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CCS(=O)(=O)N1CCC(c2c[nH]c3c(C(N)=O)cc(-c4csc(C=O)c4)cc23)CC1

CCS(=O)(=O)N1CCC(c2c[nH]c3c(C(N)=O)cc(-c4csc(CN5CCCC5C)c4)cc23)CC1
Reaction #177642
DOI: 10.1039/C8SC04228D
COCCCS(=O)(=O)N1CCC(c2c[nH]c3c(C(N)=O)cc(-c4csc(CN5CCCC5)c4)cc23)CC1
Reaction #193161
DOI: 10.1039/C8SC04228D
CCS(=O)(=O)N1CCC(c2c[nH]c3c(C(N)=O)cc(-c4csc(C(C)N5CCCC5)c4)cc23)CC1
Reaction #221148
DOI: 10.1039/C8SC04228D
CCS(=O)(=O)N1CCC(c2c[nH]c3c(C(N)=O)cc(-c4csc(CN(C)Cc5c(C)n[nH]c5C)c4)cc23)CC1
Reaction #254400
DOI: 10.1039/C8SC04228D
CC(C)S(=O)(=O)N1CCC(c2c[nH]c3c(C(N)=O)cc(-c4csc(CN5CCCC5C(N)=O)c4)cc23)CC1
Reaction #260476
DOI: 10.1039/C8SC04228D
CCS(=O)(=O)N1CCC(c2c[nH]c3c(C(N)=O)cc(-c4csc(C=O)c4)cc23)CC1
Reaction #649206
title compound
المردود 89.2%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)S(=O)(=O)N1CCC(c2c[nH]c3c(C(N)=O)cc(-c4csc(C=O)c4)cc23)CC1
Reaction #649213
title compound
المردود 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)N1CCC(c2c[nH]c3c(C(N)=O)cc(-c4csc(CN5CCCC5c5ccccc5)c4)cc23)CC1
Reaction #649255
title compound
المردود 22.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCC1CCCN1Cc1cc(-c2cc(C(N)=O)c3[nH]cc(C4CCN(S(=O)(=O)CC)CC4)c3c2)cs1
Reaction #649280
title compound
المردود 38.7%DOI: 10.6084/m9.figshare.5104873.v1
CCN(C)Cc1cc(-c2cc(C(N)=O)c3[nH]cc(C4CCN(S(=O)(=O)CC)CC4)c3c2)cs1
Reaction #649286
title compound
المردود 61.4%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)N1CCC(c2c[nH]c3c(C(N)=O)cc(-c4csc([C@H](C)N5CCCC5)c4)cc23)CC1
Reaction #649387
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)N1CCC(c2c[nH]c3c(C(N)=O)cc(-c4csc([C@@H](C)N5CCCC5)c4)cc23)CC1
Reaction #649388
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)N1CCC(c2c[nH]c3c(C(N)=O)cc(-c4csc(CN5CCC[C@@H]5C)c4)cc23)CC1
Reaction #649390
title compound
المردود 17.3%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)c1cc(-c2cc(C(N)=O)c3[nH]cc(C4CCN(S(=O)(=O)CC)CC4)c3c2)cs1
Reaction #649400
3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(5-propanoyl-3-thienyl)-1H-indole-7-carboxamide
المردود 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)N1CCC(c2c[nH]c3c(C(N)=O)cc(-c4csc(C(=O)C(C)C)c4)cc23)CC1
Reaction #649408
3-[1-(ethylsulfonyl)-4-piperidinyl]-5-[5-(2-methylpropanoyl)-3-thienyl]-1H-indole-7-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)N1CCC(c2c[nH]c3c(C(N)=O)cc(-c4csc(CN5CCC[C@H]5C(F)(F)F)c4)cc23)CC1.O=C(O)C(F)(F)F
Reaction #649490
title compound
المردود 8.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)S(=O)(=O)N1CCC(c2c[nH]c3c(C(N)=O)cc(-c4csc(CN5CCC[C@@H]5CO)c4)cc23)CC1
Reaction #649491
title compound
المردود 69.7%DOI: 10.6084/m9.figshare.5104873.v1
C=CCN(C)Cc1cc(-c2cc(C(N)=O)c3[nH]cc(C4CCN(S(=O)(=O)CC)CC4)c3c2)cs1
Reaction #649496
title compound
المردود 23.1%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)N1CCC(c2c[nH]c3c(C(N)=O)cc(-c4csc(CN(C)Cc5c(C)n[nH]c5C)c4)cc23)CC1
Reaction #649497
title compound
المردود 11.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)N(C)Cc1cc(-c2cc(C(N)=O)c3[nH]cc(C4CCN(S(=O)(=O)CC)CC4)c3c2)cs1
Reaction #649499
title compound
المردود 27.9%DOI: 10.6084/m9.figshare.5104873.v1
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