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500509 DNA Methyltransferase Inhibitor V, RSC133 - Calbiochem

A cell-permeable compound that targets Dnmt1 at the cofactor SAM-binding site and enhances the efficiency of iPSC production from both murine MEF and human foreskin fibroblasts.

MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.

Synonyms: (E)-3-(3-(1H-Indol-3-yl)acrylamido)benzamide, ID133, iPSC Induction Enhancer III, Reprogramming Stimulating Compound 133, DNA MTase Inhibitor V

Primary Target: Dnmt1
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Overview

Replacement Information

Key Specifications Table

Empirical Formula
C₁₈H₁₅N₃O₂
Description
OverviewA cell-permeable indolylacrylamido-benzamide compound that is reported to target Dnmt1 at the cofactor SAM-binding site and enhance the efficiency of iPSC production from both murine MEF (10 µM starting 5 d post KSOM viral infection) and human foreskin fibroblast (10 µM starting same day as or 5 d post KSOM viral infection) cultures with accompanying cellular Dnmt1 activity reduction, affecting hFF viability only at high concentrations (78% of control post 72 h 100 µM treatment). Also shown to help maintain H9 hESCs in undifferentiated state when cultured in unconditioned media (10 µM).

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 Number500509
Brand Family Calbiochem®
Synonyms(E)-3-(3-(1H-Indol-3-yl)acrylamido)benzamide, ID133, iPSC Induction Enhancer III, Reprogramming Stimulating Compound 133, DNA MTase Inhibitor V
References
ReferencesLee, J., et al. 2012. Angew. Chem. Int. Engl. 51, 12509.
Product Information
FormLight yellow powder
Hill FormulaC₁₈H₁₅N₃O₂
Chemical formulaC₁₈H₁₅N₃O₂
ReversibleY
Structure formula ImageStructure formula Image
Quality LevelMQ100
Applications
Biological Information
Primary TargetDnmt1
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 6 months at -20°C.
Packaging Information
Transport Information
Supplemental Information
Specifications
Global Trade Identification Number
Catalog Number GTIN
500509

Documentation

DNA Methyltransferase Inhibitor V, RSC133 - Calbiochem SDS

Title

Safety Data Sheet (SDS) 

References

Reference overview
Lee, J., et al. 2012. Angew. Chem. Int. Engl. 51, 12509.

Technical Info

Title
White Paper - The Message in the Marks: Deciphering Cancer Epigenetics
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.

Revision10-January-2014 JSW
Synonyms(E)-3-(3-(1H-Indol-3-yl)acrylamido)benzamide, ID133, iPSC Induction Enhancer III, Reprogramming Stimulating Compound 133, DNA MTase Inhibitor V
DescriptionA cell-permeable indolylacrylamido-benzamide compound that is reported to target Dnmt1 at the cofactor SAM-(S-adenosyl methionine) binding site and enhance the efficiency of iPSC production from both murine MEF (by 2.1-fold at 15 d post viral KOSM transduction with 10 µM RSC133 starting 5 d post viral infection) and human foreskin fibroblast (by 3.5- and 2.9-fold 15 d post viral KOSM transduction with 10 µM RSC133 starting same day as or 5 d post viral infection, respectively) cultures with accompanying cellular Dnmt1 activity reduction (by 38% lower in 15 d viral-transduced hiPSC cultures with 10 µM RSC133 starting on d 5 post viral infection), affecting hFF viability only at high concentrations (102% and 78% of control after 72 h incubation with 50 and 100 µM RSC133, respectively, by MTT assays). Also shown to help maintain H9 hESCs in undifferentiated state when cultured in unconditioned media (17% vs 53% drop in AP+ colonies in 6 d UM cultures, respectively, with or without 10 µM RSC133).
FormLight yellow powder
Chemical formulaC₁₈H₁₅N₃O₂
Structure formulaStructure formula
Purity≥98% by HPLC
SolubilityDMSO (100 mg/ml). Use only fresh DMSO for reconstitution.
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 6 months at -20°C.
Toxicity Standard Handling
ReferencesLee, J., et al. 2012. Angew. Chem. Int. Engl. 51, 12509.