(E/Z)-Sivopixant
CAS No. 1640808-39-4
(E/Z)-Sivopixant( (E/Z)-S-600918 )
Catalog No. M28824 CAS No. 1640808-39-4
(E/Z)-Sivopixantis a potent P2X3 receptor antagonist, IC50 = 4 nM. (E/Z)-Sivopixant can be used for respiratory diseases research.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 237 | In Stock |
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| 5MG | 212 | In Stock |
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| 10MG | 316 | In Stock |
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| 25MG | 510 | In Stock |
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| 50MG | 681 | In Stock |
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| 100MG | 921 | In Stock |
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| 200MG | Get Quote | In Stock |
|
| 500MG | 1832 | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product Name(E/Z)-Sivopixant
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NoteResearch use only, not for human use.
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Brief Description(E/Z)-Sivopixantis a potent P2X3 receptor antagonist, IC50 = 4 nM. (E/Z)-Sivopixant can be used for respiratory diseases research.
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Description(E/Z)-Sivopixantis a potent P2X3 receptor antagonist, IC50 = 4 nM. (E/Z)-Sivopixant can be used for respiratory diseases research.
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In VitroATP receptors are roughly classified into an ion channel type P2X family and a G protein coupled type P2Y family. Seven types of subtypes have been reported in the P2X receptor family, and function as non-selective cation channels by forming homotrimers or heterotrimers with other P2X subtypes. Furthermore, P2X3 that the receptor is expressed in neuroepithelial bodies (NEB) of the lungs, and ATP-induced cough, etc., P2X3 receptors. It has been suggested that it is involved in information transmission in the respiratory organs.
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In Vivo——
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Synonyms(E/Z)-S-600918
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PathwayMembrane Transporter/Ion Channel
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TargetP2X Receptor
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RecptorhPPARα| human PPARγ
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Research Area——
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Indication——
Chemical Information
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CAS Number1640808-39-4
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Formula Weight507.93
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Molecular FormulaC25H22ClN5O5
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (196.88 mM)
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SMILESC(N1C(NC2=CC=C(OC3=CC=CC=N3)C=C2)=NC(=O)N(C[C@@H](C(O)=O)C)C1=O)C4=CC=C(Cl)C=C4
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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JNJ-42253432
JNJ-42253432 is an oral active P2X7 antagonist capable of penetrating the central nervous system with a pKi value of 9.1 for rat and 7.9 for human P2X7 channels.
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AZD-9056
A potent, selective, orally bioavailable P2X7 receptor antagonist; inhibits release of pro-inflammatory mediators from isolated human peripheral monocytes (IL-1β and IL-18) and human alveolar macrophages (IL-1β) with IC50 values of 10-13 nM.
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Opiranserin hydrochl...
Opiranserin (VVZ-149) hydrochloride is a dual antagonist of glycine transporter type 2 (GlyT2) and serotonin receptor 2A (5HT2A), with IC50s of 0.86 and 1.3 μM, respectively. It shows antagonistic activity on rP2X3 (IC50=0.87 μM). It is development as an injectable agent for the treatment of postoperative pain.
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