| Identification | Back Directory | [Name]
1-benzyl-3-(4-chlorophenyl)-5-MethyliMidazolidine-2,4-dione | [CAS]
37468-32-9 | [Synonyms]
ALLO-1
1-benzyl-3-(4-chlorophenyl)-5-MethyliMidazolidine-2,4-dione
3-(4-Chlorophenyl)-5-methyl-1-(phenylmethyl)-2,4-Imidazolidinedione
2,4-Imidazolidinedione, 3-(4-chlorophenyl)-5-methyl-1-(phenylmethyl)- | [Molecular Formula]
C17H15ClN2O2 | [MDL Number]
MFCD19441284 | [MOL File]
37468-32-9.mol | [Molecular Weight]
314.77 |
| Chemical Properties | Back Directory | [Boiling point ]
452.0±55.0 °C(Predicted) | [density ]
1.321±0.06 g/cm3(Predicted) | [storage temp. ]
2-8°C | [solubility ]
DMSO: >10mg/mL | [form ]
powder | [pka]
-1.30±0.40(Predicted) | [color ]
white to beige |
| Hazard Information | Back Directory | [Uses]
ALLO-1 is a small molecule antagonist that inhibits drug-resistant mutant of Smoothened (Smo), related to cancers. | [Biological Activity]
allo-1 is a smo antagonist.hedgehog (hh) proteins are important development regulators that bind the cell-surface protein, which allows the activation of a gpcr-like receptor, smoothened (smo). in vertebrates, the smo activation finally results in the activation of the zinc-finger transcription factors of the gli family. in addition, the overactivation of smo may lead to certain cancers. | [Biochem/physiol Actions]
ALLO-1 is a Smoothened (Smo) antagonist that inhibits both wild-type and mutant Smo, including D473H SMO mutant. ALLO-1 binds to a different domain of Smo than other known Smo ligands. | [in vitro]
previous study found that allo-1 and its close analog allo-2 could inhibit smo agonist hh-ag 1.5-induced luciferase expression in tm3-gli-luc cells. the potency of allo-1 did not change when either low dose or high dose of hh-ag 1.5 was used, in contrast to other known smo antagonists that are strong sag or hh-ag 1.5 competitors. moreover, it was found that in contrast to gdc-0449, both allo-1 and allo-2 inhibited wild-type and the d477g mutant with only around2-fold shift in ic50, indicating that the d477g mutation did not significantly interfere with the binding of allo-1 and allo-2 to smo. in addition, allo-1 as well as allo-2 were able to inhibit both wild-type and d473h mutant human smo with similar potencies [1]. | [IC 50]
50 nm for wile type smo | [References]
[1] tao, h. ,jin, q.,koo, d.i., et al. small molecule antagonists in distinct binding modes inhibit drug-resistant mutant of smoothened. chemistry & biology 18, 432-437 (2011). |
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Sigma-Aldrich
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Energy Chemical
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