بحث البنية الفرعية

372006

CCCC(=O)N[C@@H](C)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccccc1
Reaction #41323
N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-phenyl-propan-2-yl]butanamide
DOI: 10.6084/m9.figshare.5104873.v1
CCC[C@H](NC(=O)CO)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccccc1
Reaction #41379
N-((1R,2S)-1-(1-(4-fluorophenyl)-1H-indazol-5-yloxy)-1-phenylpentan-2-yl)-2-hydroxyacetamide
DOI: 10.6084/m9.figshare.5104873.v1
Cl.Nc1cccc2c1ccc(=O)n2CCN1CCC(NCc2ccc3c(c2)OCCO3)CC1
Reaction #68216
1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-5-aminoquinolin-2(1H)-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CNc1cccc2c1ccc(=O)n2CCN1CCC(NCc2ccc3c(c2)OCCO3)CC1.Cl
Reaction #68220
1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-5-(N-methylamino)quinolin-2(1H)-one hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-c3ccncc3CN)nc2N1C1CCCC1
Reaction #73132
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-c3ccncc3CNC(C)=O)nc2N1C1CCCC1
Reaction #73139
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-c3ccncc3CNC(=O)c3ccccc3)nc2N1C1CCCC1
Reaction #73140
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-c3ccncc3CNS(C)(=O)=O)nc2N1C1CCCC1
Reaction #73141
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H]1C(=O)N(C)c2cnc(-c3ccncc3CNS(=O)(=O)c3ccccc3)nc2N1C1CCCC1
Reaction #73142
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(S(=O)(=O)N[C@@H](CCCNC(=N)N)C(=O)N2CCC(C)CC2C(=O)O)cc1C1CCCCC1
Reaction #94591
1-[N2 -(3-cyclohexyl-4-methoxyphenylsulfonyl)-L-arginyl]-4-methyl-2-piperidinecarboxylic acid
المردود 73.4%DOI: 10.6084/m9.figshare.5104873.v1
Cl.Cl.O=C1CCCN1c1ccc(OCCCN(CCn2ccc3ccccc3c2=O)Cc2ccncc2)cc1
Reaction #156194
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCC(N2CC(NC(=O)CNc3nn(C)c4ccc(C(O)C(F)(F)F)cc34)C2)CC1
Reaction #174933
DOI: 10.1039/C8SC04228D
CCCC1(CCC)C(=O)C(C(=O)Nc2ccc(OCc3ccccc3)cc2S(N)(=O)=O)=C(O)c2ccccc21
Reaction #184605
DOI: 10.1039/C8SC04228D
CS(=O)(=O)c1ccccc1OC1CCN(c2ccnc3ccc(-c4cn(C(c5ccccc5)(c5ccccc5)c5ccccc5)nc4C(F)(F)F)cc23)CC1
Reaction #184951
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NCCC(C(=O)Nc1ccc2c(c1)c(N)nn2C(=O)OC(C)(C)C)c1ccc(Cl)c(Cl)c1
Reaction #199221
DOI: 10.1039/C8SC04228D
Cc1ccc(C(=O)Nc2ccon2)cc1-n1ccc2ccc(OCCN3CCCCC3)cc2c1=O
Reaction #200318
DOI: 10.1039/C8SC04228D
CC(=O)OCCCCCCOc1ccccc1C(=O)Nc1ccc(C(=O)N2CCCCc3ccccc32)cc1
Reaction #202710
DOI: 10.1039/C8SC04228D
Cc1ccc(S(=O)(=O)N2CCNC(=O)C2CC(=O)NC2CCCc3cc(-c4ccccc4-c4nc(C)no4)ccc32)cc1
Reaction #208130
DOI: 10.1039/C8SC04228D
[Br-]
Reaction #208932
DOI: 10.1039/C8SC04228D
CCCCOc1ccc(S(=O)(=O)C2(C(=O)O)CCN(Cc3ccncc3)CC2)cc1
Reaction #212843
DOI: 10.1039/C8SC04228D
الصفحة 1التالي