Determine the necessary mass, volume, or concentration for preparing a solution.
Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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F286996-5mg | 5mg | In stock | $70.90 | |
F286996-10mg | 10mg | In stock | $118.90 | |
F286996-25mg | 25mg | In stock | $267.90 | |
F286996-50mg | 50mg | In stock | $434.90 | |
F286996-100mg | 100mg | In stock | $587.90 | |
F286996-250mg | 250mg | In stock | $1,323.90 |
Potent PAK inhibitor
Specifications & Purity | Moligand™, ≥96% |
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Biochemical and Physiological Mechanisms | Potent p21-activated kinase (PAK) inhibitor (IC50 values of 14, 33, 39 and 575 nM for PAK1, PAK2, PAK3 and PAK4, respectively). Blocks and reverses DISC1 knockdown-induced reduction in dendritic spine size in cortical neurons. Attenuates dendritic spine |
Storage Temp | Store at -20°C |
Shipped In | Ice chest + Ice pads |
Grade | Moligand™ |
Action Type | INHIBITOR |
Mechanism of action | Inhibitor of p21 (RAC1) activated kinase 1;Inhibitor of p21 (RAC1) activated kinase 2;Inhibitor of p21 (RAC1) activated kinase 3;Inhibitor of p21 (RAC1) activated kinase 4 |
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Pubchem Sid | 488202115 |
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Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488202115 |
IUPAC Name | 6-(2,4-dichlorophenyl)-8-ethyl-2-(3-fluoro-4-piperazin-1-ylanilino)pyrido[2,3-d]pyrimidin-7-one |
INCHI | InChI=1S/C25H23Cl2FN6O/c1-2-34-23-15(11-19(24(34)35)18-5-3-16(26)12-20(18)27)14-30-25(32-23)31-17-4-6-22(21(28)13-17)33-9-7-29-8-10-33/h3-6,11-14,29H,2,7-10H2,1H3,(H,30,31,32) |
InChi Key | DHKFOIHIUYFSOF-UHFFFAOYSA-N |
Canonical SMILES | CCN1C2=NC(=NC=C2C=C(C1=O)C3=C(C=C(C=C3)Cl)Cl)NC4=CC(=C(C=C4)N5CCNCC5)F |
Isomeric SMILES | CCN1C2=NC(=NC=C2C=C(C1=O)C3=C(C=C(C=C3)Cl)Cl)NC4=CC(=C(C=C4)N5CCNCC5)F |
PubChem CID | 68060125 |
Molecular Weight | 513.39 |
PubChem CID | 68060125 |
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CAS Registry No. | 1232030-35-1 |
RCSB PDB Ligand | 981 |
PubChem SID | 488202115 |
Enter Lot Number to search for COA:
Find and download the COA for your product by matching the lot number on the packaging.
Lot Number | Certificate Type | Date | Item |
---|---|---|---|
C23311074 | Certificate of Analysis | Jan 16, 2023 | F286996 |
C23311075 | Certificate of Analysis | Jan 16, 2023 | F286996 |
C23311076 | Certificate of Analysis | Jan 16, 2023 | F286996 |
C23311077 | Certificate of Analysis | Jan 16, 2023 | F286996 |
C23311078 | Certificate of Analysis | Jan 16, 2023 | F286996 |
C23311079 | Certificate of Analysis | Jan 16, 2023 | F286996 |
C23311080 | Certificate of Analysis | Jan 16, 2023 | F286996 |
C23311081 | Certificate of Analysis | Jan 16, 2023 | F286996 |
C23311082 | Certificate of Analysis | Jan 16, 2023 | F286996 |
C23311083 | Certificate of Analysis | Jan 16, 2023 | F286996 |
C23311084 | Certificate of Analysis | Jan 16, 2023 | F286996 |
C2331390 | Certificate of Analysis | Jan 16, 2023 | F286996 |
Solubility | Solvent:DMSO, Max Conc. mg/mL: 10.27, Max Conc. mM: 20 |
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1. Dolan BM, Duron SG, Campbell DA, Vollrath B, Shankaranarayana Rao BS, Ko HY, Lin GG, Govindarajan A, Choi SY, Tonegawa S. (2013) Rescue of fragile X syndrome phenotypes in Fmr1 KO mice by the small-molecule PAK inhibitor FRAX486.. Proc Natl Acad Sci USA, 110 (14): (5671-6). [PMID:23509247] |
2. Hayashi-Takagi A, Araki Y, Nakamura M, Vollrath B, Duron SG, Yan Z, Kasai H, Huganir RL, Campbell DA, Sawa A. (2014) PAKs inhibitors ameliorate schizophrenia-associated dendritic spine deterioration in vitro and in vivo during late adolescence.. Proc Natl Acad Sci USA, 111 (17): (6461-6). [PMID:24706880] |
3. Dittmar M, Lee JS, Whig K, Segrist E, Li M, Kamalia B, Castellana L, Ayyanathan K, Cardenas-Diaz FL, Morrisey EE et al.. (2021) Drug repurposing screens reveal cell-type-specific entry pathways and FDA-approved drugs active against SARS-Cov-2.. Cell Rep, 129 (3): (108959). [PMID:33811811] |