子结构搜索

CCCCNCCCC

CCc1nn2c(-c3c(C)cc(C)cc3OC)cccc2c1N(CC1CCOCC1)CC1CC1
Reaction #9299
title compound
收率 41.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1nn2c(-c3c(C)cc(C)cc3O)cccc2c1N(CC1CC1)CC1CC1
Reaction #9316
title compound
收率 50.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cc(C)cc(C)c1-c1cccc2c(N(CC3CC3)CC3CC3)c(SC)nn12
Reaction #9317
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C)cc(C)c1-c1cccc2c(N(CC3CC3)CC3CC3)c(S(C)=O)nn12
Reaction #9319
title compound
收率 78.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C)cc(C)c1-c1cccc2c(N(CC3CC3)CC3CC3)c(S(C)(=O)=O)nn12
Reaction #9320
title compound
收率 5.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C)cc(C)c1-c1cccc2c(N(CC3CCOCC3)CC3CC3)c(OC)nn12
Reaction #9324
title compound
收率 70.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOCc1nc2c(N)nc(C)c(C)c2n1CCC1CCN(C(=O)[C@@H]2C[C@H]2c2ccccc2)CC1
Reaction #11468
desired product
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-c2csc3c(CCCN4CCC(O)CC4)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #45526
title compound
收率 26.7%DOI: 10.6084/m9.figshare.5104873.v1
CCCCOc1c(OC)ccc(S(=O)(=O)N[C@@H](CCCNC(=N)N)C(=O)N2CCC(C)CC2C(=O)O)c1OC
Reaction #74759
1-[N2 -(3-butoxy2,4-dimethoxyphenylsulfonyl)-L-arginyl]-4-methyl-2-piperidinecarboxylic acid
收率 79.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)N[C@@H](CCCNC(=N)N)C(=O)N2CCC(C)CC2C(=O)O)cc1C1CCCCC1
Reaction #94591
1-[N2 -(3-cyclohexyl-4-methoxyphenylsulfonyl)-L-arginyl]-4-methyl-2-piperidinecarboxylic acid
收率 73.4%DOI: 10.6084/m9.figshare.5104873.v1
O=CC1CC(N2CCCCC2Nc2nc(-c3c[nH]c4ncc(Cl)cc34)ncc2F)C1
Reaction #162058
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CSc1nn2c(-c3c(C)cc(C)cc3O)cccc2c1N(CC1CC1)CC1CC1
Reaction #174995
DOI: 10.1039/C8SC04228D
CCCCN(CCCC)CCNC(=O)Nc1ccc(Oc2ncnc3cc(OC)c(OC)cc23)cc1OC
Reaction #193810
DOI: 10.1039/C8SC04228D
O=C(CC1c2ccccc2-c2ccccc2N1S(=O)(=O)c1ccc(Cl)c(Cl)c1)NC1CCC(CCN2CCCC2)CC1
Reaction #205280
DOI: 10.1039/C8SC04228D
Cc1ccc(S(=O)(=O)N2CCNC(=O)C2CC(=O)NC2CCCc3cc(-c4ccccc4-c4nc(C)no4)ccc32)cc1
Reaction #208130
DOI: 10.1039/C8SC04228D
COc1cc(-c2csc3c(CCCN4CCC(O)CC4)cnc(N)c23)ccc1NC(=O)c1cc2ccccc2n1C
Reaction #211306
DOI: 10.1039/C8SC04228D
COC(=O)NC(C(=O)NCCCC[C@@H](COC(=O)[C@@H](N)C(C)C)N(CC(C)C)S(=O)(=O)c1ccc(N)cc1)C(c1ccccc1)c1ccccc1
Reaction #219886
(2S,2S)-2-amino-3-methyl-butyric acid 2-[(4-amino-benzenesulfonyl)-isobutyl-amino]-6-(2-methoxycarbonylamino-3,3-diphenyl-propionylamino)-hexyl ester
收率 47.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCS(=O)(=O)N1CCN(Cc2cnc(NC(=O)N(C3CCCCC3)C3CCC(C)CC3)s2)CC1
Reaction #224836
DOI: 10.1039/C8SC04228D
O=C(c1ccc(F)cc1)C1CCN(CC2CCC3CN(c4noc5ccccc45)CCN3C2)CC1
Reaction #228247
DOI: 10.1039/C8SC04228D
Nc1c(Cl)cc(S(=O)(=O)NC(Cc2ccc3[nH]cnc3c2)C(=O)N2CCC(C(=O)O)CC2)cc1Cl
Reaction #228353
DOI: 10.1039/C8SC04228D
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