INDEX NAME NOT YET ASSIGNED

INDEX NAME NOT YET ASSIGNED Suppliers list
Company Name: ATK CHEMICAL COMPANY LIMITED
Tel: +undefined-21-51877795
Email: ivan@atkchemical.com
Products Intro: CAS:2762422-55-7
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G.100G
Company Name: Aladdin Scientific
Tel: +1-+1(833)-552-7181
Email: sales@aladdinsci.com
Products Intro: Product Name:AC1-IN-1
CAS:2762422-55-7
Purity:99% Package:$420.9/5mg;$670.9/10mg;$1250.9/25mg;Bulk package Remarks:99%
Company Name: Shanghai Lollane Biological Technology Co.,Ltd.  
Tel: 021-52996696,15000506266 15000506266
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Products Intro: Product Name:AC1-IN-1
CAS:2762422-55-7
Purity:98% HPLC Package:5mg,10mg,50mg,100mg,1g,5g
Company Name: Shanghai Chaolan Chemical Technology Center  
Tel: QQ:65489617 15618227136
Email: info@SuperLan-chem.com
Products Intro: CAS:2762422-55-7
Purity:98% Package:5MG;10MG;50MG;100MG,1G,5G,100G
Company Name: DC Chemicals  
Tel: 021-58447131 13564518121
Email: sales@dcchemicals.com
Products Intro: Product Name:AC1-IN-38
CAS:2762422-55-7
Purity:98% HPLC Package:100mg,250mg,1g
INDEX NAME NOT YET ASSIGNED Basic information
Product Name:INDEX NAME NOT YET ASSIGNED
Synonyms:AC1-IN-1;Adenylyl cyclase,Adenylate Cyclase,Inhibitor,AC1IN1,Chronic Pain,inhibit,antiallodynic,nontoxic,HEK293 cells,AC1 IN 1,CNS-penetration;AC1-IN-38
CAS:2762422-55-7
MF:C18H18FN5O2
MW:355.37
EINECS:
Product Categories:
Mol File:2762422-55-7.mol
INDEX NAME NOT YET ASSIGNED Structure
INDEX NAME NOT YET ASSIGNED Chemical Properties
density 1.36±0.1 g/cm3(Predicted)
pka7.00±0.50(Predicted)
form Solid
color White to off-white
Safety Information
MSDS Information
INDEX NAME NOT YET ASSIGNED Usage And Synthesis
Biological ActivityAC1-IN-1 is a potent and selective Adenylyl cyclase type 1 (AC1) inhibitor with an IC50 of 0.54 μM. AC1-IN-1 displays modest antiallodynic effects in a mouse model of inflammatory pain. AC1-IN-1 has CNS activity[1]. AC1-IN-1 (compound 38; HEK293 cells; 30 μM, 1 hours) shows nontoxic to this human cell line[1]. AC1-IN-1 (5.6 mg/kg; i.v.) displays modest, yet statistically significant, antiallodynic effects at 1 h post-treatment compared to the 0 min (allodynic) time point[1].
References[1]. Scott JA, et al. Optimization of a Pyrimidinone Series for Selective Inhibition of Ca2+/Calmodulin-Stimulated Adenylyl Cyclase 1 Activity for the Treatment of Chronic Pain. J Med Chem. 2022; 65(6):4667-4686.
INDEX NAME NOT YET ASSIGNED Preparation Products And Raw materials
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