部分構造検索

866101

CCC(C)(C)C(=O)C(=O)N1CCCC1C(=O)NNc1ccccn1
Reaction #7999
1-(3,3-Dimethyl-2-oxo-pentanoyl)-pyrrolidine-2-carboxylic acid N′-pyridine-2-yl-hydrazide
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(F)(F)F)cc(NNC(=O)C2CCCCN2C(=O)C(=O)c2cccs2)n1
Reaction #8001
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(NC(=O)[C@H](CC2CCCCC2)N2CC(Oc3c(F)cccc3F)=CC2=O)nc1
Reaction #47256
6-{(S)-3-cyclohexyl-2-[4-(2,6-difluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-propionylamino}-nicotinic acid methyl ester
収率 40.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(NC(=O)C(CC2CCOCC2)N2CC(Oc3c(F)cccc3F)=CC2=O)nc1
Reaction #47257
6-[2-[4-(2,6-difluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-3-(tetrahydro-pyran-4-yl)-propionylamino]-nicotinic acid methyl ester
収率 55.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(NC(=O)[C@H](CC(C)C)N2CC(Oc3c(F)cccc3F)=CC2=O)nc1
Reaction #47260
6-{(S)-2-[4-(2,6-difluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4-methyl-pentanoylamino}-nicotinic acid methyl ester
収率 20.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(NC(=O)[C@H](CC2CCCCC2)N2CC(Oc3c(F)cccc3Cl)=CC2=O)nc1
Reaction #47285
6-{(S)-2-[4-(2-chloro-6-fluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-3-cyclohexyl-propionylamino}-nicotinic acid methyl ester
収率 33.0%DOI: 10.6084/m9.figshare.5104873.v1
Cl.O=C(Nc1cnccn1)[C@H](CC1CCCCC1)N1CC(Oc2c(F)cccc2Cl)=CC1=O
Reaction #47287
(S)-2-[4-(2-chloro-6-fluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-3-cyclohexyl-N-pyrazin-2-yl-propionamide hydrochloride
収率 33.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(NC(=O)[C@H](CC2CCCCC2)N2CC(Oc3c(F)ccc(Cl)c3F)=CC2=O)nc1
Reaction #47289
6-{(S)-2-[4-(3-chloro-2,6-difluoro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-3-cyclohexyl-propionylamino}-nicotinic acid methyl ester
収率 24.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N)c2cc(C(=O)Nc3ccc(CNC(=O)c4ccccn4)cc3)ccc2n1
Reaction #47794
title compound
収率 36.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(N)c2cc(C(=O)Nc3ccc(CNC(=O)c4ccnc(Cl)c4)cc3)ccc2n1
Reaction #47795
title compound
収率 76.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(C)c1ccccc1NC(=O)c1ccsc1I
Reaction #48241
N-[2-(1,3-dimethylbutyl)phenyl]-2-iodothiophene-3-carboxamide
収率 21.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC(C)c1ccccc1NC(=O)c1ccoc1I
Reaction #48242
N-[2-(1,3-dimethylbutyl)phenyl]-2-iodo-3-furamide
収率 19.2%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(OCc2ccccc2)c(CO)c1
Reaction #60606
4-benzyloxy-3-hydroxymethylaniline
DOI: 10.6084/m9.figshare.5104873.v1
C=C(C)c1cc(C(=O)N2Cc3cccc(OCCCN4CCOCC4)c3C2)c(OCc2ccccc2)cc1OCc1ccccc1
Reaction #69713
(2,4-bis-benzyloxy-5-isopropenyl-phenyl)-[4-(3-morpholin-4-yl-propoxy)-1,3-dihydro-isoindol-2-yl]-methanone
DOI: 10.6084/m9.figshare.5104873.v1
O=Cc1ccc(C(=O)NCCC(=O)O)cc1
Reaction #77821
3-(4-formylbenzoylamino)propionic Acid
DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCCC(CO)C1)C1(c2ccc(Cl)cc2)CCC1
Reaction #78924
amide
収率 43.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(N1CCCC(CO)C1)C1(c2ccc(Cl)cc2)CCCC1
Reaction #78934
desired compound
収率 156.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C1CCCN(C(=O)C2(c3ccc(Cl)cc3)CC2)C1
Reaction #78936
amide
収率 167.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2ccn(C(=O)C(OC)c3ccc(N4CCOCC4)cc3)n2)cc1OC
Reaction #84856
1-(3-(3,4-dimethoxyphenyl)-1H-pyrazol-1-yl)-2-methoxy-2-(4-morpholinophenyl)ethanone
収率 489.8%DOI: 10.6084/m9.figshare.5104873.v1
Cc1nccn1-c1ccc(C(=O)N(C2CC2)C2CCN(c3ncc(C(F)(F)F)cc3F)CC2)cc1
Reaction #156067
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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