Substructure Search

CC(C)NC(C)C

CCNC(=O)[C@H]1O[C@@H](n2cnc3c(NCC(c4cccc(C)c4)c4cccc(C)c4)nc(C(=O)NCCNC(=O)NCCN(C(C)C)C(C)C)nc32)[C@H](O)[C@@H]1O
Reaction #10527
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CN1C2CC(OC(=O)C(O)(c3cccs3)c3cccs3)CC1C1OC12
Reaction #42722
title compound
Yield 42.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-c3cc[n+]([O-])cc3)nc2N1C1CCCC1
Reaction #73103
title compound
Yield 6.4%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-n3cnc(CC#N)c3)nc2N1C1CCCC1
Reaction #73110
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-n3cnc(C(=O)O)c3)nc2N1C1CCCC1
Reaction #73111
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-n3cc(C(=O)N(C)C)cn3)nc2N1C1CCCC1
Reaction #73112
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-n3cnc(C(=O)N4CCOCC4)c3)nc2N1C1CCCC1
Reaction #73113
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-n3cnc(C(=O)NC)c3)nc2N1C1CCCC1
Reaction #73114
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-n3cnc(-c4cscn4)c3)nc2N1C1CCCC1
Reaction #73115
title compound
Yield 18.7%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-n3ccc(C(=O)NC)n3)nc2N1C1CCCC1
Reaction #73116
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-n3cnc(CCN)c3)nc2N1C1CCCC1
Reaction #73117
title compound
Yield 42.2%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-n3ccc(C(N)=O)n3)nc2N1C1CCCC1
Reaction #73118
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-n3cnc(C(N)=O)c3)nc2N1C1CCCC1
Reaction #73119
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-n3ccnc3-c3nccs3)nc2N1C1CCCC1
Reaction #73121
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-n3ccnc3C3CC3)nc2N1C1CCCC1
Reaction #73167
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-n3ccnc3Cl)nc2N1C1CCCC1
Reaction #73168
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-n3ccc4ccccc43)nc2N1C1CCCC1
Reaction #73175
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN1[C@H]2CC[C@@H]1[C@@H](c1ncc(-c3ccccc3)s1)[C@@H](c1ccc(Cl)cc1)C2.Cl
Reaction #77842
3β-(4-Chlorophenyl)-2β-(5-phenylthiazol-2-yl)-tropane Hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Clc1nc(N2C3CCC2COC3)c(Cl)c(N2C3CCC2COC3)n1
Reaction #162634
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(-c2nc(N3C4CCC3COC4)c(Cl)c(N3C4CCC3COC4)n2)cc1
Reaction #162635
title compound
Yield 61.3%DOI: 10.6084/m9.figshare.5104873.v1
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