VU0119498

• CAT Number: I038139
• CAS Number: 79183-37-2
• Molecular Formula: C15H10BrNO2
• Molecular Weight: 316.15
• Purity: 98%
• Synonyms: VU0119498, VU 0119498, VU-0119498
• Target: Neuronal Signaling
• Solubility: Soluble in DMSO
• Appearance: Solid powder
• Storage: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
• IUPAC Name: 1-[(4-bromophenyl)methyl]indole-2,3-dione
• InChI: InChI=1S/C15H10BrNO2/c16-11-7-5-10(6-8-11)9-17-13-4-2-1-3-12(13)14(18)15(17)19/h1-8H,9H2
• InChIKey: DELLOEULSHGYCG-UHFFFAOYSA-N
• SMILES: O=C1N(CC2=CC=C(Br)C=C2)C3=C(C=CC=C3)C1=O

VU0119498 (CAT: I038139) is a compound that acts as an agonist of the M1 muscarinic receptor and a positive allosteric modulator (PAM) of pan mAChR M3 and M5 receptors. It exhibits an EC50 value of 3.1 μM for M1 receptor activation. By targeting these receptors, VU0119498 can modulate cholinergic neurotransmission in the central nervous system. Additionally, VU0119498 has shown potential as a neuroprotective agent, suggesting its ability to protect neuronal cells from damage or degeneration.

Reference

1: Bridges TM, Kennedy JP, Hopkins CR, Conn PJ, Lindsley CW. Heterobiaryl and heterobiaryl ether derived M5 positive allosteric modulators. Bioorg Med Chem Lett. 2010 Oct 1;20(19):5617-22. doi: 10.1016/j.bmcl.2010.08.042. Epub 2010 Aug 12. PubMed PMID: 20801651; PubMed Central PMCID: PMC3179183.
2: Bridges TM, Phillip Kennedy J, Noetzel MJ, Breininger ML, Gentry PR, Conn PJ, Lindsley CW. Chemical lead optimization of a pan Gq mAChR M1, M3, M5 positive allosteric modulator (PAM) lead. Part II: development of a potent and highly selective M1 PAM. Bioorg Med Chem Lett. 2010 Mar 15;20(6):1972-5. doi: 10.1016/j.bmcl.2010.01.109. Epub 2010 Feb 1. PubMed PMID: 20156687; PubMed Central PMCID: PMC2834874.
3: Bridges TM, Kennedy JP, Cho HP, Breininger ML, Gentry PR, Hopkins CR, Conn PJ, Lindsley CW. Chemical lead optimization of a pan G(q) mAChR M(1), M(3), M(5) positive allosteric modulator (PAM) lead. Part I: Development of the first highly selective M(5) PAM. Bioorg Med Chem Lett. 2010 Jan 15;20(2):558-62. doi: 10.1016/j.bmcl.2009.11.089. Epub 2009 Nov 22. PubMed PMID: 20004578; PubMed Central PMCID: PMC3177601.
4: Bridges TM, Marlo JE, Niswender CM, Jones CK, Jadhav SB, Gentry PR, Plumley HC, Weaver CD, Conn PJ, Lindsley CW. Discovery of the first highly M5-preferring muscarinic acetylcholine receptor ligand, an M5 positive allosteric modulator derived from a series of 5-trifluoromethoxy N-benzyl isatins. J Med Chem. 2009 Jun 11;52(11):3445-8. doi: 10.1021/jm900286j. PubMed PMID: 19438238; PubMed Central PMCID: PMC3875304.