Busqueda de Subestructura

35419

CCC(Nc1nc(N)c2ncn([C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)c2n1)c1ccccc1
Reaction #50343
secondary amine
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncnc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Reaction #50344
Adenosine
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Nc1nc(N)c2ncn([C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)c2n1)c1ccccc1
Reaction #50345
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC(Nc1nc(N)c2ncn([C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)c2n1)c1ccccc1
Reaction #50346
secondary amine
Rendimiento 74.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(Nc1nc(N)c2ncn([C@H]3O[C@H](CO)[C@@H](O)[C@H]3O)c2n1)c1ccccc1
Reaction #50347
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC(Nc1nc(N)c2ncn([C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)c2n1)c1ccccc1
Reaction #50348
secondary amine
Rendimiento 34.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(Nc2nc3c(ncn3COC(CO)CO)c(=O)[nH]2)(c2ccccc2)c2ccccc2)cc1.N#N
Reaction #92950
N2 (4-methoxyphenyldiphenylmethyl)-9-(1,3-dihydroxy-2-propoxymethyl)guanine
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(Nc2nc3c(ncn3COC(CO)CO)c(=O)[nH]2)(c2ccccc2)c2ccccc2)cc1.N#N
Reaction #93384
N2 (4-methoxyphenyldiphenylmethyl)-9-(1,3-dihydroxy-2-propoxymethyl)guanine
Rendimiento 100.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC(=O)OCC(COC(=O)CCCCCCC)OCn1cnc2c(=O)[nH]c(NC(c3ccccc3)(c3ccccc3)c3ccc(OC)cc3)nc21.N#N
Reaction #93385
N2 (4-methoxyphenyldiphenylmethyl)-9-(1,3-din-octanoyloxy-2-propoxymethyl)guanine
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC(=O)OCC(COC(=O)CCCCCCC)OCn1cnc2c(=O)[nH]c(N)nc21
Reaction #93386
9-(1,3-di-n-octanoyloxy-2-propoxymethyl)guanine
Rendimiento 63.2%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(NC2CC2)c2ncn([C@@H]3O[C@H](CO)[C@@H](O)[C@]34CCO4)c2n1
Reaction #164462
6-cyclopropylamino-nucleoside
Rendimiento 76.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C(Nc2nc(OC)c3ncn(C4OC(COC(c5ccccc5)(c5ccc(OC)cc5)c5ccc(OC)cc5)C(OC(=O)OCc5ccccc5)C4(C)F)c3n2)(c2ccccc2)c2ccc(OC)cc2)cc1
Reaction #209070
DOI: 10.1039/C8SC04228D
CCCCCCCC(=O)OCC(COC(=O)CCCCCCC)OCn1cnc2c(=O)[nH]c(N)nc21
Reaction #209447
DOI: 10.1039/C8SC04228D
CC(Nc1nc(CO)c2ncn(-c3cc(C4CC4)[nH]n3)c2n1)c1ccc(F)cc1
Reaction #222391
DOI: 10.1039/C8SC04228D
O=C(Nc1nc2c(ncn2CC(O)CF)c(=O)[nH]1)c1ccccc1
Reaction #223755
DOI: 10.1039/C8SC04228D
Nc1nc(NCc2ccccc2)nc2[nH]cnc12
Reaction #293207
DOI: 10.1039/C8SC04228D
O=c1c2nc[nH]c2nc2n1CCN2Cc1ccc(Cl)cc1
Reaction #323195
desired product
DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=N[C@]1(CO)O[C@@H](n2cnc3c(=O)[nH]c(N)nc32)[C@H](F)[C@@H]1O
Reaction #417953
( 27 )
Rendimiento 61.3%DOI: 10.6084/m9.figshare.5104873.v1
CN[C@@H]1[C@H](O)[C@H](NC)[C@H]2O[C@@]3(O)C(=O)C[C@@H](C)O[C@H]3O[C@@H]2[C@H]1O
Reaction #423211
Spectinomycin
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1nc2c(ncn2C2C(=O)N(O)C2CO)c(=O)[nH]1)c1ccccc1
Reaction #449055
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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