Recherche de Sous-structure

1346122

COc1cc2c(CC(=O)N3CCC(Cc4ccccc4)CC3)cnc(CNC(=O)OC(C)(C)C)c2cc1OC
Reaction #42967
{-4-[2-(4-benzyl-piperidin-1-yl)-2-oxo-ethyl]-6,7-dimethoxy-isoquinolin-1-ylmethyl}-carbamic acid tert-butyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(CC(=O)N3CCC(Cc4ccccc4)CC3)cnc(CN)c2cc1OC.Cl
Reaction #42968
2-(1-aminomethyl-6,7-dimethoxy-isoquinolin-4-yl)-1-(4-benzyl-piperidin-1-yl)-ethanone hydrochloride
Rendement 100.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.N#CC1(Cc2ccccc2)CCN(CCCC2(c3ccc(Cl)c(Cl)c3)CCCN(C(=O)c3ccccc3)C2)CC1.O
Reaction #78341
expected product
Rendement 105.6%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.Cl.Cl.NCC1(Cc2ccccc2)CCN(CCCC2(c3ccc(Cl)c(Cl)c3)CCCN(C(=O)c3ccccc3)C2)CC1.NCC1(Cc2ccccc2)CCN(CCCC2(c3ccc(Cl)c(Cl)c3)CCCN(C(=O)c3ccccc3)C2)CC1.O
Reaction #78342
expected product
Rendement 111.8%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O.O=C(c1ccccc1)N1CCCC(CCCN2CCC(OCCO)(c3ccccc3)CC2)(c2ccc(Cl)c(Cl)c2)C1
Reaction #78349
expected product
Rendement 128.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OCCOC1(c2ccccc2)CCN(CCCC2(c3ccc(Cl)c(Cl)c3)CCCN(C(=O)c3ccccc3)C2)CC1.Cl
Reaction #78350
expected product
DOI: 10.6084/m9.figshare.5104873.v1
NC1(c2ccccc2)CCN(CCCC2(c3ccc(Cl)c(Cl)c3)CCCN(C(=O)c3ccccc3)C2)CC1
Reaction #78351
expected product
Rendement 74.6%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O.O=C(NC1(c2ccccc2)CCN(CCCC2(c3ccc(Cl)c(Cl)c3)CCCN(C(=O)c3ccccc3)C2)CC1)c1cccs1
Reaction #78352
expected product
Rendement 101.6%DOI: 10.6084/m9.figshare.5104873.v1
C=CC(=O)N1CCC[C@@H](n2c(NC(=O)c3cccc(C(F)(F)F)c3)nc3cc(C(N)=O)ccc32)C1
Reaction #88356
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CN(C(=O)c1ccc(Cl)cc1)C1CCN(C(=O)C2CCN(C(=O)CF)CC2)CC1c1ccc(Cl)c(Cl)c1
Reaction #177398
DOI: 10.1039/C8SC04228D
CN(C(=O)c1ccc(Cl)cc1)C1CCN(C(=O)C2CCOCC2NC(=O)c2ccccc2)CC1c1ccc(Cl)c(Cl)c1
Reaction #181391
DOI: 10.1039/C8SC04228D
CN(C(=O)c1ccc(Cl)cc1)C1CCN(C(=O)C2CCN(C3CC3)CC2)CC1c1ccc(Cl)c(Cl)c1
Reaction #185563
DOI: 10.1039/C8SC04228D
CCCCCCNc1nc2ccccc2n1C1CCN(C(=O)c2ccc(CCCC)cc2)CC1
Reaction #186781
DOI: 10.1039/C8SC04228D
O=C(c1cc(C(F)(F)F)cc(C(F)(F)F)c1)N1CCC(NCc2ccnc3ccccc23)CC1Cc1ccccc1
Reaction #188101
DOI: 10.1039/C8SC04228D
O=C(c1cc(C(F)(F)F)cc(C(F)(F)F)c1)N1CCC(NCc2ccnc3ccccc23)CC1Cc1ccccc1
Reaction #190350
DOI: 10.1039/C8SC04228D
O=C(c1cc(-c2ccccc2)nc(-c2ccccc2)c1)N1CCC(N2CCCC(C(=O)N3CCNCC3)C2)CC1
Reaction #190483
DOI: 10.1039/C8SC04228D
CN(C(=O)c1ccc(Cl)cc1)C1CCN(C(=O)C2CCN(C(=O)C3CC3)CC2)CC1c1ccc(Cl)c(Cl)c1
Reaction #193320
DOI: 10.1039/C8SC04228D
C=CCN1CC(C)N(C(c2cccc(O)c2)c2cccc(C(=O)N3CCC4(CC3)OCCO4)c2)CC1C
Reaction #194055
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NCC(=O)N1CCC(CO)(C(=O)O)CC1
Reaction #232508
DOI: 10.1039/C8SC04228D
O=C(CCc1ccccc1)N1CCC2(CC1)NC(Cc1ccccc1)C(=O)N2Cc1ccccc1
Reaction #238670
DOI: 10.1039/C8SC04228D
Page 1Suivant