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1359248

CN(C)S(=O)(=O)N1CCN(C(=O)c2cnc(NC(=O)N(C3CCCCC3)C3CCCCC3)s2)CC1
Reaction #184113
DOI: 10.1039/C8SC04228D
O=C(Nc1ncc(CN2CCN(S(=O)(=O)Cc3ccccc3)CC2)s1)N(C1CCCCC1)C1CCCCC1
Reaction #207778
DOI: 10.1039/C8SC04228D
COC(=O)CCS(=O)(=O)N1CCN(Cc2cnc(NC(=O)N(C3CCCCC3)C3CCC(C)CC3)s2)CC1
Reaction #224836
DOI: 10.1039/C8SC04228D
CC(C)S(=O)(=O)N1CCN(Cc2cnc(NC(=O)N(C3CCCCC3)C3CCCCC3)s2)CC1
Reaction #231895
DOI: 10.1039/C8SC04228D
CC1CCC(N(C(=O)Nc2ncc(CN3CCN(S(=O)(=O)N(C)C)CC3)s2)C2CCCCC2)CC1
Reaction #246959
DOI: 10.1039/C8SC04228D
CCCCS(=O)(=O)N1CCN(Cc2cnc(NC(=O)N(C3CCCCC3)C3CCCCC3)s2)CC1
Reaction #248016
DOI: 10.1039/C8SC04228D
CCS(=O)(=O)N1CCN(Cc2cnc(NC(=O)N(C3CCCCC3)C3CCCCC3)s2)CC1
Reaction #293842
DOI: 10.1039/C8SC04228D
CCS(=O)(=O)N1CCN(Cc2cnc(NC(=O)N(C3CCCCC3)[C@H]3CC[C@H](C)CC3)s2)CC1
Reaction #341009
Trans-1-cyclohexyl-3-[5-(4-ethanesulfonyl-piperazin-1-ylmethyl)-thiazol-2-yl]-1-(4-methyl-cyclohexyl)-urea
DOI: 10.6084/m9.figshare.5104873.v1
CN(C)S(=O)(=O)N1CCN(Cc2cnc(NC(=O)N(C3CCCCC3)[C@H]3CC[C@H](C)CC3)s2)CC1
Reaction #341010
Trans-4-{2-[3-cyclohexyl-3-(4-methyl-cyclohexyl)-ureido]-thiazol-5-ylmethyl}-piperazine-1-sulfonic acid dimethylamide
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)CCS(=O)(=O)N1CCN(Cc2cnc(NC(=O)N(C3CCCCC3)[C@H]3CC[C@H](C)CC3)s2)CC1
Reaction #341011
Trans-3-(4-{2-[3-cyclohexyl-3-(4-methyl-cyclohexyl)-ureido]-thiazol-5-ylmethyl}-piperazine-1-sulfonyl)-propionic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CN(Cc2cnc(NC(=O)N(C3CCCCC3)C3CCCCC3)s2)CCN1
Reaction #341020
desired product
Выход 40.0%DOI: 10.6084/m9.figshare.5104873.v1
CCC(=O)N1CCN(Cc2cnc(NC(=O)N(C3CCCCC3)C3CCCCC3)s2)CC1
Reaction #341031
desired product
Выход 15.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)N1CCN(Cc2cnc(NC(=O)N(C3CCCCC3)C3CCCCC3)s2)CC1
Reaction #341032
desired product
Выход 55.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)N1CCN(Cc2cnc(NC(=O)N(C3CCCCC3)C3CCCCC3)s2)CC1
Reaction #341033
desired product
Выход 38.6%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)N1CCN(Cc2cnc(NC(=O)N(C3CCCCC3)C3CCCCC3)s2)CC1
Reaction #341034
desired product
Выход 44.2%DOI: 10.6084/m9.figshare.5104873.v1
CCCS(=O)(=O)N1CCN(Cc2cnc(NC(=O)N(C3CCCCC3)C3CCCCC3)s2)CC1
Reaction #341035
desired product
Выход 27.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)S(=O)(=O)N1CCN(Cc2cnc(NC(=O)N(C3CCCCC3)C3CCCCC3)s2)CC1
Reaction #341036
desired product
Выход 44.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCS(=O)(=O)N1CCN(Cc2cnc(NC(=O)N(C3CCCCC3)C3CCCCC3)s2)CC1
Reaction #341037
desired product
Выход 61.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ncc(CN2CCN(S(=O)(=O)c3ccccc3)CC2)s1)N(C1CCCCC1)C1CCCCC1
Reaction #341038
desired product
Выход 84.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ncc(CN2CCN(S(=O)(=O)Cc3ccccc3)CC2)s1)N(C1CCCCC1)C1CCCCC1
Reaction #341039
desired product
Выход 29.0%DOI: 10.6084/m9.figshare.5104873.v1
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