子结构搜索

330

CNC(=O)C(Cc1ccc2ccccc2c1)N1CCNC(CCO[Si](C)(C)C(C)(C)C)C1=O
Reaction #8626
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)N1CC2CC1CN2c1cnc(-c2nn(Cc3ccccc3F)c3ncccc23)nc1
Reaction #8682
1-(2-Fluorobenzyl)-3-[5-(5-isopropyl-2,5-diazabicyclo[2.2.1]hept-2-yl)-2-pyrimidinyl]-1H-pyrazol[3,4-b]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CC(CN1CCN(C(=O)c2cc(C(F)(F)F)cc(C(F)(F)F)c2)[C@H](Cc2c[nH]c3ccccc23)C1)=NOCCN(C)C
Reaction #10262
1-{(2R)-1-[3,5-bis(trifluoromethyl)benzoyl]-2-(1H-indol-3-ylmethyl)-piperazin-4-yl}-2-propanone O-[2-(dimethylamino)-ethyl]oxime
收率 104.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1cc(C(F)(F)F)cc(C(F)(F)F)c1)N1CCN(CC=NOCCN2CCOCC2)C[C@H]1Cc1c[nH]c2ccccc12
Reaction #10263
2-{(2R)-1-[3,5-bis(trifluoromethyl)benzoyl]-2-(1H-indol-3-ylmethyl)-piperazin-4-yl}-ethanal O-[2-(morpholin-4-yl)ethyl]oxime
收率 96.6%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)C(=O)NCCN1C(=O)c1oc(C(F)(F)F)cc1N
Reaction #47208
4-(4-amino-2-(trifluoromethyl)furan-5-carbonyl)-3,3-dimethylpiperazin-2-one
收率 6.8%DOI: 10.6084/m9.figshare.5104873.v1
CNC(=O)C1CN(CCCC(c2ccc(F)cc2)c2ccc(F)cc2)CCN1CC(=O)Nc1c(C)cc(N)cc1C
Reaction #63621
N-(4-amino-2,6-dimethylphenyl)-4-[4,4-bis(4-fluorophenyl)butyl]-2-[(methylamino)carbonyl]-1-piperazineacetamide
DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(-c2ccccc2)c2nc(-c3ccc(N4CC(C)NC(C)C4)cc3)cc(OC)c12
Reaction #155922
6-[4-(3,5-dimethyl-piperazin-1-yl)-phenyl]-3-ethyl-4-methoxy-1-phenyl-1H-pyrazolo[3,4-b]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cc(-c2ccc(N3CCNCC3)cc2)nc2c1c(CC)nn2-c1ccccc1
Reaction #155927
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cc(-c2ccc(N3CC(C)NC(C)C3)cc2)nc2c1c(CC)nn2-c1ccccc1
Reaction #155928
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1C(=O)N(CCCC(=O)N2CCC3(CC3)C(O)C2)CCN1C(=O)Nc1ccc(C(F)(F)F)cc1
Reaction #176558
DOI: 10.1039/C8SC04228D
COc1ccc2c(c1)C=C(c1nc(C(=O)N3C4CCC3CN(C)C4)co1)Cn1c-2c(C2CCCCC2)c2ccc(C(=O)NS(=O)(=O)N(C)C)cc21
Reaction #183413
DOI: 10.1039/C8SC04228D
CCCCCN(CCCCC)C(=O)N1CCN(C(=O)N(c2ccccc2)c2cccc(Cl)c2)C(C(=O)O)C1
Reaction #183606
DOI: 10.1039/C8SC04228D
O=C(NCC1CC1)Nc1ccc(C(=O)N2CCN(Cc3ccc(C(O)(C(F)(F)F)C(F)(F)F)cc3)CC2C(=O)O)cc1
Reaction #187769
DOI: 10.1039/C8SC04228D
CC1CN(c2c(F)cc3cc4c(=O)c(C(=O)O)cn(C)c4nc3c2F)CCN1
Reaction #192597
DOI: 10.1039/C8SC04228D
CC1CN(Cc2ccc(C(O)(C(F)(F)F)C(F)(F)F)cc2)CCN1C(=O)c1ccc(NC(=O)NCC2CC2)cc1
Reaction #195380
DOI: 10.1039/C8SC04228D
CC(C)(C)OC(=O)NCc1cc(Cl)c(NC(=O)CN2CCN(CCCCC(c3ccc(F)cc3)c3ccc(F)cc3)CC2C(N)=O)c(Cl)c1
Reaction #196096
DOI: 10.1039/C8SC04228D
COc1cc(N2CCN(C(=O)Cn3nc(-c4ccccn4)c(Cl)c3C)C(C)C2)c(F)cc1Cl
Reaction #196339
DOI: 10.1039/C8SC04228D
Cc1ccc(C2CN(c3cc4c(cc3F)ncc3c4c(=O)c(C(=O)O)cn3C)CCN2)cc1C
Reaction #202950
DOI: 10.1039/C8SC04228D
O=C(c1cc(C(F)(F)F)cc(C(F)(F)F)c1)N1CCN(CC=NOCCN2CCOCC2)CC1Cc1c[nH]c2ccccc12
Reaction #209063
DOI: 10.1039/C8SC04228D
CCc1nc2c(cnn2CC)c(NC2CCOCC2)c1CNC(=O)c1cccc(C(=O)NCc2ccc(Cl)c(-c3cccc(CN4CC5CC4CN5)c3)c2)c1
Reaction #209905
DOI: 10.1039/C8SC04228D
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