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is more active than Thalidomide and is much more stable for hydrolysis
Formula: C19H21IN2O
InChi: InChI=1S/C38H40O18/c1-50-22-11-16(3-9-19(22)41)4-10-27(43)52-15-26-31(45)33(47)35(49)38(55-26)56-37-34(48)30(44)25(14-39)54-36(37)29-23(51-2)13-24-28(32(29)46)20(42)12-21(53-24)17-5-7-18(40)8-6-17/h3-13
In the acute quinpirole rats
no time-dependent inactivation of the five major cytochrome P450 enzymes is discernible with CP-671
(S)-Tomoxetine-d3 hydrochloride xy-3-prenyl-2-naphthoate is more active than ThalidomideProduct 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
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