Substructure Search

348

O=C(c1ccc(F)cc1)C1CCN(CCN(C(=O)c2ccc(NC(=O)C(F)(F)F)cc2)c2cccnc2)CC1
Reaction #2614
title compound
Yield 81.2%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)C1CN(CC(=O)Nc2c(Cl)cccc2Cl)CCN1CCCC(=O)C(c1ccccc1)c1ccccc1.O
Reaction #63624
3-(aminocarbonyl)-N-(2,6-dichlorophenyl)-4-(4-oxo-5,5-diphenylpentyl)-1-piperazineacetamide monohydrate
Yield 3.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2c(c1)N(CCN1CCC(NCc3ccc4c(c3)OCCO4)CC1)C(=O)CC2.Cl
Reaction #68288
1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-7-methoxy-3,4-dihydroquinolin-2(1H)-one hydrochloride
Yield 135.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCCC(CN2CCN(c3ccccc3Cl)CC2)C1)C1(c2ccc(Cl)cc2)CCC1
Reaction #78927
7
Yield 42.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCCC(CN2CCN(c3ccccc3F)CC2)C1)C1(c2ccc(Cl)cc2)CCC1
Reaction #78928
8
Yield 46.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCCC(CN2CCN(c3ccccc3O)CC2)C1)C1(c2ccc(Cl)cc2)CCC1
Reaction #78931
12
Yield 32.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(=O)n(-c2ccc(N3CCOCC3)c(F)c2)c(CCCOc2cccc(F)c2)n1
Reaction #84532
title compound
Yield 49.5%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=C1CCCN1c1ccc(OCCCN(CCn2ccc3ccccc3c2=O)Cc2ccncc2)cc1
Reaction #156194
title compound
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
Yield 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
Yield 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
Yield 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
Yield 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
Yield 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
Yield 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
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