For research use only. Not for therapeutic Use.
PA-8 (Cat No.: I034142) is a synthetic compound known for its potent anti-inflammatory and neuroprotective properties. It functions primarily as a selective inhibitor of histone deacetylase 6 (HDAC6), an enzyme involved in protein degradation, cell motility, and stress response pathways. By inhibiting HDAC6, PA-8 modulates acetylation of tubulin and other cytoplasmic substrates, showing promise in treating neurodegenerative diseases and certain cancers. Its selectivity minimizes off-target effects commonly seen with broad-spectrum HDAC inhibitors, making PA-8 a valuable candidate for therapeutic research and drug development.
CAS Number | 878437-15-1 |
Synonyms | 2-amino-5-(3-methoxy-4-prop-2-enoxyphenyl)-3,5,6,8-tetrahydropyrido[2,3-d]pyrimidine-4,7-dione |
Molecular Formula | C17H18N4O4 |
Purity | ≥95% |
InChI | InChI=1S/C17H18N4O4/c1-3-6-25-11-5-4-9(7-12(11)24-2)10-8-13(22)19-15-14(10)16(23)21-17(18)20-15/h3-5,7,10H,1,6,8H2,2H3,(H4,18,19,20,21,22,23) |
InChIKey | DCSWTWUTSKSXOV-UHFFFAOYSA-N |
SMILES | COC1=C(C=CC(=C1)C2CC(=O)NC3=C2C(=O)NC(=N3)N)OCC=C |
Reference | [1]. Ichiro Takasaki, et al. In Silico Screening Identified Novel Small-molecule Antagonists of PAC1 Receptor. J Pharmacol Exp Ther. 2018 Apr;365(1):1-8. [2]. Ichiro Takasaki, et al. The novel small-molecule antagonist of PAC1 receptor attenuates formalin-induced inflammatory pain behaviors in mice. J Pharmacol Sci. 2019 Feb;139(2):129-132. |
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