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MRS 2219 , CAS No.14141-47-0, Allosteric modulator of P2X1

  • Moligand™
Item Number
M338731
Grouped product items
SKUSizeAvailabilityPrice Qty
M338731-10mg
10mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$118.90
M338731-50mg
50mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$470.90

a cyclic pyridoxine-α4, 5-monophosphate compound

View related series
P2X1 Allosteric modulator

Basic Description

SynonymsMRS 2219|14141-47-0|Pyridoxine-4,5-cyclic phosphate|MRS-2220|CHEMBL74121|Pyridoxol, cyclic 3,4-(hydrogen phosphate)|4-hydroxy-10-methyl-4-oxo-3,5-dioxa-9-aza-4$l^{5}-phosphabicyclo[5.4.0]undeca-1(11),7,9-trien-11-ol|MRS2219|NCGC00025036-01|Tocris-1203|GTP
Specifications & PurityMoligand™
Storage TempStore at 2-8°C,Desiccated
Shipped InWet ice
GradeMoligand™
Action TypeALLOSTERIC MODULATOR
Mechanism of actionAllosteric modulator of P2X1
Product Description

MRS 2219 is a cyclic pyridoxine-alpha4, 5-monophosphate, compound. Selective potentiator of ATP-evoked responses at rat P2X1 receptors (EC|50|= 5.9 μM).

Associated Targets

CYP1A2 Tchem Cytochrome P450 1A2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CYP2D6 Tclin Cytochrome P450 2D6 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CYP2C19 Tchem Cytochrome P450 2C19 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CYP3A4 Tclin Cytochrome P450 3A4 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CYP2C9 Tchem Cytochrome P450 2C9 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

KMT2A Tchem Histone-lysine N-methyltransferase 2A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

P2RX3 Tclin P2X purinoceptor 3 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

P2RX4 Tchem P2X purinoceptor 4 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

P2RY1 Tchem P2Y purinoceptor 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

P2RX2 Tchem P2X purinoceptor 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

KDM4E Tchem Lysine-specific demethylase 4E 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

P2RX1 Tchem P2X purinoceptor 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name 3-hydroxy-8-methyl-3-oxo-1,5-dihydro-[1,3,2]dioxaphosphepino[5,6-c]pyridin-9-ol
INCHI InChI=1S/C8H10NO5P/c1-5-8(10)7-4-14-15(11,12)13-3-6(7)2-9-5/h2,10H,3-4H2,1H3,(H,11,12)
InChi Key KCAJHODRYGNBSX-UHFFFAOYSA-N
Canonical SMILES CC1=NC=C2COP(=O)(OCC2=C1O)O
Isomeric SMILES CC1=NC=C2COP(=O)(OCC2=C1O)O
PubChem CID 3960826
Molecular Weight 231.14

Certificates

Certificate of Analysis(COA)

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Chemical and Physical Properties

SolubilitySoluble to 100 mM in 1eq. NaOH, Phosphate buffered saline to 5 mM

Related Documents

Solution Calculators