CDK Depict

CN1C=NC2=C1C(=O)N(C(=O)N2C)C caffeine
[Cs+].[O-]C(=O)[O-].[Cs+] Cs2CO3
[Li+].[Al+3].[H-].[H-].[H-].[H-] LiAlH4
Cl[Pt@SP1](Cl)([NH3])[NH3] cis-platin
O=[N+]([O-])[Co@]([NH3])([NH3])([NH3])([NH3])[N+]([O-])(=O) trans-[Co(NH3)4(NO2)2]
Cl*.Cl*.c1ccccc1-c1ccccc1 |m:1:4.5.6.7.8.9,3:10.11.12.13.14.15| dichlorobiphenyl
CCOCCOCCO |Sg:n:3,4,5::ht| PEGn
*c1ccccc1 |$_AP1$| phenyl
CC(C)[C@H](N*)C(*)=O |$;;;;;_AP1;;_AP2;$| valine monomer
c1(:*:c2c(:*:c1*)C(N(N2)*)=O)* |$;Y;;;X;;R10;;;;Z;;R11$| US 2007/0129374 (I)
C*.C*.C1=CC=CC=C1C=2C(C=CN3C2C=*C(=*3)C**)=O.C* |$;R2;;R3;;;;;;;;;;;;;;W;;A;;X;R4;;;R1$,m:0:5.4.9.8.7.6,2:7.6.5.4.9.8,24:4.9.8.7.6.5,Sg:n:20:m:ht| US 2007/0129372 (I)
[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].CCCCc1ccc(CO[C@H]2O[C@H](COS(=O)(=O)[O-])[C@@H](OS(=O)(=O)[O-])[C@H](OS(=O)(=O)[O-])[C@@H]2O[C@H]3O[C@H](COS(=O)(=O)[O-])[C@@H](OS(=O)(=O)[O-])[C@H](O[C@H]4O[C@H](COS(=O)(=O)[O-])[C@@H](OS(=O)(=O)[O-])[C@H](O[C@H]5O[C@H](COS(=O)(=O)[O-])[C@@H](OS(=O)(=O)[O-])[C@H](OS(=O)(=O)[O-])[C@@H]5OS(=O)(=O)[O-])[C@@H]4OS(=O)(=O)[O-])[C@@H]3OS(=O)(=O)[O-])cc1 CHEMBL590010
CCO.[CH3:1][C:2](=[O:3])[OH:4]>[H+]>CC[O:4][C:2](=[O:3])[CH3:1].O Ethyl esterification [1.7.3]
[CH3:9][CH:8]([CH3:10])[c:7]1[cH:11][cH:12][cH:13][cH:14][cH:15]1.[CH2:3]([CH2:4][C:5](=[O:6])Cl)[CH2:2][Cl:1]>[Al+3].[Cl-].[Cl-].[Cl-].C(Cl)Cl>[CH3:9][CH:8]([CH3:10])[c:7]1[cH:11][cH:12][c:13]([cH:14][cH:15]1)[C:5](=[O:6])[CH2:4][CH2:3][CH2:2][Cl:1] |f:2.3.4.5| Friedel-Crafts acylation [3.10.1]