RU-SKI 43 (hydrochloride)


CAS No. : 1782573-67-4

1782573-67-4
Price and Availability of CAS No. : 1782573-67-4
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5mg $132 In-stock
10mg $192 In-stock
25mg $451 In-stock
50mg $828 In-stock
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Cat. No. : HY-18366A
M.Wt: 423.01
Formula: C22H31ClN2O2S
Purity: >98 %
Solubility: DMSO : ≥ 51 mg/mL;H2O : 2.5 mg/mL (ultrasonic)
Introduction of 1782573-67-4 :

RU-SKI 43 hydrochloride is a potent and selective Hedgehog acyltransferase (Hhat) inhibitor with an IC50 of 850 nM. RU-SKI 43 hydrochloride reduces Gli-1 activation through Smoothened-independent non-canonical signaling and decreases Akt and mTOR pathway activity. RU-SKI 43 hydrochloride has anti-cancer activity[1]. IC50 & Target: IC50: 850 nM (Hhat)[1] In Vitro: RU-SKI 43 hydrochloride (10 μM; for 6 days) strongly decreases cell proliferation (83% in AsPC-1 cells) in AsPC-1 and Panc-1 cells[2].
RU-SKI 43 hydrochloride (10 or 20 μM; 5 hours) causes dose-dependent inhibition of Shh palmitoylation following only 5 hours[1].
RU-SKI 43 hydrochloride (10 μM; for 72 hours) causes a 40% decrease in Gli-1 levels in AsPC-1 cells[2].
RU-SKI 43 hydrochloride (10 μM; 48 hours) results in decreased phosphorylation (47-67%) of four proteins in the Akt pathway, including Akt (phosphorylation at both Thr307 and Ser473), PRAS40, Bad and GSK-3β. RU-SKI 43 treatment also decreases phosphorylation of mTOR and S6, members of the mTOR signaling pathway[2].
RU-SKI 43 hydrochloride behaves as an uncompetitive inhibitor (Ki=7.4 μM) with respect to Shh, and as a noncompetitive inhibitor (Ki=6.9 μM) with respect to 125I-iodo-palmitoylCoA[1].
In Vivo: RU-SKI 43 hydrochloride has a t1/2 of 17 min in mouse plasma after IV administration[1].

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