Substructure Search

C1=CC(=CC=C1N)F

C[C@H](NC(=O)c1ccccc1)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccccc1
Reaction #41314
N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-phenyl-propan-2-yl]benzamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc([C@@H](Oc2ccc3c(cnn3-c3ccc(F)cc3)c2)[C@H](C)NC(=O)c2ccc(C(F)(F)F)cc2)c1
Reaction #41371
N-((1R,2S)-1-(1-(4-fluorophenyl)-1H-indazol-5-yloxy)-1-(3-methoxyphenyl)propan-2-yl)-4-(trifluoromethyl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)C1(C)CC1)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccc2c(c1)OCCO2
Reaction #41431
N-((1R,2S)-1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-1-(1-(4-fluorophenyl)-1H-indazol-5-yloxy)propan-2-yl)-1-methylcyclopropanecarboxamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CCN(Cc2cc(Oc3ccc4c(ccn4C(=O)Nc4ccc(F)c(C(F)(F)F)c4)c3)ncn2)CC1
Reaction #73392
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(F)c(F)c2c1[nH]c(=O)n2-c1ccc(F)cc1I
Reaction #160606
6,7-Difluoro-1-(4-fluoro-2-iodophenyl)-4-methoxy-1H-benzo[d]imidazol-2(3H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(c2ccc(F)c(-c3nc4cc(C)ccc4n3C(=O)OC(C)(C)C)c2)CC1
Reaction #164263
title compound
Yield 99.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCN(c2ccc(F)c(-c3nc4cc(Cl)ccc4n3C(=O)OC(C)(C)C)c2)CC1
Reaction #164265
title compound
Yield 24.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(O)C1CCN(c2ccc(F)c(-c3nc4cc(Cl)ccc4[nH]3)c2)CC1
Reaction #164266
title compound
Yield 138.1%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
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)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
CC(C)C(=O)Nc1ccc(F)c(C2CCN(CCCNC(=O)C3(c4ccc(F)cc4)CCCCC3)CC2)c1
Reaction #174299
DOI: 10.1039/C8SC04228D
COc1cc2c(Oc3ccc(NC(=O)Nc4ccc(F)cc4F)c(Cl)c3)ccnc2cc1OCCN(C)CCO
Reaction #177766
DOI: 10.1039/C8SC04228D
COC(=O)CCCCCNC(=O)c1ccc(C=NN=C2C(=O)Nc3ccc(F)cc32)cc1
Reaction #177885
DOI: 10.1039/C8SC04228D
CC(=O)N(CCCN1C(=O)c2ccccc2C1=O)c1ccc(-c2cc(=O)c3c(N)c(F)cc(F)c3o2)cc1F
Reaction #180707
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(F)cc1)C1(C(=O)Nc2ccc(O)cc2F)CC1
Reaction #183706
DOI: 10.1039/C8SC04228D
O=C(O)C1CCN(Cc2cc(Oc3ccc4c(ccn4C(=O)Nc4ccc(F)c(C(F)(F)F)c4)c3)ncn2)CC1
Reaction #187616
DOI: 10.1039/C8SC04228D
CCCc1cc(C(=O)OCC)n(CC(=O)N2CCN(c3ccc(F)cc3)CC2)n1
Reaction #190389
DOI: 10.1039/C8SC04228D
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