بحث البنية الفرعية

CNCCCc1ccncc1

S=C1N(CCCc2ccncc2)CCN1CCc1ccccc1
Reaction #11565
titled compound
المردود 19.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCC(O)c1ccncc1
Reaction #11571
titled compound
المردود 55.3%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCN(CCC12CC3CC(CC(C3)C1)C2)C(=O)NCCC(O)c1ccncc1
Reaction #46685
1-[2-(1-Adamantyl)ethyl]-3-[3-hydroxy-3-(4-pyridyl)propyl]-1-pentylurea
DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)N1CCC(c2ccncc2)CC1
Reaction #61628
benzyl 4-(pyridin-4-yl)piperidine-1-carboxylate
المردود 74.2%DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1cc(C2(C(F)(F)F)CCNC2)cc(C(F)(F)F)n1
Reaction #70910
2,6-bis(trifluoromethyl)-4-[3-(trifluoromethyl)pyrrolidin-3-yl]pyridine
المردود 70.1%DOI: 10.6084/m9.figshare.5104873.v1
C[C@H](NC(=O)C1CC1)c1ccc(N2CCC(c3cc(C(F)(F)F)nc(C(F)(F)F)c3)(C(F)(F)F)C2)cc1
Reaction #70911
N-[(1S)-1-(4-{3-[2,6-bis(trifluoromethyl)pyridin-4-yl]-3-(trifluoromethyl)pyrrolidin-1-yl}phenyl)ethyl]cyclopropanecarboxamide
المردود 100.9%DOI: 10.6084/m9.figshare.5104873.v1
c1cc(C2(c3ccc(-c4cn[nH]c4)cc3)CCNCC2)ccn1
Reaction #73841
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cn(C2CC2)c2cc(N3CCC(c4ccncc4)C3)c(F)cc2c1=O
Reaction #82766
title compound
المردود 52.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1ccc(NC(=O)C(Cc2ccncc2)n2ccc(-c3cc(Cl)ccc3Br)cc2=O)cc1
Reaction #85253
4-({2-[4-(2-Bromo-5-chlorophenyl)-2-oxopyridin-1(2H)-yl]-3-(pyridin-4-yl)propanoyl}amino)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1C(C)CC(c2ccncc2N)CC1NC(=O)OC(C)(C)C
Reaction #160768
(+/−)-4-(3-aminopyridin-4-yl)-2-(tert-butoxycarbonylamino)-6-methylcyclohexyl acetate
المردود 59.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H]1C[C@H](NC(=O)OC(C)(C)C)C[C@H](c2ccncc2NC(=O)c2csc(Br)n2)C1
Reaction #160788
tert-butyl (1S,3R,5S)-3-(3-(2-bromothiazole-4-carboxamido)pyridin-4-yl)-5-methylcyclohexylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1onc(-c2ccccc2)c1COc1cc(C2=CCN(C)CC2)ccn1
Reaction #170345
title compound
المردود 17.0%DOI: 10.6084/m9.figshare.5104873.v1
CN(C)c1cc(NC(=O)OC(C)(C)C)c(NC(=O)CC(=O)c2ccnc(C#N)c2)cc1C(F)(F)F
Reaction #181172
DOI: 10.1039/C8SC04228D
N#Cc1cc(C2=Nc3ccc(C#Cc4ccccc4)cc3NC(=O)C2)ccn1
Reaction #182738
DOI: 10.1039/C8SC04228D
CCOc1cc2c(cc1C(F)(F)F)NC(=O)CC(c1ccnc(-c3cccnc3)c1)=N2
Reaction #183262
DOI: 10.1039/C8SC04228D
CCOC(=O)CCN(C)CCCc1ccncc1
Reaction #184243
DOI: 10.1039/C8SC04228D
N#Cc1cc(C2=Nc3cc(N4CCSCC4)c(C(F)(F)F)cc3NC(=O)C2)ccn1
Reaction #184287
DOI: 10.1039/C8SC04228D
O=C(O)c1cn(C2CC2)c2cc(N3CCC(c4ccncc4)C3)c(F)cc2c1=O
Reaction #185859
DOI: 10.1039/C8SC04228D
Cc1cc2nc(NC(=O)C3CC3c3ccncc3)cc(-c3ccccc3)n2n1
Reaction #197733
DOI: 10.1039/C8SC04228D
Cl
Reaction #198775
DOI: 10.1039/C8SC04228D
الصفحة 1التالي