ML 141 (Synonyms: CID2950007) |
Katalog-Nr.GC14800 |
ML 141 (CID-2950007) ist ein potenter, allosterischer, selektiver und reversibler nicht-kompetitiver Inhibitor der Cdc42-GTPase. ML 141 hemmt den Cdc42-Wildtyp und die Cdc42-Q61L-Mutante mit EC50-Werten von 2,1 bzw. 2,6 μM. ML 141 zeigt eine niedrige mikromolare Wirksamkeit und Selektivität gegenüber anderen Mitgliedern der Rho-Familie von GTPasen (Rac1, Rab2, Rab7). ML 141 zeigt in mehreren Zelllinien keine Zytotoxizität.
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 71203-35-5
Sample solution is provided at 25 µL, 10mM.
ML141(CID-2950007) is a potent, selective and reversible non-competitive inhibitor of Cdc42 GTPase(IC50=200 nM) with low micromolar potency and selectivity against other members of the Rho family of GTPases (Rac1, Rab2, Rab7). IC50 value: 200 nM [1]Target: Cdc42 inhibitorin vitro: In the primary HTS bead-based assay using 1 mM EDTA and 100 nM BODIPY-FL-GTP, potency for CID2950007 was IC50 = 2.6 and 5.4 μM for Cdc42 wild type and activated mutant, respectively [1]. ML141 exposure also enhanced the ability of TMX to suppress BLBC cell growth, through both induction of cell death and suppression of cell division [2]. in vivo: Treatment with ML141 + TMX caused a suppression of further tumour growth in vivo [2]. Parallel suppression of the conserved brain CDC42 activity by intracerebroventricular ML141 injection caused acute anxiety in mice [3]. using a pilocarpine-induced epileptic model, we found that pretreatment with ML141, a specific inhibitor of Cdc42, reduces seizure severity [4].
References:
[1]. Surviladze Z, et al. A Potent and Selective Inhibitor of Cdc42 GTPase. Probe Reports from the NIH Molecular Libraries Program
[2]. Chen HY, et al. Inhibition of redox/Fyn/c-Cbl pathway function by Cdc42 controls tumour initiation capacity and tamoxifen sensitivity in basal-like breast cancer cells. EMBO Mol Med. 2013 May;5(5):723-36.
[3]. Hanin G, et al. Competing targets of microRNA-608 affect anxiety and hypertension. Hum Mol Genet. 2014 Sep 1;23(17):4569-80.
[4]. Zhang Y, et al. Inhibition of the small GTPase Cdc42 in regulation of epileptic-seizure in rats. Neuroscience. 2015 Mar 19;289:381-91.
Cas No. | 71203-35-5 | SDF | |
Überlieferungen | CID2950007 | ||
Chemical Name | 4-(5-(4-methoxyphenyl)-3-phenyl-4,5-dihydro-1H-pyrazol-1-yl)benzenesulfonamide | ||
Canonical SMILES | COC1=CC=C(C2CC(C3=CC=CC=C3)=NN2C4=CC=C(S(N)(=O)=O)C=C4)C=C1 | ||
Formula | C22H21N3O3S | M.Wt | 407.49 |
Löslichkeit | DMF: 30 mg/mL,DMF:PBS (pH 7.2) (1:4): 0.2 mg/mL,DMSO: 20 mg/mL | Storage | Store at -20°C |
General tips | Please select the appropriate solvent to prepare the stock solution according to the
solubility of the product in different solvents; once the solution is prepared, please store it in
separate packages to avoid product failure caused by repeated freezing and thawing.Storage method
and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored
at -20°C, please use it within 1 month. To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time. |
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Shipping Condition | Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request. |
Prepare stock solution | |||
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1 mg | 5 mg | 10 mg |
1 mM | 2.454 mL | 12.2702 mL | 24.5405 mL |
5 mM | 0.4908 mL | 2.454 mL | 4.9081 mL |
10 mM | 0.2454 mL | 1.227 mL | 2.454 mL |
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Quality Control & SDS
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- Purity: >98.50%
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Average Rating: 5
(Based on Reviews and 8 reference(s) in Google Scholar.)GLPBIO products are for RESEARCH USE ONLY. Please make sure your review or question is research based.
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