HEPES

CN1CCC[C@H]1c1cccnc1
Reaction #1858
(S)-(-)-nicotine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN1CCC[C@H]1c1cccnc1
Reaction #2817
(S)-(-)-nicotine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
CN1CCC[C@H]1c1cccnc1
Reaction #5022
(S)-(-)-nicotine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CN1CCC[C@H]1c1cccnc1
Reaction #6467
(S)-(-)-nicotine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
CNCCCN1c2ccccc2CCc2ccccc21
Reaction #57129
desipramine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CN1CCC[C@H]1c1cccnc1
Reaction #80685
(S)-(-)-nicotine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
NCCCC[C@H](N)C(=O)O
Reaction #162269
Lysine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=S(=O)(O)CCN1CCN(CCO)CC1.[Cl-].[Na+]
Reaction #167530
HEPES NaCl
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_09
O=P([O-])([O-])[O-].O=P([O-])([O-])[O-].[Ca+2].[Ca+2].[Ca+2]
Reaction #316503
calcium phosphate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CC(=O)N[C@H]1C(O)O[C@H](CO)[C@@H](O[C@@H]2O[C@H](CO[C@]3(C(=O)O)C[C@H](O)[C@@H](N)[C@H]([C@H](O)[C@H](O)CO)O3)[C@H](O)[C@H](O)[C@H]2O)[C@@H]1O
Reaction #320727
Neuα2,6Galβ1,4GlcNAc
Ausbeute 97.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CN1CCC[C@H]1c1cccnc1
Reaction #322444
(S)-(-)-nicotine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_01
CN1CCC[C@H]1c1cccnc1
Reaction #336467
(S)-(-)-nicotine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_05
CC(C)=CCC/C(C)=C/CC/C(C)=C/CC/C=C(\C)CC/C=C(\C)CCC=C(C)C
Reaction #345322
Squalene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_11
CCc1c2c(nc3ccc(O)cc13)-c1cc3c(c(=O)n1C2)COC(=O)[C@]3(O)CC
Reaction #358224
SN-38
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
O=c1ccc2ccccc2o1
Reaction #358229
coumarin
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
CCC[C@@H]1C[C@H](OC)C[C@H](C)C[C@@H]2C[C@@H](OC(=O)/C=C\CCc3coc(/C=C\CNC(=O)OC)n3)C[C@H](CC(=O)O1)O2
Reaction #436784
Neopeltolide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
CC(O)[C@H](C)[C@H](N)C(=O)O
Reaction #470402
4-hydroxyisoleucine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CC(O)[C@H](C)[C@H](N)C(=O)O
Reaction #470403
4-hydroxyisoleucine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
CCc1c2c(nc3ccc(O)cc13)-c1cc3c(c(=O)n1C2)COC(=O)[C@]3(O)CC
Reaction #479208
SN-38
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_10
CN1CCC[C@H]1c1cccnc1
Reaction #482013
(S)-(−)-nicotine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_08
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