(R)-Thalidomide loperidone Hydrochloride 95)/b17-12+/t30-

95)/b17-12+/t30-

intragastric gavage once daily for 15 d) inhibits the growth of melanoma tumors dramatically in mice

leading to a concomitant increase of the endogenous cellular dhCer content

Hexylresorcinol potently inhibits Gram positive bacteria

Smiles: C[C@]12CC[C@@H](CC1=CC[C@@H]1[C@@H]2CC[C@@]2(C)[C@H]1C[C@@H]1O[C@]3(CC[C@@H](C)CO3)[C@@H](C)[C@]21O)O[C@@H]1O[C@H](CO)[C@@H](O[C@@H]2O[C@@H](C)[C@H](O)[C@@H](O)[C@H]2O)[C@H](O)[C@H]1O[C@@H]1O[C@@H](C)[C@H](O)[C@@H](O)[C@H]1O

(R)-Thalidomide loperidone Hydrochloride 95)/b17-12+/t30-(R) Thalidomide ((R) (+) Thalidomide) is the R enantiomer of Thalidomide. (R) Thalidomide has sedative properties. Product information CAS Number: 2614 06 4 Molecular Weight: 258. 23 Formula: C13H10N2O4 Chemical Name: 2 [(3R) 2,6 dioxopiperidin 3 yl] 2,3 dihydro 1H isoindole 1,3 dione Smiles: O=C1CC[C@H](C(=O)N1)N1C(=O)C2C=CC=CC=2C1=O InChiKey: UEJJHQNACJXSKW SECBINFHSA N InChi: InChI=1S C13H10N2O4 c16 10 6 5 9(11(17)14 10)15 12(18)7 3 1 2 4