子结构搜索

1095857

O=C(O)[C@H](CC1CCCCC1)N1CC(Oc2c(F)cccc2Cl)=CC1=O
Reaction #47282
(S)-2-[4-(2-chloro-6-fluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-3-cyclohexyl-propionic acid
收率 97.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CC1CCCCC1)N1CC(Oc2cccc(Cl)c2Cl)=CC1=O
Reaction #47480
(S)-3-cyclohexyl-2-[4-(2,3-dichloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid methyl ester
收率 17.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@H](CC1CCCCC1)N1CC(Oc2cccc(Cl)c2Cl)=CC1=O
Reaction #47481
(S)-3-cyclohexyl-2-[4-(2,3-dichloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid
收率 77.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CC1CCCCC1)N1CC(Oc2cc(Cl)ccc2Cl)=CC1=O
Reaction #47515
(S)-3-cyclohexyl-2-[4-(2,5-dichloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid methyl ester
收率 15.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@H](CC1CCCCC1)N1CC(Oc2cc(Cl)ccc2Cl)=CC1=O
Reaction #47516
(S)-3-cyclohexyl-2-[4-(2,5-dichloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid
收率 84.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CC1CCCCC1)N1CC(Oc2ccc(Cl)cc2Cl)=CC1=O
Reaction #47520
(S)-3-cyclohexyl-2-[4-(2,4-dichloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid methyl ester
收率 33.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@H](CC1CCCCC1)N1CC(Oc2ccc(Cl)cc2Cl)=CC1=O
Reaction #47521
(S)-3-cyclohexyl-2-[4-(2,4-dichloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionic acid
收率 78.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)[C@H](CC1CCCCC1)N1CC(Oc2cccc(Cl)c2)=CC1=O
Reaction #47544
(S)-2-[4-(3-chloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-3-cyclohexyl-propionic acid methyl ester
收率 35.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)[C@H](CC1CCCCC1)N1CC(Oc2cccc(Cl)c2)=CC1=O
Reaction #47545
(S)-2-[4-(3-chloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-3-cyclohexyl-propionic acid
收率 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Nc2cc(Cl)cc(Cl)c2C2C=CCC12
Reaction #75639
Compound 1
收率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C1Nc2cc(Cl)cc(Cl)c2C2C=CCC12
Reaction #75640
7,9-dichloro-3a,4,5,9b-tetrahydro-3H-cyclopenta[c]quinoline-4-carboxylic Acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Nc2cc(Cl)cc(Cl)c2C2c3ccccc3CCC12
Reaction #75646
Compound 12
收率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(c2cc(C)cc(C)c2)c2c(Cl)cc(Cl)cc2N1
Reaction #75656
Compound 24
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(c2ccc(C(C)(C)C)cc2)c2c(Cl)cc(Cl)cc2N1
Reaction #75657
Compound 25
收率 89.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(c2ccccc2F)c2c(Cl)cc(Cl)cc2N1
Reaction #75658
Compound 26
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(c2ccccc2Cl)c2c(Cl)cc(Cl)cc2N1
Reaction #75665
Compound 33
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(c2ccccc2Br)c2c(Cl)cc(Cl)cc2N1
Reaction #75668
Compound 36
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(c2ccc(Br)cc2)c2c(Cl)cc(Cl)cc2N1
Reaction #75671
Compound 39
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CC(c2cccc(C(F)(F)F)c2)c2c(Cl)cc(Cl)cc2N1
Reaction #75673
Compound 41
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1Nc2cc(Cl)cc(Cl)c2C(c2ccccc2)C1C
Reaction #75674
Compound 42
DOI: 10.6084/m9.figshare.5104873.v1
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