بحث البنية الفرعية

C1CCN(C1)C2CCNCC2

Cl.Cl.O=c1c(-c2cccnc2)c[nH]n1-c1cc(N2CCC(N3CCCC3)CC2)ncn1
Reaction #66180
4-Pyridin-3-yl-2-[6-(4-pyrrolidin-1-ylpiperidin-1-yl)pyrimidin-4-yl]-1,2-dihydro-3H-pyrazol-3-one dihydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
C1CCN(C2CCNCC2)C1
Reaction #81438
4-pyrrolidino-piperidine
المردود 57.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)c2cc(N3CCC(N4CCCC4)CC3)ccc2C(=O)c2c1[nH]c1cc(C#N)ccc21
Reaction #90013
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(c2ccc(C(=O)N3CCC(N4CCCC4)CC3)cc2)OC1(C)C
Reaction #167730
boronic acid
المردود 42.0%DOI: 10.6084/m9.figshare.5104873.v1
c1ccc(-c2nc3ccc(N4CCC(N5CCCC5)CC4)nn3c2-c2ccncc2)cc1
Reaction #167918
2-Phenyl-3-pyrid-4-yl-6-(4-pyrrolidin-1-ylpiperid-1-yl)imidazo[1,2-b]pyridazine
DOI: 10.6084/m9.figshare.5104873.v1
c1cncc(-c2ccc(N3CCC(N4CCCC4)CC3)nn2)c1
Reaction #168122
title compound
DOI: 10.6084/m9.figshare.5104873.v1
c1cc(-c2ccc(N3CCC(N4CCCC4)CC3)nn2)ccn1
Reaction #168123
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cc(Oc2ccc([N+](=O)[O-])cc2)ccn1)N1CCC(N2CCCC2)CC1
Reaction #173575
DOI: 10.1039/C8SC04228D
Cn1ccnc1Sc1ccc(Nc2c(C#N)cnc3cc(N4CCC(N5CCCC5)CC4)c([N+](=O)[O-])cc23)cc1Cl
Reaction #174760
DOI: 10.1039/C8SC04228D
Cc1ccc(S(=O)(=O)n2ccc3c(-c4c(-c5ccc(F)cc5)nc5ccc(N6CCC(N7CCCC7)CC6)nn45)ccnc32)cc1
Reaction #176559
DOI: 10.1039/C8SC04228D
OCCC1(N2CCCC2)CCNCC1
Reaction #177316
DOI: 10.1039/C8SC04228D
N#CCN1CCC(N2CCCC2)CC1
Reaction #191028
DOI: 10.1039/C8SC04228D
CCc1cc(-c2cccc(CN3CCC(N4CCCC4)CC3)n2)c(C)[nH]c1=O
Reaction #193010
DOI: 10.1039/C8SC04228D
CCCC1CN(C(C)C)CCC1N1CCC(N)C1=O
Reaction #197828
DOI: 10.1039/C8SC04228D
O=C(Cc1ccccc1)NC(=O)Nc1ccc(Oc2ccnc(NC(=O)N3CCC(N4CCCC4)CC3)c2)c(F)c1
Reaction #199098
DOI: 10.1039/C8SC04228D
O=C(Nc1cc(Oc2ccc3c(ccn3C(=O)NC3CC3)c2)ccn1)N1CCCCC1
Reaction #206823
DOI: 10.1039/C8SC04228D
O=C(Nc1cc(Oc2ccc3c(ccn3C(=O)NC3CC3)c2)ccn1)N1CCCCC1
Reaction #206919
DOI: 10.1039/C8SC04228D
Cc1nn(-c2ccc(OC(F)(F)F)cc2)c(C)c1C(=O)N1CCC(N2CCCC2)CC1
Reaction #207855
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)N1CCC(N2CCC(Cc3c(Cl)cc(-c4ccc(C(=O)N5CCC(C(F)(F)F)CC5)cc4)cc3Cl)C2=O)CC1
Reaction #207990
DOI: 10.1039/C8SC04228D
COC(=O)c1cc(NC(=O)C2CCC(=O)N2C2CCN(Cc3ccc(Cl)c(C)c3)CC2)cc(-c2nnnn2C)c1
Reaction #210246
DOI: 10.1039/C8SC04228D
الصفحة 1التالي