533982 Sigma-AldrichDock5 Inhibitor, C21 - CAS 54129-15-6 - Calbiochem
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Overview
Key Spec Table
CAS # | Empirical Formula |
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54129-15-6 | C₁₂H₉Cl₂NO₂S |
Products
Catalogue Number | Packaging | Qty/Pack | |
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5339820001 | Glass bottle | 50 mg |
Description | |
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Overview | A cell-permeable, bioavailable, non-toxic benzenesulfonamide compound that directly blocks Dock5-mediated Rac activation (kcat/KM = 7.9 x 104 & 9.5 x 104 M-1s-1 for Rac1 & Rac2 by Dock5-DHR2, respectively) with selectivity over RhoA and Cdc42. At higher concentrations, affects Dock1 and Dock2 guanine nucleotide exchange factor activity. Shown to reversibly perturb podosome organization and inhibit osteoclastic bone degradation in a dose-dependent manner. Efficiently prevents both arthritis and metastasis-induced bone loss while preserving bone formation in several osteolytic disease mouse model (25 mg/kg, i.p. or i.v., 5 days a week for 4 weeks). Unlike alendronate (Cat. No. 126855), C21 does not impair bone formation. Please note that the molecular weight for this compound is batch-specific due to variable water content. Please refer to the vial label or the certificate of analysis for the batch-specific molecular weight. The molecular weight provided represents the baseline molecular weight without water. |
Catalogue Number | 533982 |
Brand Family | Calbiochem® |
Synonyms | N-(3,5-Dichlorophenyl)benzenesulfonamide |
References | |
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References | Vives, V., et al. 2015. Nat. Commun. 6, 6218. Vives, V., et al. 2011. J. Bone Miner. Res. 26, 1099. |
Product Information | |
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CAS number | 54129-15-6 |
Form | Grey powder |
Hill Formula | C₁₂H₉Cl₂NO₂S |
Chemical formula | C₁₂H₉Cl₂NO₂S |
Reversible | Y |
Quality Level | MQ100 |
Biological Information | |
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Primary Target | Dock5 |
Purity | ≥98% by HPLC |
Physicochemical Information | |
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Cell permeable | Y |
Packaging Information | |
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Packaged under inert gas | Packaged under inert gas |
Global Trade Item Number | |
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Catalogue Number | GTIN |
5339820001 | 04055977281729 |