بحث البنية الفرعية

CC(=O)N1CCC(N)CC1.Cl

C[C@H]1C[C@H](Nc2cc(=O)[nH]c3cc(F)c(F)cc23)CCN1C(=O)c1cnn(C)c1Cl
Reaction #629
المردود 49.5%
C[C@H]1C[C@H](Nc2cc(=O)[nH]c3cc(F)c(F)cc23)CCN1C(=O)c1cnn(C)c1Cl
Reaction #630
المردود 23.1%
C[C@H]1C[C@H](Nc2cc(=O)[nH]c3cc(F)c(F)cc23)CCN1C(=O)c1cnn(C)c1Cl
Reaction #735
المردود 8.5%
CC(C)(C)OC(=O)NC1CCN(CC(c2ccc(Cl)c(Cl)c2)C2(O)CCCCC2)CC1
Reaction #57084
tert-butyl {1-[2-(3,4-dichlorophenyl)-2-(1-hydroxycyclohexyl)ethyl]piperidin-4-yl}carbamate
المردود 53.0%DOI: 10.6084/m9.figshare.5104873.v1
CO[C@@H]1CN(C(=O)CCl)CC[C@@H]1NC(=O)OCc1ccccc1
Reaction #72091
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CC(=O)N1CC[C@H](NC(=O)OCc2ccccc2)[C@H](OC)C1)C(C)=O
Reaction #72092
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NC1CCN(C(=O)c2ccc(-c3nnc4n3-c3cccnc3Nc3ccccc3-4)cc2)CC1
Reaction #72504
(4-(9H-benzo[f]pyrido[2,3-b][1,2,4]triazolo[4,3-d][1,4]diazepin-3-yl)phenyl)(4-aminopiperidin-1-yl)methanone hydrochloride
المردود 88.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CCC(NN)CC1.Cl
Reaction #72927
title compound
المردود 77.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N1CC[C@@H](n2cnc3c(cc(Cc4ccc(Cl)nc4)c4ccccc43)c2=O)[C@H](O)C1
Reaction #169655
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)C(CC(=O)N1CCC(N2Cc3cc(O)ccc3NC2=O)CC1)Cc1cc(Cl)c(N)c(C(F)(F)F)c1
Reaction #173009
DOI: 10.1039/C8SC04228D
Nc1c(Cl)cc(CC(OC(=O)N2CCC(N3CCc4ccccc4NC3=O)CC2)C(=O)N2CCC(N3CCCC3C(=O)O)CC2)cc1C(F)(F)F
Reaction #173746
DOI: 10.1039/C8SC04228D
Nc1c(Cl)cc(CC(CO)CC(=O)N2CCC(N3CCc4ccccc4NC3=O)CC2)cc1C(F)(F)F
Reaction #176626
DOI: 10.1039/C8SC04228D
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
CN1CCN(C2CCN(C(=O)C(CC(=O)N3CCC(N4Cc5ccccc5NC4=O)CC3)Cc3cc(Cl)c(N)c(C(F)(F)F)c3)CC2)CC1
Reaction #180969
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
CC(=O)N1CCC(NC(=O)c2cnc3n2C(C)(Cc2ccc(C#N)cc2)C(=O)N3c2cc(Cl)cc(Cl)c2)(C(=O)NC2(c3ccccn3)CC2)CC1
Reaction #190233
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
CC(=O)N1CCC(n2cc(-c3cnc(N)c4oc(Cl)cc34)cn2)CC1
Reaction #194620
DOI: 10.1039/C8SC04228D
O=C(c1cc(Cl)cc(Cl)c1)N1CCC(NCc2ccnc3ccccc23)CC1Cc1ccccc1
Reaction #194705
DOI: 10.1039/C8SC04228D
CNc1ncc(-c2cnn(C3CCN(C(C)=O)CC3)c2)c2cc(Cl)oc12
Reaction #196562
DOI: 10.1039/C8SC04228D
الصفحة 1التالي