1-benzyl-N-(furan-2-ylmethyl)benzimidazol-2-amine

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Company Name: Zhejiang J&C Biological Technology Co.,Limited
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Products Intro: Product Name:AC1903 AC-1903
CAS:831234-13-0
Purity:99% Package:5KG;1KG Remarks:AC1903 AC-1903
Company Name: InvivoChem
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Products Intro: Product Name:AC1903
CAS:831234-13-0
Purity:98% Package:25mg Remarks:V10018
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Products Intro: Product Name:VX809
CAS:831234-13-0
Purity:98% HPLC Package:10mg,500mg,1g,5g,25g,more
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Products Intro: Product Name:AC1903
CAS:831234-13-0
Package:10 mg;25 mg;5 mg;50 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: Aladdin Scientific
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Products Intro: Product Name:AC 1903
CAS:831234-13-0
Purity:>=98%(HPLC) Package:$63.9/5mg;$107.9/10mg;$236.9/25mg;$414.9/50mg;$747.9/100mg;Bulk package Remarks:98%(HPLC)
1-benzyl-N-(furan-2-ylmethyl)benzimidazol-2-amine Basic information
Product Name:1-benzyl-N-(furan-2-ylmethyl)benzimidazol-2-amine
Synonyms:1-benzyl-N-(furan-2-ylmethyl)benzimidazol-2-amine;AC1903;1H-Benzimidazol-2-amine, N-(2-furanylmethyl)-1-(phenylmethyl)-;AC1903 >=98% (HPLC);1-benzyl-N-(furan-2-ylmethyl)-1H-benzo[d]imidazol-2-amine;1-Benzyl-N-[(furan-2-yl)methyl]-1H-1,3-benzodiazol-2-amine;Inhibitor,glomerulosclerosis,proteinuria,inhibit,TRP Channel,ros,focal segmental,AC 1903,Transient receptor potential channels,AC-1903,FSGS,AC1903,kidney disease,podocyte loss,HEK-293;AC1903 AC-1903
CAS:831234-13-0
MF:C19H17N3O
MW:303.36
EINECS:
Product Categories:
Mol File:831234-13-0.mol
1-benzyl-N-(furan-2-ylmethyl)benzimidazol-2-amine Structure
1-benzyl-N-(furan-2-ylmethyl)benzimidazol-2-amine Chemical Properties
Boiling point 512.4±60.0 °C(Predicted)
density 1.20±0.1 g/cm3(Predicted)
storage temp. -20°C
solubility Soluble in DMSO (up to 30 mg/ml) or in Ethanol (up to 25 mg/ml)
pka6.09±0.10(Predicted)
form solid
color Beige
Stability:Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20°C for up to 3 months.
Safety Information
MSDS Information
1-benzyl-N-(furan-2-ylmethyl)benzimidazol-2-amine Usage And Synthesis
DescriptionAC1903 is an inhibitor of transient receptor potential canonical channel 5 (TRPC5; IC50 = 14.7 μM). It is selective for TRPC5 over TRPC4 and TRPC6 at concentrations up to 100 and 30 μM, respectively. It inhibits TRPC5 in a concentration-dependent manner in HEK293 cells when used at concentrations ranging from 1 to 100 μM. AC1903 (30 μM) inhibits angiotensin II-induced production of reactive oxygen species (ROS) in wild-type podocytes and podocytes expressing a mutant angiotensin II type 1 (AT1) receptor that cannot be inactivated and endocytosed. It also suppresses proteinuria as well as reduces pseudocyst formation and podocyte loss in an AT1 receptor transgenic rat model of kidney disease when administered at a dose of 50 mg/kg twice per day. In a model of hypertension-induced focal segmental glomerulosclerosis (FSGS) using Dahl salt-sensitive rats, AC1903 decreases the rate of proteinuria when administered at the beginning of a high-salt diet and prevents progression when administered one week following initiation of a high-salt diet.
UsesAC1903 is a TRPC5 inhibitor with valuable potential for the treatment of progressive kidney diseases. AC1903 inhibits TRPC5 ion channels and suppresses progressive kidney diseases via TRPC5-AT1R related genetic pathways. ?AC1903 also provides therapeutic benefit in a rat model of hypertensive proteinuric kidney disease.
storageStore at -20°C
References1) Zhou?et al.?(2017),?A small-molecule inhibitor of TRPC5 ion channels suppresses progressive kidney disease in animal models; Science,?358?1332
1-benzyl-N-(furan-2-ylmethyl)benzimidazol-2-amine Preparation Products And Raw materials
Tag:1-benzyl-N-(furan-2-ylmethyl)benzimidazol-2-amine(831234-13-0) Related Product Information
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