Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C10H14N2O2S |
Molecular Weight | 226.295 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@@H](S)[C@@H](CC1=CN=C(N)C=C1)C(O)=O
InChI
InChIKey=GYIYAOUGKJSCCG-HTRCEHHLSA-N
InChI=1S/C10H14N2O2S/c1-6(15)8(10(13)14)4-7-2-3-9(11)12-5-7/h2-3,5-6,8,15H,4H2,1H3,(H2,11,12)(H,13,14)/t6-,8-/m1/s1
Approval Year
PubMed
Title | Date | PubMed |
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Colominic acid: a novel chiral selector for capillary electrophoresis of basic drugs. | 2002 Jul 12 |
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Transformation of opium poppy (Papaver somniferum L.) with antisense berberine bridge enzyme gene (anti-bbe) via somatic embryogenesis results in an altered ratio of alkaloids in latex but not in roots. | 2004 Dec |
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Instability of pancuronium in postmortem blood and liver taken after a fatal intramuscular Pavulon injection. | 2004 Jul 16 |
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Synthesis and biological evaluation of N-methyl-laudanosine iodide analogues as potential SK channel blockers. | 2005 Feb 15 |
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Simultaneous determination of atracurium and its metabolite laudanosine in post-mortem fluids by liquid chromatography/multiple-stage mass spectrometry on an ion trap. | 2007 |
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Laudanosine has no effects on respiratory activity but induces non-respiratory excitement activity in isolated brainstem-spinal cord preparation of neonatal rats. | 2010 |
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87609775
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DB05712
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84KQ4M4N8B
Created by
admin on Sat Dec 16 12:12:50 GMT 2023 , Edited by admin on Sat Dec 16 12:12:50 GMT 2023
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775274-06-1
Created by
admin on Sat Dec 16 12:12:50 GMT 2023 , Edited by admin on Sat Dec 16 12:12:50 GMT 2023
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ACTIVE MOIETY