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ChemicalBook--->CAS DataBase List--->212631-79-3

212631-79-3

212631-79-3 Structure

212631-79-3 Structure
IdentificationBack Directory
[Name]

PD184352
[CAS]

212631-79-3
[Synonyms]

CS-333
Ci-1040
PD184352
PD 184352, >=98%
PD184352 USP/EP/BP
CI-1040, PD-184352
PD 184352;CI-1040;PD-184352
CI1040;PD-184352; CI 1040 (PD184352)
2-[(2-CHLORO-4-IODOPHENYL) AMINO]-N-(CYCLOPROPYLME
2-(2-CHLORO-4-IODOANILINO)-N-(CYCLOPROPYLMETHOXY)-3,4-DIFLUOROBENZAMIDE
3,4-Difluoro-2-(2-chloro-4-iodophenylaMino)-N-cyclopropylMethoxybenzaMide
2-[(2-Chloro-4-iodophenyl)amino]-N-(cyclopropylmethoxy)-3,4-difluorobenzamide
Benzamide, 2-[(2-chloro-4-iodophenyl)amino]-N-(cyclopropylmethoxy)-3,4-difluoro-
CI-10402-(2-chloro-4-iodophenylamino)-N-(cyclopropylmethoxy)-3,4-difluorobenzamide
2-(2-Chloro-4-iodophenylamino)-N-(cyclopropylmethoxy)-3,4-difluorobenzamide PD184352
[Molecular Formula]

C17H14ClF2IN2O2
[MDL Number]

MFCD02683961
[MOL File]

212631-79-3.mol
[Molecular Weight]

478.66
Chemical PropertiesBack Directory
[Melting point ]

166-169°C
[density ]

1.747±0.06 g/cm3(Predicted)
[storage temp. ]

-20°C Freezer
[solubility ]

DMSO: ≥30mg/mL
[form ]

powder
[pka]

-5.58±0.50(Predicted)
[color ]

white to tan
Safety DataBack Directory
[Hazard Codes ]

N
[Risk Statements ]

50/53
[Safety Statements ]

60-61
[RIDADR ]

UN 3077 9 / PGIII
[WGK Germany ]

3
[HS Code ]

2924297099
Hazard InformationBack Directory
[Chemical Properties]

Off-White to Pale Beige Solid
[Uses]

An inhibitor of ERK signaling pathway. A MAP kinase inhibitor
[Definition]

ChEBI: 2-(2-chloro-4-iodoanilino)-N-(cyclopropylmethoxy)-3,4-difluorobenzamide is an aminobenzoic acid.
[Biological Activity]

Potent and selective inhibitor of MAPK (ERK kinase 1; MEK1) activation (IC50=300nM in vitro, IC50=2nM in vivo). Suppresses activation of MAPK but does not block its activity. Strongly suppresses growth of human implanted colon tumors in mice.
[Biochem/physiol Actions]

PD184352 (CI-1040) is a highly selective non-competitive inhibitor of MEK (MKK1; MAPK kinase) and the closely related MKK2. It has anti-cancer activity, suppresses the ERK pathway, and has been used along with other classes of inhibitors to establish embryonic stem cell lines.
[Enzyme inhibitor]

This substituted benzamide (FW = 478.66 g/mol), also known as 2- (chloro- 4-iodophenylamino) -N-cyclopropylmethoxy-3,4-difluorobenzamide and CI- 1040, inhibits ERK activation, IC50 = 16 nM.
[storage]

Store at -20°C
[References]

[1] frémin c, meloche s. from basic research to clinical development of mek1/2 inhibitors for cancer therapy. j hematol oncol. 2010 feb 11;3:8. doi: 10.1186/1756-8722-3-8.
Spectrum DetailBack Directory
[Spectrum Detail]

PD184352(212631-79-3)1HNMR
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