Benzolamide

Benzolamide Suppliers list
Company Name: TargetMol Chemicals Inc.  Gold
Tel: 4008200310 15002144251
Email: marketing@tsbiochem.com
Company Name: Jiangsu Aikon Biopharmaceutical R&D co.,Ltd.  
Tel: 025-66113011 13913916777
Email: cfzhang@aikonchem.com
Company Name: Sichuan Yuehe Bio-Pharmaceutical Co.,Ltd  
Tel: 028-82729560 17365561851
Email: tangzhichen@yuehepharm.com
Company Name: Shanghai EFE Biological Technology Co., Ltd.  
Tel: 021-65675885 18964387627
Email: info@efebio.com
Company Name: Shanghai YuanYe Biotechnology Co., Ltd.  
Tel: 15026964105
Email: 2881489226@qq.com

Benzolamide manufacturers

  • Benzolamide
  • Benzolamide pictures
  • $47.00
  • 2026-07-27
  • CAS:3368-13-6
  • Purity: 99.31%
  • Supply Ability: 10g
Benzolamide Basic information
Product Name:Benzolamide
Synonyms:5-(phenylsulfonylamino)-1,3,4-thiadiazole-2-sulfonamide;2-benzenesulfonamido-1,3,4-thiadiazole-5-sulfonamide;Benzolamide;1,3,4-Thiadiazole-2-sulfonamide, 5-[(phenylsulfonyl)amino]-;5-(Phenylsulfonamido)-1,3,4-thiadiazole-2-sulfonamide;W 1803;W-1803;Benzolamide,Inhibitor,Carbonate dehydratase,seizures,CAS3,glaucoma,inhibit,Carbonic Anhydrase
CAS:3368-13-6
MF:C8H8N4O4S3
MW:320.37
EINECS:
Product Categories:
Mol File:3368-13-6.mol
Benzolamide Structure
Benzolamide Chemical Properties
Melting point 239.5°C (rough estimate)
Boiling point 585.9±33.0 °C(Predicted)
density 1.6772 (rough estimate)
refractive index 1.5690 (estimate)
storage temp. 4°C, protect from light
solubility DMSO : 250 mg/mL (780.35 mM; Need ultrasonic)
form Solid
pka4.42±0.40(Predicted)
color White to light yellow
Water Solubility 384.4mg/L(25 ºC)
Safety Information
MSDS Information
Benzolamide Usage And Synthesis
UsesBenzolamide (CL11366) is a potent carbonic anhydrase (CA) inhibitor, with Kis of 15 nM, 9 nM, 94 nM and 78 nM for hCA I, hCA II, EcoCAγ and VchCAγ, respectively. Benzolamide also inhibits CAS3, with a Ki of 54 nM. Benzolamide can be used for the research of glaucoma and seizures[1][2][3].
in vivo

Benzolamide (90 μmol/kg; i.p.) decreases brain pH and suppresses electrographic post-asphyxia seizures in rats[3].

Animal Model:Male and female Wistar Han rats (11-day-old)[3]
Dosage:90 μmol/kg
Administration:A single i.p.
Result:Induced a fast brain acidosis of a comparable magnitude.
Suppressed electrographic seizures after asphyxia by slowing down the recovery of brain pH.
IC 50CA Ⅱ
References[1] Prete SD, et, al. Escherichia coli γ-carbonic anhydrase: characterisation and effects of simple aromatic/heterocyclic sulphonamide inhibitors. J Enzyme Inhib Med Chem. 2020 Dec;35(1):1545-1554. DOI:10.1080/14756366.2020.1800670
[2] Vullo D, et, al. Sulfonamide Inhibition Studies of the β-Class Carbonic Anhydrase CAS3 from the Filamentous Ascomycete Sordaria macrospora. Molecules. 2020 Feb 25;25(5):1036. DOI:10.3390/molecules25051036
[3] Pospelov AS, et, al. Carbonic anhydrase inhibitors suppress seizures in a rat model of birth asphyxia. Epilepsia. 2021 Jun 27. DOI:10.1111/epi.16963
Benzolamide Preparation Products And Raw materials
Tag:Benzolamide(3368-13-6) Related Product Information
Fluconazole aniline 5-AMINO-1,3,4-THIADIAZOLE-2-SULFONAMIDE Benzolamide Benzenesulfonamide, N-[5-(methylthio)-1,3,4-thiadiazol-2-yl]- CARBONIC ANHYDRASE 9 PROTEIN, MOUSE (HEK293, HIS) Carbonic Anhydrase 14 Protein, Mouse (HEK293, His)