部分構造検索

485618

Cc1ccc(CCN2CCCC(C(C(N)=O)(c3ccccc3)c3ccccc3)C2)cc1
Reaction #49674
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)C(c1ccccc1)(c1ccccc1)C1CCCN(CCc2ccc(Cl)cc2)C1
Reaction #49676
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC(=O)C(c1ccccc1)(c1ccccc1)C1CCCN(CCc2ccc(O)cc2)C1
Reaction #49677
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(CCCCN2CCCCCC2Cc2ccc(Cl)cc2)cc1
Reaction #55713
title compound
収率 62.2%DOI: 10.6084/m9.figshare.5104873.v1
CN(Cc1ccccc1)C(=O)CCC(=O)N1CCC[C@H]1C(=O)C(=O)O.O
Reaction #64145
title compound
収率 150.4%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)C(=O)[C@@H]1CCCN1C(=O)CCC(=O)N(C)Cc1ccccc1
Reaction #64146
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(Cc1ccccc1)C(=O)CCC(=O)N1CCC[C@H]1C(O)C(=O)OCc1ccccc1
Reaction #64147
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCC(O)[C@@H]1CCCN1C(=O)CCC(=O)N(C)Cc1ccccc1
Reaction #64151
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(Cc1ccccc1)C(=O)CCC(=O)N1CCC[C@H]1C(O)c1ccccc1
Reaction #64152
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)N1CCC[C@H]1[C@H](OC)[C@@H](C)C(=O)N[C@@H](Cc1ccccc1)c1nccs1)OC)N(C)C(=O)[C@@H](NC(=O)C(C)(C)N)C(C)C
Reaction #84178
#54
収率 75.3%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)N1CCC[C@H]1[C@H](OC)[C@@H](C)C(=O)N[C@@H](Cc1ccccc1)c1nccs1)OC)N(C)C(=O)[C@@H](NC(=O)C1(N)CCCC1)C(C)C
Reaction #161924
#47
収率 96.5%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)N1CCC[C@H]1[C@H](OC)[C@@H](C)C(=O)N[C@@H](Cc1ccccc1)c1nccs1)OC)N(C)C(=O)[C@@H](NC(=O)C1(N)CC1)C(C)C
Reaction #161925
#51
収率 40.5%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)N1CCC[C@H]1[C@H](OC)[C@@H](C)C(=O)N[C@@H](Cc1ccccc1)c1nccs1)OC)N(C)C(=O)[C@@H](NC(=O)C(C)(C)N)C(C)C
Reaction #161927
#54
収率 75.3%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)N1CCC[C@H]1[C@H](OC)[C@@H](C)C(=O)N[C@@H](Cc1ccccc1)C(=O)OC)OC)N(C)C(=O)[C@@H](NC(=O)C(C)(C)NC(=O)OCC1c2ccccc2-c2ccccc21)C(C)C
Reaction #161937
N-[(9H-fluoren-9-ylmethoxy)carbonyl]-2-methylalanyl-N-[(3R,4S,5S)-3-methoxy-1-{(2S)-2-[(1R,2R)-1-methoxy-3-{[(2S)-1-methoxy-1-oxo-3-phenylpropan-2-yl]amino}-2-methyl-3-oxopropyl]pyrrolidin-1-yl}-5-methyl-1-oxoheptan-4-yl]-N-methyl-L-valinamide
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)N1CCC[C@H]1[C@H](OC)[C@@H](C)C(=O)N[C@@H](Cc1ccccc1)c1nccs1)OC)N(C)C(=O)[C@@H](N)C(C)C
Reaction #161942
#86
収率 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)N1CCC[C@H]1[C@H](OC)[C@@H](C)C(=O)NC(C(=O)OC)C1Cc2ccccc21)OC)N(C)C(=O)[C@@H](NC(=O)C(C)(C)NC(=O)OCC1c2ccccc2-c2ccccc21)C(C)C
Reaction #161952
#106
収率 76.3%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)N1CCC[C@H]1[C@H](OC)[C@@H](C)C(=O)N[C@H](C)[C@@H](O)c1ccccc1)OC)N(C)C(=O)[C@@H](N)C(C)C
Reaction #161969
#133
収率 43.2%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)N1CCC[C@H]1[C@H](OC)[C@@H](C)C(=O)NCCC1C=CC=CC=C1)OC)N(C)C(=O)[C@@H](NC(=O)OCC1c2ccccc2-c2ccccc21)C(C)C
Reaction #161984
#175
収率 68.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)N1CCC[C@H]1[C@H](OC)[C@@H](C)C(=O)NCCC1C=CC=CC=C1)OC)N(C)C(=O)[C@@H](N)C(C)C
Reaction #161985
#176
収率 87.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@@H]([C@@H](CC(=O)N1CCC[C@H]1[C@H](OC)[C@@H](C)C(=O)N[C@@H](Cc1ccccc1)C(=O)O)OC)N(C)C(=O)[C@@H](NC(=O)C(C)(C)N(C)C(=O)CCCCN1C(=O)C=CC1=O)C(C)C
Reaction #162004
mv#115
収率 3.3%DOI: 10.6084/m9.figshare.5104873.v1
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