بحث البنية الفرعية

CO.C1CCOC1

COC[C@H]1O[C@@H](n2cnc3c(NC4CCCC4)ncnc32)[C@H](O)[C@@H]1O
Reaction #6761
N6-cyclopentyl-5′-O-methyladenosine
DOI: 10.6084/m9.figshare.5104873.v1
COC[C@H]1O[C@@H](n2cnc3c(NCc4cccc(I)c4)ncnc32)[C@H](O)[C@@H]1O
Reaction #6762
N6-(3-iodobenzyl)-5′-O-methyladenosine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC[C@H]1O[C@@H](n2cnc3c(NC4CCCC4)ncnc32)[C@H](O)[C@@H]1O
Reaction #6765
N6-cyclopentyl-5′-O-ethyladenosine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC[C@H]1O[C@@H](n2cnc3c(NCc4cccc(I)c4)ncnc32)[C@H](O)[C@@H]1O
Reaction #6766
N6-(3-Iodobenzyl)-5′-O-Ethyladenosine
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C2CCC(OC)O2)cc(OC)c1OC
Reaction #50766
2-(3,4,5-trimethoxyphenyl)-5 -methoxytetrahydrofuran
المردود 27.3%DOI: 10.6084/m9.figshare.5104873.v1
Cl.NCC12CN(c3c(F)c(F)c4c(=O)c(C(=O)O)cn(C5CC5)c4c3F)CC1CCO2
Reaction #82161
7-(1-aminomethyl-2-oxa-7-aza-bicyclo[3.3.0]-oct-7-yl)-1-cyclopropyl-5,6,8-trifluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NCC12CN(c3cc4c(cc3F)c(=O)c(C(=O)O)cn4[C@@H]3C[C@@H]3F)CC1CCO2
Reaction #82163
7-(1-aminomethyl-2-oxa-7-aza-bicyclo[3.3.0]oct-7-yl)-6-fluoro-1-(cis-2-fluorocyclopropyl)-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NCC12CN(c3cc4c(cc3F)c(=O)c(C(=O)O)cn4-c3ccc(F)cc3F)CC1CCO2
Reaction #82165
7-(1-aminomethyl-2-oxa-7-azabicyclo[3.3.0]oct-7-yl)-1-(2,4-difluorophenyl)-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1C2C(=O)OC(=O)C12
Reaction #82988
2,4-dioxo-3-oxabicyclo[3.1.0]hexane-6-carboxylic acid
المردود 83.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(/C=C/CC(C)CCCC(C)(C)OC)=C1COC(=O)C1
Reaction #95403
aimed compound
المردود 52.1%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
O=C([O-])CCC(=O)[O-].c1ccc([S+](c2ccccc2)c2ccccc2)cc1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #163392
triphenylsulfonium succinic acid salt
DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])CCC(=O)[O-].c1ccc([S+](c2ccccc2)c2ccccc2)cc1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #163393
triphenylsulfonium succinic acid salt
DOI: 10.6084/m9.figshare.5104873.v1
O=C([O-])CCC(=O)[O-].c1ccc([S+](c2ccccc2)c2ccccc2)cc1.c1ccc([S+](c2ccccc2)c2ccccc2)cc1
Reaction #163394
triphenylsulfonium succinic acid salt
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)OC1CC(n2cc(C#C[Si](C)(C)C)c3c(CCc4ccccc4)ncnc32)OC1CO[Si](C)(C)C(C)(C)C
Reaction #178143
DOI: 10.1039/C8SC04228D
c1cnc(Oc2ccc(Nc3nc4ccccc4s3)cc2)c(C2CCOC2)c1
Reaction #186050
DOI: 10.1039/C8SC04228D
COc1cc(C2CCC(OCCCN)O2)cc(OC)c1OC
Reaction #203180
DOI: 10.1039/C8SC04228D
CCCCCCCC(C=CC1C(O)CC2OC(O)CC21)OC1CCCCO1
Reaction #207394
DOI: 10.1039/C8SC04228D
CS(=O)(=O)OCC1CCC2(CC2)O1
Reaction #208674
DOI: 10.1039/C8SC04228D
Cl
Reaction #209126
DOI: 10.1039/C8SC04228D
الصفحة 1التالي