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1040167

OCc1ccc(CN2CCCN(Cc3ccc(Oc4ccccc4)cc3)CC2)cc1
Reaction #44790
[4-[[hexahydro-4-[(4-phenoxyphenyl)methyl]-1H-1,4-diazepin-1-yl]methyl]phenyl]methanol
Выход 78.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CN2CCC(N(C)CCc3ccc(Oc4ccccc4)cc3)CC2)cc1
Reaction #44799
methyl 4-[[4-[methyl[2-(4-phenoxyphenyl)ethyl]amino]-1-piperidinyl]methyl]benzoate
DOI: 10.6084/m9.figshare.5104873.v1
CN(CCc1ccc(Oc2ccccc2)cc1)C1CCN(Cc2ccc(C(=O)O)cc2)CC1
Reaction #44800
4-[[4-[methyl[2-(4-phenoxyphenyl)ethyl]amino]-1-piperidinyl]methyl]benzoic acid
Выход 12.7%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CN(C)C[C@H]2CCCN2Cc2ccc(Oc3ccc(Br)cc3)cc2)cc1
Reaction #44804
methyl 4-[[[[(R)-1-[[4-(4-bromophenoxy)phenyl]methyl]-2-pyrrolidinyl]methyl]methylamino]methyl]benzoate
Выход 94.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CN2CCC[C@@H]2CN(C)Cc2ccc(Oc3ccc(Br)cc3)cc2)cc1
Reaction #44807
methyl 4-[[(R)-2-[[[[4-(4-bromophenoxy)phenyl]methyl]methyl-amino]methyl]-1-pyrrolidinyl]methyl]benzoate
Выход 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(Cc1ccc(Oc2ccc(Br)cc2)cc1)C[C@H]1CCCN1Cc1ccc(C(=O)O)cc1
Reaction #44808
4-[[(R)-2-[[[[4-(4-bromophenoxy)phenyl]methyl]methylamino]methyl]-1-pyrrolidinyl]methyl]benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CN2C[C@@H]3C[C@H]2CN3Cc2ccc(OCC(F)(F)C(F)F)cc2)cc1
Reaction #44812
methyl 4-[[(1S,4S)-5-[[4-(2,2,3,3-tetrafluoropropoxy)phenyl]methyl]-2,5-diazabicyclo[2.2.1]hept-2-yl]methyl]benzoate
Выход 35.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(CN2C[C@@H]3C[C@H]2CN3Cc2ccc(OCC(F)(F)C(F)F)cc2)cc1
Reaction #44813
4-[[(1S,4S)-5-[[4-(2,2,3,3-tetrafluoropropoxy)phenyl]methyl]-2,5-diazabicyclo[2.2.1]hept-2-yl]methyl]benzoic acid
Выход 52.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CCc2cc(NC(=O)c3ccc(CN4CCC(F)CC4)cc3)[nH]n2)cc(OC)c1
Reaction #45007
title compound
Выход 16.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(CCc2cc(NC(=O)c3ccc(CN4CCCC(F)C4)cc3)n[nH]2)cc(OC)c1
Reaction #45020
title compound
Выход 16.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C(=O)Nc2ccc3c(c2)CC(=O)N3)cc1
Reaction #52595
5-(4-methoxycarbonylbenzamido)-2oxindole
Выход 81.0%DOI: 10.6084/m9.figshare.5104873.v1
NC1CCCc2cc(CO)ccc21
Reaction #60390
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc2c(c1)CNC2.O=C(O)C(F)(F)F
Reaction #69685
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(CN(C(=O)N[C@@H](C)c2ccc(Cl)cc2)c2ccc(C3CCCCC3)cc2)cc1
Reaction #77823
4-[3-[1(S)-(4-Chlorophenyl)ethyl]1-(4-cyclohexylphenyl)ureidomethyl]benzoic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)N(Cc1ccc(C(=O)O)cc1)c1ccc(C2CCCCC2)cc1)c1ccc(Cl)cc1
Reaction #77824
4-[3-[1(S)-(4-Chlorophenyl)ethyl]1-(4-cyclohexylphenyl)ureidomethyl]benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(C(Nc2ccccc2)C(=O)O[C@H]2CN3CCC2CC3)cc1
Reaction #164201
desired compound
Выход 21.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(Cn2nc(OC)c3ccc(NC(=O)OC4CCCC4)cc32)c(OC)c1
Reaction #175310
DOI: 10.1039/C8SC04228D
CC(C)Oc1cc(CO)ccc1Cn1nc(-c2ccccc2)cc1-c1ccccc1
Reaction #177347
DOI: 10.1039/C8SC04228D
COC(=O)c1ccc(CN2CCCCc3ccccc32)cc1OC
Reaction #177937
DOI: 10.1039/C8SC04228D
CCOC(=O)c1ccc(C(C)n2nc(-c3cc(Cl)cc(Cl)c3)cc2-c2ccc3cc(OC)ccc3c2)cc1
Reaction #178241
DOI: 10.1039/C8SC04228D
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