1469777-40-9
1469777-40-9
Chemical Structure
Lumateperone metabolite 1
- CAS. Nr.: 1469777-40-9
- Formula:C23H28FN3O
- Molecular Weight:381.49
InChIKey: NUJKRFFWQXVMAM-QUCQDJGISA-N
SMILES: OC(C1=CC=C(C=C1)F)CCCN2C[C@@]3([H])C4=CC=CC5=C4N(CCN5)[C@@]3([H])CC2
Biological Activity: Lumateperone metabolite 1 (Formula T) is a metabolite of Lumateperone (HY-17637)[1]. Lumateperone (ITI-007) is an orally active 5-HT2A receptor antagonist (Ki = 0.54 nM), a partial agonist of presynaptic D2 receptors and an antagonist of postsynaptic D2 receptors (Ki = 32 nM), and a dopamine D1 receptor modulator[2][3]
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Lumateperone metabolite 1 | 98.26% | Lumateperone metabolite 1 (Formula T) is a metabolite of Lumateperone (HY-17637). Lumateperone (ITI-007) is an orally active 5-HT2A receptor antagonist (Ki = 0.54 nM), a partial agonist of presynaptic D2 receptors and an antagonist of postsynaptic D2 receptors (Ki = 32 nM), and a dopamine D1 receptor modulator | ||||||||||||||||||||
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References
- [1]. Sharon Mates, et al. Organic compounds. WO2015154025A1.
- [2]. Jinyuan Zhang, et al. Identification of Trovafloxacin, Ozanimod, and Ozenoxacin as Potent c-Myc G-quadruplex Stabilizers to Suppress c-Myc Transcription and Myeloma Growth. Mol Inform. 2022 Mar 30:e2200011. [Content Brief]
- [3]. J Titulaer, et al. Lumateperone-mediated effects on prefrontal glutamatergic receptor-mediated neurotransmission: A dopamine D1 receptor dependent mechanism. Eur Neuropsychopharmacol. 2022 Jul 22;62:22-35. [Content Brief]
