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  • DC Chemicals Limited
  • China
  • Product Name: ML-141
  • Price: $400.0/100mg $800.0/250mg $1500.0/1g
  • Purity: 98.0%
  • Stocking Period: 3 Day
  • Contact: Tony Cao

71203-35-5

71203-35-5 structure
71203-35-5 structure
  • Name: ML 141
  • Chemical Name: 4-[5-(4-Methoxyphenyl)-3-phenyl-4,5-dihydro-1H-pyrazol-1-yl]benze nesulfonamide
  • CAS Number: 71203-35-5
  • Molecular Formula: C22H21N3O3S
  • Molecular Weight: 407.485
  • Catalog: Biochemical Inhibitor Cell Cycle Rho inhibitor
  • Create Date: 2016-01-20 01:16:30
  • Modify Date: 2024-01-10 15:44:21
  • 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].

Name 4-[5-(4-Methoxyphenyl)-3-phenyl-4,5-dihydro-1H-pyrazol-1-yl]benze nesulfonamide
Synonyms 4-[3-(4-methoxyphenyl)-5-phenyl-3,4-dihydropyrazol-2-yl]benzenesulfonamide
4-[3-(4-Methoxyphenyl)-1-propyl]piperidine
Benzenesulfonamide, 4-[4,5-dihydro-5-(4-methoxyphenyl)-3-phenyl-1H-pyrazol-1-yl]-
4-[5-(4-Methoxyphenyl)-3-phenyl-4,5-dihydro-1H-pyrazol-1-yl]benzenesulfonamide
Piperidine,4-[3-(4-methoxyphenyl)propyl]
4-(5-(4-methoxyphenyl)-3-phenyl-4,5-dihydro-1H-pyrazol-1-yl)benzenesulfonamide
ML-141
ML141
Description 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].
Related Catalog
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.

Density 1.3±0.1 g/cm3
Boiling Point 622.9±65.0 °C at 760 mmHg
Melting Point 216 °C
Molecular Formula C22H21N3O3S
Molecular Weight 407.485
Flash Point 330.5±34.3 °C
Exact Mass 407.130371
PSA 93.37000
LogP 1.82
Appearance white to beige
Vapour Pressure 0.0±1.8 mmHg at 25°C
Index of Refraction 1.652
Storage condition 2-8°C
Water Solubility DMSO: soluble5mg/mL (warmed, clear solution)
Hazard Codes Xi
RIDADR NONH for all modes of transport

~66%

71203-35-5 structure

71203-35-5

Literature: Faid-Allah, Hassan M.; Mokhtar, Hassan M. Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1988 , vol. 27, # 1-12 p. 245 - 249

~64%

71203-35-5 structure

71203-35-5

Literature: Feid-Allah Pharmazie, 1981 , vol. 36, # 11 p. 754 - 756

~71%

71203-35-5 structure

71203-35-5

Literature: Faid-Allah, Hassan M.; Mokhtar, Hassan M. Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1988 , vol. 27, # 1-12 p. 245 - 249

~%

71203-35-5 structure

71203-35-5

Literature: Faid-Allah, Hassan M.; Mokhtar, Hassan M. Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1988 , vol. 27, # 1-12 p. 245 - 249

~%

71203-35-5 structure

71203-35-5

Literature: Faid-Allah, Hassan M.; Mokhtar, Hassan M. Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 1988 , vol. 27, # 1-12 p. 245 - 249