部分構造検索

60593

O=C1Cc2ccc(C(=O)c3ccccc3)cc2N1
Reaction #4570
6-benzoyloxindole
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2ccc3c(c2)NC(=O)C3)c1
Reaction #52603
6-(3-methoxypheny)-2-oxindole
収率 69.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2ccc3c(c2)NC(=O)C3=Cc2cc(C(C)C)c(OC)c(C(C)C)c2)c1
Reaction #52722
3-(3,5-diisopropyl-4-methoxybenzylidene)-6-(3-methoxyphenyl)-1,3-dihydroindol-2-one
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cccc(-c2ccc3c(c2)NC(=O)C3)c1
Reaction #52737
6-(3-ethoxyphenyl)-2-oxindole
収率 91.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cccc(-c2ccc3c(c2)NC(=O)C3=Cc2cc(C(C)C)c(OC)c(C(C)C)c2)c1
Reaction #52738
3-(3,5-diisopropyl-4-methoxybenzylidene)-6-(3-ethoxyphenyl)-1,3-dihydroindol-2-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1-c1ccc2c(c1)NC(=O)C2=Cc1[nH]c(C)cc1CCC(=O)O
Reaction #52748
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2ccc3c(c2)NC(=O)C3=Cc2[nH]c3c(c2CCC(=O)O)CCCC3)c1
Reaction #52793
3-{2-[6-(3-methoxyphenyl)-2-oxo-1,2-dihydroindol-3-ylidenemethyl]-4,5,6,7-tetrahydro-1H-indol-3-yl}-propionic acid
収率 82.1%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ccc3c(c2)NC(=O)C3=Cc2[nH]c3c(c2CCC(=O)O)CCCC3)cc1
Reaction #52794
3-{2-[6-(4-Methoxyphenyl)-2-oxo-1,2-dihydroindol-3-ylidenemethyl]-4,5,6,7-tetrahydro-1H-indol-3-yl}-propionic acid
収率 30.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1-c1ccc2c(c1)NC(=O)C2=Cc1[nH]c2c(c1CCC(=O)O)CCCC2
Reaction #52798
3-{2-[6-(2-methoxyphenyl)-2-oxo-1,2-dihydroindol-3-ylidenemethyl]-4,5,6,7-tetrahydro-1H-indol-3yl}-propionic acid
収率 35.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2ccc3c(c2)NC(=O)C3=Cc2[nH]c(C(=O)O)c(C)c2CCC(=O)O)c1
Reaction #52828
4-(2-Carboxyethyl)-5-[6-(3-methoxyphenyl)-2-oxo-1,2-dihydroindol-3-ylidenemethyl]-3-methyl-1H-pyrrole-2-carboxylic acid
収率 92.6%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cccc(-c2ccc3c(c2)NC(=O)C3=Cc2[nH]c(C(=O)O)c(C)c2CCC(=O)O)c1
Reaction #52830
4-(2-Carboxyethyl)-5-[6-(3-ethoxyphenyl)-2-oxo-1,2-dihydroindol-3-ylidenemethyl]-3-methyl-1H-pyrrole-2-carboxylic acid
収率 80.4%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCN1CCc2c(C)c(NS(=O)(=O)NC(=O)OC)c(C)c(NC(=O)C(C)(C)C)c21
Reaction #61876
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCN1CCc2c(C)c(NS(=O)(=O)NC(=O)OC(C)(C)C)c(C)c(NC(=O)C(C)(C)C)c21
Reaction #61877
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCN1CCc2c(C)c(NS(N)(=O)=O)c(C)c(NC(=O)C(C)(C)C)c21.Cl
Reaction #61878
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCCCN1CCc2c(C)c(NC(N)=O)c(C)c(NC(=O)C(C)(C)C)c21.Cl
Reaction #61879
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(=O)Nc2cc(-c3nc4ccccc4[nH]3)ccc21
Reaction #64678
grey crystals
収率 10.3%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ccc3c(c2)NC(=O)C3=Cc2cc3cc(OCCN4CCCC4)ccc3[nH]2)cc1
Reaction #77361
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2ccc3c(c2)NC(=O)C3=Cc2cc3cc(OCCN4CCCC4)ccc3[nH]2)c1
Reaction #77362
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1-c1ccc2c(c1)NC(=O)C2=Cc1cc2cc(OCCN3CCCC3)ccc2[nH]1
Reaction #77363
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ccc3c(c2)NC(=O)C3=Cc2cc3cc(OCCN4CCOCC4)ccc3[nH]2)cc1
Reaction #77364
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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