بحث البنية الفرعية

1177542

O=C(c1cc(Cl)cc(Cl)c1)N1CCC(NCc2ccnc3ccccc23)CC1Cc1ccccc1
Reaction #194705
DOI: 10.1039/C8SC04228D
O=C(c1cc(Cl)cc(Cl)c1)N1CCC(NC(c2ccccc2)c2ccccc2)CC1Cc1ccccc1
Reaction #211604
DOI: 10.1039/C8SC04228D
O=C(c1cc(Cl)cc(Cl)c1)N1CC[C@H](NCc2ccnc3ccccc23)C[C@H]1Cc1ccccc1
Reaction #351802
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc(Cl)cc(Cl)c1)N1CC[C@H](N(Cc2ccnc3ccccc23)C(=O)C(F)(F)F)C[C@H]1Cc1ccccc1
Reaction #351803
(2R*,4S*)-2-Benzyl-1-(3,5-dichlorobenzoyl)-N-(4-quinolylmethyl)-N-trifluoroacetyl-4-piperidinamine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc(Cl)cc(Cl)c1)N1CC[C@H](NCc2ccnc3ccccc23)C[C@H]1Cc1ccccc1
Reaction #351841
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(Cc1ccnc2ccccc12)[C@H]1CCN(C(=O)c2cc(Cl)cc(Cl)c2)[C@H](Cc2ccccc2)C1
Reaction #351865
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #351866
crystals
المردود 66.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #351867
residue
المردود 52.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc(Cl)cc(Cl)c1)N1CC[C@H](NCCc2ccccc2)C[C@H]1Cc1ccccc1
Reaction #351868
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc(Cl)cc(Cl)c1)N1CC[C@H](N(CCc2ccccc2)C(=O)C(F)(F)F)C[C@H]1Cc1ccccc1
Reaction #351870
title compound
المردود 60.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H]1CCN(C(=O)c2cc(Cl)cc(Cl)c2)[C@H](Cc2ccccc2)C1)c1ccc2ccccc2c1
Reaction #351873
title compound
المردود 96.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H]1CCN(C(=O)c2cc(Cl)cc(Cl)c2)[C@H](Cc2ccccc2)C1)c1ccnc2ccccc12
Reaction #351874
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H]1CCN(C(=O)c2cc(Cl)cc(Cl)c2)[C@H](Cc2ccccc2)C1)c1c[nH]c2ccccc12
Reaction #351875
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H]1CCN(C(=O)c2cc(Cl)cc(Cl)c2)[C@H](Cc2ccccc2)C1)c1cc2ccccc2[nH]1
Reaction #351876
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2[nH]c(C(=O)N[C@H]3CCN(C(=O)c4cc(Cl)cc(Cl)c4)[C@H](Cc4ccccc4)C3)cc2c1
Reaction #351877
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H]1CCN(C(=O)c2cc(Cl)cc(Cl)c2)[C@H](Cc2ccccc2)C1)c1cccc2ccccc12
Reaction #351878
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cc1ccccc1)N[C@H]1CCN(C(=O)c2cc(Cl)cc(Cl)c2)[C@H](Cc2ccccc2)C1
Reaction #351879
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1CN[C@H]1CCN(C(=O)c2cc(Cl)cc(Cl)c2)[C@H](Cc2ccccc2)C1
Reaction #351880
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc(Cl)cc(Cl)c1)N1CC[C@H](NCc2cc3ccccc3o2)C[C@H]1Cc1ccccc1
Reaction #351881
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc2[nH]cc(CN[C@H]3CCN(C(=O)c4cc(Cl)cc(Cl)c4)[C@H](Cc4ccccc4)C3)c2c1
Reaction #351882
title compound
DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي