Seletracetam lithium bromide uanide hydrochloride Smiles: C[C@@H]1C[C@H]2[C@@H]3C[C@H](F)C4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@H]1C(=O)COC(=O)CCCC

Smiles: C[C@@H]1C[C@H]2[C@@H]3C[C@H](F)C4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@H]1C(=O)COC(=O)CCCC

thereby blocking the conversion of cholesterol to pregnenolone and the peripheral aromatization of androgenic precursors into estrogens

InChi: InChI=1S/C18H13F3N4O2/c19-18(20

3)35-21(26)20-34-19-18-33-17-16-32-15-14-31-13-12-30-11-10-29-9-8-28-7-6-27-5-4-24-25-23/h4-20H2

InChiKey: AWSXISOALMMMQQ-UHFFFAOYSA-N

Seletracetam lithium bromide uanide hydrochloride Smiles: C[C@@H]1C[C@H]2[C@@H]3C[C@H](F)C4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]2(C)[C@H]1C(=O)COC(=O)CCCCSeletracetam (Ucb 44212) lithium bromide, an analog of the antiepileptic agent Levetiracetam, is a SV2A modulator for the research of epilepsy. Product information CAS Number: 2024584 38 9 Molecular Weight: 275. 65 Formula: C20H28BrF4LiN4O4 Chemical Name: bis((2S) 2 [(4S) 4 (2,2 difluoroethenyl) 2 oxopyrrolidin 1 yl]butanamide); bromolithium Smiles: [Li]Br. CC[C@@H](C(N)=O)N1C[C@@H](CC1=O)C=C(F)F. CC[C@@H](C(N)=O)N1C[C@@H](CC1=O)C=C(F)F InChiKey: