MK-8353, 99.94%

cas: 1184173-73-6 — see every product listed under this CAS number, including other names

MK-8353, 99.94% (CAS 1184173-73-6) is a chemical reagent available from Chemat. Available pack sizes: 100 mg, 10mM/1mL, 50 mg, 1 mg, 10 mg, 25 mg, 5 mg. Offered by: MedChemExpress.

brandMedChemExpress
catalog numberHY-111407-100 mg
cas1184173-73-6
size100 mg
availability In stock
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Available pack sizes

brand size price
MedChemExpress 100 mg 8757.84 Pln
MedChemExpress 10mM/1mL 1531.78 Pln
MedChemExpress 50 mg 5878.56 Pln
MedChemExpress 1 mg 556.54 Pln
MedChemExpress 10 mg 1782.55 Pln
MedChemExpress 25 mg 3719.10 Pln
MedChemExpress 5 mg 1044.16 Pln

properties

delivery time 2-3 weeks
purity99.94%

MK-8353 is a member of the class of indazoles that is 1H-indazole substituted by a 6-(propan-2-yloxy)pyridin-3-yl group at position 3 and by a {[(3S)-3-(methylsulfanyl)-1-(2-{4-[4-(1-methyl-1H-1,2,4-triazol-3-yl)phenyl]-3,6-dihydropyridin-1(2H)-yl}-2-oxoethyl)pyrrolidin-3-yl]carbonyl}amino group at position 5. It is a potent and selective inhibitor of ERK1 and ERK2 in vitro (IC50 values of 23.0 nM and 8.8 nM, respectively). The drug is being developed by Merck Sharp & Dohme and is currently in clinical development for the treatment of advanced/metastatic solid tumors. It has a role as an antineoplastic agent, an apoptosis inducer and an EC 2.7.11.24 (mitogen-activated protein kinase) inhibitor. It is a secondary carboxamide, a tertiary carboxamide, a member of pyridines, an aromatic ether, a member of triazoles, a member of indazoles, a pyrrolidinecarboxamide, a N-alkylpyrrolidine, a dihydropyridine and a methyl sulfide.

Source: ChEBI

Identity
Molecular formulaC37H41N9O3S
Molecular weight691.8 g/mol
IUPAC name(3S)-3-methylsulfanyl-1-[2-[4-[4-(1-methyl-1,2,4-triazol-3-yl)phenyl]-3,6-dihydro-2H-pyridin-1-yl]-2-oxoethyl]-N-[3-(6-propan-2-yloxy-3-pyridinyl)-1H-indazol-5-yl]pyrrolidine-3-carboxamide
InChIKeyKPQQGHGDBBJGFA-QNGWXLTQSA-N
SMILESCC(C)OC1=NC=C(C=C1)C2=NNC3=C2C=C(C=C3)NC(=O)[C@@]4(CCN(C4)CC(=O)N5CCC(=CC5)C6=CC=C(C=C6)C7=NN(C=N7)C)SC

Computed by PubChem (NCBI)

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