部分構造検索

CC(CCO)OC

Nc1ncnc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O
Reaction #3749
Adenosine
DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H]1O[C@@H](n2cnc3c(NCc4cccc(I)c4)nc(Cl)nc32)[C@H](O)[C@@H]1O
Reaction #6764
N6-(3-iodobenzyl)-2-Chloro-5′-O-methyladenosine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC[C@H]1O[C@@H](n2cnc3c(NCc4cccc(I)c4)ncnc32)[C@H](O)[C@@H]1O
Reaction #6766
N6-(3-Iodobenzyl)-5′-O-Ethyladenosine
DOI: 10.6084/m9.figshare.5104873.v1
O=P([O-])([O-])[O-]
Reaction #7441
Phosphate
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)C1OC(n2cnc3c(N)nc(C#CCC4CCC(C(=O)NC)CC4)nc32)C(O)C1O
Reaction #44343
JR3065
収率 48.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)C1OC(n2cnc3c(N)nc(C#CC4(O)CCCC(C)C4)nc32)C(O)C1O
Reaction #44345
5-[6-Amino-2-(1-hydroxy-3-methyl-cyclohexylethynyl)-purin-9-yl]-3,4-dihydroxytetrahydrofuran-2-carboxylic acid ethylamide
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 #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
収率 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
収率 34.6%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ncnc2c1ncn2[C@@H]1O[C@H](C(O)C(=O)OCc2ccccc2)[C@@H](O)[C@H]1O
Reaction #56257
Adenosine-5'-carboxylic acid benzyl ester
DOI: 10.6084/m9.figshare.5104873.v1
[N-]=[N+]=NCO[C@H]1C[C@H](n2cnc3c(NC(=O)c4ccccc4)ncnc32)O[C@@H]1CO
Reaction #86787
9a
収率 48.1%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCC=CC1OCC(C)C(OC)C1OC(=O)CNC(=O)OC(C)(C)C
Reaction #187520
DOI: 10.1039/C8SC04228D
Cc1ccc(-c2ccc(CNc3nc4c(N)ncnc4n3C3OC(CO)C(O)C3O)cc2)cc1
Reaction #188105
DOI: 10.1039/C8SC04228D
Cc1ccc(NC(=O)C(CCO)Oc2ncnc3c2cnn3-c2ncccc2Cl)nc1
Reaction #190724
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCCCCCNC1OC(CO)C(O)C(O)C1O
Reaction #212646
DOI: 10.1039/C8SC04228D
[CH2-]C(C)=O
Reaction #231235
DOI: 10.1039/C8SC04228D
CCCCCCCCCCCCCCNC1OC(CO)C(O)C(O)C1O
Reaction #232402
DOI: 10.1039/C8SC04228D
1 ページ次のページ