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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
Structure of AZD-9684

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

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Colominic acid: a novel chiral selector for capillary electrophoresis of basic drugs.
2002 Jul 12
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
Instability of pancuronium in postmortem blood and liver taken after a fatal intramuscular Pavulon injection.
2004 Jul 16
Synthesis and biological evaluation of N-methyl-laudanosine iodide analogues as potential SK channel blockers.
2005 Feb 15
Simultaneous determination of atracurium and its metabolite laudanosine in post-mortem fluids by liquid chromatography/multiple-stage mass spectrometry on an ion trap.
2007
Laudanosine has no effects on respiratory activity but induces non-respiratory excitement activity in isolated brainstem-spinal cord preparation of neonatal rats.
2010
Name Type Language
AZD-9684
Code English
(2S,3R)-2-((6-AMINO-3-PYRIDYL)METHYL)-3-SULFANYL-BUTANOIC ACID
Systematic Name English
3-PYRIDINEPROPANOIC ACID, 6-AMINO-.ALPHA.-((1R)-1-MERCAPTOETHYL)-, (.ALPHA.S)-
Systematic Name English
(.ALPHA.S)-6-AMINO-.ALPHA.-((1R)-1-MERCAPTOETHYL)-3-PYRIDINEPROPANOIC ACID
Systematic Name English
AZD9684
Code English
Code System Code Type Description
PUBCHEM
87609775
Created by admin on Sat Dec 16 12:12:50 GMT 2023 , Edited by admin on Sat Dec 16 12:12:50 GMT 2023
PRIMARY
DRUG BANK
DB05712
Created by admin on Sat Dec 16 12:12:50 GMT 2023 , Edited by admin on Sat Dec 16 12:12:50 GMT 2023
PRIMARY
FDA UNII
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
PRIMARY
CAS
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
PRIMARY