+86-27-65522453 sales@sun-shinechem.com

AF-353

Catalog No.: 16071021
Cas No.: 865305-30-2
Purity : 98% by HPLC 
16071021 - AF-353 | CAS 865305-30-2

Catalog number : 16071021

CAS number : 865305-30-2

Molecular Formula : C14H17IN4O2 

Molecular Weight : 400.21 

Iupac Chemical Name : 2,4-PyriMidinediaMine, 5-[5-iodo-4-Methoxy-2-(1-Methylethyl)phenoxy]- 

Smile : IC=1C(=CC(=C(OC=2C(=NC(=NC2)N)N)C1)C(C)C)OC

InChiKey : AATPYXMXFBBKFO-UHFFFAOYSA-N

PackagingPriceAvailabilityPurityEstimated Shipping Time
BulkEnquiryEnquiry
Request Bulk Quote Download MSDSTel:+86-27-65522453 | Email:sales@sun-shinechem.com
SynonymsAF-353 
Molecular FormulaC14H17IN4O2 
Molecular Weight400.21 
AppearanceSolid powder 
Purity98% by HPLC 
SolubilitySoluble in DMSO 
Storage-20 ºC for 3 years 
Shipping ConditionShipped under ambient temperature 
SmileIC=1C(=CC(=C(OC=2C(=NC(=NC2)N)N)C1)C(C)C)OC
InChiKeyAATPYXMXFBBKFO-UHFFFAOYSA-N
InChiInChI=1S/C14H17IN4O2/c1-7(2)8-4-11(20-3)9(15)5-10(8)21-12-6-18-14(17)19-13(12)16/h4-7H,1-3H3,(H4,16,17,18,19)
Coming soon.
AF-353 is a novel, potent and orally bioavailable P2X3/P2X2/3 receptor antagonist, inhibits human and rat P2X3 (pIC50= 8.0). IC50 value: pIC50 = 8.0 (pIC50, for P2X3) Target: P2X3/P2X2/3 receptor in vitro: AF-353 is a highly potent inhibitor of ,-meATP-evoked intracellular calcium flux in cell lines expressing recombinant rat and human P2X3 and human P2X2/3 channels. AF-353 also blocks human P2X2/3 channel function with marginally reduced potency (pIC50 = 7.3). [1] in vivo: SCI rats has significantly higher frequencies for field potentials and NVC than NL rats. Intravesical ATP increases field potential frequency in control but not SCI rats, while systemic AF-353 significantly reduces this parameter in both groups. AF-353 also reduces the inter-contractile interval in control but not in SCI rats; however, the frequency of NVC in SCI rats was significantly reduced 

865305-30-2 - Request Bulk Quote

×
865305-30-2 - Request Bulk Quote
Change