Dorzolamide hydrochloride NEW
| Price | $35 | $48 | $68 |
| Package | 25mg | 50mg | 100mg |
| Min. Order: | |
| Supply Ability: | 10g |
| Update Time: | 2024-11-19 |
Product Details
| Product Name: Dorzolamide hydrochloride | CAS No.: 130693-82-2 |
| Purity: ≥95% | Supply Ability: 10g |
| Release date: 2024/11/19 |
Product Introduction
Bioactivity
| Name | Dorzolamide hydrochloride |
| Description | Dorzolamide hydrochloride (MK507 hydrochloride) is the hydrochloride salt form of dorzolamide, an inhibitor of carbonic anhydrase, a zinc-containing enzyme that catalyzes the rapid conversion of carbon dioxide and water into carbonic acid, protons and bicarbonate ions. Distributed throughout many cells and tissues, various carbonic anhydrases play important roles in mineral and metabolic homeostasis. |
| In vitro | In rabbits, Dorzolamide hydrochloride significantly reduces intraocular pressure (IOP) and is effective at night as well. Dorzolamide substantially decreases IOP in glaucoma-afflicted monkeys by 22%, 30%, and 37%. The combination of Dorzolamide (administered topically to the eye for 1 to 5 days) and oral methazolamide (administered from day 3 to day 5) significantly lower IOP, with this effect persisting on days 1, 3, and 5. Compared to the regimen of twice-daily oral methazolamide and 2% Dorzolamide, applying Dorzolamide (2%) topically three times a day achieves a similar reduction in IOP. |
| In vivo | Dorzolamide induces dilation of retinal blood vessels through three distinct mechanisms that directly cause precontraction, independent of extracellular pH changes. It acts as a potent inhibitor of carbonic anhydrase (CA) II, penetrating the sclera and cornea to reach the ciliary processes and reduce the formation of HCO3 and aqueous humor. |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
| Solubility Information | H2O : 13.3 mg/mL (36.9 mM) DMSO : 1 mg/mL (2.77 mM) |
| Keywords | tumor | solid | MK-507 Hydrochloride | MK507 Hydrochloride | MK-507 | MK507 | MK 507 Hydrochloride | MK 507 | L-671152 Hydrochloride | L671152 Hydrochloride | L-671152 | L671152 | L 671152 Hydrochloride | L 671152 | Inhibitor | inhibit | EAC | Dorzolamide Hydrochloride | Dorzolamide hydrochloride | Dorzolamide | Carbonic Anhydrase | Carbonate dehydratase | CA-II | anti-tumor |
| Inhibitors Related | Benzenesulfonamide | Urea | Cyclamic acid sodium | Hydrochlorothiazide | Orthanilamide | Tioxolone | Zonisamide | Histone acetyltransferase p300 Inhibitor 4c | EMAC10101d | pNNP | Levosimendan | Trichlormethiazide |
| Related Compound Libraries | FDA-Approved & Pharmacopeia Drug Library | Target-Focused Phenotypic Screening Library | Bioactive Compound Library | ReFRAME Related Library | Anti-Cancer Metabolism Compound Library | Drug Repurposing Compound Library | Inhibitor Library | FDA-Approved Drug Library | Metabolism Compound Library | Clinical Compound Library | Bioactive Compounds Library Max | Anti-Metabolism Disease Compound Library |
Company Profile Introduction
Target Molecule Corp. (TargetMol) is a global high-tech enterprise, headquartered in Boston, MA, specializing in chemical and biological research product and service to meet the research needs of global customers.
TargetMol has evolved into one of the biggest global compound library and small molecule suppliers and a customer based on 40+ countries. TargetMol offers over 80 types of compound libraries and a wide range of high-quality research chemicals including inhibitors, activator, natural compounds, peptides, inhibitory antibodies, and novel life-science kits, for laboratory and scientific use. Besides, virtual screening service is also available for customers who would like to conduct the computer-aided drug discovery.
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