Home Imidazoles 162758-04-5
162758-04-5,MFCD01320376
Catalog No.:AA001TBG

162758-04-5 | O-(2-(5-((3AS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamido)ethyl) methanesulfonothioate

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1mg
≥95%
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$46.00   $32.00
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5mg
≥95%
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$199.00   $139.00
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10mg
≥95%
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$329.00   $230.00
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  • Technical Information
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  • Literature
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  • Technical Information
  • Properties
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Technical Information
Catalog Number:
AA001TBG
Chemical Name:
O-(2-(5-((3AS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamido)ethyl) methanesulfonothioate
CAS Number:
162758-04-5
Molecular Formula:
C13H23N3O4S3
Molecular Weight:
381.5344
MDL Number:
MFCD01320376
SMILES:
O=C(NCCSS(=O)(=O)C)CCCC[C@@H]1SC[C@H]2[C@@H]1NC(=O)N2
Properties
Properties
 
Form:
Solid  
MP:
95-103°C  
Storage:
-20 ℃;Inert atmosphere;  

Computed Properties
 
Complexity:
535  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
3  
Heavy Atom Count:
23  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
9  
XLogP3:
-0.1  

Literature

Title: Synthesis of hetero-telechelic alpha,omega bio-functionalized polymers.

Journal: Biomacromolecules 20100111

Title: Outward stabilization of the S4 segments in domains III and IV enhances lidocaine block of sodium channels.

Journal: The Journal of physiology 20070701

Title: Setting up for the block: the mechanism underlying lidocaine's use-dependent inhibition of sodium channels.

Journal: The Journal of physiology 20070701

Title: Inorganic mercury interacts with cysteine residues (C451 and C474) of hOCT2 to reduce its transport activity.

Journal: American journal of physiology. Renal physiology 20070501

Title: Noxious compounds activate TRPA1 ion channels through covalent modification of cysteines.

Journal: Nature 20070201

Title: Mutation of glutamate 155 of the GABAA receptor beta2 subunit produces a spontaneously open channel: a trigger for channel activation.

Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience 20041215

Title: Peroxynitrite inactivates the human dopamine transporter by modification of cysteine 342: potential mechanism of neurotoxicity in dopamine neurons.

Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience 20020601

Title: Conserved cysteine residues in the extracellular loop of the human P2X(1) receptor form disulfide bonds and are involved in receptor trafficking to the cell surface.

Journal: Molecular pharmacology 20020201

Title: Investigating the surface expression of the renal type IIa Na+/Pi-cotransporter in Xenopus laevis oocytes.

Journal: The Journal of membrane biology 20010301

Title: Structure and dynamics of the GABA binding pocket: A narrowing cleft that constricts during activation.

Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience 20010101

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SDS
Tags:162758-04-5 Molecular Formula|162758-04-5 MDL|162758-04-5 SMILES|162758-04-5 O-(2-(5-((3AS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamido)ethyl) methanesulfonothioate