Recherche de Sous-structure

985939

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Reaction #744078
solid
Rendement 105.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cnc2ccc(=O)n(CCN3CCC(NCc4cc5c(nn4)OCCO5)CC3)c2c1.Cl
Reaction #744079
title compound
Rendement 242.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1cnc2ccc(=O)n(CCN3CCC(NCc4ccc5c(n4)NC(=O)CO5)CC3)c2c1.Cl
Reaction #744081
title compound
Rendement 71.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cnc2ccc(=O)n(CCN3CCC(NCc4cc5c(cn4)OCCC5)CC3)c2c1.Cl
Reaction #744082
title compound
Rendement 75.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cnc2ccc(=O)n(CCN3CC[C@H](N)[C@H](O)C3)c2c1.Cl.Cl
Reaction #744160
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cnc2ccc(=O)n(CCN3CC[C@H](NCc4cc5c(cn4)OCCO5)[C@H](O)C3)c2c1.Cl
Reaction #744161
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cnc2ccc(=O)n(CCN3CC[C@@H](N)[C@@H](O)C3)c2c1.Cl.Cl
Reaction #744213
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cnc2ccc(=O)n(CCN3CC[C@@H](NCc4cc5c(cn4)OCCO5)[C@@H](O)C3)c2c1.Cl
Reaction #744214
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cnc2ccc(=O)n(CCN3CC[C@H](NCc4cnc(CO)c(Cl)c4)[C@H](O)C3)c2c1.Cl
Reaction #1968921
1-{2-[(3R,4S)-4-({[5-chloro-6-(hydroxymethyl)-3-pyridinyl]methyl}amino)-3-hydroxy-1-piperidinyl]ethyl}-7-(methyloxy)-1,5-naphthyridin-2(1H)-one hydrochloride
Rendement 148.8%DOI: 10.6084/m9.figshare.5104873.v1