S-Venlafaxine (C007B-572953)

S-Venlafaxine is an optically active version of Venlafaxine . Venlafaxine is a derivative of phenylethylamine which is reported to facilitate neurotransmission within the central nervous system via blocking the presynaptic reuptake of neuroamines such as serotonin (5-hydroxytryptamine; 5-HT) and noradrenaline (norepinephrine). Venlafaxine is also reported to be a weak inhibitor of dopamine reuptake.|In vitro|studies indicate that Venlafaxine does not demonstrate significant activity for muscarinic, histaminergic or α-1 adrenergic receptors. The metabolism of venlafaxine is reported to occur by cytochrome P450 (CYP) enzyme CYP2D6 yielding O-desmethylvenlafaxine. A lesser metabolite, N-desmethylvenlafaxine is produced by CYP3A4.

Specifictaions: ≥95%

MDL Number: C17H27NO2

Molecular Formula: 277.4

PubChem CID: 11846746

Isomeric SMILES: CN(C)C[C@H](C1=CC=C(C=C1)OC)C2(CCCCC2)O

Related Documents: https://ald-pub-files.oss-cn-shanghai.aliyuncs.com/aladdinsci/pdp/sds/1/S357810-SCI_80b460e799b55b6a5a5cf220bb3847d7.pdf