ST3932

ST3932 Suppliers list
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354 +1-00000000000
Email: marketing@targetmol.com
Products Intro: Product Name:ST3932
CAS:1246018-21-2
Purity:98.00% Package:100 mg;500 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: Twochem Co.Ltd.  
Tel: 021-58111628 15800915896
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Products Intro: Product Name:ST3932
CAS:1246018-21-2
Purity:98%+ Package:0.1g;1g;5g
Company Name: Tianjin Kaifu Pharmaceutical Technology Co., Ltd.  
Tel: 18081075745
Email: chemflowtech@sina.com
Products Intro: Product Name:ST3932
CAS:1246018-21-2
Purity:98% HPLC Package:100mg;1g;10g;100g
Company Name: DC Chemicals  
Tel: 021-58447131 13564518121
Email: sales@dcchemicals.com
Products Intro: Product Name:ST3932
CAS:1246018-21-2
Purity:98% HPLC Package:100mg,250mg,1g
Company Name: cjbscvictory  
Tel: 13348960310 13348960310
Email: 3003867561@qq.com
Products Intro: Product Name:ST3932
CAS:1246018-21-2
Purity:98% Package:5mg;10mg;20mg;50mg;100mg;200mg
ST3932 Basic information
Product Name:ST3932
Synonyms:ST3932;ST-3932,ST3932;9H-Purine-2-propanol, 6-amino-α,9-dimethyl-8-(2H-1,2,3-triazol-2-yl)-
CAS:1246018-21-2
MF:C12H16N8O
MW:288.32
EINECS:
Product Categories:
Mol File:1246018-21-2.mol
ST3932 Structure
ST3932 Chemical Properties
Boiling point 482.7±55.0 °C(Predicted)
density 1.62±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility Soluble in DMSO
pka14.96±0.20(Predicted)
Safety Information
MSDS Information
ST3932 Usage And Synthesis
Description

ST3932 is a metabolite of ST1535, acts as an antagonist of adenosine A2A receptor, with Kis of 8 nM and 33 nM for A2A and A1 receptors, respectively.

ST3932 is a metabolite of ST1535, acts as an antagonist of adenosine A2A receptor, with Kis of 8 nM and 33 nM for A2A and A1 receptors, respectively. ST3932 inhibits agonist-induced cAMP accumulation with an IC50 value of 450 nM[1].

ST3932 (10, 20, 40 mg/kg, p.o.) antagonizes haloperidol-induced catalepsy, and increases motor activity in mice. ST3932 (20, 40 mg/kg, i.p.) significantly increases the number of contralateral turns induced by l-DOPA in rats[1].

References

[1]. ST3932, et al. Animal models of Parkinson?s disease: Effects of two adenosine A2A receptor antagonists ST4206 and ST3932, metabolites of 2-n-Butyl-9-methyl-8-[1,2,3]triazol-2-yl-9H-purin-6-ylamine (ST1535). Eur J Pharmacol. 2015 Aug 15;761:353-61.

ST3932 Preparation Products And Raw materials
Preparation Products2-Butanone, 4-[6-amino-9-methyl-8-(2H-1,2,3-triazol-2-yl)-9H-purin-2-yl]-
Tag:ST3932(1246018-21-2) Related Product Information