部分構造検索

14

CCOC(=O)c1cc2c(N3CCN(Cc4ccccc4)CC3)cccc2o1
Reaction #328
収率 0.0%
CCOC(=O)c1cnc(Nc2cc(Cl)ccn2)o1
Reaction #447
収率 0.0%
CCOC(=O)c1cnc(Nc2cc(Cl)ccn2)o1
Reaction #448
収率 0.0%
CC(=O)Nc1cc(Nc2cc(NC3CC3)n3ncc(C#N)c3n2)ccc1N1CC[C@@H](N)C1
Reaction #466
収率 17.8%
Cc1cc2ccc(OC(F)(F)F)cc2n1-c1cccc(OCc2ccccc2)c1
Reaction #525
収率 59.1%
Cc1cc2ccc(OC(F)(F)F)cc2n1-c1cccc(OCc2ccccc2)c1
Reaction #526
収率 62.5%
COc1cccc(-n2c(C)cc3ccc(OC(F)(F)F)cc32)c1
Reaction #530
収率 65.5%
Cc1cc2ccc(OC(F)(F)F)cc2n1-c1cccc(OCc2ccccc2)c1
Reaction #541
収率 40.2%
Cc1cc2ccc(OC(F)(F)F)cc2n1-c1cccc(OCc2ccccc2)c1
Reaction #542
収率 10.4%
CC(=O)Nc1cc(Nc2cc(NC3CC3)n3ncc(C#N)c3n2)c(F)cc1C
Reaction #702
収率 20.6%
CC(=O)Nc1cc(Nc2cc(NC3CC3)n3ncc(C#N)c3n2)ccc1N(C)CCN(C)C
Reaction #711
収率 15.6%
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)c(F)cc1C1CC1
Reaction #790
収率 23.9%
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)c(F)cc1C1CC1
Reaction #791
収率 11.9%
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)c(F)cc1C1CC1
Reaction #792
収率 3.5%
CC(=O)Nc1cc(Nc2cc(NC3CC3)n3ncc(C#N)c3n2)ncc1C
Reaction #821
収率 10.6%
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)ccc1C
Reaction #824
収率 16.5%
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)ccc1C1CC1
Reaction #832
収率 7.0%
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)ccc1C1CC1
Reaction #833
収率 0.0%
CC(=O)Nc1cc(Nc2cc(NC3COC3)n3ncc(C#N)c3n2)ccc1C1CC1
Reaction #834
収率 8.7%
COc1cc(-c2nc3ccccc3o2)ccc1-c1ccc(N2CCOCC2)cn1
Reaction #7887
2-[3-methoxy-4-(5-morpholin-4-ylpyridin-2-yl)phenyl]-1,3-benzoxazole
DOI: 10.6084/m9.figshare.5104873.v1
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