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CCCCCNCCCCC

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
O=C(CCC(Nc1ncnc2cc(C(=O)N3CCCC3)c(Cl)cc12)c1nc2cc(Cl)ccc2[nH]1)NC1CCCC1
Reaction #62447
6-chloro-4-[1-(5-chloro-1H-benzimidazol-2-yl)-3-(cyclopentylamino-carbonyl)-propyl-amino]-7-(pyrrolidin-1-yl-carbonyl)-quinazoline
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
Выход 79.6%DOI: 10.6084/m9.figshare.5104873.v1
CCC(C)[C@H](N)C(=O)N1CCC(F)(F)CC1.Cl
Reaction #78044
(S)-2-amino-1-(4,4-difluoro-piperidin-1-yl)-3-methyl-pentan-1-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(NS(=O)(=O)c1ccccc1)C(=O)N1CCC[C@H]1C(=O)O
Reaction #86300
solid
Выход 99.6%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
Выход 73.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1sc(Br)cc1N(C(=O)C1CCC(C)CC1)C1CCC(O)CC1
Reaction #160340
5-Bromo-3-[(4-hydroxy-cyclohexyl)-(4-methyl-cyclohexanecarbonyl)-amino]-thiophene-2-carboxylic acid methyl ester
Выход 77.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1sc(-c2cccc(F)c2)cc1N(C(=O)C1CCC(C)CC1)C1CCC(O)CC1
Reaction #160341
5-(3-Fluoro-phenyl)-3-[(4-hydroxy-cyclohexyl)-(4-methyl-cyclohexanecarbonyl)-amino]-thiophene-2-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1sc(Br)cc1N(C(=O)C1CCC(C)CC1)C1CCC(=O)CC1
Reaction #182311
DOI: 10.1039/C8SC04228D
CN(C)S(=O)(=O)N1CCN(C(=O)c2cnc(NC(=O)N(C3CCCCC3)C3CCCCC3)s2)CC1
Reaction #184113
DOI: 10.1039/C8SC04228D
CCCCCN(CC(=O)N1CCCCC1)C(=O)C(CCC(=O)O)CS(=O)(=O)c1ccc2ccccc2c1
Reaction #197636
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NC(CC(N)=O)C(=O)NC(Cc1ccccc1)C(O)CN1CCCC1C(F)(F)F
Reaction #206464
DOI: 10.1039/C8SC04228D
COc1ccc(C2=NN(CCCCCN)C(=O)C3CC=CCC23)cc1OC
Reaction #208112
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
CCCCCN(CCOC(C)=O)C(=O)C(CCC(=O)O)CS(=O)(=O)c1ccc2ccccc2c1
Reaction #225245
DOI: 10.1039/C8SC04228D
O=C(c1ccc(F)cc1)C1CCN(CC2CCC3CN(c4noc5ccccc45)CCN3C2)CC1
Reaction #228247
DOI: 10.1039/C8SC04228D
O=C(CCCc1ccccc1)N1CCCC1C(=O)N1CCCC1C(O)CS(=O)c1ccccc1
Reaction #232821
DOI: 10.1039/C8SC04228D
COC(=O)c1sc(C#CC(C)(C)C)cc1N(C(=O)C1CCC(C)CC1)C1CCC(O)CC1
Reaction #250258
DOI: 10.1039/C8SC04228D
COc1cc(C(F)(F)F)cc(SC)c1C(=O)NC1CCCC1NC1CCCC1
Reaction #251907
DOI: 10.1039/C8SC04228D
COC(=O)c1sccc1N(C(=O)C1CCC(C)CC1)C1CCC(O)CC1
Reaction #253364
DOI: 10.1039/C8SC04228D
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