بحث البنية الفرعية

852212

C[C@@H](C(=O)N1CCCCC1)N1CC[C@H](NS(=O)(=O)/C=C/c2ccc(Cl)cc2)C1=O
Reaction #7395
title compound
المردود 21.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](C(=O)N1CCOCC1)N1CC[C@H](NS(=O)(=O)/C=C/c2ccc(Cl)c(O)c2)C1=O
Reaction #7419
title compound
المردود 83.8%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CN1C(=O)[C@H](NC(=O)c2cc3cc(Cl)ccc3[nH]2)Cc2ccccc21
Reaction #11674
title compound
المردود 26.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CN1C(=O)[C@@H](NC(=O)c2cc3cc(Cl)ccc3[nH]2)Cc2ccccc21
Reaction #11675
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CN1C(=O)[C@H](NC(=O)c2cc3cc(Cl)ccc3[nH]2)Cc2ccccc21
Reaction #11676
title compound
المردود 95.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CN1C(=O)[C@@H](NC(=O)c2cc3cc(Cl)ccc3[nH]2)Cc2ccccc21
Reaction #11677
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H]1Cc2ccccc2N(CCO)C1=O)c1cc2cc(Cl)ccc2[nH]1
Reaction #11678
title compound
المردود 19.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)CN1C(=O)[C@H](NC(=O)c2cc3cc(Cl)ccc3[nH]2)Cc2ccccc21
Reaction #11679
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)CN1C(=O)[C@@H](NC(=O)c2cc3cc(Cl)ccc3[nH]2)Cc2ccccc21
Reaction #11680
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N[C@@H]1CC[C@@H](c2cccc(F)c2F)CN(Cc2ccccn2)C1=O
Reaction #48424
title compound
المردود 99.6%DOI: 10.6084/m9.figshare.5104873.v1
N[C@@H]1CC[C@@H](c2cccc(F)c2F)CN(Cc2ccccn2)C1=O
Reaction #48425
(3R,6S)-3-Amino-6-(2,3-difluorophenyl)-1-(pyridin-2-ylmethyl)azepan-2-on
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CN1C(=O)[C@H](NC(=O)c2cc3cc(Cl)ccc3[nH]2)Cc2ccccc21
Reaction #59399
title compound
المردود 26.3%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CN1C(=O)[C@@H](NC(=O)c2cc3cc(Cl)ccc3[nH]2)Cc2ccccc21
Reaction #59400
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CN1C(=O)[C@H](NC(=O)c2cc3cc(Cl)ccc3[nH]2)Cc2ccccc21
Reaction #59401
title compound
المردود 95.6%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CN1C(=O)[C@@H](NC(=O)c2cc3cc(Cl)ccc3[nH]2)Cc2ccccc21
Reaction #59402
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N[C@H]1Cc2ccccc2N(CCO)C1=O)c1cc2cc(Cl)ccc2[nH]1
Reaction #59403
title compound
المردود 19.0%DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)CN1C(=O)[C@H](NC(=O)c2cc3cc(Cl)ccc3[nH]2)Cc2ccccc21
Reaction #59404
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)CN1C(=O)[C@@H](NC(=O)c2cc3cc(Cl)ccc3[nH]2)Cc2ccccc21
Reaction #59405
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(N(C)CC(=O)N(C)C)c2sc(NC(=O)c3ccc(F)cc3)nc12
Reaction #80151
N-[7-(Dimethylcarbamoylmethyl-methyl-amino)-4-methoxy-benzothiazol-2-yl]-4-fluoro-benzamide
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC(=O)N(C)C)c1ccc(OC)c2nc(NC(=O)c3ccc(F)cc3)sc12
Reaction #80155
N-[7-(Dimethylcarbamoylmethyl-ethyl-amino)-4-methoxy-benzothiazol-2-yl]-4-fluoro-benzamide
DOI: 10.6084/m9.figshare.5104873.v1
الصفحة 1التالي