Participa en 235 reacciones

11983

CCCCCNCCC12CC3CC(CC(C3)C1)C2.Cl
Reaction #11528
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CCCCCNC(=O)[C@@H](N)CO
Reaction #81636
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CCCCCNC(=O)c1nnc(N2CCN(C(=O)c3ccccc3C(F)(F)F)CC2)o1
Reaction #191018
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCNC(=O)Nc1ccc(Oc2ncnc3cc(OC)c(OC)cc23)cc1Cl
Reaction #192361
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCNc1nc(N)nc(C)c1Cc1ccccc1
Reaction #195848
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCNc1nc(Cl)nc2c1ncn2C1CCCC1
Reaction #197174
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCCCCNC(=O)NCCCCC
Reaction #209233
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCNc1nc(N)nc(C)c1Cc1ccc(C(=O)OC)cc1OC
Reaction #213277
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCCCCNCc1ccc(Oc2ccc(C(N)=O)nc2)c(F)c1
Reaction #218023
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCCCCNCc1ccc(Oc2ccc(C(N)=O)nc2)c(Cl)c1
Reaction #218028
title compound
Rendimiento 64.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCCCCNCc1ccc(Oc2ccc(C(N)=O)cn2)c(OC)c1
Reaction #218039
title compound
Rendimiento 67.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCCCCNCc1ccc(Oc2ccc(C(N)=O)cn2)c(F)c1F
Reaction #218142
title compound
Rendimiento 83.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCCCCNCc1ccc(Oc2cnc(C(N)=O)cn2)c(OC)c1
Reaction #218158
title compound
Rendimiento 71.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCCCCNCc1ccc(Oc2cnc(C(N)=O)cn2)c(F)c1
Reaction #218176
title compound
Rendimiento 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCCCCNC(=O)c1ccc2c(c1)nc(COc1ccccc1)n2Cc1ccc(OC(F)(F)F)cc1
Reaction #218395
2-Phenoxymethyl-1-(4-trifluoromethoxy-benzyl)-1H-benzoimidazole-5-carboxylic acid pentylamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CCCCCNCCC12CC3CC(CC(C3)C1)C2
Reaction #222435
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCNCc1ccc(Oc2ccc(C(N)=O)cn2)c(F)c1F
Reaction #240179
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCNC(=O)c1ccc(Cl)nn1
Reaction #241674
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCNc1nc(N)nc(C)c1Cc1ccc(C(=O)OC)cc1F
Reaction #250174
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CCCCCNC(=O)c1cn2nc(N3CCN(C(=O)c4ccccc4C(F)(F)F)CC3)ccc2n1
Reaction #250933
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
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