Recherche de Sous-structure

CC1=C(SC(=N1)N)C.Cl

Cc1nc(NC(=O)CCl)sc1-c1ccnc(Nc2cccc([N+](=O)[O-])c2)n1
Reaction #60644
2-Chloro-N-{4-methyl-5-[2-(3-nitro-phenylamino)-pyrimidin-4-yl]-thiazol-2-yl}-acetamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nc(NC(=O)CCl)sc1-c1ccnc(Nc2ccc(F)cc2)n1
Reaction #60645
2-Chloro-N-{5-[2-(4-fluoro-phenylamino)-pyrimidin-4-yl]-4-methyl-thiazol-2-yl}-acetamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1sc(NC(N)=NCC(F)(F)F)nc1CCCCN.Cl.Cl
Reaction #63084
2-[2-(2,2,2-trifluoroethyl)guanidino]-4-(4-aminobutyl)-5-methylthiazole dihydrochloride
Rendement 128.6%DOI: 10.6084/m9.figshare.5104873.v1
C=Cc1nc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OC)C2)sc1C(=O)OCC
Reaction #71731
title compound
Rendement 21.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@@H]2CCN(c3ncc(C)s3)C[C@@H]2OC)nc1Cl
Reaction #71798
title compound
Rendement 100.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OCC)C2)nc1C(=O)O
Reaction #71800
title compound
Rendement 99.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OCC)C2)nc1C(=O)NCCOC
Reaction #71801
title compound
Rendement 72.5%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OCC)C2)nc1C(=O)NC
Reaction #71806
title compound
Rendement 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@@H]1CN(c2nc(C(=O)NCCOC)c(C(=O)OCC)s2)CC[C@@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #71808
title compound
Rendement 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N2CC[C@@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](N)C2)nc1C
Reaction #71818
title compound
Rendement 100.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3nc(C)c(C(=O)O)s3)C[C@H]2OCC(F)F)nc1Cl
Reaction #71973
title compound
Rendement 71.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3nc(C)c(C(=O)O)s3)C[C@H]2OCCF)nc1Cl
Reaction #71978
title compound
Rendement 93.2%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3nc(C)c(C(=O)O)s3)C[C@H]2OCCCF)nc1Cl
Reaction #71993
title compound
Rendement 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OC(C)C)C2)nc1C(=O)NCCOC
Reaction #72020
title compound
Rendement 74.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3nc(C(=O)NCCOC)c(C(=O)O)s3)C[C@H]2OC(C)C)nc1Cl
Reaction #72021
title compound
Rendement 98.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3nc(C)c(C(=O)O)s3)C[C@H]2Cl)nc1Cl
Reaction #72120
title compound
Rendement 34.2%DOI: 10.6084/m9.figshare.5104873.v1
CCN[C@@H]1CN(c2nc(C)c(C(=O)OCC)s2)CC[C@H]1NC(=O)c1nc(Cl)c(CC)[nH]1
Reaction #72140
title compound
Rendement 41.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N2CC(NC(=O)c3nc(Cl)c(CC)[nH]3)C2)nc1C(C)C
Reaction #72162
title compound
Rendement 41.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)NC2CN(c3nc(C(C)C)c(C(=O)O)s3)C2)nc1Cl
Reaction #72163
title compound
Rendement 80.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1sc(N2CC(N(C)C(=O)c3nc(Cl)c(CC)[nH]3)C2)nc1C
Reaction #72181
title compound
Rendement 91.0%DOI: 10.6084/m9.figshare.5104873.v1
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