ChemicalBook >> CAS DataBase List >>MethanesulfonaMide, N-[3-[[[2-[(2,3-dihydro-2-oxo-1H-indol-5-yl)aMino]-5-(trifluoroMethyl)-4-pyriMidinyl]aMino]Methyl]-2-pyridinyl]-N-Methyl-, hydrochloride (1:1)

MethanesulfonaMide, N-[3-[[[2-[(2,3-dihydro-2-oxo-1H-indol-5-yl)aMino]-5-(trifluoroMethyl)-4-pyriMidinyl]aMino]Methyl]-2-pyridinyl]-N-Methyl-, hydrochloride (1:1)

CAS No.
939791-41-0
Chemical Name:
MethanesulfonaMide, N-[3-[[[2-[(2,3-dihydro-2-oxo-1H-indol-5-yl)aMino]-5-(trifluoroMethyl)-4-pyriMidinyl]aMino]Methyl]-2-pyridinyl]-N-Methyl-, hydrochloride (1:1)
Synonyms
PF-562271 HCl ,S7357;PF-562271 hydrochloride;PF562271 HCL;PF 562271 HCL;PF562271 hydrochloride. PF271, PF-271, PF 271;N-methyl-N-(3-{[2-(2-oxo-2,3-dihydro-1H-indol-5-ylamino)-5-trifluoromethylpyrimidin-4-ylamino]methyl}pyridin-2-yl)methanesulfonamide hydrochloride;PF562271; PF562271; PF-562271; PF562,271; PF562,271; PF-562,271; PF-00562271; PF00562271; PF 00562271; PF562271 HYDROCHLORIDE. PF271, PF-271, PF 271;N-methyl-N-[3-[[[2-[(2-oxo-1,3-dihydroindol-5-yl)amino]-5-(trifluoromethyl)pyrimidin-4-yl]amino]methyl]pyridin-2-yl]methanesulfonamide:hydrochloride;MethanesulfonaMide, N-[3-[[[2-[(2,3-dihydro-2-oxo-1H-indol-5-yl)aMino]-5-(trifluoroMethyl)-4-pyriMidinyl]aMino]Methyl]-2-pyridinyl]-N-Methyl-, hydrochloride (1:1);Proline-rich tyrosine kinase 2,Ewing,inhibit,Antitumor,PF-562271,Focal adhesion kinase,Sarcoma,FAK,VS-6062(hydrochloride),PTK2 protein tyrosine kinase 2,Pyk2,PF562271 hydrochloride,PTK2,PF 562271,PF562271,Cancer,PF 562271 hydrochloride,Inhibitor,Breast
CBNumber:
CB82667582
Molecular Formula:
C21H21ClF3N7O3S
Molecular Weight:
543.95
MDL Number:
MFCD17170115
MOL File:
939791-41-0.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-04-24 14:58:19
Product description Number Pack Size Price
PF-562271 HCl PMB79141 10mg $527.8
PF-562271 HCl PMB79141 25mg $989.5
PF-562271 HCl PMB79141 50mg $1583.5
PF-562271 HCl PMB79141 100mg $2535
PF-562271 hydrochloride 98.10% CS-0008668 5mg $171
More product size

MethanesulfonaMide, N-[3-[[[2-[(2,3-dihydro-2-oxo-1H-indol-5-yl)aMino]-5-(trifluoroMethyl)-4-pyriMidinyl]aMino]Methyl]-2-pyridinyl]-N-Methyl-, hydrochloride (1:1) Properties

storage temp. Store at -20°C
solubility ≥26.35 mg/mL in DMSO with gentle warming; insoluble in H2O; insoluble in EtOH
form solid

MethanesulfonaMide, N-[3-[[[2-[(2,3-dihydro-2-oxo-1H-indol-5-yl)aMino]-5-(trifluoroMethyl)-4-pyriMidinyl]aMino]Methyl]-2-pyridinyl]-N-Methyl-, hydrochloride (1:1) price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biosynth PMB79141 PF-562271 HCl 939791-41-0 10mg $527.8 2026-06-04 Buy
Biosynth PMB79141 PF-562271 HCl 939791-41-0 25mg $989.5 2026-06-04 Buy
Biosynth PMB79141 PF-562271 HCl 939791-41-0 50mg $1583.5 2026-06-04 Buy
Biosynth PMB79141 PF-562271 HCl 939791-41-0 100mg $2535 2026-06-04 Buy
ChemScene CS-0008668 PF-562271 hydrochloride 98.10% 939791-41-0 5mg $171 2026-06-04 Buy
Product number Packaging Price Buy
PMB79141 10mg $527.8 Buy
PMB79141 25mg $989.5 Buy
PMB79141 50mg $1583.5 Buy
PMB79141 100mg $2535 Buy
CS-0008668 5mg $171 Buy

MethanesulfonaMide, N-[3-[[[2-[(2,3-dihydro-2-oxo-1H-indol-5-yl)aMino]-5-(trifluoroMethyl)-4-pyriMidinyl]aMino]Methyl]-2-pyridinyl]-N-Methyl-, hydrochloride (1:1) Chemical Properties,Uses,Production

Uses

PF-562271 (VS-6062) hydrochloride is a potent, ATP-competitive and reversible FAK and Pyk2 kinase inhibitor with IC50s of 1.5 nM and 13 nM, respectively[1].

Biological Activity

pf-562271 is a potent, atp-competitive and reversible inhibitor of both focal adhesion kinase (fak), a non-receptor tyrosine kinase involved in a variety of cellular events, and proline-rich tyrosine kinase 2 (pyk2), an fak homolog containing 48% amino acid identity, with half maximal inhibitory concentration (ic50) of 1.5 nmol/l and 14 nmol/l respectively. as a potential therapeutic agent either alone or in combination with other agents for the treatment of cancer, pf-562271 has been reported to effectively inhibit the proliferation of tumors in both xenograft and transgenic mouse models, in which it dose-dependently inhibits fak phosphorylation in tumor-bearing mice with half maximal effective concentration (ec50) of 93 ng/ml.

in vivo

PF-562271 inhibits FAK phosphorylation in vivo in a dose-dependent fashion (calculated EC50 of 93 ng/mL, total) after p.o. administration to tumor-bearing mice[1]. Rats that receive PF-562271 demonstrate a decrease in tumor growth after 2 weeks of treatment with signs of bone healing as evidenced by the deposition of new bone (cortical and cancellous) at sites previously damaged by the tumor[3].

References

[1]stokes jb, adair sj, slack-davis jk, walters dm, tilghman rw, hershey ed, lowrey b, thomas ks, bouton ah, hwang rf, stelow eb, parsons jt, bauer tw. inhibition of focal adhesion kinase by pf-562,271 inhibits the growth and metastasis of pancreatic cancer concomitant with altering the tumor microenvironment. mol cancer ther. 2011 nov;10(11):2135-45. doi: 10.1158/1535-7163.mct-11-0261. epub 2011 sep 8.
[2]roberts wg, ung e, whalen p, cooper b, hulford c, autry c, richter d, emerson e, lin j, kath j, coleman k, yao l, martinez-alsina l, lorenzen m, berliner m, luzzio m, patel n, schmitt e, lagreca s, jani j, wessel m, marr e, griffor m, vajdos f. antitumor activity and pharmacology of a selective focal adhesion kinase inhibitor, pf-562,271. cancer res. 2008 mar 15;68(6):1935-44. doi: 10.1158/0008-5472.can-07-5155.

MethanesulfonaMide, N-[3-[[[2-[(2,3-dihydro-2-oxo-1H-indol-5-yl)aMino]-5-(trifluoroMethyl)-4-pyriMidinyl]aMino]Methyl]-2-pyridinyl]-N-Methyl-, hydrochloride (1:1) Preparation Products And Raw materials

Raw materials

Preparation Products

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MethanesulfonaMide, N-[3-[[[2-[(2,3-dihydro-2-oxo-1H-indol-5-yl)aMino]-5-(trifluoroMethyl)-4-pyriMidinyl]aMino]Methyl]-2-pyridinyl]-N-Methyl-, hydrochloride (1:1) Spectrum

MethanesulfonaMide, N-[3-[[[2-[(2,3-dihydro-2-oxo-1H-indol-5-yl)aMino]-5-(trifluoroMethyl)-4-pyriMidinyl]aMino]Methyl]-2-pyridinyl]-N-Methyl-, hydrochloride (1:1) N-methyl-N-[3-[[[2-[(2-oxo-1,3-dihydroindol-5-yl)amino]-5-(trifluoromethyl)pyrimidin-4-yl]amino]methyl]pyridin-2-yl]methanesulfonamide:hydrochloride PF562271 hydrochloride. PF271, PF-271, PF 271 PF562271; PF562271; PF-562271; PF562,271; PF562,271; PF-562,271; PF-00562271; PF00562271; PF 00562271; PF562271 HYDROCHLORIDE. PF271, PF-271, PF 271 PF562271 HCL;PF 562271 HCL N-methyl-N-(3-{[2-(2-oxo-2,3-dihydro-1H-indol-5-ylamino)-5-trifluoromethylpyrimidin-4-ylamino]methyl}pyridin-2-yl)methanesulfonamide hydrochloride PF-562271 hydrochloride Proline-rich tyrosine kinase 2,Ewing,inhibit,Antitumor,PF-562271,Focal adhesion kinase,Sarcoma,FAK,VS-6062(hydrochloride),PTK2 protein tyrosine kinase 2,Pyk2,PF562271 hydrochloride,PTK2,PF 562271,PF562271,Cancer,PF 562271 hydrochloride,Inhibitor,Breast PF-562271 HCl ,S7357 939791-41-0 C21H20F3N7O3SClH