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Enpp/Carbonic anhydrase-IN-1
Enpp/Carbonic anhydrase-IN-1
CAS No. 2883495-35-8
Enpp/Carbonic anhydrase-IN-1( —— )
Catalog No. M35976 CAS No. 2883495-35-8
Enpp/Carbonic anhydrase-IN-1 (compound 1e) is a potent inhibitor of Enpp and carbonic anhydrase, exhibiting IC50s of 1.36, 1.35, 3.00, 0.88, and 1.02 μM for NPP1, NPP2, NPP3, CA-II, and CA-IX respectively.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 36 | Get Quote |
|
| 10MG | 55 | Get Quote |
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| 25MG | 109 | Get Quote |
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| 50MG | 181 | Get Quote |
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| 100MG | 291 | Get Quote |
|
| 200MG | 410 | Get Quote |
|
| 500MG | Get Quote | Get Quote |
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| 1G | Get Quote | Get Quote |
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Biological Information
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Product NameEnpp/Carbonic anhydrase-IN-1
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NoteResearch use only, not for human use.
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Brief DescriptionEnpp/Carbonic anhydrase-IN-1 (compound 1e) is a potent inhibitor of Enpp and carbonic anhydrase, exhibiting IC50s of 1.36, 1.35, 3.00, 0.88, and 1.02 μM for NPP1, NPP2, NPP3, CA-II, and CA-IX respectively.
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DescriptionEnpp/Carbonic anhydrase-IN-1 (compound 1e) is a potent Enpp and carbonic anhydrase inhibitor with IC50s of 1.36, 1.35, 3.00, 0.88, 1.02 μM for NPP1, NPP2, NPP3, CA-II, CA-IX respectively. Enpp/Carbonic anhydrase-IN-1 shows antiproliferative activity for cancer cells and low cytotoxic against normal cells. Enpp/Carbonic anhydrase-IN-1 induces Apoptosis.
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In VitroEnpp/Carbonic anhydrase-IN-1 (compound 1e) (0-100 μM; ) inhibits some cancer cells growth with IC50s of 0.32, 0.40, 0.58, 0.87, 0.40, 0.96 μM for K-562, RPMI-8226, SR, COLO 205, HT-29, SF-539 cells, respectively.Enpp/Carbonic anhydrase-IN-1 (0-2 μM) shows low cytotoxic against normal breast epithelial cells (HME1) and normal skin fibroblast cells (F180) with IC50s of > 50 μM.Enpp/Carbonic anhydrase-IN-1 (0.32, 0.64 μM) induces apoptosis in a dose-dependent manner at K-562 cells.Cell Proliferation Assay Cell Line:K-562, RPMI-8226, SR, COLO 205, HT-29, SF-539 cells Concentration:0-100 μM Incubation Time:Result:Inhibited the cell growth with IC50s of 0.32, 0.40, 0.58, 0.87, 0.40, 0.96 μM for K-562, RPMI-8226, SR, COLO 205, HT-29, SF-539 cells, respectively.Apoptosis Analysis Cell Line:K-562 cells Concentration:0.32, 0.64 μM Incubation Time:Result:Induced apoptosis in a dose-dependent manner.
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In Vivo——
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Synonyms——
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PathwayMembrane Transporter/Ion Channel
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TargetCarbonic Anhydrase
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RecptorCarbonic Anhydrase | PDE
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Research Area——
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Indication——
Chemical Information
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CAS Number2883495-35-8
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Formula Weight411.51
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Molecular FormulaC23H25NO4S
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (243.01 mM; Ultrasonic (<50°C)
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SMILESO=C(Nc1ccc(OS(=O)(=O)c2ccccc2)cc1)C12CC3CC(CC(C3)C1)C2
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Chemical Name——
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. Afnan I.Shahin, et al. Design and synthesis of new adamantyl derivatives as promising antiproliferative agents. European Journal of Medicinal Chemistry, 2022.
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