子结构搜索

3776

O=C(Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1)C1CCCO1
Reaction #3697
crystals
收率 33.2%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccccc1OC1=CC(=O)N([C@@H](CC2CCCO2)C(=O)Nc2ccn(CC(C)(C)O)n2)C1
Reaction #47249
(S)-N-[1-(2-hydroxy-2-methyl-propyl)-1H-pyrazol-3-yl]-2-[4-(2-methoxy-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-3-(tetrahydro-furan-2-yl)-propionamide
收率 36.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCN(C(=O)C2C3CCC(O3)C2C(=O)Cl)CC1
Reaction #73456
3-(4-Methylpiperazine-1-carbonyl)-7-oxa-bicyclo[2,2,1]heptane-2-carbonyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1)C1CCCO1
Reaction #83519
crystals
收率 33.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C1O[C@@]2(Cc3ccccc3)CC[C@H](C(=O)N3CCN(c4ccccc4)CC3)[C@@H]1C2
Reaction #89769
crude product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NO)[C@H]1C[C@](O)(Cc2ccccc2)CC[C@@H]1C(=O)N1CCN(c2ccccc2)CC1
Reaction #89770
product
收率 26.0%DOI: 10.6084/m9.figshare.5104873.v1
COCC(C)N1CCCN(c2ccc(N3CCc4cc(OC[C@H]5CCCO5)ccc4C3=O)cc2OC)CC1
Reaction #156650
2-{3-Methoxy-4-[4-(2-methoxy-1-methyl-ethyl)-[1,4]diazepan-1-yl]-phenyl}-6-[(R)-1-(tetrahydrofuran-2-yl)methoxy]-3,4-dihydro-2H-isoquinolin-1-one
DOI: 10.6084/m9.figshare.5104873.v1
CN1CCCN(c2ccc(N3CCc4cc(OC[C@H]5CCCO5)ccc4C3=O)cc2)CC1
Reaction #156658
2-[4-(4-Methyl-[1,4]diazepan-1-yl)-phenyl]-6-[(R)-1-(tetrahydrofuran-2-yl)methoxy]-3,4-dihydro-2H-isoquinolin-1-one
DOI: 10.6084/m9.figshare.5104873.v1
CNC1CCCN(c2ccc(-n3ccc4cc(OC[C@@H]5CCCO5)ccc4c3=O)cc2)C1
Reaction #156673
2-[4-(3-Methylamino-piperidin-1-yl)-phenyl]-6-[(S)-1-(tetrahydrofuran-2-yl)methoxy]-2H-isoquinolin-1-one
DOI: 10.6084/m9.figshare.5104873.v1
COCCCN[C@@H]1CCN(c2ccc(N3CCc4cc(OC[C@@H]5CCCO5)ccc4C3=O)cc2F)C1
Reaction #156690
2-{3-Fluoro-4-[(R)-3-(3-methoxy-propylamino)-pyrrolidin-1-yl]-phenyl}-6-[(S)-1-(tetrahydro-furan-2-yl)methoxy]-3,4-dihydro-2H-isoquinolin-1-one
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2ccc(CC[C@@H]3O[C@H](O)[C@H](O)[C@@H]3CCN3C(=O)c4ccccc4C3=O)cc2)cc1F
Reaction #171215
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(NC(=O)c1c(F)c(F)c(N)c(F)c1F)C(=O)N1CCCC1C(=O)NC1CC(=O)OC1OCc1ccccc1
Reaction #193364
DOI: 10.1039/C8SC04228D
O=C1CCC(N2C(=O)c3cccc(OCc4ccc(CN5CC6CCC(C5)O6)cc4)c3C2=O)C(=O)N1
Reaction #197492
DOI: 10.1039/C8SC04228D
CN(C)C(=O)CN(CCc1cccc(OCc2ccccc2)c1)CC1CCOC1
Reaction #208307
DOI: 10.1039/C8SC04228D
CN1CCN(C(=O)C2C3CCC(O3)C2C(=O)Cl)CC1
Reaction #212138
DOI: 10.1039/C8SC04228D
CN(C(=O)C1CCCO1)C(CN)c1csc(NC(=O)NCc2cccc(F)c2)n1
Reaction #221090
DOI: 10.1039/C8SC04228D
CC(C)Oc1cc(C(=O)NC(Cc2ccccc2)C(O)CC(C)C(=O)NCCC2=CCCCC2)cc(N2CCCC2=O)c1
Reaction #227734
DOI: 10.1039/C8SC04228D
CN1CCN(C(=O)C2CC(N(C(=O)C3CCCO3)C3CCC(C)(C)CC3)CN2C(=O)C2CN(C3CC3)CC2c2ccc(Cl)cc2)CC1
Reaction #235038
DOI: 10.1039/C8SC04228D
O=C(Nc1ccc(C(=O)N2Cc3cccn3Cc3ccccc32)cc1)C1CCCO1
Reaction #240752
DOI: 10.1039/C8SC04228D
CS(=O)(=O)N1CC2CCCCC(NC(=O)c3ccccc3)C(=O)N2C(C(=O)NC2CC(=O)OC2O)C1
Reaction #242721
DOI: 10.1039/C8SC04228D
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