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InChi: InChI=1S/C23H18ClF2N3O3S/c1-2-9-33(31
Formula: C23H29F3N4O8
CCOC(=O)[C@H](NC(=O)[C@H](CSCC1C=CC=CC=1)NC(=O)CC[C@H](N)C(=O)OCC)C1C=CC=CC=1
a nucleic acid AMP derivative
24 hours) cells were characterized by a striking heterogeneity of the peroxisomal population with the occurrence of dumbbell-shaped and cup-shaped peroxisomal profiles in MH1C1cells
(R, R)-Palonosetron Hydrochloride 1139 InChi: InChI=1S/C23H18ClF2N3O3S/c1-2-9-33(31(R,R) Palonosetron Hydrochloride is the active enantiomer of Palonosetron. Product information CAS Number: 135729 75 8 Molecular Weight: 332. 87 Formula: C19H25ClN2O Chemical Name: (5R) 3 [(3R) 1 azabicyclo[2. 2. 2]octan 3 yl] 3 azatricyclo[7. 3. 1. 0,]trideca 1(12),9(13),10 trien 2 one hydrochloride Smiles: Cl. O=C1C2=CC=CC3CCC[C@@H](CN1[C@H]1CN4CCC1CC4)C=32 InChiKey: OLDRWYVIKMSFFB NBLXOJGSSA N InChi: InChI=1S C19H24N2O. ClH c22 19 16 6 2 4 14 3 1 5
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