research use only
Cat.No.S7719
| Related Targets | CDK HSP PD-1/PD-L1 ROCK Wee1 DNA/RNA Synthesis Microtubule Associated Ras KRas Aurora Kinase |
|---|---|
| Other Rho Inhibitors | NSC 23766 Trihydrochloride EHop-016 ML141 (CID-2950007) EHT 1864 2HCl ZCL278 MBQ-167 CCG-203971 CID44216842 1A-116 Rhosin hydrochloride |
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In vitro |
DMSO
: 90 mg/mL
(197.91 mM)
Ethanol : 4 mg/mL Water : Insoluble |
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In vivo |
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Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.
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| Molecular Weight | 454.75 | Formula | C18H13ClF6N2O3 |
Storage (From the date of receipt) | |
|---|---|---|---|---|---|
| CAS No. | 285986-88-1 | Download SDF | Storage of Stock Solutions |
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| Synonyms | N/A | Smiles | CC(C(=O)NC1=CC=C(C=C1)Cl)ONC(=O)C2=CC(=CC(=C2)C(F)(F)F)C(F)(F)F | ||
| Targets/IC50/Ki |
RhoA
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|---|---|
| In vitro |
CCG-1423 selectively inhibits SRF-mediated transcription activated by Rho pathway signaling, and specifically inhibits LPA-stimulated DNA synthesis. This compound also selectively inhibits the proliferation of RhoC-overexpressing melanoma cells (A375M2 and SK-Mel-147), and strongly suppresses the Rho-dependent invasion by PC-3 cells. It in combination with LY294002 enhances differentiation of mouse embryonic stem cells into intermediate mesoderm through BMP7-positive cells. In H9c2 cells, this chemical inhibits MRTF nuclear localization, and completely blocks STARS proximal reporter activity. This compound, as a Rho/MRTF/SRF pathway inhibitor, also represses both matrix-stiffness and TGF-beta-induced fibrogenesis in human colonic myofibroblasts.
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References |
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