Product Name | BM30 |
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Description | BM30 is the first potent peptidomimetic inhibitor for N-terminal methyltransferase1/2 (NTMT1/2). BM30 has a half-maximal inhibitory concentration of 0.89 ± 0.10 μM, is a competitive inhibitor to the peptide substrate and is noncompetitive to the cofactor S-adenosylmethionine. BM30 exhibits over 100-fold selectivity for NTMT1/2 among a panel of 41 methyl transferases, showing great potential for high selectivity when targeting the peptide substrate binding site of NTMT1/2. Its cell-permeable analogue DC432 is also available, which can decrease the N-terminal methylation level of the regulator of chromosome condensation 1 and SET proteins in HCT116 cells. |
Synonyms | BM30, EI-010, EI010, N-terminal methyltransferase1/2, NTMT1/2 |
Molecular Weight | 532.64 Da |
Target | Transferases |
Amino Acid Sequence | XPKR-NH2 |
Form | Freeze dried solid |
Purity | >95% by HPLC |
Storage | Store desiccated, frozen and in the dark |
Notes | Modifications: X is 4-hydroxyphenylacetyl, C terminal amide |
References | Mackie et al (2020) Selective Peptidomimetic Inhibitors of NTMT1/2: Rational Design, Synthesis, Characterization, and Crystallographic Studies. J Med Chem. 63(17) 9512 PMID: 32689795 |
Supplier | Isca Biochemicals Limited |
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