NAD+

O[C@@H](c1ccccc1)C(F)(F)F
Reaction #433618
(S)-2,2,2-trifluoro-1-phenylethanol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_02
N=c1c2ncn3c2ncn1[C@@H]1O[C@H](COP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H]3[C@H](O)[C@@H]2O)[C@@H](O)[C@H]1O
Reaction #462850
cADPR
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_01
NC(=O)C1=CN([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)OC[C@H]3O[C@@H](n4cnc5c(N)ncnc54)[C@H](O)[C@@H]3O)[C@@H](O)[C@H]2O)C=CC1
Reaction #546917
NADH
Ausbeute 24.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
NC(=O)C1=CN([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)OC[C@H]3O[C@@H](n4cnc5c(N)ncnc54)[C@H](O)[C@@H]3O)[C@@H](O)[C@H]2O)C=CC1
Reaction #546918
NADH
Ausbeute 19.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_03
NC(=O)C1=CN([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)OC[C@H]3O[C@@H](n4cnc5c(N)ncnc54)[C@H](OP(=O)(O)O)[C@@H]3O)[C@@H](O)[C@H]2O)C=CC1
Reaction #570951
NADPH
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_07
NC(=O)C1=CN([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)OC[C@H]3O[C@@H](n4cnc5c(N)ncnc54)[C@H](O)[C@@H]3O)[C@@H](O)[C@H]2O)C=CC1
Reaction #721257
NADH
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_04
Nc1ncnc2nc[nH]c12
Reaction #1067307
adenine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1987_01
NC(=O)C1=CN([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)OC[C@H]3O[C@@H](n4cnc5c(N)ncnc54)[C@H](O)[C@@H]3O)[C@@H](O)[C@H]2O)C=CC1.O=C1CCC(=O)N1Cl
Reaction #1117642
NAD NCS
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_04
C[C@H](O)c1ccccc1
Reaction #1178407
(S)-phenylethanol
Ausbeute 96.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
C[C@H](O)c1ccccc1
Reaction #1178408
(S)-phenylethanol
Ausbeute 97.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
C[C@H](O)c1ccccc1
Reaction #1178409
(S)-phenylethanol
Ausbeute 96.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
NC(=O)C1=CN([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)OC[C@H]3O[C@@H](n4cnc5c(N)ncnc54)[C@H](O)[C@@H]3O)[C@@H](O)[C@H]2O)C=CC1
Reaction #1446307
NADH
Ausbeute 24.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_07
NC(=O)C1=CN([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)OC[C@H]3O[C@@H](n4cnc5c(N)ncnc54)[C@H](O)[C@@H]3O)[C@@H](O)[C@H]2O)C=CC1
Reaction #1446308
NADH
Ausbeute 19.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_07
CCC(C)(C)[C@H](N)C(=O)O
Reaction #1466404
(S)-3-methyl-isoleucine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_09
CC(O)C(=O)[O-]
Reaction #1664797
lactate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_09
CC(O)C(=O)[O-]
Reaction #1664798
lactate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_09
NC(=O)c1ccc[n+]([C@@H]2O[C@H](COP(=O)(O)OP(=O)(O)OC[C@H]3O[C@@H](n4cnc5c(N)ncnc54)[C@H](OP(=O)(O)O)[C@@H]3O)[C@@H](O)[C@H]2O)c1
Reaction #1742340
NADP+
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_10
Nc1ncnc2nc[nH]c12
Reaction #1767697
adenine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1981_06
—
Reaction #1850398
alcohol
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_09
N[C@@H](CCC(=O)O)C(=O)O
Reaction #1902919
glutamic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_04
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