BAY-1797
- Product Name
- BAY-1797
- CAS No.
- 2055602-83-8
- Chemical Name
- BAY-1797
- Synonyms
- BAY-1797;BAY-1797, 10 mM in DMSO;Benzeneacetamide, N-[3-(aminosulfonyl)-4-(3-chlorophenoxy)phenyl]-;paw,ion,inhibit,anti-inflammatory,CFA,Complete,P2XRs,BAY-1797,Freund’s,selective,channel,P2X Receptor,inflamed,Inhibitor,BAY1797,Adjuvant,BAY 1797,P2X,anti-nociceptive
- CBNumber
- CB98022694
- Molecular Formula
- C20H17ClN2O4S
- Formula Weight
- 416.88
- MOL File
- 2055602-83-8.mol
BAY-1797 Property
- Density
- 1.414±0.06 g/cm3(Predicted)
- storage temp.
- -20°C
- solubility
- Soluble in DMSO (>25 mg/ml)
- pka
- 9.84±0.60(Predicted)
- form
- solid
- color
- Pale brown
- Stability:
- Stable for 2 years as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months.
- InChIKey
- CSJYMAFXYMYNCK-UHFFFAOYSA-N
- SMILES
- ClC1=CC=CC(OC2=C(C=C(NC(CC3=CC=CC=C3)=O)C=C2)S(=O)(N)=O)=C1
Safety
- WGK Germany
- WGK 3
- Storage Class
- 11 - Combustible Solids
N-Bromosuccinimide Price
- Product number
- SML2817
- Product name
- BAY-1797
- Purity
- ≥98% (HPLC)
- Packaging
- 5 mg
- Price
- $111
- Updated
- 2026/03/19
- Product number
- SML2817
- Product name
- BAY-1797
- Purity
- ≥98% (HPLC)
- Packaging
- 25 mg
- Price
- $356
- Updated
- 2026/03/19
- Product number
- CS-0109406
- Product name
- BAY-1797
- Purity
- 98.66%
- Packaging
- 50mg
- Price
- $695
- Updated
- 2021/12/16
- Product number
- CS-0109406
- Product name
- BAY-1797
- Purity
- 98.66%
- Packaging
- 100mg
- Price
- $1250
- Updated
- 2021/12/16
- Product number
- CS-0109406
- Product name
- BAY-1797
- Purity
- 98.66%
- Packaging
- 5mg
- Price
- $205
- Updated
- 2021/12/16
BAY-1797 Chemical Properties,Usage,Production
Description
BAY-1797 (2055602-83-8) is a selective P2X4 receptor antagonist (IC50 = 211 nM HEK cellular assay; P2X4 calcium influx based assays – hIC50 = 108 nM, mIC50 = 112 nM, rIC50 = 233 nM).1 Displayed antinociceptive and anti-inflammatory effects in mouse CFA inflammatory pain models.
Uses
BAY-1797 is a potent, orally active, and selective P2X4 antagonist, with an IC50 of 211 nM against human P2X4. BAY-1797 displays no or very weak activity on the other P2X ion channels. BAY-1797 shows anti-nociceptive and anti-inflammatory effects[1].
in vivo
BAY-1797 (12.5-50 mg/kg; p.o.) shows a significant induction of PGE2 levels in the inflamed paw in the mouse Complete Freund’s Adjuvant (CFA) inflammatory pain model[1].
BAY-1797 (50 mg/kg; once daily for multiple p.o. administrations) induces a significant reduction of the ipsilateral paw load 24 and 48 h after CFA injection[1].
BAY-1797 treatment shows the AUCnorm, Vss and t1/2 are 1.06 kg h/L, 3.67 L/kg and 2.64 hours, respectively[1].
| Animal Model: | Female adult C57BL/6N mice (CFA inflammatory pain model)[1] |
| Dosage: | 12.5, 25, 50 mg/kg |
| Administration: | p.o.; once |
| Result: | Dose-dependently reduced PGE2 concentration in inflamed paw. |
| Animal Model: | Rat male Wistar[1] |
| Dosage: | 1 mg/kg |
| Administration: | i.v. (Pharmacokinetic Analysis) |
| Result: | The AUCnorm, Vss and t1/2 were 1.06 kg h/L, 3.67 L/kg and 2.64 hours, respectively. |
IC 50
P2X4 Receptor
storage
Store at -20°C
References
[1] STEFAN WERNER*. Discovery and Characterization of the Potent and Selective P2X4 Inhibitor N-[4-(3-Chlorophenoxy)-3-sulfamoylphenyl]-2-phenylacetamide (BAY-1797) and Structure-Guided Amelioration of Its CYP3A4 Induction Profile[J]. Journal of Medicinal Chemistry, 2019, 62 24: 11194-11217. DOI:10.1021/acs.jmedchem.9b01304
BAY-1797 Preparation Products And Raw materials
Raw materials
Preparation Products
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