부분 구조 검색

C1CCCC(CC1)NC2CCCCC2

O=C(O)CSc1cnc(NC(=O)N(C2CCCCCC2)C2CCC(c3ccccc3)CC2)s1
Reaction #229178
DOI: 10.1039/C8SC04228D
CCN(CC)C(=O)N(C1CCCCC1)C1CC2CCC(C1)N2C(=O)C(Cc1ccc(Cl)cc1)NCC1CC(O)CN1C(=O)OC(C)(C)C
Reaction #233819
DOI: 10.1039/C8SC04228D
CC(C)C1CCC(N(C(=O)Nc2ncc(SCC(=O)O)s2)C2CCCCCC2)CC1
Reaction #254609
DOI: 10.1039/C8SC04228D
COC(=O)CCS(=O)(=O)N1CCN(Cc2cnc(NC(=O)N(C3CCCCCC3)C3CCC(C)CC3)s2)CC1
Reaction #300881
DOI: 10.1039/C8SC04228D
O=C(O)CSc1cnc(NC(=O)N(C2CCCCCC2)C2CCCCC2)s1
Reaction #340999
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CC[C@H](N(C(=O)Nc2ncc(SCC(=O)O)s2)C2CCCCCC2)CC1
Reaction #341000
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCS(=O)(=O)N1CCN(Cc2cnc(NC(=O)N(C3CCCCCC3)[C@H]3CC[C@H](C)CC3)s2)CC1
Reaction #341012
Trans-3-(4-{2-[3-cycloheptyl-3-(4-methyl-cyclohexyl)-ureido]-thiazol-5-ylmethyl}-piperazine-1-sulfonyl)-propionic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cnc(NC(=O)N(C2CCCCC2)C2CCCCC2)s1
Reaction #341065
1,1-dicyclohexyl-3-(5-formyl-thiazol-2-yl)-urea
수율 34.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CC[C@H](N(C(=O)Nc2ncc(SCCC(=O)O)s2)C2CCCCCC2)CC1
Reaction #341078
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCSc1cnc(NC(=O)N(C2CCCCCC2)C2CCCCC2)s1
Reaction #341110
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C(=O)N(C1CCCCC1)C1CC2CCC(C1)N2C(=O)C(Cc1ccc(Cl)cc1)NCC1CC(O)CN1
Reaction #370184
DOI: 10.1039/C8SC04228D
O=C(O)CSc1cnc(NC(=O)N(C2CCCCCC2)C2CCCCC2)s1
Reaction #619130
title compound
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CC[C@H](N(C(=O)Nc2ncc(SCC(=O)O)s2)C2CCCCCC2)CC1
Reaction #619131
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCS(=O)(=O)N1CCN(Cc2cnc(NC(=O)N(C3CCCCCC3)[C@H]3CC[C@H](C)CC3)s2)CC1
Reaction #619141
Trans-3-(4-{2-[3-cycloheptyl-3-(4-methyl-cyclohexyl)-ureido]-thiazol-5-ylmethyl}-piperazine-1-sulfonyl)-propionic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1cnc(NC(=O)N(C2CCCCC2)C2CCCCC2)s1
Reaction #619191
1,1-dicyclohexyl-3-(5-formyl-thiazol-2-yl)-urea
수율 34.3%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H]1CC[C@H](N(C(=O)Nc2ncc(SCCC(=O)O)s2)C2CCCCCC2)CC1
Reaction #619204
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)CCSc1cnc(NC(=O)N(C2CCCCCC2)C2CCCCC2)s1
Reaction #619234
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)C(=O)N(C1CCCCC1)C1CC2CCC(C1)N2C(=O)C(Cc1ccc(Cl)cc1)NC1CCOCC1
Reaction #754046
DOI: 10.1039/C8SC04228D
c1cc2[nH]ncc2cc1NC1CCC(NC2CCCCCC2)CC1
Reaction #773930
DOI: 10.1039/C8SC04228D
CC(C)(C)[C@H]1CC[C@H](N(C(=O)Nc2ncc(SCC(=O)O)s2)C2CCCCCC2)CC1
Reaction #818616
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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