DATP

—
Reaction #65236
DNA
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_05
Nc1ncnc2c1ncn2[C@@H]1O[C@H](COP(=O)(O)OP(=O)(O)OP(=O)(O)O)[C@@H](O)[C@H]1O
Reaction #440590
ATP
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
Nc1ncnc2c1ncn2[C@@H]1O[C@H](COP(=O)(O)OP(=O)(O)OP(=O)(O)O)[C@@H](O)[C@H]1O
Reaction #440596
ATP
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
Nc1ncnc2c1ncn2[C@@H]1O[C@H](COP(=O)(O)OP(=O)(O)OP(=O)(O)O)[C@@H](O)[C@H]1O
Reaction #440690
ATP
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_06
O=c1ccn([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O2)c(=O)[nH]1
Reaction #452419
dUTP
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2000_10
Nc1ccccc1C(=O)[O-].Nc1ncnc2c1ncn2[C@H]1C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O1
Reaction #569560
Anthranilate dATP
Ausbeute 80.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_08
O=c1ccn([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O2)c(=O)[nH]1
Reaction #645247
dUTP
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_11
O=c1ccn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)c(=O)[nH]1
Reaction #670135
Uridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_07
Nc1ncnc2c1ncn2[C@@H]1O[C@H](COP(=O)(O)OP(=O)(O)OP(=O)(O)O)[C@@H](O)[C@H]1O
Reaction #929037
ATP
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_04
O=c1ccn([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O2)c(=O)[nH]1
Reaction #973859
dUTP
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_08
O=c1ccn([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O2)c(=O)[nH]1
Reaction #1259207
dUTP
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_11
O=c1ccn([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O2)c(=O)[nH]1
Reaction #1382730
dUTP
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_07
O=c1ccn([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O2)c(=O)[nH]1
Reaction #1435715
dUTP
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2007_05
O=c1ccn([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O2)c(=O)[nH]1
Reaction #1451103
dUTP
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_02
O=c1ccn([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O2)c(=O)[nH]1
Reaction #1502843
dUTP
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_06
CC(=O)[O-].NC(CO)(CO)CO
Reaction #1527017
Tris·acetate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1996_03
Nc1ncnc2c1ncn2[C@@H]1O[C@H](COP(=O)(O)OP(=O)(O)OP(=O)(O)O)[C@@H](O)[C@H]1O
Reaction #1669686
ATP
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_05
Nc1ncnc2c1ncn2[C@@H]1O[C@H](COP(=O)(O)OP(=O)(O)OP(=O)(O)O)[C@@H](O)[C@H]1O
Reaction #1669687
ATP
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_05
O=c1ccn([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O2)c(=O)[nH]1
Reaction #1729174
dUTP
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_02
NCCCCNCCCN
Reaction #1770836
Spermidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_06
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