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A-366, MedChemExpress
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Quantity:
5 mg
10 mg
50 mg
Unit Size:
10mg
50mg
5mg
Description
A-366 shows >1000-fold selectivity over 21 other methyltransferases. A-366 is also a potent, nanomolar inhibitor of the Spindlin1-H3K4me3-interaction (IC50=182.6 nM). A-366 displays high affinity at human histamine H3 receptor (Ki=17 nM) and shows subtype selectivity among subsets of the histaminergic and dopaminergic receptor families.
Specifications
Specifications
| Chemical Name or Material | A-366 |
| CAS | 1527503-11-2 |
| Color | Yellow |
| Purity Grade Notes | Research |
| Molecular Formula | C19H27N3O2 |
| Quantity | 50 mg |
| Solubility Information | DMSO : 50 mg/mL (151.77 mM; Need ultrasonic) |
| SMILES | COC1=CC2=C(N=C(N)C23CCC3)C=C1OCCCN4CCCC4 |
| Molecular Weight (g/mol) | 329.44 |
| Formula Weight | 329.44 |
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Research purposes only
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