Levocetirizine Dihydrochloride Catalog No.:M14939-2 Smiles: C[C@@H]1O[C@@H](O[C@@H]2[C@@H](CO[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)O[C@@H](O[C@H]3CC[C@]4(C)[C@H]5C=C[C@]67OC[C@@]8(CCC(C)(C)C[C@H]86)[C@@H](O)C[C@@]7(C)[C@]5(C)CC[C@H]4C3(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@H](O)[C@H]1O

Smiles: C[C@@H]1O[C@@H](O[C@@H]2[C@@H](CO[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)O[C@@H](O[C@H]3CC[C@]4(C)[C@H]5C=C[C@]67OC[C@@]8(CCC(C)(C)C[C@H]86)[C@@H](O)C[C@@]7(C)[C@]5(C)CC[C@H]4C3(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@H](O)[C@H]1O

Smiles: C(NCCNCC1C=CC(=CC=1)C1C=CC=CN=1)C1C=CC(=CC=1)C1C=CC=CN=1

Effects of Sphondin

Dihydrochelerythrine appeared to be less cytotoxic since the viability of cells exposed to 20 microM dihydrochelerythrine for 24h was reduced only to 53%

difluprednate is sometimes abbreviated DFBA

Levocetirizine Dihydrochloride Catalog No.:M14939-2 Smiles: C[C@@H]1O[C@@H](O[C@@H]2[C@@H](CO[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)O[C@@H](O[C@H]3CC[C@]4(C)[C@H]5C=C[C@]67OC[C@@]8(CCC(C)(C)C[C@H]86)[C@@H](O)C[C@@]7(C)[C@]5(C)CC[C@H]4C3(C)C)[C@H](O)[C@H]2O)[C@H](O)[C@H](O)[C@H]1OLevocetirizine (Xyzal, ( ) Cetirizine) is the active R enantiomer of cetirizine and represents a new second generation histamine H1 antagonist. Product information CAS Number: 130018 87 0 Molecular Weight: 461. 81 Formula: C21H27Cl3N2O3 Chemical Name: 2 (2 {4 [(4 chlorophenyl)(phenyl)methyl]piperazin 1 yl}ethoxy)acetic acid dihydrochloride Smiles: Cl. Cl. OC(=O)COCCN1CCN(CC1)C(C1C=CC=CC=1)C1C=CC(Cl)=CC=1 InChiKey: PGLIUCLTXOYQMV UHFFFAOYSA N InChi: