子结构搜索

CCCNCCC

C#CC(=O)NC1CCCN(C(=O)[C@H](C)N2CC[C@H](NS(=O)(=O)c3ccc4cc(Cl)ccc4c3)C2=O)C1
Reaction #7399
title compound
收率 115.5%DOI: 10.6084/m9.figshare.5104873.v1
COCCC(=O)N[C@@H](C)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccccc1
Reaction #41312
N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-phenyl-propan-2-yl]-3-methoxy-propanamide
DOI: 10.6084/m9.figshare.5104873.v1
CCCC(=O)N[C@@H](C)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccccc1
Reaction #41323
N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-phenyl-propan-2-yl]butanamide
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2nnc(NC3CC4CCC(C3)N4Cc3ccc4ccccc4c3)c3cc(OC)ccc23)cc1
Reaction #58207
7-Methoxy-4-(4-methoxyphenyl)-N-[8-(naphthalen-2-ylmethyl)-8-azabicyclo[3.2.1]oct-3-yl]phthalazin-1-amine
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-c3ccncc3CN)nc2N1C1CCCC1
Reaction #73132
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-c3ccncc3CNC(C)=O)nc2N1C1CCCC1
Reaction #73139
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-c3ccncc3CNC(=O)c3ccccc3)nc2N1C1CCCC1
Reaction #73140
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-c3ccncc3CNS(C)(=O)=O)nc2N1C1CCCC1
Reaction #73141
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-c3ccncc3CNS(=O)(=O)c3ccccc3)nc2N1C1CCCC1
Reaction #73142
title compound
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
COc1ccc(S(=O)(=O)[C@@H]2C[C@@H](C(=O)NC3(C#N)CC3)N(C(=O)C3(c4ccc(Cl)cn4)CN(C)C3)C2)c(Cl)c1
Reaction #156710
(2S,4R)-4-(2-Chloro-4-methoxy-benzenesulfonyl)-1-[3-(5-chloro-pyridin-2-yl)-1-methyl-azetidine-3-carbonyl]-pyrrolidine-2-carboxylic acid (1-cyano-cyclopropyl)-amide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(C[N+]12CCC(CC1)[C@@H](OC(=O)C(NCc1ccc(F)cc1)c1ccccc1)C2)c1cccs1.[Cl-]
Reaction #164227
title compound
收率 68.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCC(N2CC(NC(=O)CNc3nn(C)c4ccc(C(O)C(F)(F)F)cc34)C2)CC1
Reaction #174933
DOI: 10.1039/C8SC04228D
CC(C)N1CC2N(C(=O)C(NC(=O)c3ccc(C(F)(F)F)nc3)CN2S(=O)(=O)c2ccc(Cl)cc2Cl)C(Cc2ccc(Cl)cc2)C1=O
Reaction #179255
DOI: 10.1039/C8SC04228D
COc1ccc(S(=O)(=O)N2CCC(=O)N3C(Cc4ccc(Cl)cc4)C(=O)N(C(C)C)CC32)cc1
Reaction #196499
DOI: 10.1039/C8SC04228D
CC1(C)CN(C(=O)c2ncc(Cl)cc2NS(=O)(=O)c2ccc(Cl)c(C(F)(F)F)c2)CCC1O
Reaction #196638
DOI: 10.1039/C8SC04228D
CCCCOCCOc1ccc(-c2ccc3c(c2)C=C(C(=O)Nc2ccc(S(=O)Cc4cccnc4)c(Cl)c2)CCN3CC(C)C)cc1
Reaction #202954
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
COc1ccc(Cl)cc1S(=O)(=O)N1CC(NC(=O)C2CC2)C(=O)N2C(Cc3ccc(Cl)cc3)C(=O)N(C(C)C)CC21
Reaction #213801
DOI: 10.1039/C8SC04228D
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