Reaction Details |
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Target | Protein arginine N-methyltransferase 3 [N508S] |
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Ligand | BDBM50353131 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_768495 (CHEMBL1832318) |
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IC50 | >10000±n/a nM |
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Citation | Liu, F; Barsyte-Lovejoy, D; Allali-Hassani, A; He, Y; Herold, JM; Chen, X; Yates, CM; Frye, SV; Brown, PJ; Huang, J; Vedadi, M; Arrowsmith, CH; Jin, J Optimization of cellular activity of G9a inhibitors 7-aminoalkoxy-quinazolines. J Med Chem54:6139-50 (2011) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Protein arginine N-methyltransferase 3 [N508S] |
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Name: | Protein arginine N-methyltransferase 3 [N508S] |
Synonyms: | ANM3_HUMAN | HRMT1L3 | Heterogeneous nuclear ribonucleoprotein methyltransferase-like protein 3 | PRMT3 | Protein arginine N-methyltransferase 3 | Protein arginine N-methyltransferase 3 (PRMT3) |
Type: | Protein |
Mol. Mass.: | 59859.85 |
Organism: | Homo sapiens (Human) |
Description: | O60678[N508S] |
Residue: | 531 |
Sequence: | MCSLASGATGGRGAVENEEDLPELSDSGDEAAWEDEDDADLPHGKQQTPCLFCNRLFTSA
EETFSHCKSEHQFNIDSMVHKHGLEFYGYIKLINFIRLKNPTVEYMNSIYNPVPWEKEEY
LKPVLEDDLLLQFDVEDLYEPVSVPFSYPNGLSENTSVVEKLKHMEARALSAEAALARAR
EDLQKMKQFAQDFVMHTDVRTCSSSTSVIADLQEDEDGVYFSSYGHYGIHEEMLKDKIRT
ESYRDFIYQNPHIFKDKVVLDVGCGTGILSMFAAKAGAKKVLGVDQSEILYQAMDIIRLN
KLEDTITLIKGKIEEVHLPVEKVDVIISEWMGYFLLFESMLDSVLYAKNKYLAKGGSVYP
DICTISLVAVSDVNKHADRIAFWDDVYGFKMSCMKKAVIPEAVVEVLDPKTLISEPCGIK
HIDCHTTSISDLEFSSDFTLKITRTSMCTAIAGYFDIYFEKNCHNRVVFSTGPQSTKTHW
KQTVFLLEKPFSVKAGEALKGKVTVHKSKKDPRSLTVTLTLNNSTQTYGLQ
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BDBM50353131 |
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n/a |
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Name | BDBM50353131 |
Synonyms: | CHEMBL1829304 |
Type | Small organic molecule |
Emp. Form. | C36H59N7O2 |
Mol. Mass. | 621.8994 |
SMILES | COc1cc2c(NC3CCN(CC3)C3CCCCC3)nc(nc2cc1OCCCN1CCCCC1)N1CCCN(CC1)C(C)C |
Structure |
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