budesonide

CCCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@]5(C)[C@H]4[C@@H](O)C[C@]3(C)[C@]2(C(=O)CO)O1.CCCCCCCCCCCCOC(=O)[O-]
Reaction #939034
budesonide dodecylcarbonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_08
CCCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@]5(C)[C@H]4[C@@H](O)C[C@]3(C)[C@]2(C(=O)CO)O1.CCCCCCCCCCCCCCCCOC(=O)[O-]
Reaction #939035
budesonide hexadecylcarbonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_08
CCCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@]5(C)[C@H]4[C@@H](O)C[C@]3(C)[C@]2(C(=O)CO)O1.CCCCCCCCCCOC(=O)[O-]
Reaction #939036
budesonide decylcarbonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_08
CCCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@]5(C)[C@H]4[C@@H](O)C[C@]3(C)[C@]2(C(=O)CO)O1.CCCCNC(=O)[O-]
Reaction #939037
budesonide butylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_08
CCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@]5(C)[C@H]4[C@@H](O)C[C@]3(C)[C@]2(C(=O)CO)O1
Reaction #1009259
Budenoside
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_03
CCCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@]5(C)[C@H]4[C@@H](O)C[C@]3(C)[C@]2(C(=O)CO)O1.CCCCCCCCCCCCCCCCOC(=O)[O-]
Reaction #1831970
Budesonide Hexadecylcarbonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_03
CCCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@]5(C)[C@H]4[C@@H](O)C[C@]3(C)[C@]2(C(=O)CO)O1.CCCCCCCCCCOC(=O)[O-]
Reaction #1831971
Budesonide Decylcarbonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_03
CCCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@]5(C)[C@H]4[C@@H](O)C[C@]3(C)[C@]2(C(=O)CO)O1.CCCCNC(=O)[O-]
Reaction #1831972
Budesonide Butylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_03
CCCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@]5(C)[C@H]4[C@@H](O)C[C@]3(C)[C@]2(C(=O)CO)O1.CCCCCCCCCCCCOC(=O)[O-]
Reaction #2180484
Budesonide Dodecylcarbonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_05
CCCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@]5(C)[C@H]4[C@@H](O)C[C@]3(C)[C@]2(C(=O)CO)O1.CCCCCCCCCCCCCCCCOC(=O)[O-]
Reaction #2180485
Budesonide Hexadecylcarbonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_05
CCCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@]5(C)[C@H]4[C@@H](O)C[C@]3(C)[C@]2(C(=O)CO)O1.CCCCCCCCCCOC(=O)[O-]
Reaction #2180486
Budesonide Decylcarbonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_05
CCCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@]5(C)[C@H]4[C@@H](O)C[C@]3(C)[C@]2(C(=O)CO)O1.CCCCNC(=O)[O-]
Reaction #2180487
Budesonide Butylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_05
CCCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@]5(C)[C@H]4[C@@H](O)C[C@]3(C)[C@]2(C(=O)CO)O1.CCCCCCCCCCCCOC(=O)[O-]
Reaction #2456971
Budesonide Dodecylcarbonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_04
CCCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@]5(C)[C@H]4[C@@H](O)C[C@]3(C)[C@]2(C(=O)CO)O1.CCCCCCCCCCCCCCCCOC(=O)[O-]
Reaction #2456972
Budesonide Hexadecylcarbonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_04
CCCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@]5(C)[C@H]4[C@@H](O)C[C@]3(C)[C@]2(C(=O)CO)O1.CCCCCCCCCCOC(=O)[O-]
Reaction #2456973
Budesonide Decylcarbonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_04
CCCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@]5(C)[C@H]4[C@@H](O)C[C@]3(C)[C@]2(C(=O)CO)O1.CCCCNC(=O)[O-]
Reaction #2456974
Budesonide Butylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_04
CCCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@]5(C)[C@H]4[C@@H](O)C[C@]3(C)[C@]2(C(=O)CO)O1.CCCCCCCCCCCCCCCCOC(=O)[O-]
Reaction #2463791
Budesonide Hexadecylcarbonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_12
CCCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@]5(C)[C@H]4[C@@H](O)C[C@]3(C)[C@]2(C(=O)CO)O1.CCCCCCCCCCOC(=O)[O-]
Reaction #2463792
Budesonide Decylcarbonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_12
CCCC1O[C@@H]2C[C@H]3[C@@H]4CCC5=CC(=O)C=C[C@]5(C)[C@H]4[C@@H](O)C[C@]3(C)[C@]2(C(=O)CO)O1.CCCCNC(=O)[O-]
Reaction #2463793
Budesonide Butylcarbamate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_12