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ML141

Chemical Structure : ML141

CAS No.: 71203-35-5

ML141 (ML-141;CID-2950007)

Catalog No.: PC-43180Not For Human Use, Lab Use Only.

ML141 (CID-2950007) is a potent, selective, reversible non-competitive inhibitor of Cdc42 GTPase with IC50 of 200 nM in biochemical assays, shows no appreciable inhibitory activity against Rac1, Rab2, Rab7 or Ras.

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Biological Activity

ML141 (CID-2950007) is a potent, selective, reversible non-competitive inhibitor of Cdc42 GTPase with IC50 of 200 nM in biochemical assays, shows no appreciable inhibitory activity against Rac1, Rab2, Rab7 or Ras.
ML141 also exhibits IC50 of 2.6 and 5.4 uM for Cdc42 wild type and activated mutant in the primary HTS bead-based assays.
ML141 enhances G-CSF-induced hematopoietic stem and progenitor cell mobilization, also significantly protects neuroblastoma cells from metformin-induced apoptosis.

Physicochemical Properties

M.Wt 407.4854
Formula C22H21N3O3S
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
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Solubility

DMSO: ≥ 55 mg/mL

Chemical Name/SMILES

Benzenesulfonamide, 4-[4,5-dihydro-5-(4-methoxyphenyl)-3-phenyl-1H-pyrazol-1-yl]-

References

1. Surviladze Z, et al. Probe Reports from the NIH Molecular Libraries Program [Internet].

2. Chen HY, et al. EMBO Mol Med. 2013 May;5(5):723-36.

3. Zhang Y, et al. Neuroscience. 2015 Mar 19;289:381-91.

4. Chen C, et al. Int J Hematol. 2015 Jan;101(1):5-12.

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