| Identification | Back Directory | [Name]
KUC103479N-02 | [CAS]
1222513-26-9 | [Synonyms]
KSC-221-15
CID44216842
KUC103479N-02
CID44216842 >=98% (HPLC)
CID44216842, 10 mM in DMSO
4-[3-(4-Bromophenyl)-5-(3-methoxyphenyl)-3,4-dihydropyrazol-2-yl]benzenesulfonamide
4-(5-(4-Bromophenyl)-3-(3-methoxyphenyl)-4,5-dihydro-1H-pyrazol-1-yl)benzenesulfonamide
4-[5-(4-bromophenyl)-4,5-dihydro-3-(3-methoxyphenyl)-1H-pyrazol-1-yl]-benzenesulfonamide
Benzenesulfonamide, 4-[5-(4-bromophenyl)-4,5-dihydro-3-(3-methoxyphenyl)-1H-pyrazol-1-yl]-
diseases,neutrophils,ovarian,disorders,Cdc42,fibroblasts,breast,hepatitis C,CID 44216842,retardation,Inhibitor,CID44216842,Ras,cancer,kidney epithelia,mental,inhibit,immune,virus,neurological,CID-44216842 | [Molecular Formula]
C22H20BrN3O3S | [MDL Number]
MFCD28009507 | [MOL File]
1222513-26-9.mol | [Molecular Weight]
486.38 |
| Hazard Information | Back Directory | [Uses]
CID44216842 (Cdc42-IN-1) is a potent Cdc42-selective guanine nucleotide binding lead inhibitor. The EC50s for Cdc42 WT and Cdc42Q61L mutant are 1.0 and 1.2 μM in GTP binding assay, respectively. The EC50s for Cdc42 WT and Cdc42Q61L mutant are 0.3 and 0.5 μM in GDP binding assay, respectively. Use as a molecular probe[1]. | [Biological Activity]
CID44216842 is a potent and selective non-competitive allosteric inhibitor of Cdc42 GTPase th at does not inhabit Rho and Rac. CID44216842 inhibits Cdc42 dependent filopodia formation and cell migration. | [References]
[1] Lin Hong, et al. Characterization of a Cdc42 Protein Inhibitor and Its Use as a Molecular Probe. J Biol Chem. 2013 Mar 22;288(12):8531-43. DOI:10.1074/jbc.M112.435941 |
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BOC Sciences
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1-631-485-4226; 16314854226 |
| Website: |
https://www.bocsci.com |
| Company Name: |
Energy Chemical
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021-58432009 400-005-6266 |
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http://www.energy-chemical.com |
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InvivoChem
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13549236410 |
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https://www.invivochem.cn/ |
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