子结构搜索

1405576

CCOCc1nc2c(N)nc3cc(-c4cccnc4)ccc3c2n1CC1CCN(C(=O)C2CCCO2)CC1
Reaction #9490
2-ethoxymethyl-7-(pyridin-3-yl)-1-{[1-(tetrahydrofuran-2-ylcarbonyl)piperidin-4-yl]methyl}-1H-imidazo[4,5-c]quinolin-4-amine
收率 69.5%DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)[C@H]1O[C@@H](OC)[C@@H]2OC(C)(C)O[C@@H]21
Reaction #10539
title compound
收率 94.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1nc(NCC(c2ccccc2)c2ccccc2)c2ncn([C@@H]3O[C@H](C(=O)O)[C@H]4OC(C)(C)O[C@H]43)c2n1
Reaction #10565
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCNC(=O)[C@H]1O[C@@H](n2cnc3c(NCC(c4ccccc4)c4ccccc4)nc(C(=O)OCC)nc32)[C@@H]2OC(C)(C)O[C@@H]21
Reaction #10566
title compound
收率 78.9%DOI: 10.6084/m9.figshare.5104873.v1
Nc1nc(I)nc2c1ncn2[C@@H]1O[C@H](C(=O)O)[C@@H](O)[C@H]1O
Reaction #44333
6.8
收率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(OCc1ccccc1)N1CCN(C(=O)[C@H]2C[C@H](Br)CO2)CC1
Reaction #83067
desired product
收率 57.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C[C@H](NC(=O)[C@H](C)NC(=O)[C@H]2CCCO2)C(=O)N[C@@H](Cc2ccccc2)C(=O)[C@@]2(C)CO2)cc1
Reaction #87206
(R)-N-((S)-1-(((S)-3-(4-methoxyphenyl)-1-(((S)-1-((R)-2-methyloxiran-2-yl)-1-oxo-3-phenylpropan-2-yl)amino)-1-oxopropan-2-yl)amino)-1-oxopropan-2-yl)tetrahydrofuran-2-carboxamide
收率 57.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1ccc(Cl)c(-c2nn(-c3ccc(C(F)(F)F)cc3)c(=O)[nH]2)c1)[C@H]1CCCO1
Reaction #87787
desired title product
收率 28.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CNC(=O)[C@H]2CCCO2)c(C)c1-c1nn(-c2ccc(C(F)(F)F)cc2)c(=O)[nH]1
Reaction #87792
title product
收率 26.8%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1cc(-c2nn(-c3ccc(C(F)(F)F)cc3)c(=O)[nH]2)c(Cl)cc1F)[C@H]1CCCO1
Reaction #87803
desired product
收率 13.3%DOI: 10.6084/m9.figshare.5104873.v1
O=C([C@H]1CCCO1)N1CC[C@@H](Nc2nc(N3CCN(c4ccc(Cl)cc4)CC3)nc3c2S(=O)CC3)C1
Reaction #157298
((R)-3-{2-[4-(4-chloro-phenyl)-piperazin-1-yl]-5-oxo-6,7-dihydro-5H-5λ4-thieno[3,2-d]pyrimidin-4-ylamino}-pyrrolidin-1-yl)-(R)-tetrahydro-furan-2-yl-methanone
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(NC(=O)C2CCCO2)cc1-c1ccc(C(=O)NCC2CC2)cc1
Reaction #178624
DOI: 10.1039/C8SC04228D
O=C(C1CCCO1)N1CCNCC1
Reaction #184016
DOI: 10.1039/C8SC04228D
COC(=O)C1CCC(C(=O)CSC2C(NC(=O)Cc3ccccc3)C(=O)N2C(O)C(=O)OCc2ccc(OC)cc2)O1
Reaction #185896
DOI: 10.1039/C8SC04228D
CC1(C)OC2C(C(=O)NNC(=O)C(C)(C)C)OC(n3cnc4c(Cl)ncnc43)C2O1
Reaction #197237
DOI: 10.1039/C8SC04228D
O=C1CCC(Cl)(C(=O)OCc2ccc([N+](=O)[O-])cc2)O1
Reaction #198027
DOI: 10.1039/C8SC04228D
CC1(C)OC2C(C(=O)O)OC(n3cnc4c(N)nc(I)nc43)C2O1
Reaction #199795
DOI: 10.1039/C8SC04228D
COc1cc2nc(N3CCN(C(=O)C4CCCO4)CC3)nc(N)c2cc1OC
Reaction #200633
DOI: 10.1039/C8SC04228D
COC(O[Si](C)(C)C)=C1CCCO1
Reaction #201664
DOI: 10.1039/C8SC04228D
COC(=O)C1CCC(O)O1
Reaction #205026
DOI: 10.1039/C8SC04228D
第 1 页下一页