Dorzolamide hydrochloride
CAS No. 130693-82-2
Dorzolamide hydrochloride( L-671,152 | MK-507 )
Catalog No. M11227 CAS No. 130693-82-2
Dorzolamide Hcl(L671152 Hcl; MK507 Hcl) is an anti-glaucoma agent, which is a carbonic anhydrase inhibitor.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 25MG | 33 | In Stock |
|
| 50MG | 45 | In Stock |
|
| 100MG | 63 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | 212 | In Stock |
|
| 1G | 313 | In Stock |
|
Biological Information
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Product NameDorzolamide hydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionDorzolamide Hcl(L671152 Hcl; MK507 Hcl) is an anti-glaucoma agent, which is a carbonic anhydrase inhibitor.
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DescriptionDorzolamide Hcl(L671152 Hcl; MK507 Hcl) is an anti-glaucoma agent, which is a carbonic anhydrase inhibitor.(In Vitro):Component A, caused by an inward flux of CO2 and its subsequent hydration by CA-II, is blocked by Dorzolamide in a dose-dependent manner with an 50% inhibitory concentration IC50 of 2.4 μM (95% confidence interval: 0.5-10.85 μM).(In Vivo):Dorzolamide (3, 10, or 30 mg/kg/day, ip) synergized mitomycin C exhibits anti-tumor activity in EAC solid tumor models. Dorzolamide produces a dose-dependent decrease in the calculated ratio (relative value of 57.3±1, 25.5±1.8, and 24.3± 0.7 %, respectively).
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In Vitro——
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In Vivo——
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SynonymsL-671,152 | MK-507
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PathwayMembrane Transporter/Ion Channel
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TargetCarbonic Anhydrase
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RecptorCarbonic anhydrase I| Carbonic anhydrase II| Carbonic anhydrase IV
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Research AreaOther Indications
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Indication——
Chemical Information
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CAS Number130693-82-2
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Formula Weight360.9
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Molecular FormulaC10H17ClN2O4S3
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Purity>98% (HPLC)
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SolubilityWater: 14 mg/mL (38.79 mM)
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SMILESO=S(C(S1)=CC([C@@H](NCC)C[C@@H]2C)=C1S2(=O)=O)(N)=O.[H]Cl
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Chemical Name(4S,6S)-4-(ethylamino)-6-methyl-5,6-dihydro-4H-thieno[2,3-b]thiopyran-2-sulfonamide 7,7-dioxide hydrochloride
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Maren TH, et al. J Ocul Pharmacol Ther, 1997, 13(1), 23-30.
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