Substructure Search

3603

CCCn1cnc(C(N)=O)c1N
Reaction #3740
title compound
Yield 61.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCn1cnc(C(N)=O)c1NC(=O)c1ccccc1OCC
Reaction #3741
title compound
Yield 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)OC[C@H]1O[C@@H](n2cnc(C(N)=O)c2N)[C@H](OC(=O)CC)[C@@H]1OC(=O)CC
Reaction #214529
5-amino-1-(2,3,5,-tri-O-propionyl-β-D-ribofuranosyl)imidazole-4-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCn1cnc(C(N)=O)c1NC(=O)c1ccccc1OCC
Reaction #391745
DOI: 10.1039/C8SC04228D
O=c1[nH]nnc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Reaction #489502
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]nnc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Reaction #800910
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC1C(O)C(CO)OC1n1cnc(C(N)=O)c1N
Reaction #894942
DOI: 10.1039/C8SC04228D
CCC(=O)OC[C@H]1O[C@@H](n2cnc(C#N)c2N)[C@H](OC(=O)CC)[C@@H]1OC(=O)CC
Reaction #934945
5-amino-1-(2,3,5-tri-O-propionyl-β-D-ribofuranosyl)imidazole-4-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ncn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)c1N
Reaction #934946
5-amino-1-β-D-ribofuranosylimidazole-4-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cnc(C(N)=O)c1N
Reaction #967134
5-amino-1-(2-O-methyl-β-D-ribofuranosyl)imidazole-4-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1ncn([C@@H]2O[C@H](CCl)[C@@H](O)[C@H]2O)c1N
Reaction #967135
5-amino-1-(5-chloro-5-deoxy-.beta.-D-ribofuranosyl)imidazole-4-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CCO[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cnc(C(N)=O)c1N
Reaction #967136
5-amino-1-(2-O-ethyl-β-D-ribofuranosyl) imidazole-4-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)c1ncn(C2OC(CO)C(O)C2O)c1NC(N)=S
Reaction #1047637
DOI: 10.1039/C8SC04228D
N#Cc1ncn(C2OC(CO)C(O)C2O)c1N
Reaction #1321531
DOI: 10.1039/C8SC04228D
CCCn1c(C)nc(C(N)=O)c1N
Reaction #1442738
title compound
Yield 45.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCn1c(Cc2ccccc2)nc(C(N)=O)c1N
Reaction #1442739
title compound
Yield 21.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCn1c(Cc2ccccc2)nc(C(N)=O)c1NC(=O)c1ccccc1OCC
Reaction #1442740
title compound
Yield 36.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCn1c(C)nc(C(N)=O)c1N
Reaction #1444737
title compound
Yield 45.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCn1c(Cc2ccccc2)nc(C(N)=O)c1N
Reaction #1444738
title compound
Yield 21.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCn1c(Cc2ccccc2)nc(C(N)=O)c1NC(=O)c1ccccc1OCC
Reaction #1444739
title compound
Yield 36.0%DOI: 10.6084/m9.figshare.5104873.v1
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