Dorzolamide
For Laboratory Research Only. Not for Clinical or Personal Use.
- Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
- Dry Ice Shipment: No


Dorzolamide
Description:
Dorzolamide (L671152) is a potent carbonic anhydrase II inhibitor, with IC50 values of 0.18 nM and 600 nM for red blood cell CA-II and CA-I respectively. Dorzolamide possesses anti-tumor activity[1].Product Name Alternative:
L671152; MK507UNSPSC:
12352005Hazard Statement:
H302Target:
Carbonic AnhydraseType:
Reference compoundRelated Pathways:
Metabolic Enzyme/ProteaseField of Research:
CancerAssay Protocol:
https://www.medchemexpress.com/Dorzolamide.htmlSolubility:
10 mM in DMSOSmiles:
O=S(C(S1)=CC2=C1S([C@@H](C)C[C@@H]2NCC)(=O)=O)(N)=OMolecular Formula:
C10H16N2O4S3Molecular Weight:
324.44Precautions:
P264-P270-P330-P501References & Citations:
[1]J Biollaz, et al. Whole-blood pharmacokinetics and metabolic effects of the topical carbonic anhydrase inhibitor dorzolamide. Eur J Clin Pharmacol. 1995;47 (5) :455-60.|[2]Sangly P Srinivas, et al. Inhibition of carbonic anhydrase activity in cultured bovine corneal endothelial cells by dorzolamide. Invest Ophthalmol Vis Sci. 2002 Oct;43 (10) :3273-8.|[3]Belal M Ali, et al. Dorzolamide synergizes the antitumor activity of mitomycin C against Ehrlich's carcinoma grown in mice: role of thioredoxin-interacting protein. Naunyn Schmiedebergs Arch Pharmacol. 2015 Dec;388 (12) :1271-82.Shipping Conditions:
Room temperatureScientific Category:
Reference compound1Clinical Information:
LaunchedIsoform:
CA IICitation 01:
Anal Chem. 2020 Dec 15;92 (24) :15745-15756.|ETH Zurich. 2020 Dec.|J Pharm Biomed Anal. 2021 Feb 20:195:113870.|ACS Environ Au. 2025 Aug 8.|Anal Chem. 2025 Jun 3;97 (21) :11099-11109.|Cell Rep. 2024 Nov 27;43 (12) :114996.|Sci Data. 2024 Sep 19;11 (1) :1024.CAS Number:
120279-96-1
