Busqueda de Subestructura

39004

CS(=O)(=O)c1ccc(-c2cc(C(F)(F)F)nc(NC3CCOCC3)n2)cc1
Reaction #6792
title compound
Rendimiento 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(c1nc(-c2ccc(S(C)(=O)=O)cc2)cc(C(F)(F)F)n1)C1CCOCC1
Reaction #6793
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Clc1nc(NCC(c2ccccc2)c2ccccc2)c2ncn(C3CCCCO3)c2n1
Reaction #10531
title compound
Rendimiento 104.1%DOI: 10.6084/m9.figshare.5104873.v1
CSc1nc(NCC(c2ccccc2)c2ccccc2)c2ncn(C3CCCCO3)c2n1
Reaction #10532
title compound
Rendimiento 99.8%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1nc(NCC(c2ccccc2)c2ccccc2)c2ncn(C3CCCCO3)c2n1
Reaction #10533
title compound
Rendimiento 75.7%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1nc(NCC(c2ccccc2)c2ccccc2)c2ncn(C3CCCCO3)c2n1
Reaction #10534
title compound
Rendimiento 95.1%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1nc(NCC(c2ccccc2)c2ccccc2)c2nc[nH]c2n1
Reaction #10535
title compound
Rendimiento 99.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc(NCC(c2ccccc2)c2ccccc2)c2ncn(C3CCCCO3)c2n1
Reaction #10561
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc(NCC(c2ccccc2)c2ccccc2)c2nc[nH]c2n1
Reaction #10562
title compound
Rendimiento 100.6%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Cc2cccc3cc(C4(O)O[C@H](COCc5ccccc5)[C@@H](OCc5ccccc5)[C@H](OCc5ccccc5)[C@H]4OCc4ccccc4)sc23)cc1
Reaction #43688
title compound
Rendimiento 69.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Cc2cccc3cc([C@@H]4O[C@H](COCc5ccccc5)[C@@H](OCc5ccccc5)[C@H](OCc5ccccc5)[C@H]4OCc4ccccc4)sc23)cc1
Reaction #43689
title compound
Rendimiento 80.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Cc2cccc3cc([C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)sc23)cc1
Reaction #43690
title compound
Rendimiento 32.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(NC(=O)C(CC2CCOCC2)N2CC(Oc3c(F)cccc3F)=CC2=O)nc1
Reaction #47257
6-[2-[4-(2,6-difluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-3-(tetrahydro-pyran-4-yl)-propionylamino]-nicotinic acid methyl ester
Rendimiento 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(O)Cn1ccc(NC(=O)C(CC2CCOCC2)N2CC(Oc3c(F)cccc3F)=CC2=O)n1
Reaction #47258
2-[4-(2,6-difluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-N-[1-(2-hydroxy-2-methyl-propyl)-1H-pyrazol-3-yl]-3-(tetrahydro-pyran-4-yl)-propionamide
Rendimiento 68.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccn(CC(=O)Nc2cc(-c3cccc4[nH]ccc34)cc3[nH]ncc23)n1
Reaction #70526
title compound
Rendimiento 31.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(S(=O)(=O)Nc2ncns2)ccc1Oc1ccc(C(F)(F)F)cc1C1CCOCC1
Reaction #74526
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Nc1n[nH]cc1-c1cc(Cl)ccc1Oc1cc(F)c(S(=O)(=O)Nc2ccncn2)cc1Cl
Reaction #74550
white solid
Rendimiento 108.5%DOI: 10.6084/m9.figshare.5104873.v1
Nc1n[nH]cc1-c1cc(Cl)ccc1Oc1cc(F)c(S(=O)(=O)Nc2cccnn2)cc1Cl
Reaction #74552
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCN(c1ccncn1)S(=O)(=O)c1cc(Cl)c(Oc2ccc(Cl)cc2-c2cn(C3CCCCO3)nc2N)cc1F
Reaction #74678
colorless oil
Rendimiento 97.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(COc1cccc(-c2nc(Nc3ccc4[nH]ncc4c3)c3ccccc3n2)c1)NC1CCOCC1
Reaction #89869
2-(3-(4-(1H-indazol-5-ylamino)quinazolin-2-yl)phenoxy)-N-(tetrahydro-2H-pyran-4-yl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1
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