子结构搜索

c1ccc(C2CCNC2)cc1

NCc1ccc(C2CCN(c3c(F)c(N)c4c(=O)c(C(=O)O)cn(C5CC5)c4c3F)C2)cc1
Reaction #82754
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CNCc1ccc(C2CCN(c3c(F)c(N)c4c(=O)c(C(=O)O)cn(C5CC5)c4c3F)C2)cc1
Reaction #82757
title compound
收率 51.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC1=N[C@@]2(c3cccc(NC(=O)c4ccc(F)cn4)c3)CN(c3ncc(F)cn3)C[C@H]2CS1)c1ccccc1
Reaction #164764
title compound
收率 41.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cnc(C(=O)Nc2cccc([C@]34CN(c5ncc(F)cn5)C[C@H]3CSC(NC(=O)c3ccccc3)=N4)c2)cn1
Reaction #164766
title compound
收率 92.4%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(C(=O)Nc2cccc([C@]34CN(c5ncc(F)cn5)C[C@H]3CSC(NC(=O)c3ccccc3)=N4)c2)nc1
Reaction #164770
title compound
收率 92.9%DOI: 10.6084/m9.figshare.5104873.v1
NC1=NC2(c3cc(NC(=O)c4ccc(F)cn4)ccc3F)CN(c3ncc(F)cn3)CC2CS1
Reaction #164773
title compound
收率 186.9%DOI: 10.6084/m9.figshare.5104873.v1
NC1=N[C@@]2(c3cccc(NC(=O)c4ccc(F)cn4)c3)CN(c3ncc(F)cn3)C[C@H]2CS1
Reaction #164774
N-[3-[(4aR,7aS)-2-amino-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazin-7a-yl]phenyl]-5-fluoro-pyridine-2-carboxamide
收率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cnc(C(=O)Nc2cccc([C@]34CN(c5ncc(F)cn5)C[C@H]3CSC(N)=N4)c2)cn1
Reaction #164775
N-[3-[(4aR,7aS)-2-amino-6-(5-fluoropyrimidin-2-yl)-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazin-7a-yl]phenyl]-5-methoxy-pyrazine-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NC1=N[C@@]2(c3cc(NC(=O)c4ccc(F)cn4)ccc3F)CN(c3ncc(F)cn3)C[C@H]2CS1
Reaction #164776
title compound
收率 38.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cnc(C(=O)Nc2ccc(F)c([C@]34CN(c5ncc(F)cn5)C[C@H]3CSC(N)=N4)c2)cn1.Cl
Reaction #164777
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.N#Cc1ccc(C(=O)Nc2cccc([C@]34CN(c5ncc(F)cn5)C[C@H]3CSC(N)=N4)c2)nc1
Reaction #164778
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NC1=N[C@@]2(c3cccc(NC(=O)c4ncc(F)cc4F)c3)CN(c3ncc(F)cn3)C[C@H]2CS1
Reaction #164779
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.N#Cc1ccc(C(=O)Nc2ccc(F)c([C@]34CN(c5ncc(F)cn5)C[C@H]3CSC(N)=N4)c2)nc1
Reaction #164780
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NC1=N[C@@]2(c3cc(NC(=O)c4ncc(F)cc4F)ccc3F)CN(c3ncc(F)cn3)C[C@H]2CS1
Reaction #164781
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc2ccccc2n1Cc1ccc(Cl)cc1)N1CCC(C(=O)N2CCC(c3ccccc3)C2)CC1
Reaction #170854
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc([C@@H]2CN(Cc3ccccc3)C[C@H]2/C=C/C(=O)OC(C)(C)C)c1
Reaction #172143
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)N(C)C1CN(C(=O)C2CCOCC2)CC1c1ccc(F)cc1)c1cc(Br)cc(C(F)(F)F)c1
Reaction #179102
DOI: 10.1039/C8SC04228D
C=CCCCCCC(NC(=O)OC(C)(C)C)C(=O)N1CC(SCCCC)(c2ccc(-c3ccccc3)cc2)CC1C(=O)OC
Reaction #179173
DOI: 10.1039/C8SC04228D
CCOCCn1c(N2CCCN(CCC3(c4ccccc4)CCN(C(=S)c4cc(C)ccc4OC)C3)CC2)nc2ccccc21
Reaction #181931
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)CCN1C(=O)C2(CC(=O)N(Cc3ccccc3)C2=O)c2cc(Cl)ccc21
Reaction #182222
DOI: 10.1039/C8SC04228D
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