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Product Name :
Salfaprodil

Description:
Salfaprodil (Neu2000 potassium) is an NR2B-selective and uncompetitive antagonist of N-methyl-D-aspartate (NMDA). Salfaprodil is also a free radical scavenger. Salfaprodil has excellent neuroprotection against NMDA- and free radical-induced cell death.

CAS:
916214-57-8

Molecular Weight:
421.31

Formula:
C15H7F7KNO3

Chemical Name:
potassium 2-hydroxy-5-({[2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl]methyl}amino)benzoate

Smiles :
[K+].[O-]C(=O)C1=CC(=CC=C1O)NCC1C(F)=C(F)C(=C(F)C=1F)C(F)(F)F

InChiKey:
KLOANMLPWLPVSW-UHFFFAOYSA-M

InChi :
InChI=1S/C15H8F7NO3.K/c16-10-7(11(17)13(19)9(12(10)18)15(20,21)22)4-23-5-1-2-8(24)6(3-5)14(25)26;/h1-3,23-24H,4H2,(H,25,26);/q;+1/p-1

Purity:
≥98% (or refer to the Certificate of Analysis)

Shipping Condition:
Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis

Storage Condition :
Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.

Shelf Life:
≥12 months if stored properly.

Stock Solution Storage:
0 – 4 oC for 1 month or refer to the Certificate of Analysis.

Additional information:
Salfaprodil (Neu2000 potassium) is an NR2B-selective and uncompetitive antagonist of N-methyl-D-aspartate (NMDA). Salfaprodil is also a free radical scavenger. Salfaprodil has excellent neuroprotection against NMDA- and free radical-induced cell death.|Product information|CAS Number: 916214-57-8|Molecular Weight: 421.31|Formula: C15H7F7KNO3|Chemical Name: potassium 2-hydroxy-5-({[2,3,5,6-tetrafluoro-4-(trifluoromethyl)phenyl]methyl}amino)benzoate|Smiles: [K+].[O-]C(=O)C1=CC(=CC=C1O)NCC1C(F)=C(F)C(=C(F)C=1F)C(F)(F)F|InChiKey: KLOANMLPWLPVSW-UHFFFAOYSA-M|InChi: InChI=1S/C15H8F7NO3.K/c16-10-7(11(17)13(19)9(12(10)18)15(20,21)22)4-23-5-1-2-8(24)6(3-5)14(25)26;/h1-3,23-24H,4H2,(H,25,26);/q;+1/p-1|Technical Data|Appearance: Solid Power|Purity: ≥98% (or refer to the Certificate of Analysis)|Solubility: DMSO : 200 mg/mL (474.71 mM; Need ultrasonic).|Shipping Condition: Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis|Storage Condition: Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.|Shelf Life: ≥12 months if stored properly.|Stock Solution Storage: 0 – 4 oC for 1 month or refer to the Certificate of Analysis.|Drug Formulation: To be determined|HS Tariff Code: 382200|How to use|In Vitro:|Salfaprodil (10-300 μM) shows apparent neuroprotection against 300 μM N-methyl-d-aspartate (NMDA) at doses as low as 30 μM.{{Elinzanetant} site|{Elinzanetant} GPCR/G Protein|{Elinzanetant} Purity & Documentation|{Elinzanetant} In Vitro|{Elinzanetant} supplier|{Elinzanetant} Epigenetic Reader Domain} Salfaprodil (10-500 μM) inhibits the electrophysiologic response of cultured cortical neurons to 300 μM NMDA in a concentration-dependent manner.{{Anacardic Acid} MedChemExpress|{Anacardic Acid} Histone Acetyltransferase|{Anacardic Acid} Technical Information|{Anacardic Acid} Description|{Anacardic Acid} manufacturer|{Anacardic Acid} Cancer} Salfaprodil (0.PMID:23659187 1-1 μM) produces a marked reduction of Fe2+-induced neurotoxicity, even at doses of 0.1 to 0.3 μM. Salfaprodil (0.1-1 μM) blocks the degeneration of neurons and glia in cortical cell cultures. Salfaprodil (0-350 μM) effectively scavenges superoxide radicals (IC50=63.07±1.44 μM), nitric oxide (IC50=155.8±4.88 μM), and hydroxyl radicals (IC50=58.45±1.74 μM). Salfaprodil (0.78-12.5 μM) decreases the amount of antimycin A-induced ROS/RNS formation in a dose-dependent manner, with an IC50 of 2.21±0.11 μM. Salfaprodil (0.19-12.5 μM) inhibits malondialdehyde (MDA) formation with an IC50 of 2.72±0.26 μM. Salfaprodil (0-125 μM) effectively reduces iron-ascorbate-induced lipid peroxidation (IC50=24.56±0.07 μM).|In Vivo:|Salfaprodil (0.5-20 mg/kg; i.v.) reduces cerebral infarct evolving 24 h after 60-mins occlusion of the middle cerebral artery occlusion (MCAO) substantially and dose dependently. Salfaprodil (5 mg/kg; i.v.) protects white matter such as axons and myelin as well as gray matter from ischemic brain injury.|Products are for research use only. Not for human use.|

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Author: nucleoside analogue