Hydrochlorothiazide-15N2,13C,d2氢氯噻嗪-15N2,13C,d2,2140316-81-8

Hydrochlorothiazide-15N2,13C,d

2氢氯噻嗪-15N2,13C,d2,2140316-81-8
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  • 询价
  • MedChemExpress(MCE)已认证
  • 美国
  • HY-B0252S3
  • 2025年12月05日
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    • 详细信息
    • 技术资料
    • 保存条件

      Please store the product under the recommended conditions in the Certificate of Analysis.

    • 英文名

      HCTZ-<sup>15</sup>N<sub>2</sub>,<sup>13</sup>C,d<sub>2</sub>

    • 库存

      货期:询盘

    • 供应商

      MedChemExpress LLC

    • CAS号

      2140316-81-8

    • 规格

      1 mg///5 mg

    Hydrochlorothiazide-15N2,13C,d2 产品活性:Hydrochlorothiazide-15N2,13C,d2 是 15N 和氘代标记的 Hydrochlorothiazide (HY-B0252)。Hydrochlorothiazide (HCTZ) 是一种口服有效的噻嗪类的利尿药,可抑制转化 TGF-β/Smad 信号通路。Hydrochlorothiazide 通过打开钙激活钾 (KCA) 通道具有直接的血管松弛作用。Hydrochlorothiazide 改善心脏功能,减少纤维化并具有降压作用。 产品来源: www.medchemexpress.cn/hydrochlorothiazide-15n2-13c-d2.html 研究领域:Membrane Transporter/Ion Channel | TGF-beta/Smad | Stem Cell/Wnt | Others 作用靶点:Potassium Channel | TGF-beta/Smad | Isotope-Labeled Compounds In Vitro: Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs.Hydrochlorothiazide belongs to thiazide class of diuretics. It reduces blood volume by acting on the kidneys to reduce sodium (Na) reabsorption in the distal convoluted tubule. The major site of action in the nephron appears on an electroneutral Na+-Cl co-transporter by competing for the chloride site on the transporter. By impairing Na transport in the distal convoluted tubule, hydrochlorothiazide induces a natriuresis and concomitant water loss. Thiazides increase the reabsorption of calcium in this segment in a manner unrelated to sodium transport. Additionally, by other mechanisms, Hydrochlorothiazide is believed to lower peripheral vascular resistance. In Vivo: Hydrochlorothiazide (HCTZ; orally bygavage; 12.5 mg/kg/d; 8 weeks) has improved cardiac function, reduced cardiac interstitial fibrosis and collagen volume fraction, decreased expression of AT1, TGF-β and Smad2 in the cardiac tissues in adult male Sprague Dawley rats. In addition, hydrochlorothiazide reduces plasma angiotensin II and aldosterone levels. Furthermore, hydrochlorothiazide inhibits angiotensin II-induced TGF-β1 and Smad2 protein expression in the neonatal rat ventricular fibroblasts. 相关产品:Nigericin sodium salt | Yoda 1 | BAPTA-AM | Pirfenidone | Minocycline hydrochloride | SIS3 | Branaplam | Rosuvastatin Calcium | SCH-23390 hydrochloride | Halofuginone | Glibenclamide | Quinidine (15% dihydroquinidine) | SRI-011381 hydrochloride | Asiaticoside | Carbamazepine | Tetrandrine | Kartogenin | E-4031 | Trimethylamine N-oxide | DCPIB | Minoxidil | Amiodarone hydrochloride | 20(S)-Ginsenoside Rg3 | Guanosine 5'-diphosphate disodium salt | Tannic acid | Quinine | TRAM-34 | SKF-96365 hydrochloride | (±)-Naringenin

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