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Submit ReviewMU 1700 trihydrochloride is a potent and selective ALK2 and ALK1 inhibitor (IC50 values are 6 nM and 13 nM, respectively in biochemical assays). It is also a potent ALK6 inhibitor (IC50 = 41 nM). It shows selectivity for ALK over >360 other kinases. It shows favorable pharmacokinetic for in vivo use. MU 1700 trihydrochloride is orally bioavailable. It is cell membrane permeable and brain penetrant.
This probe is supplied in conjunction with the Structural Genomics Consortium. For further characterization details, please visit the MU 1700 probe summary on the SGC website.
M. Wt | 515.86 |
Formula | C26H22N4O.3HCl |
Storage | Store at -20°C |
Purity | ≥98% (HPLC) |
InChI Key | RRVVHPUANQAUJY-UHFFFAOYSA-N |
Smiles | C12=C(C=CC=C2)N=CC=C1C3=COC4=C3N=CC(C5=CC=C(C=C5)N6CCNCC6)=C4.Cl.Cl.Cl |
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Solvent | Max Conc. mg/mL | Max Conc. mM | |
---|---|---|---|
Solubility | |||
DMSO | 5.16 | 10 | |
water | 25.79 | 50 |
The following data is based on the product molecular weight 515.86. Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
---|---|---|---|
0.5 mM | 3.88 mL | 19.39 mL | 38.77 mL |
2.5 mM | 0.78 mL | 3.88 mL | 7.75 mL |
5 mM | 0.39 mL | 1.94 mL | 3.88 mL |
25 mM | 0.08 mL | 0.39 mL | 0.78 mL |
References are publications that support the biological activity of the product.
Němec et al (2024) Discovery of two highly selective structurally orthogonal chemical probes for activin receptor-like kinases 1 and 2. J.Med.Chem. 67 12632 PMID: 39023313
If you know of a relevant reference for MU 1700 trihydrochloride, please let us know.
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