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Chemical Structure : BI-9321
CAS No.: 2387510-86-1
Catalog No.: PC-72293Not For Human Use, Lab Use Only.
BI-9321 (BI 9321) is a potent, selective and cellular active inhibitor of the NSD3-PWWP1 domain with SPR Kd of 166 nM.
| Packing | Price | Stock | Quantity |
|---|---|---|---|
| 5 mg | $128 | In stock | |
| 10 mg | $198 | In stock | |
| 25 mg | $348 | In stock | |
| 50 mg | Get quote | ||
| 100 mg | Get quote |
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BI-9321 (BI 9321) is a potent, selective and cellular active inhibitor of the NSD3-PWWP1 domain with SPR Kd of 166 nM.
BI-9321 displays no significant inhibition against a selection of 31 diverse kinases, closest family members NSD2-PWWP1, BRD4 and KDM1B.
BI-9321 targets the methyl-lysine binding site of the PWWP1 domain with sub-micromolar in vitro activity and cellular target engagement at 1 uM.
BI-9321 downregulated Myc messenger RNA expression and reduces proliferation in MOLM-13 cells, BI-9321 inhibited proliferation of both MOLM-13 (IC50=26.8 uM) and RN2 cells (IC50=13 uM).
BI-9321 enhanced the JQ1-dependent proliferation phenotype in the MOLM-13 cell line.
| M.Wt | 360.436 | |
| Formula | C22H21FN4 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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| Chemical Name/SMILES |
(4-(5-(7-fluoroquinolin-4-yl)-1-methyl-1H-imidazol-4-yl)-3,5-dimethylphenyl)methanamine |
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1. Böttcher J, et al. Nat Chem Biol. 2019 Aug;15(8):822-829.
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