子结构搜索

CC(O)CCc1ccccc1

CCCCN(C)Cc1cc(C)cc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)CNCc2cccc(C(C)C)c2)c1.Cl.Cl
Reaction #42395
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C#CC(=O)OC(C)(C)C
Reaction #42560
solid
收率 106.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N[C@@H](Cc1cc(F)cc(F)c1)[C@H](OCc1ccccc1)[C@H]1CO[C@H](OCCCC2CCCC2)CN1.O=C(O)C(F)(F)F
Reaction #48616
title compound
DOI: 10.6084/m9.figshare.5104873.v1
N[C@H](CO)[C@@H](OCc1ccccc1)[C@H](Cc1cccc(OCc2ccccc2)c1)N(Cc1ccccc1)Cc1ccccc1
Reaction #48628
crude desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H](CCC2CCCCC2)OC[C@@H]1[C@@H](O)[C@@H](N)Cc1cc(F)cc(F)c1
Reaction #48643
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H](CO)OC[C@@H]1[C@@H](O)[C@@H](N)Cc1cc(F)cc(F)c1
Reaction #48656
desired compound
收率 88.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H](COC2CCCCC2)OC[C@@H]1[C@@H](OCc1ccccc1)[C@H](Cc1cc(F)cc(F)c1)N(Cc1ccccc1)Cc1ccccc1
Reaction #48659
desired compound
收率 84.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@H](COC2CCCCC2)OC[C@@H]1[C@@H](O)[C@@H](N)Cc1cc(F)cc(F)c1
Reaction #48660
desired compound
收率 97.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)CO[C@H]1CN(C(=O)OC(C)(C)C)[C@@H]([C@@H](O)[C@@H](N)Cc2cc(F)cc(F)c2)CO1
Reaction #48690
title compound
收率 93.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1C[C@@H](OC(C)(CF)CF)OC[C@@H]1[C@@H](O)[C@@H](N)Cc1cc(O)cc(F)c1
Reaction #48750
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C1N[C@@H](Cc2cc(F)cc(F)c2)[C@@H]([C@H]2C[C@H](O)CN2C(c2ccccc2)c2ccccc2)O1
Reaction #49216
title compound
收率 29.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1N[C@@H](Cc2cc(F)cc(F)c2)[C@@H]([C@H]2C[C@H](O)CN2C(c2ccccc2)c2ccccc2)O1
Reaction #49217
title compound
收率 95.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C)C(=O)c1cccc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@@H](OCCC)CN2)c1
Reaction #49233
title compound
收率 80.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@H]1CN[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)c2cccc(C(=O)N(CCC)CCC)c2)C1
Reaction #49234
title compound
收率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C)C(=O)c1cccc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2CC(O)(c3ccccc3)CN2)c1
Reaction #49236
title compound
收率 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCN(C)C(=O)c1cc(C)cc(C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@@H](OCCC)CN2)c1
Reaction #49240
title compound
收率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCO[C@H]1CN[C@@H]([C@@H](O)[C@H](Cc2cc(F)cc(F)c2)NC(=O)c2cc(C)cc(C(=O)N(CCC)CCC)c2)C1
Reaction #49241
title compound
收率 90.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC[C@@H](Cc2ccccc2)N1C(=O)[C@H](CC1CCCC1)[C@@H](O)CCc1ccccc1
Reaction #58580
3
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@H](CC1CCCC1)[C@@H](O)CCc1ccccc1
Reaction #58581
desired acid 4
收率 166.4%DOI: 10.6084/m9.figshare.5104873.v1
CN1C(=O)C(NC(=O)[C@H](CC2CC2)[C@@H](O)CCc2cc(F)cc(F)c2)N=C(c2ccccn2)c2ccccc21
Reaction #58583
3-(2-(R)-cyclopropylmethyl-5-(3,5-difluorophenyl)-3(S)-hydroxyl-1-oxopentyl)amino-1-methyl-5-(pyridin-2-yl)-2,3-dihydro-1H-1,4-benzodiazepin-2-one
DOI: 10.6084/m9.figshare.5104873.v1
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