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CCC(C)CN

COc1cccc(-c2c(C)n(Cc3c(F)cccc3F)c(=O)n(C[C@H](NC(=O)OC(C)(C)C)C3CCCCC3)c2=O)c1F
Reaction #56779
compound 4c
Rendimiento 32.3%DOI: 10.6084/m9.figshare.5104873.v1
NC1=c2ccsc2=NCN1c1ccc(NC(=O)C2(c3ccc(Cl)c(Cl)c3)CC2)cc1
Reaction #60774
title compound
DOI: 10.6084/m9.figshare.5104873.v1
NC1=c2ccsc2=NCN1c1ccc(NC(=O)C2(c3cc(F)ccc3F)CC2)cc1
Reaction #60775
4-Amino-3-(4-((1-(2,5-difluorophenyl)-cyclopropanecarbonyl)amino)phenyl)thieno[2,3-d]pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1
C#CCN1CCC(OC)(c2cccc(OCc3ccc4c(ccc(=O)n4C)c3)c2)C1
Reaction #65830
3-methoxy-3-[3-(1-methyl-2-oxo-1,2-dihydroquinolin-6-ylmethoxy)phenyl]-1-(prop-2-ynyl)pyrrolidine
Rendimiento 21.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1)C(C)C)C(=O)N[C@@H](Cc1c[nH]cn1)C(N)=O
Reaction #93624
title compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #93651
B7
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](Cc1ccccc1)NC(=O)OCc1ccccc1)C(C)C)C(=O)N[C@@H](Cc1c[nH]cn1)C(N)=O
Reaction #93655
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cccc(-c2c(C)n(Cc3c(F)cccc3F)c(=O)n(CC(NC(=O)OC(C)(C)C)C3CCCCC3)c2=O)c1F
Reaction #174938
DOI: 10.1039/C8SC04228D
CCC(CC)(NC(=O)c1ccc(C(F)(F)F)c(OCC2CCOCC2)n1)C(=O)N(C)C
Reaction #185323
DOI: 10.1039/C8SC04228D
COc1ccccc1C1(O)CC(CC#N)CC2CN(C(=O)Cc3ccccc3O)CC21
Reaction #195572
DOI: 10.1039/C8SC04228D
CCOCCn1c(NC2CCN(CCC3(c4ccc(Cl)c(Cl)c4)CCCN(C(=O)c4cc(OC)c(OC)c(OC)c4)C3)CC2)nc2ccccc21
Reaction #196540
DOI: 10.1039/C8SC04228D
CC(=O)C1CC(C(=O)OC(C)(C)C)N(C(=O)CNC(=O)Nc2cccc(C)c2)C1c1ccccc1
Reaction #200723
DOI: 10.1039/C8SC04228D
Cn1c(=O)c(CN(C(=O)C2CCCCC2)C2(C)CCNC2)cc2ccccc21
Reaction #204629
DOI: 10.1039/C8SC04228D
COC(=O)NCC1CCC(C(=O)N2CC(c3ccc(F)cc3)C(N(C)C(=O)N(C)c3cc(C(F)(F)F)cc(C(F)(F)F)c3)C2)CC1
Reaction #205365
DOI: 10.1039/C8SC04228D
CC[C@@H](C)[C@@]1(NC(C)=O)CCN([C@@H](CCc2ccccc2)C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2CCCCN2)C1=O
Reaction #220132
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](C)[C@@]1(NC(C)=O)CCN([C@@H](CCc2ccccc2)C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@H](Oc3ccccc3)CN2)C1=O
Reaction #220133
title compound
Rendimiento 73.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](C)[C@@]1(NC(C)=O)CCN([C@@H](CCc2ccccc2)C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@H](Oc3ccccn3)CN2)C1=O
Reaction #220135
title compound
Rendimiento 52.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](C)[C@@]1(NC(C)=O)CCN([C@@H](CCc2ccccc2)C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@H](Oc3ccccn3)CN2)C1=O
Reaction #220136
title compound
Rendimiento 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](C)[C@@]1(NC(C)=O)CCN([C@@H](CCc2ccccc2)C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@@H](Oc3ccccc3)CN2)C1=O
Reaction #220138
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC[C@@H](C)[C@@]1(NC(C)=O)CCN([C@@H](CCc2ccccc2)C(=O)N[C@@H](Cc2cc(F)cc(F)c2)[C@H](O)[C@H]2C[C@@H](Oc3ccccn3)CN2)C1=O
Reaction #220140
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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