بحث البنية الفرعية

584217

CCNC(=O)[C@H]1O[C@@H](n2cnc3c(NCC(c4cccc(C)c4)c4cccc(C)c4)nc(C(=O)NCCNC(=O)NCCN(C(C)C)C(C)C)nc32)[C@H](O)[C@@H]1O
Reaction #10527
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)[C@H]1O[C@@H](n2cnc3c(NCC(c4cccc(C)c4)c4cccc(C)c4)nc(I)nc32)[C@H](OC(=O)c2ccccc2)[C@@H]1OC(=O)c1ccccc1
Reaction #10555
title compound
المردود 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)[C@H]1O[C@@H](n2cnc3c(NCC(c4cccc(Cl)c4)c4cccc(Cl)c4)nc(I)nc32)[C@H](OC(=O)c2ccccc2)[C@@H]1OC(=O)c1ccccc1
Reaction #10556
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)C1OC(n2cnc3c(N)nc(C#CC4(O)CCCCC4C)nc32)C(O)C1O
Reaction #44344
5-[6-Amino-2-(1-hydroxy-2-methyl-cyclohexylethynyl)-purin-9-yl]-3,4-dihydroxytetrahydrofuran-2-carboxylic acid ethylamide
المردود 65.0%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
CCNC(=O)C1OC(n2cnc3c(NCC(c4cccc(Cl)c4)c4cccc(Cl)c4)nc(I)nc32)C(OC(=O)c2ccccc2)C1OC(=O)c1ccccc1
Reaction #287764
DOI: 10.1039/C8SC04228D
CCNC(=O)C1OC(n2cnc3c(NCC(c4ccc(Cl)cc4)c4ccc(Cl)cc4)nc(C#N)nc32)C(OC(=O)c2ccccc2)C1OC(=O)c1ccccc1
Reaction #399997
DOI: 10.1039/C8SC04228D
CCNC(=O)C1OC(n2cnc3c(NC(CO)Cc4ccccc4)nc(I)nc32)C(OC(=O)c2ccccc2)C1OC(=O)c1ccccc1
Reaction #404616
DOI: 10.1039/C8SC04228D
CCNC(=O)[C@H]1O[C@@H](n2cnc3c(NCC(c4cccc(C)c4)c4cccc(C)c4)nc(C(=O)NCCNC(=O)NCCN(C(C)C)C(C)C)nc32)[C@H](O)[C@@H]1O
Reaction #440798
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)[C@H]1O[C@@H](n2cnc3c(N)nc(C#CCC4CCC(C(=O)OC)CC4)nc32)[C@H](O)[C@@H]1O
Reaction #517578
DWH-146e
المردود 24.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)[C@H]1O[C@@H](n2cnc3c(N)nc(C#CCC4CCC(COC(C)=O)CC4)nc32)[C@H](O)[C@@H]1O
Reaction #517579
[4-(3-{9[(4S,5S,2R,3R)-5-(N-ethylcarbamoyl)-3,4-dihydroxyoxolan-2-yl]-6-aminopurin-2-yl}prop-2-ynyl)cyclohexyl]methyl acetate
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)[C@H]1O[C@@H](n2cnc3c(NCC(c4ccc(Cl)cc4)c4ccc(Cl)cc4)nc(I)nc32)[C@H](OC(=O)c2ccccc2)[C@@H]1OC(=O)c1ccccc1
Reaction #984307
title compound
المردود 48.9%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)[C@H]1O[C@@H](n2cnc3c(NCC(c4ccc(Cl)cc4)c4ccc(Cl)cc4)nc(C#N)nc32)[C@H](OC(=O)c2ccccc2)[C@@H]1OC(=O)c1ccccc1
Reaction #984308
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)C1OC(n2cnc3c(NCC(c4ccc(Cl)cc4)c4ccc(Cl)cc4)nc(I)nc32)C(OC(=O)c2ccccc2)C1OC(=O)c1ccccc1
Reaction #1025901
DOI: 10.1039/C8SC04228D
CCNC(=O)[C@H]1O[C@@H](n2cnc3c(NC4CCCCC4)nc(C(=O)NCCN4CCCCC4)nc32)[C@H](O)[C@@H]1O
Reaction #1147725
compound
المردود 58.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)[C@H]1O[C@@H](n2cnc3c(NCC(Cc4ccccc4)Cc4ccccc4)nc(I)nc32)[C@H](OC(=O)c2ccccc2)[C@@H]1OC(=O)c1ccccc1
Reaction #1147737
title compound
المردود 83.0%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)[C@H]1O[C@@H](n2cnc3c(NC(CC)CC)nc(I)nc32)[C@H](OC(=O)c2ccccc2)[C@@H]1OC(=O)c1ccccc1
Reaction #1147738
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)[C@H]1O[C@@H](n2cnc3c(N[C@H](CO)Cc4ccccc4)nc(I)nc32)[C@H](OC(=O)c2ccccc2)[C@@H]1OC(=O)c1ccccc1
Reaction #1147739
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)[C@H]1O[C@@H](n2cnc3c(NCC4c5ccccc5-c5ccccc54)nc(I)nc32)[C@H](OC(=O)c2ccccc2)[C@@H]1OC(=O)c1ccccc1
Reaction #1147740
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)[C@H]1O[C@@H](n2cnc3c(NC4CCCCC4)nc(I)nc32)[C@H](OC(=O)c2ccccc2)[C@@H]1OC(=O)c1ccccc1
Reaction #1147741
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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