Chemical structure of CAS 391210-10-9

N-((2R)-2,3-Dihydroxypropoxy)-3,4-difluoro-2-((2-fluoro-4-iodophenyl)amino)benzamide

CAS No.391210-10-9
MDL No.MFCD08435926
MFC16H14F3IN2O4
MW482.19
InChI KeySUDAHWBOROXANE-SECBINFHSA-N

Pricing & Availability

Pack SizePurityPriceAvailabilityAction
- -On RequestOn Request
Custom synthesis and bulk supply options are available upon request.

Product Information

PD 0325901 is a hydroxamic acid ester derived from benzhydroxamic acid (N-hydroxybenzamide), with the hydroxamic acid group converted to a 2,3-dihydroxypropyl ester. The benzene ring is substituted at position 2 with a (2-fluoro-4-iodophenyl)amino group and at positions 3 and 4 with fluorines (R enantiomer). It functions as an EC 2.7.12.2 (mitogen-activated protein kinase kinase) inhibitor and an antineoplastic agent. It is also a secondary amino compound, a monofluorobenzene, an organoiodine compound, a propane-1,2-diol, and a difluorobenzene.

CAS No.391210-10-9
Product NameN-((2R)-2,3-Dihydroxypropoxy)-3,4-difluoro-2-((2-fluoro-4-iodophenyl)amino)benzamide

Biological Targets

MAP2K1·MAP2K2

Associated Conditions

cancer·low grade glioma·colorectal cancer·neurofibromatosis type 1·neoplasm·
* The information provided here is compiled from public sources and is for reference only.