子结构搜索

1280011

COC(=O)c1nc(-c2cscc2N)nc(O)c1O.O=C(O)C(F)(F)F
Reaction #8802
methyl 2-(3-amino-4-thienyl)-4,5-dihydroxy-pyrimidine-6-carboxylate trifluoroacetate
收率 99.0%DOI: 10.6084/m9.figshare.5104873.v1
Ic1ccnc(Oc2cncnc2)c1
Reaction #68846
5-(4-Iodo-pyridin-2-yloxy)-Pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
COc1cnc(Oc2cc3c(cc2OC)CCN(CC(=O)NC2CCc4ccccc42)C3Cc2ccc(OC)c(OC)c2)nc1
Reaction #77132
2-[1-(3,4-dimethoxy-benzyl)-6-methoxy-7-(5-methoxy-pyrimidin-2-yloxy)-3,4-dihydro-1H-isoquinolin-2-yl]-N-(indan-1-yl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(CNC(=O)c2nc3n(c(=O)c2O)CC2(CO)CCC3(NC(=O)C(=O)N(C)C)CC2)ccc1F
Reaction #162909
title compound
收率 55.2%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(CNC(=O)c2nc3n(c(=O)c2O)CC2(CC#N)CCC3(N(C)C(=O)C(=O)N(C)C)CC2)ccc1F
Reaction #162911
title compound
收率 19.3%DOI: 10.6084/m9.figshare.5104873.v1
COCC12CCC(N(C)C(=O)C(=O)N(C)C)(CC1)c1nc(C(=O)NCc3ccc(F)c(C)c3)c(O)c(=O)n1C2
Reaction #162913
title compound
收率 3.8%DOI: 10.6084/m9.figshare.5104873.v1
N#CC(Cc1ccc(F)cc1)NC(=O)c1nc2n(c(=O)c1OCc1ccccc1)CC1CCC2(NC(=O)OCc2ccccc2)CC1
Reaction #167871
title compound
收率 62.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC12CCC(CC1)Cn1c2nc(-c2nc(Cl)c(Cc3ccc(F)cc3)[nH]2)c(OCc2ccccc2)c1=O)OCc1ccccc1
Reaction #167872
title compound
收率 42.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CNC(=O)c1nc2n(c(=O)c1OCc1ccccc1)CC1CCC2(NC(=O)OCc2ccccc2)CC1)Cc1ccc(F)cc1
Reaction #167873
title compound
收率 77.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NC12CCC(CC1)Cn1c2nc(-c2ncc(Cc3ccc(F)cc3)s2)c(OCc2ccccc2)c1=O)OCc1ccccc1
Reaction #167874
title compound
收率 50.2%DOI: 10.6084/m9.figshare.5104873.v1
NC12CCC(CC1)Cn1c2nc(-c2nnc(Cc3ccc(F)cc3)o2)c(O)c1=O
Reaction #167877
title compound
收率 78.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(CNC(=O)c1nc2n(c(=O)c1OCc1ccccc1)CC1CCC2(NC(=O)OCc2ccccc2)CC1)Cc1ccc(F)cc1
Reaction #167878
title compound
收率 59.0%DOI: 10.6084/m9.figshare.5104873.v1
NC12CCC(CC1)Cn1c2nc(C(=O)NCC(=O)Cc2ccc(F)cc2)c(O)c1=O
Reaction #167879
title compound
收率 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)C(=O)NC12CCC(CC1)Cn1c2nc(C(=O)NCC(=O)Cc2ccc(F)cc2)c(O)c1=O
Reaction #167880
title compound
收率 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)C(=O)NC12CCC(CC1)Cn1c2nc(C(=O)NCC(=O)Cc2ccc(F)cc2)c(OCc2ccccc2)c1=O
Reaction #167881
title compound
收率 59.5%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)C(=O)NC12CCC(CC1)Cn1c2nc(-c2ncc(Cc3ccc(F)cc3)o2)c(OCc2ccccc2)c1=O
Reaction #167882
title compound
收率 53.6%DOI: 10.6084/m9.figshare.5104873.v1
NC12CCC(CC1)Cn1c2nc(-c2nc(Cc3ccc(F)cc3)c[nH]2)c(O)c1=O
Reaction #167883
title compound
收率 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)C(=O)NC12CCC(CC1)Cn1c2nc(-c2nc(Cc3ccc(F)cc3)c[nH]2)c(O)c1=O
Reaction #167884
title compound
收率 8.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(=O)NC23CCC(CC2)Cn2c3nc(-c3nc(Cc4ccc(F)cc4)c[nH]3)c(O)c2=O)no1
Reaction #167885
title compound
收率 39.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)C(=O)C(=O)NC12CCC(CC1)Cn1c2nc(-c2nnc(Cc3ccc(F)cc3)o2)c(O)c1=O
Reaction #167887
title compound
收率 22.6%DOI: 10.6084/m9.figshare.5104873.v1
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