Substructure Search

17497

CCCCC(O)(CCC)N(c1ccnc(C)c1OC)C1CCCCC1
Reaction #1105
4-[(4-Hydroxy-4-n-octyl)cyclohexylamino]-3-methoxy-2-methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCC(N(C(=O)Nc2ncc(SCC(=O)O)s2)C2CCC2)CC1
Reaction #174023
DOI: 10.1039/C8SC04228D
COP1(=O)CCC(NC2CCC(N(C(=O)C3CCC(C)CC3)c3cc(C#CC(C)(C)C)sc3C(=O)O)CC2)CC1
Reaction #177839
DOI: 10.1039/C8SC04228D
CC(C)N(C)C1CCC(NC(=O)OC(C)(C)C)CC1
Reaction #190592
DOI: 10.1039/C8SC04228D
CC1CCC(N(C(=O)Nc2ncc(CN3CCN(S(=O)(=O)N(C)C)CC3)s2)C2CCN(C(=O)c3ccc(F)cc3)CC2)CC1
Reaction #191479
DOI: 10.1039/C8SC04228D
CC(C)NC1CCC(CNC(=O)OC(C)(C)C)CC1
Reaction #192234
DOI: 10.1039/C8SC04228D
CN1C(=O)N(C2CCN(C3CCNCC3)CC2)C2CCCCC21
Reaction #192868
DOI: 10.1039/C8SC04228D
COC(=O)C1CC(N(C)C(C)C)CCC1N1CCC(Nc2ncnc3ccc(C(F)(F)F)cc23)C1=O
Reaction #205040
DOI: 10.1039/C8SC04228D
O=C(Nc1ncc(CN2CCN(S(=O)(=O)Cc3ccccc3)CC2)s1)N(C1CCCCC1)C1CCCCC1
Reaction #207778
DOI: 10.1039/C8SC04228D
CC(C)S(=O)(=O)NC1CCN(Cc2cnc(NC(=O)N(C3CCCCC3)C3CCCCC3)s2)CC1
Reaction #208074
DOI: 10.1039/C8SC04228D
COC(=O)CCS(=O)(=O)N1CCN(Cc2cnc(NC(=O)N(C3CCCCC3)C3CCC(C)CC3)s2)CC1
Reaction #224836
DOI: 10.1039/C8SC04228D
CCCC(CSc1ccc(F)cc1)N(CC)C1CCC(c2ccc3[nH]c(=O)oc3c2)CC1
Reaction #227053
DOI: 10.1039/C8SC04228D
CC(=O)C(C)(C)C(=O)N(C1CCC(C)(C)CC1)C1CCN(C(=O)OC(C)(C)C)C1
Reaction #228852
DOI: 10.1039/C8SC04228D
CCN(C)C(=O)C1CC(N(C(=O)C2CCCO2)C2CCC(C)(C)CC2)CN1C(=O)OC(C)(C)C
Reaction #231300
DOI: 10.1039/C8SC04228D
CC(O)C(C)(C)C(=O)N(C1CCC(C)(C)CC1)C1CCN(C(=O)OC(C)(C)C)C1
Reaction #237519
DOI: 10.1039/C8SC04228D
CC1CCC(N(C(=O)C(C)(C)C)C2CC(C#N)N(C(=O)OC(C)(C)C)C2)CC1
Reaction #243598
DOI: 10.1039/C8SC04228D
CC1(C)CCC(N(C(=O)C(C)(C)CO)C2CCN(C(=O)C3CN(C(C)(C)C)CC3c3ccc(Cl)cc3)C2)CC1
Reaction #245295
DOI: 10.1039/C8SC04228D
CCCCS(=O)(=O)N1CCN(Cc2cnc(NC(=O)N(C3CCCCC3)C3CCCCC3)s2)CC1
Reaction #248016
DOI: 10.1039/C8SC04228D
COCCNC(=O)c1nc(NC2CCCCC2N)c2cc(C)ccc2n1
Reaction #248290
DOI: 10.1039/C8SC04228D
N#Cc1ccc2c(c1)N(CCC1CCC(N)CC1)C(=O)CO2
Reaction #248715
DOI: 10.1039/C8SC04228D
Page 1Next