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CAS RN: 48208-26-0 | Product Number: P2023
N-Phthalyl-L-tryptophan
Purity: >98.0%(T)(HPLC)
Synonyms:
- RG 108
Product Documents:
Size | Unit Price | Belgium | Japan* | Quantity |
---|---|---|---|---|
50MG |
€79.00
|
1 | 16 |
|
200MG |
€261.00
|
6 | ≥40 |
|
*Stock available in Belgium will be delivered in 1 to 3 days
*Stock available in Japan will be delivered in 1 to 2 weeks (excludes regulated items and dry ice shipments).
Product Number | P2023 |
Purity / Analysis Method | >98.0%(T)(HPLC) |
Molecular Formula / Molecular Weight | C__1__9H__1__4N__2O__4 = 334.33 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Frozen (<0°C) |
Condition to Avoid | Heat Sensitive |
CAS RN | 48208-26-0 |
Reaxys Registry Number | 4552782 |
PubChem Substance ID | 253661522 |
MDL Number | MFCD08705332 |
Specifications
Appearance | Light yellow to Amber to Dark green powder to crystaline |
Purity(HPLC) | min. 98.0 area% |
Purity(Neutralization titration) | min. 98.0 % |
Specific rotation [a]20/D | -268 to -273 deg(C=1, EtOH) |
Properties (reference)
Melting Point | 181 °C |
Specific Rotation | -271° (C=1,EtOH) |
Solubility (slightly sol. in) | Methanol |
GHS
Related Laws:
Transport Information:
HS Number | 2933998090 |
Application
Research on regenerative medicine
RG 108 enhances reprogramming of human1) and mouse2,3) somatic cells to iPS cells.
References
- 1) Butyrate greatly enhances derivation of human induced pluripotent stem cells by promoting epigenetic remodeling and the expression of pluripotency-associated genes
- 2) Efficient non-viral reprogramming of myoblasts to stemness with a single small molecule to generate cardiac progenitor cells
- 3) Induction of pluripotent stem cells from mouse embryonic fibroblasts by Oct4 and Klf4 with small-molecule compounds
Application
RG108: A Non-Nucleoside DNA Methyltransferase (DNMT) Inhibitor
DNA methylation regulates epigenetic gene expression in normal and malignant cells. N-phthaloyl-L-tryptophan (RG108) is a non-nucleoside DNA methyltransferase (DNMT) inhibitor. RG108 significantly reduces the methylation of genomic DNA in cells without any detectable toxicity, distinguishing it from nucleoside-based DNA DNMT inhibitors like 5-azacytidine [A2033], 5-aza-2’-deoxycytidine [A2232] and zebularine [Z0022]. RG108 is useful for the experimental modulation of epigenetic gene regulation.
References
- Epigenetic Reactivation of Tumor Suppressor Genes by a Novel Small-Molecule Inhibitor of Human DNA Methyltransferases
- Functional Diversity of DNA Methyltransferase Inhibitors in Human Cancer Cell Lines
- Antileukemic activity of combined epigenetic agents, DNMT inhibitors zebularine and RG108 with HDAC inhibitors, against promyelocytic leukemia HL-60 cells
- DNA methyltransferase inhibitor RG108 and histone deacetylase inhibitors cooperate to enhance NB4 cell differentiation and E-cadherin re-expression by chromatin remodelling
- Epigenetic-based therapies in cancer: progress to date (a review)
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