6-Chloro-7-deazapurine-β-D-riboside HPC-Me-CO-CH2-PEG3-NH2 Smiles: CNC(=O)C1=CC(=CC=N1)OC1=CC(F)=C(C=C1)NC(=O)NC1=CC(=NN1C1=CC2=CC=CN=C2C=C1)C(C)(C)C

Smiles: CNC(=O)C1=CC(=CC=N1)OC1=CC(F)=C(C=C1)NC(=O)NC1=CC(=NN1C1=CC2=CC=CN=C2C=C1)C(C)(C)C

and affacts T cell subpopulations in TAChR-immunized Lewis rats

InChi: InChI=1S/C17H20ClN5O3/c1-19-15-12(18)10-20-17(22-15)21-13-4-3-11(9-14(13)25-2)16(24)23-5-7-26-8-6-23/h3-4

6 nM in A431 cells

6-Chloro-7-deazapurine-β-D-riboside HPC-Me-CO-CH2-PEG3-NH2 Smiles: CNC(=O)C1=CC(=CC=N1)OC1=CC(F)=C(C=C1)NC(=O)NC1=CC(=NN1C1=CC2=CC=CN=C2C=C1)C(C)(C)CChloro 7 deazapurine D riboside is a nucleoside derivative and has antifungal activity. Product information CAS Number: 16754 80 6 Molecular Weight: 285. 68 Formula: C11H12ClN3O4 Chemical Name: (2R,3R,4S,5R) 2 {4 chloro 7H pyrrolo[2,3 d]pyrimidin 7 yl} 5 (hydroxymethyl)oxolane 3,4 diol Smiles: OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N1C=CC2C(Cl)=NC=NC1=2 InChiKey: BFDDOTZWMOKUCD KCGFPETGSA N InChi: InChI=1S C11H12ClN3O4 c12 9 5 1 2 15(10(5)14 4 13 9)11