Substructure Search

Nc1cccnc1S

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Reaction #11433
Formula XII
DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C1CSc2ncc(CNC3CCN(C[C@@H]4Cn5c(=O)ccc6ncc(F)c4c65)CC3)cc2N1
Reaction #43624
title compound
Yield 39.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1nc(C)ccc1NC(=O)CCCCCCCCBr
Reaction #51160
9-bromo-N-(6-methyl-2-methylthio-3-pyridyl)nonanamide
Yield 27.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1cc(C)nc(SC)c1NC(=O)CBr
Reaction #51161
2-bromo-N-[2,4-bis(methylthio)-6-methyl-3-pyridyl]acetamide
Yield 13.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1cc(C)nc(SC)c1NC(=O)CCCBr
Reaction #51162
4-bromo-N-[2,4-bis(methylthio)-6-methyl-3-pyridyl]butanamide
Yield 66.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cccnc1SCCSc1ccccc1
Reaction #173019
DOI: 10.1039/C8SC04228D
COc1cc(C)nc(OC)c1NC(=O)CN1CCN(CCSc2nc3ccccc3o2)CC1
Reaction #174343
DOI: 10.1039/C8SC04228D
Cc1cc(N2CCOCC2)c(NC(=O)CN2CCN(CCSc3nc4cccc(C(F)(F)F)c4o3)CC2)c(N2CCOCC2)n1
Reaction #177717
DOI: 10.1039/C8SC04228D
O=C1CSc2ncc(C(=O)O)cc2N1
Reaction #185481
DOI: 10.1039/C8SC04228D
CN1CNc2cccnc2S1(=O)=O
Reaction #187225
DOI: 10.1039/C8SC04228D
O=C1CSc2ncc(C(=O)O)cc2N1
Reaction #187972
DOI: 10.1039/C8SC04228D
Cc1cc(N2CCOCC2)c(NC(=O)CN2CCN(CCSc3nc4ccccc4o3)CC2)c(N2CCOCC2)n1
Reaction #194747
DOI: 10.1039/C8SC04228D
CCSc1nc(N)ccc1[N+](=O)[O-]
Reaction #196103
DOI: 10.1039/C8SC04228D
Cc1c(OS(=O)(=O)C(F)(F)F)c([N+](=O)[O-])c2n(c1=O)CCS2
Reaction #197337
DOI: 10.1039/C8SC04228D
Nc1ccnc(N(Cc2ccccc2)Cc2ccccc2)c1[N+](=O)[O-]
Reaction #200588
DOI: 10.1039/C8SC04228D
CN1C=NS(=O)(=O)c2ncccc21
Reaction #221726
DOI: 10.1039/C8SC04228D
CSc1cc(C)nc(SC)c1NC(=O)CN1CCN(CCOS(C)(=O)=O)CC1
Reaction #222074
DOI: 10.1039/C8SC04228D
CCOC(=O)C1=CNc2cccnc2S1
Reaction #225962
DOI: 10.1039/C8SC04228D
CCN1C=NS(=O)(=O)c2ncc(C)cc21
Reaction #230521
DOI: 10.1039/C8SC04228D
Cc1cnc2c(c1)N(C)CNS2(=O)=O
Reaction #236964
DOI: 10.1039/C8SC04228D
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