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CCCNCC

COCCC(=O)N[C@@H](C)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccccc1
Reaction #41312
N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-phenyl-propan-2-yl]-3-methoxy-propanamide
DOI: 10.6084/m9.figshare.5104873.v1
COCC(=O)N[C@@H](C)[C@H](Oc1ccc2c(cnn2-c2ccc(F)cc2)c1)c1ccccc1
Reaction #41313
N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-phenyl-propan-2-yl]-2-methoxy-acetamide
DOI: 10.6084/m9.figshare.5104873.v1
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
COc1cc2c(Nc3cccc4c(Cl)coc34)ncnc2cc1OCC(O)CN1CCOCC1.Cl.Cl
Reaction #51058
title compound
Ausbeute 157.7%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc2c(Nc3c(Cl)ccc4c(Br)coc34)ncnc2cc1OCCCN1CCOCC1
Reaction #51062
title compound
Ausbeute 66.4%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(CN(C)CC(O)c2cc(F)c(F)c(F)c2)sc2c(=O)c(C(=O)NCc3ccc(Cl)cc3)cn(C)c12
Reaction #51942
title compound
Ausbeute 50.4%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)N1CCN(CCC(=O)Nc2cccc(-c3nc(Nc4ccc5[nH]ncc5c4)c4ccccc4n3)c2)CC1
Reaction #89831
N-(3-(4-(1H-indazol-5-ylamino)quinazolin-2-yl)phenyl)-3-(4-isopropylpiperazin-1-yl)propanamide
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
Ausbeute 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
CCCc1cc(C(=O)N[C@H](Cc2ccccc2)[C@@H](O)C(=O)O)nn1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)=O)cc1
Reaction #158840
title compound
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1
CCCc1cc(C(=O)NC(Cc2ccccc2)C(O)C(=O)O)nn1Cc1ccc(-c2ccccc2S(=O)(=O)NC(C)=O)nc1
Reaction #184351
DOI: 10.1039/C8SC04228D
C=C(C)c1ccc(N(CCc2ccc(OC(C)(C)C(=O)OCC)cc2)Cc2ccc(C(F)(F)F)cc2)nc1
Reaction #188238
DOI: 10.1039/C8SC04228D
CC(C)(c1ccc(Cl)cc1)C(NC(=O)c1ccc(I)cc1NS(=O)(=O)c1cccc2nsnc12)C(=O)O
Reaction #197846
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
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