| Weight | 508.645 g/mol |
|---|---|
| Formula | C23H36N6O5S |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 5 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 9 |
21S-Argatroban (121785-71-5, 121785-72-6)
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- Complete 1H and 13C assignments of (21R) and (21S) diastereomers of argatroban. (Magnetic Resonance in Chemistry, 2008)
- Chemoenzymatic synthesis of the enantiomerically pure 1,2,3,4-tetrahydroquinoline moiety of the antithrombotic (21R)- and (21S)-argatroban (Tetrahedron-asymmetry, 2013)
- Crystallographic, spectroscopic, and theoretical investigation of the efficiently separated 21R and 21S-diastereoisomers of argatroban. (Chirality, 2013)
- Optically pure (r) and (s) 3- methyl-1,2,3,4-biological catalytic synthesis of tetrahydroquinoline, and the anti-thrombotic (21r) - and (21s) - argatroban its use as synthons for preparing (2014)
- Biocatalyzed synthesis of the optically pure (r) and (s) 3-methyl-1,2,3,4-tetrahydroquinoline and their use as chiral synthons for the preparation of the antithrombotic (21r)- and (21s)-argatroban (2016)
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SMILESCC1CCN(C(C1)C(=O)O)C(=O)C(CCCN=C(N)N)NS(=O)(=O)C2=CC=CC3=C2NCC(C3)C
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InChIKeyKXNPVXPOPUZYGB-UHFFFAOYSA-N
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