452-35-7
452-35-7
Chemical Structure
Ethoxzolamide
Synonym(s): Redupresin; L-643786; PNU-4191
- CAS No.: 452-35-7
- Formula:C9H10N2O3S2
- Molecular Weight:258.32
IUPAC Name: 6-ethoxybenzo[d]thiazole-2-sulfonamide
InChIKey: OUZWUKMCLIBBOG-UHFFFAOYSA-N
SMILES: O=S(C1=NC2=CC=C(OCC)C=C2S1)(N)=O
Biological Activity: Ethoxzolamide is a carbonic anhydrase inhibitor with Ki of 1 nM.
| Cat. No. | Nom du produit | Pureté | Description | Pricing | |||||||||||||||||||
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Ethoxzolamide | 99.85% | Ethoxzolamide is a carbonic anhydrase inhibitor with Ki of 1 nM. | ||||||||||||||||||||
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Ethoxzolamide (Standard) | ≥98% | Ethoxzolamide (Standard) is the analytical standard of Ethoxzolamide. This product is intended for research and analytical applications. Ethoxzolamide is a carbonic anhydrase inhibitor with Ki of 1 nM. | ||||||||||||||||||||
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Ethoxzolamide-d5 | Ethoxzolamide-d5 (Redupresin-d5) is deuterium labeled Ethoxzolamide. Ethoxzolamide is a carbonic anhydrase inhibitor with Ki of 1 nM. | |||||||||||||||||||||
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Flaviviruses-IN-1 | Flaviviruses-IN-1 is an inhibitor of several viruses belonging to the Flaviviridae family, with activity to inhibit viral infection. Flaviviruses-IN-1 is able to specifically inhibit multiple viruses of the Flaviviridae family. The mechanism of action of Flaviviruses-IN-1 is related to the modulation of the host cell immune response to viral infection. Flaviviruses-IN-1 was identified as a potential candidate compound in a high-throughput screening. Flaviviruses-IN-1 provides a new strategy for inhibiting infections caused by the Flaviviridae family. | |||||||||||||||||||||
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L-645151 | L-645151 is a carbonic anhydrase inhibitor with ocular penetration and hypotensive activity. L-645151 lowers the elevated intraocular pressure (IOP) of o-chymotripsinized (o-CT) rabbit eyes. L-645151 is promising for research of an ocular hypotensive agent. | |||||||||||||||||||||
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Ethacridine | 98.60% | Ethacridine is a poly(ADP-ribose) glycohydrolase (PARG) inhibitor and an activator of the transcriptional coactivator. Ethacridine induces thyroid cancer cells apoptosis and promotes differentiation in thyroid follicular cells. | ||||||||||||||||||||
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Diamthazole | Diamthazole (Dimazole) is an antifungal agent. Diamthazole can be used for the research of infection. | |||||||||||||||||||||
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Diamthazole hydrochloride | 99.86% | Diamthazole (Dimazole) hydrochloride is an antifungal agent. Diamthazole hydrochloride can be used for the research of infection. | ||||||||||||||||||||
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Frentizole | 98.48% | Frentizole, an FDA-approved immunosuppressant, is a Aβ-ABAD (binding alcohol dehydrogenase) interaction inhibitor with an IC50 value of 200 μM. Frentizole is used in studies of diseases related to rheumatoid arthritis and systemic lupus erythematosus. | ||||||||||||||||||||
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N-Hydroxy riluzole | N-Hydroxy riluzole is a metabolite of the antiglutamatergic agent Riluzole (HY-B0211). | |||||||||||||||||||||
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Riluzole hydrochloride | 99.87% | Riluzole hydrochloride is an anticonvulsant agent and belongs to the family of use-dependent Na+ channel blocker which can also inhibit GABA uptake with an IC50 of 43 μM. | ||||||||||||||||||||
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Actinoquinol | 99.20% | Actinoquinol is a UVB absorber that can be helpful for the human eye in the defence against photooxidative and other oxidative processes. | ||||||||||||||||||||
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