71 SMILES Strings for Ornithine decarboxylase

Compound Name
SMILES String
CC(C)(CN)C(C)(CN)C(O)=O
CC(C)(CN)C(CN)C(O)=O
CC(C)(C[NH3+])C(C)(C)C[NH3+]
CC(C)(C[NH3+])CC[NH3+]
CC(C)NCC(O)CON
CC(CN)(CCN)C(O)=O
CC(CN)C(C)(CN)C(O)=O
CC(CN)C(CN)C(O)=O
CC(C[NH3+])C(C)(C)C[NH3+]
CC(C[NH3+])C(C)C[NH3+]
CC(N)(CCCN)C(O)=O
CC(N)(CCCNCCCN)C(O)=O
CC(N)(\C=C\CN)C(O)=O
CC(N)C(C)CCN
CC(N)CC(C)CN
CC1(C)Oc2ccc(C(=O)\C=C\c3ccc(O)cc3)c(O)c2C=C1 |c:24|
CN(C)CC(O)CON
CN(C)CCCCN
CNCC(O)CON
CNCCCC(C)(N)C(O)=O
COc1cc(OC)c(cc1OC)C1COc2c(ccc3OC(C)(C)C=Cc23)C1=O |c:25|
COc1cc(OC)c(cc1OC)C1COc2c(ccc3OC(C)(C)[C@@H](O)[C@@H](O)c23)C1=O |r|
COc1cc(\C=C\C(=O)c2ccc3OC(C)(C)C=Cc3c2O)ccc1O |c:17|
COc1cc(\C=C\c2cc(OC)c3C=CC(C)(C)Oc3c2)ccc1O |c:13|
COc1cc(\C=C\c2ccc(O)cc2)cc2OC(C)(C)C=Cc12 |c:21|
COc1cc(\C=C\c2ccc3C=CC(C)(C)Oc3c2)cc(OC)c1OC |c:11|
COc1ccc2oc(cc(=O)c2c1OC)-c1c(OC)cccc1OC
CS(=O)(=O)OC(CN)CON
C[C@H](N)CC[C@H](N)C#C
Cc1ncc(COP(O)(O)=O)c(\C=N\OCC(F)CN)c1O
Cc1ncc(COP(O)(O)=O)c(\C=N\OCC(O)CN)c1O
Cl.C[C@@](N)(CCCN)C(O)=O |r|
Cl.C[C@](N)(CCCN)C(O)=O |r|
Cl.NCCCC(N)c1nnn[nH]1
NCC(Cl)CON
NCC(F)CNN
NCC(F)CON
NCC(O)CON
NCCC(CN)C(O)=O
NCCCC(N)(C(F)F)C(O)=O
NCCCC(N)(CF)C(O)=O
NCCCC(N)C(F)F
NCCCC(N)CF
NCCCCNCCCN
NCCC[C@@](N)(C(F)F)C(O)=O |r|
NCCC[C@@](N)(CF)C(O)=O |r|
NCCC[C@H](N)C(O)=O |r|
NCCC[C@H](NN)C(O)=O |r|
NC[C@@H](O)CON
NC[C@H](O)CON
NC\C=C\C(N)(C(F)F)C(O)=O
NC\C=C\C(N)(CF)C(O)=O
NC\C=C\C(N)C(F)F
NC\C=C\C(N)C(O)=O
NC\C=C\C(N)CF
NOCC(O)CNCC#C
NOCC(O)CNCC=C
NOCC(O)CON
N[C@@H](CCCNC(=O)CCl)C(O)=O |r|
N[C@H]1CC[C@@](N)(CC1)C(O)=O |r,wU:4.8,wD:1.0,(19.99,-29.56,;19.99,-28.02,;21.32,-27.25,;21.32,-25.71,;19.99,-24.94,;20.74,-23.6,;18.66,-25.71,;18.66,-27.25,;19.19,-23.6,;17.65,-23.63,;19.93,-22.26,)|
Oc1ccc(\C=C\c2cc(O)cc(O)c2)cc1
Oc1ccc(cc1)-c1coc2cc(O)cc(O)c2c1=O
[#6]-[#8]-c1cc(ccc1-[#8])-[#6@@H]-1-[#6]-[#6](=O)-c2c(-[#8])c(-[#6]\[#6]=[#6](\[#6])-[#6])c3-[#8]C([#6])([#6])[#6]=[#6]-c3c2-[#8]-1 |r,c:28|
[#6]-[#8]-c1ccc(cc1-[#8])-[#6@@H]-1-[#6]-[#6](=O)-c2c(-[#8])c(-[#6]\[#6]=[#6](\[#6])-[#6])c3-[#8]C([#6])([#6])[#6]=[#6]-c3c2-[#8]-1 |r,c:28|
[#6]-[#8]-c1ccc(cc1-[#8]-[#6])-[#6@@H]-1-[#6]-[#6](=O)-c2c(-[#8])c(-[#6]\[#6]=[#6](\[#6])-[#6])c3-[#8]C([#6])([#6])[#6]=[#6]-c3c2-[#8]-1 |r,c:29|
[#6]-[#8]-c1ccc(cc1-[#8]-[#6])-[#6@@H]-1-[#6]-[#6](=O)-c2cc(-[#6]\[#6]=[#6](\[#6])-[#6])c3-[#8]C([#6])([#6])[#6]=[#6]-c3c2-[#8]-1 |r,c:28|
[H][C@]12CC[C@@](C)(O1)O[C@@]([H])([C@H](C)[C@H](O)[C@H](C)[C@@H](O)[C@@H](C)\C=C\C=C(\C)C(N)=O)[C@@H]2C |r|
[H][C@]12CC[C@@](C)(O1)O[C@@]([H])([C@H](C)[C@H](O)[C@H](C)[C@@H](O)[C@@H](C)\C=C\C=C(\CO)C(N)=O)[C@@H]2C |r|
[NH3+]CC(F)(F)CC([NH3+])C#C