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Dantrolene sodium salt - 10mM in DMSO, high purity , CAS No.14663-23-1, Ryanodine receptor 3 antagonist

    Grade & Purity:
  • 10mM in DMSO
En stock
Item Number
D421701
Articles du produit groupé
SKU Taille
Disponibilité
Prix Qté
D421701-1ml
1ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
167,90$US

Ryanodine receptor antagonist. Calcium channel inhibitor

Description générale

Synonymes DANTROLENE SODIUM | Dantrolene sodium salt | 14663-23-1 | Dantrolene, Sodium Salt | Dantrolene (sodium) | Dantrolene Sodium (anhydrous) | Dantrium | Dantrolene sodium anhydrous | Dantamacrin | EINECS 238-706-8 | UNII-28F0G1E0VF | Ryanodex | 28F0G1E0VF | Sodium dantrolene | 1-((5-(p-
Spécifications et pureté 10mM in DMSO
Mécanismes biochimiques et physiologiques Ryanodine receptor antagonist. Calcium channel inhibitor. Reduces calcium flux across the sarcoplasmic reticulum. Displays selectivity for RYR1 and RYR3 over RYR2. Crosses the blood-brain barrier and active in vivo.
Température de stockage Store at -80°C
Expédié en
Ice chest + Ice pads
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Type d'action ANTAGONIST
Mécanisme d'action Ryanodine receptor 3 antagonist
Product Description

Dantrolene is a small molecule inhibitor of the Ryanodine receptor and a calcium channel protein inhibitor.Blockade of Ca2+ release from the sarcoendoplasmic reticulum, strongly related to excitation and contraction of muscles, generates a muscle relaxant effect correlated with Dantrolene. The neurotoxicity presented by pronounced glutamate activity is correlated to excessive rises in cytoplasmic Ca2+ levels, and Dantrolene is accordingly indicated as a neuroprotective agent against neurotrasmitter-induced excitotoxicity. Dantrolene, Sodium Salt is an inhibitor of RyR-1 and RyR-3.
A calcium channel protein inhibitor.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic acids and derivatives
Classe Carboxylic acids and derivatives
Subclass Amino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives
Direct Parent Alpha amino acids and derivatives
Alternative Parents Nitrobenzenes  Nitroaromatic compounds  Imidazolinones  Furans  Heteroaromatic compounds  N-acylimines  Propargyl-type 1,3-dipolar organic compounds  Oxacyclic compounds  Azacyclic compounds  Organic oxoazanium compounds  Organic oxides  Hydrocarbon derivatives  Organic sodium salts  Organic zwitterions  Carbonyl compounds  Organopnictogen compounds  
Molecular Framework Aromatic heteromonocyclic compounds
Substituents Alpha-amino acid or derivatives - Nitrobenzene - Nitroaromatic compound - Monocyclic benzene moiety - Imidazolinone - Benzenoid - Furan - 2-imidazoline - Heteroaromatic compound - C-nitro compound - Organic nitro compound - N-acylimine - Oxacycle - Azacycle - Organic oxoazanium - Organic alkali metal salt - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organoheterocyclic compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Carbonyl group - Organic zwitterion - Organic sodium salt - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organic nitrogen compound - Aromatic heteromonocyclic compound
Description This compound belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof.
External Descriptors Not available

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Cibles associées (non humaines)

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Mécanismes d'action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name Références

Noms et identifiants

IUPAC Name sodium;3-[(E)-[5-(4-nitrophenyl)furan-2-yl]methylideneamino]-2-oxo-4H-imidazol-5-olate
INCHI InChI=1S/C14H10N4O5.Na/c19-13-8-17(14(20)16-13)15-7-11-5-6-12(23-11)9-1-3-10(4-2-9)18(21)22;/h1-7H,8H2,(H,16,19,20);/q;+1/p-1/b15-7+;
InChIKey KSRLIXGNPXAZHD-HAZZGOGXSA-M
Smiles C1C(=NC(=O)N1N=CC2=CC=C(O2)C3=CC=C(C=C3)[N+](=O)[O-])[O-].[Na+]
Isomères SMILES C1C(=NC(=O)N1/N=C/C2=CC=C(O2)C3=CC=C(C=C3)[N+](=O)[O-])[O-].[Na+]
WGK Allemagne 2
RTECS MU3875000
Poids moléculaire 336.23
Reaxy-Rn 5698800
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=5698800&ln=

Certificats (CoA, COO, BSE/TSE et tableau d'analyse)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Propriétés chimiques et physiques

Poids moléculaire 336.230 g/mol
XLogP3
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 6
Rotatable Bond Count 3
Exact Mass 336.047 Da
Monoisotopic Mass 336.047 Da
Topological Polar Surface Area 127.000 Ų
Heavy Atom Count 24
Formal Charge 0
Complexity 536.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 1
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 1
Covalently-Bonded Unit Count 2

Calculateurs de solution

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