Powder: -20°C for 3 years | In solvent: -80°C for 1 year
FIDAS-5, a potent and orally active methionine S-adenosyltransferase 2A (MAT2A) inhibitor with an IC50 of 2.1 μM, competitively inhibits S-adenosylmethionine (SAM) binding to MAT2A. It exhibits anticancer activities.
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
1 mg | In stock | $ 54.00 | |
2 mg | In stock | $ 77.00 | |
5 mg | In stock | $ 118.00 | |
10 mg | In stock | $ 196.00 | |
25 mg | In stock | $ 349.00 | |
50 mg | In stock | $ 538.00 | |
100 mg | In stock | $ 778.00 | |
500 mg | In stock | $ 1,490.00 | |
1 mL * 10 mM (in DMSO) | In stock | $ 115.00 |
Description | FIDAS-5, a potent and orally active methionine S-adenosyltransferase 2A (MAT2A) inhibitor with an IC50 of 2.1 μM, competitively inhibits S-adenosylmethionine (SAM) binding to MAT2A. It exhibits anticancer activities. |
Targets&IC50 | Mat2A:2.1 μM |
In vitro | FIDAS-5 induces the expression of cell cycle inhibitor, p21WAF1/CIP1. FIDAS-5 (3 μM; 36 h) treatment reduces the levels of both S-adenosylmethionine (SAM) and S-adenosylhomocysteine (SAH) in LS174T cells.FIDAS-5 (3 μM; 7 days; LS174T cells) treatment significantly inhibits the proliferation of LS174T cells. FIDAS-5 (3 μM) treatment inhibits the expression of c-Myc and cyclinD1 in LS174T CRC cells. |
In vivo | Mice are treated with FIDAS-5 (20 mg/kg) for 1 week.?The liver SAM levels are significantly reduced.FIDAS-5 (20 mg/kg; oral gavage; daily; for two weeks; athymic nude mice) treatment significantly inhibits the growth of xenograft tumors, with minimal difference in body weight. |
Molecular Weight | 261.72 |
Formula | C15H13ClFN |
CAS No. | 1391934-98-7 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 125 mg/mL (477.61 mM), Sonication is recommended.
You can also refer to dose conversion for different animals. More
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FIDAS-5 1391934-98-7 Others p21WAF1/CIP1 S-adenosylmethionine inhibit MAT2A anti-proliferation SAH Inhibitor anti-cancer CyclinD1 FIDAS5 c-Myc SAM FIDAS 5 colorectal inhibitor