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Dotinurad

Dotinurad Suppliers list
Company Name: Shandong Jikun Biopharmaceutical Co., Ltd.  Gold
Tel: 15020996564 16658695017
Email: sales@jikungroup.com
Company Name: Wuhan HSN Pharmaresearch CO., LTD.  Gold
Tel: 027-81525288 18086100502
Email: linwell@126.com
Company Name: Jinan Guoding Pharmaceutical Technology Co., Ltd.  Gold
Tel: 053167801621 15665775653
Email: sales@guodingpharma.com
Company Name: Shanghai Wishpharma Co.,Ltd.  Gold
Tel: 021-56789108 18550363168
Email: 95413064@qq.com
Company Name: Huadong Microbiology Co., Ltd.  Gold
Tel: 15858880160
Email: dingya@eastchinapharm.com

Dotinurad manufacturers

  • Dotinurad
  • Dotinurad pictures
  • 2026-09-15
  • CAS:1285572-51-1
  • Min. Order: 1g
  • Purity: More Than 99%
  • Supply Ability: 50kg/Month
  • Dotinurad.
  • Dotinurad. pictures
  • 2026-09-15
  • CAS:1285572-51-1
  • Min. Order: 1g
  • Purity: More Than 99%
  • Supply Ability: 50kg/Month
  • Dotinurad
  • Dotinurad pictures
  • $132.00
  • 2026-08-06
  • CAS:1285572-51-1
  • Purity: 98.95%
  • Supply Ability: 10g
Dotinurad Basic information
FDA Approval
Product Name:Dotinurad
Synonyms:Dotinurad;Methanone, (3,5-dichloro-4-hydroxyphenyl)(1,1-dioxido-3(2H)-benzothiazolyl)-;Dotinurad (FYU-981);uricosuric,Inhibitor,Dotinurad,URAT1,urate,reabsorption,SLC22A12,Urate transporter 1,inhibit,transporter;(3,5-Dichloro-4-hydroxyphenyl)(1,1-dioxido-3(2H)-benzothiazolyl)methanone;3-(3,5-dichloro-4-hydroxybenzoyl)-1,1-dioxo-2,3-dihydro-1,3-benzothiazole;Dotinurad, 10 mM in DMSO;Doltenolil control
CAS:1285572-51-1
MF:C14H9Cl2NO4S
MW:358.2
EINECS:
Product Categories:API
Mol File:1285572-51-1.mol
Dotinurad Structure
Dotinurad Chemical Properties
Melting point 188 - 191°C
Boiling point 614.8±55.0 °C(Predicted)
density 1.662±0.06 g/cm3(Predicted)
storage temp. -20°C Freezer, Under inert atmosphere
solubility Chloroform (Slightly, Sonicated), DMSO (Sparingly)
pka4.60±0.25(Predicted)
form Solid
color White to Off-White
InChIInChI=1S/C14H9Cl2NO4S/c15-9-5-8(6-10(16)13(9)18)14(19)17-7-22(20,21)12-4-2-1-3-11(12)17/h1-6,18H,7H2
InChIKeyVOFLAIHEELWYGO-UHFFFAOYSA-N
SMILESC(C1=CC(Cl)=C(O)C(Cl)=C1)(N1C2=CC=CC=C2S(=O)(=O)C1)=O
Safety Information
MSDS Information
Dotinurad Usage And Synthesis
FDA ApprovalDotinurad was approved by the FDA in 2015.
DescriptionDotinurad is an organic compound with the chemical Name (3,5-dichloro-4-hydroxyphenyl)(1,1-dioxidobenzo[d]thiazol-3(2H)-yl)methanone. This compound is a newer urate-lowering agent that suppresses uric acid reabsorption through the selective inhibition of urate transporter 1 (URAT1) in the proximal renal tubules, and it was first approved in Japan in 2020 for the treatment of hyperuricemia, irrespective of gout[1].
UsesDotinurad is a useful drug for treating hyperuricemia and gout.
Brand nameURECE
PharmacokineticsThe plasma concentration of dotinurad increased in a dose-dependent manner with Cmax and AUC0–24h values of 107 μg/ml and 780 μg.h/ml, respectively, at a dose of 30 mg/kg. Dotinurad dose-dependently lowered the plasma urate levels with its maximum effect at 8 h. Changes in plasma urate level between 0 and 8 h (ΔPUA) were lower than that of control by 0.28, 0.97 (p < 0.05), and 1.79 mg/dl (p < 0.01), at doses of 1, 5, and 30 mg/kg, respectively. Furthermore, dotinurad dose-dependently increased FEUA. The 0–4 h FEUA increased by 180%, at a dose of 30 mg/kg compared to the control (p < 0.01)[3].    
SynthesisAminothiophenol (152) reacts with hydrated formaldehyde to give dihydrobenzothiazole 153. Acid chloride 155 is generated from acid 154. Dihydrobenzothiazole 153 is condensed with acid chloride 155 to form amide 156. Thiazole is oxidized using mCPBA. Methyl ether is removed in the presence of lithium chloride to give doxenolide.
Dotinurad
AdvantagesDotinurad, as a selective urate reabsorption inhibitor, is anticipated to be more effective in inhibiting urate reabsorption compared to conventional urate-lowering agents. It demonstrates noninferiority to benzbromarone or febuxostat in reducing serum urate levels in hyperuricemic patients with or without gout. Moreover, its effectiveness remains uncompromised in patients with mild to moderate renal or hepatic impairment. In a long-term study, a majority of patients achieved the target serum urate level of ≤6 mg/dL when administered a maintenance dose of 2 or 4 mg once daily. No safety concerns, such as liver injury, were observed. Consequently, Dotinurad is expected to serve as a new therapeutic option for hyperuricemic patients, regardless of the presence of gout [2].
References[1] Tanaka A, et al. Clinical effects of a selective urate reabsorption inhibitor dotinurad in patients with hyperuricemia and treated hypertension: a multicenter, prospective, exploratory study (DIANA). European Journal of Medical Research, 2023; 238.
[2] Ishikawa T, et al. Dotinurad: a novel selective urate reabsorption inhibitor for the treatment of hyperuricemia and gout. Expert Opinion on Pharmacotherapy, 2021; 22: 1397-1406.
[3] Taniguchi T, et al. Pharmacological Evaluation of Dotinurad, a Selective Urate Reabsorption Inhibitor. Journal of Pharmacology and Experimental Therapeutics, 2019; 162-170.
Dotinurad Preparation Products And Raw materials
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