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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 | Same Day | 2-3 Business Days | Other Lead Time |
Shipping Information
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---|---|---|---|---|---|
50MG |
NT$5,124
|
15 | 1 | Contact Us | |
200MG |
NT$13,944
|
≥40 | 0 | Contact Us |
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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 |
Packaging and Container | 200MG-Glass Bottle with Plastic Insert (View image), 50MG-Glass Bottle with Plastic Insert (View image) |
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:
H.S.code* | 2933.99-000 |
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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