酸(NAD) 降解的一种最终产物,可显著抑制PARP-1活性。 | |||
T4238 |
Glycocyamine
乙酸胍,2-Guanidinoacetic acid,Guanidoacetic acid |
Others; Endogenous Metabolite | Metabolism; Others |
Glycocyamine (2-Guanidinoacetic acid) 是一种肌酸的前体,能够为鸟类的体内平衡提供能量,也能够成为食用精氨酸的替代物。 | |||
T20793 |
Magnesium Lithospermate B
丹參酸B鎂,Monomethyl lithospermate B,丹参酸 B 镁,Lithospermate B |
Others | Others |
Magnesium Lithospermate B 是一种咖啡酸四聚体的衍生物,从Salviae miltiorrhizae 中提取得到。它能够抑制神经炎症并减轻神经变性。它被广泛用于心血管疾病的研究,并且可以防止葡萄糖引起的细胞内氧化损伤。 | |||
T0414 |
D-Mannitol
Mannite,Mannitol,D-甘露糖醇,Osmitrol |
Apoptosis; Dehydrogenase; Endogenous Metabolite | Apoptosis; Metabolism |
D-Mannitol (Mannitol) 是与山梨醇相关的利尿剂和肾脏诊断辅助剂,具有较弱的肾脏血管扩张活性。 | |||
T4904 |
1-Methylguanidine hydrochloride
|
Others; Endogenous Metabolite | Metabolism; Others |
1-Methylguanidine hydrochloride 是内源性代谢产物的一种。 | |||
TN1912 |
Marinobufogenin
南美蟾毒精,Marinobufagenin |
ATPase; EGFR | Angiogenesis; JAK/STAT signaling; Membrane transporter/Ion channel; Tyrosine Kinase/Adaptors |
Marinobufagenin, a cardiotonic steroid, its increased concentrations are important in the cardiac disease and oxidant stress state seen with renal failure. |