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374013

CCCCN(C(=O)C(C)C)c1nc(C)co1
Reaction #54761
2-(N-butylisobutyramido)-4-methyloxazole
Rendimiento 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(CC)C(=O)N(CC)c1nc(C)co1
Reaction #54762
product
Rendimiento 51.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1coc(NC(=O)CCCCl)n1
Reaction #54763
2-(4-Chlorobutyramido)-4-methyloxazole
Rendimiento 23.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1coc(N2CCCC2=O)n1
Reaction #54764
1-(4-methyloxazol-2-yl)-2-pyrrolidone
Rendimiento 41.6%DOI: 10.6084/m9.figshare.5104873.v1
CCCCNc1nc(-c2ccccc2)co1
Reaction #54765
2-(N-Butylamino)-4-phenyloxazole
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C(=O)C(C)C)c1nc(-c2ccccc2)co1
Reaction #54766
2-(N-Butyl-isobutyramido)-4-phenyloxazole
DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C(=O)C(C)C)c1nc(C)c(O)o1
Reaction #54768
5-Hydroxy-2(N-butylisobutyramido)-4-methyloxazole
DOI: 10.6084/m9.figshare.5104873.v1
Cc1coc(N(CCCC(=O)O)C(=O)C(C)C)n1
Reaction #54771
product
Rendimiento 57.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1coc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)n1
Reaction #71880
title compound
Rendimiento 79.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1coc(N2CC[C@H](N)[C@H](OC)C2)n1
Reaction #71881
title compound
Rendimiento 102.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1coc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OC)C2)n1
Reaction #71882
title compound
Rendimiento 59.5%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3nc(C(=O)O)co3)C[C@H]2OC)nc1Cl
Reaction #71883
title compound
Rendimiento 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)oc1C
Reaction #71894
title compound
Rendimiento 78.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOC(=O)c1nc(N2CC[C@H](N)[C@H](OC)C2)oc1C
Reaction #71895
title compound
Rendimiento 113.5%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3nc(C(=O)O)c(C)o3)C[C@H]2OC)nc1Cl
Reaction #71896
title compound
Rendimiento 99.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1oc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)nc1C
Reaction #71897
title compound
Rendimiento 31.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1oc(N2CC[C@H](N)[C@H](OC)C2)nc1C
Reaction #71898
title compound
Rendimiento 100.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1oc(N2CC[C@H](NC(=O)c3nc(Cl)c(CC)[nH]3)[C@H](OC)C2)nc1C
Reaction #71899
title compound
Rendimiento 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1[nH]c(C(=O)N[C@H]2CCN(c3nc(C)c(C(=O)O)o3)C[C@H]2OC)nc1Cl
Reaction #71900
title compound
Rendimiento 89.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc(N2CC[C@H](NC(=O)OCc3ccccc3)[C@H](OC)C2)oc1CC
Reaction #71916
title compound
Rendimiento 108.6%DOI: 10.6084/m9.figshare.5104873.v1
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