子结构搜索

754

COCC(C)NS(=O)(=O)c1ccc(Nc2cc(Oc3ccc(C)nc3C)ccn2)cc1
Reaction #566
收率 52.0%
CC1(C)Oc2ccc(C#N)cc2C(OC(=O)C2CCCN2S(=O)(=O)c2ccc([N+](=O)[O-])cc2)C1Br
Reaction #194838
DOI: 10.1039/C8SC04228D
CC(C)(C#N)CN1C(=O)C2(OCCCO2)c2cc(S(=O)(=O)N3CCCC3COCc3ccccc3)ccc21
Reaction #206214
DOI: 10.1039/C8SC04228D
O=C1C(=O)N(Cc2ccnc(F)c2)c2ccc(S(=O)(=O)N3CCC3COc3ccccc3)cc21
Reaction #210465
DOI: 10.1039/C8SC04228D
CC(=O)Nc1ccc(S(=O)(=O)NC2COCOCC2O)cc1
Reaction #212173
DOI: 10.1039/C8SC04228D
CN1CCN(c2cccc3c2C[C@H](NS(=O)(=O)c2ccc(N4CCOCC4)cc2)CO3)CC1
Reaction #218318
title compound
收率 61.5%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC[C@H](CCCCNC(=O)OC(C)(C)C)N(CC(C)C)S(=O)(=O)c1ccc(NC(=O)OC(C)(C)C)cc1
Reaction #219884
(2S)-acetic acid 6-tert-butoxycarbonylamino-2-[(4-tert-butoxycarbonylamino-benzenesulfonyl)-isobutyl-amino]-hexyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)N[C@H](C(=O)NCCCC[C@@H](COC(=O)c1cccnc1)N(CC(C)C)S(=O)(=O)c1ccc(N)cc1)C(c1ccccc1)c1ccccc1
Reaction #219885
title compound
收率 20.0%DOI: 10.6084/m9.figshare.5104873.v1
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
CCOC(OCC)C(CC(=O)OC(C)(C)C)NS(=O)(=O)c1ccc(NC(C)=O)cc1OC(C)Cn1ncc2ccccc21
Reaction #221992
DOI: 10.1039/C8SC04228D
CCOC(=O)C1CCC2(CCOCC2)N1
Reaction #222889
DOI: 10.1039/C8SC04228D
CCC(NC(Cc1ccc2c(c1)OCC(c1ccc(OCc3ccc(Cl)c(Cl)c3)cc1)O2)C(=O)OC)c1ccccc1
Reaction #230175
DOI: 10.1039/C8SC04228D
COC(=O)C(Cc1ccc2c(c1)OCC(c1ccc(OCc3ccc(Cl)c(Cl)c3)cc1)O2)NS(=O)(=O)c1ccc([N+](=O)[O-])cc1
Reaction #233968
DOI: 10.1039/C8SC04228D
CCOC(OCC)C(CC(=O)OC(C)(C)C)NS(=O)(=O)c1ccc([N+](=O)[O-])cc1OCc1ccccc1
Reaction #234180
DOI: 10.1039/C8SC04228D
CN1C(=O)C(=O)c2cc(S(=O)(=O)N3CCC3COc3ccccc3)ccc21
Reaction #234309
DOI: 10.1039/C8SC04228D
O=C1C(=O)N(Cc2ccccc2F)c2ccc(S(=O)(=O)N3CCC3COc3ccccc3)cc21
Reaction #245757
DOI: 10.1039/C8SC04228D
CCOC(OCC)C(CC(=O)OC(C)(C)C)NS(=O)(=O)c1ccc(N)cc1OCc1ccccc1
Reaction #248110
DOI: 10.1039/C8SC04228D
O=C1Nc2ccc(S(=O)(=O)N3CCCC3COc3ccccc3)cc2C12OCCCO2
Reaction #253272
DOI: 10.1039/C8SC04228D
COCC1CCCN1S(=O)(=O)c1ccc2c(c1)C(=O)C1=NCCCN12
Reaction #263905
DOI: 10.1039/C8SC04228D
CS(=O)(=O)Nc1cc(C(O)CNC2CCN(c3ccc(S(=O)(=O)N4CCCC4C(=O)O)cc3)CC2)ccc1O
Reaction #273746
DOI: 10.1039/C8SC04228D
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