(S)-Tomoxetine-d3 hydrochloride xy-3-prenyl-2-naphthoate Smiles: CC(C)C[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC1=CC=C(O)C=C1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCCN)NC(=O)[C@@H](N)CCCCN)[C@@H](C)CC)C(O)=O

Smiles: CC(C)C[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC1=CC=C(O)C=C1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCCN)NC(=O)[C@@H](N)CCCCN)[C@@H](C)CC)C(O)=O

no time-dependent inactivation of the five major cytochrome P450 enzymes is discernible with CP-671

CPI-455 has improved potency against KDM5A while demonstrating ~200-fold selectivity for KDM5A over KDM4C

In the acute quinpirole rats

Upregulation of orphan nuclear receptor Nur77 following PGF(2alpha)

(S)-Tomoxetine-d3 hydrochloride xy-3-prenyl-2-naphthoate Smiles: CC(C)C[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC1=CC=C(O)C=C1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCCN)NC(=O)[C@@H](N)CCCCN)[C@@H](C)CC)C(O)=OProduct information CAS Number: 1217703 95 1 Molecular Weight: 294. 83 Formula: C17H22ClNO Chemical Name: (H)methyl[(3S) 3 (2 methylphenoxy) 3 phenylpropyl]amine hydrochloride Smiles: Cl.[2H]C([2H])([2H])NCC[C@H](OC1=CC=CC=C1C)C1C=CC=CC=1 InChiKey: LUCXVPAZUDVVBT GJILKALXSA N InChi: InChI=1S C17H21NO. ClH c1 14 8 6 7 11 16(14)19 17(12 13 18 2)15 9 4 3 5 10 15; h3 11,17 18H,12 13H2,1 2H3; 1H t17 ; m0. s1 i2D3; Technical Data Appearance: Solid Power