部分構造検索

C1CCOC1.C1CCOC1

O=c1ccn([C@H]2C[C@H](O)[C@@H](CO)O2)c(=O)[nH]1.O=c1ccn([C@H]2C[C@H](O)[C@@H](CO)O2)c(=O)[nH]1
Reaction #4261
dUrd 2'-deoxyuridine
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c(=O)c2[nH]c(=O)[nH]c2[nH]1
Reaction #5857
Uric Acid
DOI: 10.6084/m9.figshare.5104873.v1
O=P([O-])([O-])[O-]
Reaction #7441
Phosphate
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #9810
salt
収率 30.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)C(=O)Nc1cnc([C@H](O)CO)cn1
Reaction #40279
(S)—N-[5-(1,2-dihydroxy-ethyl)-pyrazin-yl]-2,2-dimethyl-propionamide
収率 105.1%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@](O)(CCO)CC(=O)[O-]
Reaction #42641
mevalonate
DOI: 10.6084/m9.figshare.5104873.v1
C/C(=C\c1csc(C)n1)[C@@H]1C[C@@H]2O[C@]2(C)CCC[C@H](C)[C@H](O)[C@@H](C)C(=O)C(C)(C)[C@@H](O)CC(=O)O1
Reaction #42642
epothilone B
DOI: 10.6084/m9.figshare.5104873.v1
C/C(=C\c1csc(C)n1)[C@@H]1C[C@@H]2O[C@]2(C)CCC[C@H](C)[C@H](O)[C@@H](C)C(=O)C(C)(C)[C@@H](O)CC(=O)O1
Reaction #53255
epothilone B
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](C(=O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H]1O[C@@H](CC(=O)OO)[C@H](C)C[C@@H]1C)[C@H]1O[C@](C)([C@]2(O)O[C@](CC)([C@@H](O)CC)C[C@H]2C)C[C@@H]1C
Reaction #62575
lysocellin
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1C2CCC(O2)C1C(=O)OCc1ccccc1
Reaction #73454
10
DOI: 10.6084/m9.figshare.5104873.v1
O=P([O-])([O-])OP(=O)([O-])OP(=O)([O-])OP(=O)(O)O.O=c1ccn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)c(=O)[nH]1.O=c1ccn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)c(=O)[nH]1.[NH4+].[NH4+].[NH4+].[NH4+]
Reaction #78833
diuridine tetraphosphate tetraammonium salt
収率 30.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccccc1C1CCc2cc(O[C@H]3CC[C@H](NCC4CCOC4)CC3)ccc2O1
Reaction #88053
(tetrahydrofuran-3-ylmethyl)-[trans-4-(2-o-tolyl-chroman-6-yloxy)-cyclohexyl]-amine
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OC(=O)C2C3CCC(O3)C12
Reaction #155664
product
収率 50.6%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(-c2nc(N3CC4CCC(C3)O4)cc(N3CC4CCC(C3)O4)n2)cc1
Reaction #162600
title compound
収率 39.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(-c2nc(N3CC4CCC(C3)O4)cc(N3CC4CCC(C3)O4)n2)cc1
Reaction #162601
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(-c2cc(N3CC4CCC(C3)O4)nc(N3CC4CCC(C3)O4)n2)cc1
Reaction #162602
title compound
収率 65.6%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(-c2cc(N3CC4CCC(C3)O4)nc(N3CC4CCC(C3)O4)n2)cc1
Reaction #162603
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Oc1nc(N2CC3CCC(C2)O3)cc(N2CC3CCC(C2)O3)n1
Reaction #162606
title compound
収率 42.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1nc(N2CC3CCC(C2)O3)cc(N2CC3CCC(C2)O3)n1
Reaction #162607
title compound
収率 93.0%DOI: 10.6084/m9.figshare.5104873.v1
N=c1sc2c(n1C[C@H]1CCCO1)C1CCC(C2)O1
Reaction #165710
crude material
収率 90.5%DOI: 10.6084/m9.figshare.5104873.v1
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