Substructure Search

CC(CO)O

CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccc(C#N)cc2)SC[C@H]1OC(C)=O
Reaction #6088
expected product
Yield 17.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccc(C#N)cc2)SC[C@H]1OC(C)=O
Reaction #6089
expected product
Yield 23.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccc(C#N)cc2)SC[C@H]1OC(C)=O
Reaction #6090
expected product
Yield 64.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(S[C@@H]2SC[C@@H](O)[C@H](O)[C@H]2O)cc1
Reaction #6091
expected product
Yield 89.7%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2cccc(C#N)c2)SC[C@H]1OC(C)=O
Reaction #6098
expected product
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2cccc(C#N)c2)SC[C@H]1OC(C)=O
Reaction #6099
expected product
Yield 31.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccccc2C#N)SC[C@H]1OC(C)=O
Reaction #6101
expected product
Yield 50.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccccc2C#N)SC[C@H]1OC(C)=O
Reaction #6102
expected product
Yield 60.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccccc2)SC[C@H]1OC(C)=O
Reaction #6105
expected product
Yield 52.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)O[C@@H]1[C@@H](OC(C)=O)[C@H](Sc2ccccc2)SC[C@H]1OC(C)=O
Reaction #6106
expected product
Yield 32.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](CO)Oc1cc(Oc2ccc(-c3ncon3)cc2)cc(C(=O)Nc2ccn(C)n2)c1
Reaction #48833
title compound
Yield 84.5%DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H](C)Oc1cc(Oc2ccc(-c3ncon3)cc2)cc(C(=O)Nc2ccn(C)n2)c1
Reaction #48834
desired compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](CO)Oc1cc(Oc2cc(Cl)c(C(=O)N(C)C)cc2F)cc(C(=O)Nc2ccn(C)n2)c1
Reaction #48875
title compound
Yield 16.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ncnc2c1ncn2[C@@H]1O[C@H](CO)[C@H]1CO)c1ccccc1
Reaction #65670
6-benzamido-9-((2R,3R,4S) 3,4-bis(hydroxymethyl)-oxetan-2-yl)purine
DOI: 10.6084/m9.figshare.5104873.v1
CCCCNCC1COc2ccc(S(C)(=O)=O)cc2O1
Reaction #67194
N-{[7-(METHYLSULFONYL)-2,3-DIHYDRO-1,4-BENZODIOXIN-2-YL]METHYL}BUTAN-1-AMINE
DOI: 10.6084/m9.figshare.5104873.v1
CCN(Cc1ccccc1)C[C@H]1COc2ccc(SC)c(F)c2O1
Reaction #67300
title compound
Yield 51.3%DOI: 10.6084/m9.figshare.5104873.v1
CSc1ccc(Nc2c(C(=O)NOC[C@H](O)CO)ccc3cnsc23)c(F)c1
Reaction #166257
title compound
Yield 26.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ccc(S(=O)(=O)NC(C(=O)O)C(OCc3ccccc3)C(O)CSc3nccs3)cc2)cc1
Reaction #174962
DOI: 10.1039/C8SC04228D
CCCCNCC1COc2ccc(S(C)(=O)=O)cc2O1
Reaction #187462
DOI: 10.1039/C8SC04228D
Nc1nc(C#CC2CCCCC2)nc2c1ncn2C1OC(CO)C(O)C1O
Reaction #189708
DOI: 10.1039/C8SC04228D
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