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PZ0112

Sigma-Aldrich

PD-184161

≥98% (HPLC)

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Synonym(s):
5-Bromo-2-[(2-chloro-4-iodophenyl)amino]-N-(cyclopropylmethoxy)-3,4-difluoro-benzamide, PF-1529483, PF-3011370, UK-287074
Empirical Formula (Hill Notation):
C17H13BrClF2IN2O2
CAS Number:
212631-67-9
Molecular Weight:
557.56
MDL number:
MFCD16038897
PubChem Substance ID:
329823704

Quality Level

100

Assay

≥98% (HPLC)

form

powder

color

white to off-white

solubility

DMSO: >10 mg/mL

storage temp.

2-8°C

SMILES string

Fc1c(F)c(Nc2ccc(I)cc2Cl)c(cc1Br)C(=O)NOCC3CC3

InChI

1S/C17H13BrClF2IN2O2/c18-11-6-10(17(25)24-26-7-8-1-2-8)16(15(21)14(11)20)23-13-4-3-9(22)5-12(13)19/h3-6,8,23H,1-2,7H2,(H,24,25)

InChI key

VJNZMSLGVUSPCF-UHFFFAOYSA-N

Biochem/physiol Actions

PD-184161 is a MEK inhibitor.

Features and Benefits

This compound is featured on the MAPKKKs page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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A Dushani C U Ranasinghe et al.
Biochimica et biophysica acta. Molecular and cell biology of lipids, 1865(12), 158789-158789 (2020-08-11)
Phosphorylation of sphingosine by sphingosine kinase 1 (SPHK1) produces the bioactive sphingolipid sphingosine-1-phosphate (S1P), a microvascular and immuno-modulator associated with vascular remodeling in pulmonary arterial hypertension (PAH). The low intracellular concentration of S1P is under tight spatial-temporal control. Molecular mechanisms
Akikazu Harada et al.
eLife, 10 (2021-10-01)
Pancreatic cancer has a high mortality rate due to metastasis. Whereas KRAS is mutated in most pancreatic cancer patients, controlling KRAS or its downstream effectors has not been succeeded clinically. ARL4C is a small G protein whose expression is induced
Zhengxi Wei et al.
Toxicology and applied pharmacology, 289(1), 98-108 (2015-09-20)
Cadmium (Cd) is a carcinogenic metal which is implicated in breast cancer by epidemiological studies. It is reported to promote breast cancer cell growth in vitro through membrane receptors. The study described here examined Cd-mediated growth of non-metastatic human breast

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