PF-3758309

Last updated

PF-3758309
PF-3758309 structure.png
Identifiers
  • N-[(1S)-2-(dimethylamino)-1-phenylethyl]-6,6-dimethyl-3-[(2-methylthieno[3,2-d]pyrimidin-4-yl)amino]-1,4-dihydropyrrolo[3,4-c]pyrazole-5-carboxamide
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard 100.231.337 OOjs UI icon edit-ltr-progressive.svg
Chemical and physical data
Formula C25H30N8OS
Molar mass 490.63 g·mol−1
3D model (JSmol)
  • CC1=NC2=C(C(=N1)NC3=NNC4=C3CN(C4(C)C)C(=O)N[C@H](CN(C)C)C5=CC=CC=C5)SC=C2
  • InChI=1S/C25H30N8OS/c1-15-26-18-11-12-35-20(18)23(27-15)29-22-17-13-33(25(2,3)21(17)30-31-22)24(34)28-19(14-32(4)5)16-9-7-6-8-10-16/h6-12,19H,13-14H2,1-5H3,(H,28,34)(H2,26,27,29,30,31)/t19-/m1/s1
  • Key:AYCPARAPKDAOEN-LJQANCHMSA-N

PF-3758309 is an experimental anticancer drug which acts as an inhibitor of p21-activated kinases with highest affinity for PAK4. It shows activity against a variety of different cancer types including colon, lung and pancreatic cancers, and is in early stage clinical trials. [1] [2] [3] [4] [5] [6] [7]

References

  1. ↑ Murray BW, Guo C, Piraino J, Westwick JK, Zhang C, Lamerdin J, et al. (May 2010). "Small-molecule p21-activated kinase inhibitor PF-3758309 is a potent inhibitor of oncogenic signaling and tumor growth". Proceedings of the National Academy of Sciences of the United States of America. 107 (20): 9446–9451. Bibcode:2010PNAS..107.9446M. doi: 10.1073/pnas.0911863107 . PMC   2889050 . PMID   20439741.
  2. ↑ Senapedis W, Crochiere M, Baloglu E, Landesman Y (2016). "Therapeutic Potential of Targeting PAK Signaling". Anti-Cancer Agents in Medicinal Chemistry. 16 (1): 75–88. doi:10.2174/1871520615666150617111414. PMID   26081410.
  3. ↑ Li Z, Li X, Xu L, Tao Y, Yang C, Chen X, et al. (November 2017). "Inhibition of neuroblastoma proliferation by PF-3758309, a small-molecule inhibitor that targets p21-activated kinase 4". Oncology Reports. 38 (5): 2705–2716. doi:10.3892/or.2017.5989. PMC   5780023 . PMID   29048629.
  4. ↑ Wang K, Huynh N, Wang X, Pajic M, Parkin A, Man J, et al. (2019). "PAK inhibition by PF-3758309 enhanced the sensitivity of multiple chemotherapeutic reagents in patient-derived pancreatic cancer cell lines". American Journal of Translational Research. 11 (6): 3353–3364. PMC   6614655 . PMID   31312349.
  5. ↑ Li Y, Lu Q, Xie C, Yu Y, Zhang A (2022). "Recent advances on development of p21-activated kinase 4 inhibitors as anti-tumor agents". Frontiers in Pharmacology. 13: 956220. doi: 10.3389/fphar.2022.956220 . PMC   9465411 . PMID   36105226.
  6. ↑ Zhao CC, Zhan MN, Liu WT, Jiao Y, Zhang YY, Lei Y, et al. (November 2020). "Combined LIM kinase 1 and p21-Activated kinase 4 inhibitor treatment exhibits potent preclinical antitumor efficacy in breast cancer". Cancer Letters. 493: 120–127. doi:10.1016/j.canlet.2020.08.006. PMID   32829006.
  7. ↑ Nagel A, Huegel J, Petrilli A, Rosario R, Victoria B, Hardin HM, et al. (March 2024). "Simultaneous inhibition of PI3K and PAK in preclinical models of neurofibromatosis type 2-related schwannomatosis". Oncogene. 43 (13): 921–930. doi:10.1038/s41388-024-02958-w. PMC   10959746 . PMID   38336988.
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