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533982 Dock5 Inhibitor, C21 - CAS 54129-15-6 - Calbiochem

Overview

Replacement Information

Key Specifications Table

CAS #Empirical Formula
54129-15-6C₁₂H₉Cl₂NO₂S

Products

Catalog NumberPackaging Qty/Pack
5.33982.0001 Glass bottle 50 mg
Description
OverviewA 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 Number533982
Brand Family Calbiochem®
SynonymsN-(3,5-Dichlorophenyl)benzenesulfonamide
References
ReferencesVives, V., et al. 2015. Nat. Commun. 6, 6218.
Vives, V., et al. 2011. J. Bone Miner. Res. 26, 1099.
Product Information
CAS number54129-15-6
FormGrey powder
Hill FormulaC₁₂H₉Cl₂NO₂S
Chemical formulaC₁₂H₉Cl₂NO₂S
ReversibleY
Quality LevelMQ100
Applications
Biological Information
Primary TargetDock5
Purity≥98% by HPLC
Physicochemical Information
Cell permeableY
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Storage and Shipping Information
Ship Code Ambient Temperature Only
Toxicity Standard Handling
Storage +2°C to +8°C
Protect from Light Protect from light
Do not freeze Ok to freeze
Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Packaging Information
Packaged under inert gas Packaged under inert gas
Transport Information
Supplemental Information
Specifications
Global Trade Item Number
Catalog Number GTIN
5.33982.0001 04055977281729

Documentation

Dock5 Inhibitor, C21 - CAS 54129-15-6 - Calbiochem SDS

Title

Safety Data Sheet (SDS) 

References

Reference overview
Vives, V., et al. 2015. Nat. Commun. 6, 6218.
Vives, V., et al. 2011. J. Bone Miner. Res. 26, 1099.
Data Sheet

Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.

Revision14-July-2017 JSW
SynonymsN-(3,5-Dichlorophenyl)benzenesulfonamide
DescriptionA 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.
FormGrey powder
Intert gas (Yes/No) Packaged under inert gas
CAS number54129-15-6
Chemical formulaC₁₂H₉Cl₂NO₂S
Purity≥98% by HPLC
SolubilityDMSO (50 mg/ml)
Storage Protect from light
+2°C to +8°C
Do Not Freeze Ok to freeze
Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Toxicity Standard Handling
ReferencesVives, V., et al. 2015. Nat. Commun. 6, 6218.
Vives, V., et al. 2011. J. Bone Miner. Res. 26, 1099.