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223213

O=C1COc2ccc(-c3ccc4cc(-c5nc6cc(C(=O)O)ccc6n5C5CCCCC5)ccc4n3)cc2N1
Reaction #212233
DOI: 10.1039/C8SC04228D
O=C(O)c1ccc2c(c1)nc(-c1ccc3nc(C(=O)O)ccc3c1)n2C1CCCCC1
Reaction #232938
DOI: 10.1039/C8SC04228D
CCOC(=O)c1ccc2c(c1)nc(-c1ccc3nc(C(=O)NC(C)C(N)=O)ccc3c1)n2C1CCCCC1
Reaction #275002
DOI: 10.1039/C8SC04228D
O=C(O)c1ccc2c(c1)nc(-c1ccc3nc(CCCO)ccc3c1)n2C1CCCCC1
Reaction #373264
DOI: 10.1039/C8SC04228D
O=C(O)c1ccc2c(c1)nc(-c1ccc3nc(-c4cccc(Br)c4)ccc3c1)n2C1CCCCC1
Reaction #374112
DOI: 10.1039/C8SC04228D
O=C(O)c1ccc2c(c1)nc(-c1ccc3nc(-c4cccc(-c5ccc(Cl)cc5)c4)ccc3c1)n2C1CCCCC1
Reaction #1030529
DOI: 10.1039/C8SC04228D
NC(=O)c1cc(-c2ccc3cc(-c4nc5cc(C(=O)O)ccc5n4C4CCCCC4)ccc3n2)ccc1O
Reaction #1046256
DOI: 10.1039/C8SC04228D
O=C(O)C1CCCN1C(=O)c1ccc2c(c1)nc(-c1ccc3nc(-c4ccccc4)ccc3c1)n2C1CCCCC1
Reaction #1236913
DOI: 10.1039/C8SC04228D
CC1(C)C(CC(=O)O)CC1c1ccc2cc(-c3nc4cc(C(=O)O)ccc4n3C3CCCCC3)ccc2n1
Reaction #1287507
DOI: 10.1039/C8SC04228D
O=C(O)c1ccc2c(c1)nc(-c1ccc3nc(-c4cc(-c5ccc(Cl)c(Cl)c5)no4)ccc3c1)n2C1CCCCC1
Reaction #1321020
DOI: 10.1039/C8SC04228D
Cc1nc(-c2ccc(Cl)cc2)sc1-c1ccc2cc(-c3nc4cc(C(=O)O)ccc4n3C3CCCCC3)ccc2n1
Reaction #1652164
DOI: 10.1039/C8SC04228D
O=C(NC(CO)C(=O)O)c1ccc2c(c1)nc(-c1ccc3nc(-c4ccccc4)ccc3c1)n2C1CCCCC1
Reaction #1875590
Compound 231
Выход 36.0%DOI: 10.6084/m9.figshare.5104873.v1
NCCCCC(NC(=O)c1ccc2c(c1)nc(-c1ccc3nc(-c4ccccc4)ccc3c1)n2C1CCCCC1)C(=O)O
Reaction #1875591
Compound 232
Выход 15.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1CCCN1C(=O)c1ccc2c(c1)nc(-c1ccc3nc(-c4ccccc4)ccc3c1)n2C1CCCCC1
Reaction #1875592
Compound 233
Выход 15.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCC(NC(=O)c1ccc2c(c1)nc(-c1ccc3nc(-c4ccccc4)ccc3c1)n2C1CCCCC1)C(=O)O
Reaction #1875603
title compound
Выход 15.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc2c(c1)nc(-c1ccc3nc(-c4ccccc4-c4ccncc4)ccc3c1)n2C1CCCCC1
Reaction #1875613
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc2c(c1)nc(-c1ccc3nc(-c4cccc(C(=O)N5CCCC5)c4)ccc3c1)n2C1CCCCC1
Reaction #1875615
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ccc(Cl)cc2)c(-c2ccc3cc(-c4nc5cc(C(=O)O)ccc5n4C4CCCCC4)ccc3n2)c1
Reaction #1875622
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COCCOc1ccc(-c2ccc(Cl)cc2)c(-c2ccc3cc(-c4nc5cc(C(=O)O)ccc5n4C4CCCCC4)ccc3n2)c1
Reaction #1875623
2-{2-[4′-Chloro-4-(2-methoxy-ethoxy)-biphen-2-yl]-quinolin-6-yl}-1-cyclohexyl-1H-benzoimidazole-5-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOCCOc1ccc(-c2ccc(Cl)cc2)c(-c2ccc3cc(-c4nc5cc(C(=O)O)ccc5n4C4CCCCC4)ccc3n2)c1
Reaction #1875624
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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