BX 430

BX 430 Suppliers list
Company Name: Shanghai EFE Biological Technology Co., Ltd.  
Tel: 021-65675885 18964387627
Email: info@efebio.com
Company Name: Shanghai YuanYe Biotechnology Co., Ltd.  
Tel: 15026964105
Email: 2881489226@qq.com
Company Name: Tianjin Kailiqi Biotechnology Co., Ltd.  
Tel: 15076683720
Email: klq@cw-bio.com
Company Name: Shanghai Chaolan Chemical Technology Center  
Tel: QQ:65489617 13301690235
Email: Sales@ATKchemical.com
Company Name: Aikon International Limited  
Tel: 025-66113011 19370895928
Email: qzhang@aikonchem.com

BX 430 manufacturers

  • BX430
  • BX430 pictures
  • $38.00
  • 2026-07-14
  • CAS:688309-70-8
  • Purity: 99.95%
  • Supply Ability: 10g
  • BX430
  • BX430 pictures
  • $38.00
  • 2026-07-14
  • CAS:688309-70-8
  • Purity: 99.95%
  • Supply Ability: 10g
BX 430 Basic information
Product Name:BX 430
Synonyms:BX 430;N-[2,6-Dibromo-4-(1-methylethyl)phenyl]-N'-(3-pyridinyl)urea;Urea, N-[2,6-dibromo-4-(1-methylethyl)phenyl]-N'-3-pyridinyl-;1-(2,6-Dibromo-4-isopropylphenyl)-3-(pyridin-3-yl)urea;P2X Receptor,Ca channels,BX430,chronic,channels,species,P2XRs,Inhibitor,disease,Ca2+ channels,BX 430,cardiovascular,P2X4,receptor,specificity,inhibit,Calcium Channel,human,pain,BX-430;BX430, 10 mM in DMSO
CAS:688309-70-8
MF:C15H15Br2N3O
MW:413.11
EINECS:
Product Categories:
Mol File:688309-70-8.mol
BX 430 Structure
BX 430 Chemical Properties
Melting point 164-168°C
storage temp. 2-8°C
solubility DMSO (Slightly), Methanol (Slightly)
form Solid
color White
InChI1S/C15H15Br2N3O/c1-9(2)10-6-12(16)14(13(17)7-10)20-15(21)19-11-4-3-5-18-8-11/h3-9H,1-2H3,(H2,19,20,21)
InChIKeyJFNKIJKRXKPQCC-UHFFFAOYSA-N
SMILESBrC1=CC(C(C)C)=CC(Br)=C1NC(NC2=CC=CN=C2)=O
Safety Information
WGK Germany WGK 3
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
MSDS Information
BX 430 Usage And Synthesis
UsesBX 430 is a selective P2X4 allosteric antagonist in human and zebrafish.
Biological ActivityBX430 is a selective noncompetitive allosteric antagonist of human P2X4 receptor channels. P2X4 receptors are highly expressed in the CNS, and have been studied as a therapeutic target for neuropathic pain and inflammation, and treatment of traumatic brain injury, cerebral ischemia, and spinal cord injury. BX430 is highly selective for human P2X4, with minimal activity towards other P2X subtypes, including P2X1–P2X3, P2X5, and P2X7. BX430 is also an antagonist of zebrafish P2X4 but has no effect on r at and mouse P2X4 receptors. BX430 has an IC50 value of 540 nM.
IC 50P2X4 Receptor
storageStore at +4°C
BX 430 Preparation Products And Raw materials
Tag:BX 430(688309-70-8) Related Product Information
N-(3-(4-(3-(3-Amino-2,2-dimethyl-3-oxopropanamido)propylamino)-5-bromopyrimidin-2-ylamino)phenyl)pyrrolidine-1-carboxamide N-[3-[[5-Iodo-4-[[3-[(2-thienylcarbonyl)amino]propyl]amino]-2-pyrimidinyl]amino]phenyl]-1-pyrrolidinecarboxamide BX 513 hydrochloride Urea, N-[5-chloro-2-[2-[(2R)-4-[(4-fluorophenyl)Methyl]-2-Methyl-1-piperazinyl]-2-oxoethoxy]phenyl]- BX517(PDK1 inhibitor2) Halofuginone