ChemicalBook > CAS DataBase List > 1-benzyl-N-(furan-2-ylmethyl)benzimidazol-2-amine

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

Product Name: 1-benzyl-N-(furan-2-ylmethyl)benzimidazol-2-amine
CAS No.: 831234-13-0
Chemical Name: 1-benzyl-N-(furan-2-ylmethyl)benzimidazol-2-amine
Synonyms: AC1903;AC1903 ，S0977;AC1903 AC-1903;AC1903 >=98% (HPLC);AC1903, 10 mM in DMSO;1-benzyl-N-(furan-2-ylmethyl)benzimidazol-2-amine;1-Benzyl-N-(2-furylmethyl)-1H-benzimidazol-2-amine;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;1H-Benzimidazol-2-amine, N-(2-furanylmethyl)-1-(phenylmethyl)-
CBNumber: CB14243558
Molecular Formula: C19H17N3O
Formula Weight: 303.36
MOL File: 831234-13-0.mol

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

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)
pka: 6.09±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.
InChI: InChI=1S/C19H17N3O/c1-2-7-15(8-3-1)14-22-18-11-5-4-10-17(18)21-19(22)20-13-16-9-6-12-23-16/h1-12H,13-14H2,(H,20,21)
InChIKey: OECUWHDVQIITIS-UHFFFAOYSA-N
SMILES: C1(NCC2=CC=CO2)N(CC2=CC=CC=C2)C2=CC=CC=C2N=1

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P330Rinse mouth.

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P337+P313IF eye irritation persists: Get medical advice/attention.

P362Take off contaminated clothing and wash before reuse.

P403+P233Store in a well-ventilated place. Keep container tightly closed.

P405Store locked up.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Cayman Chemical

Product number: 25324
Product name: AC1903
Purity: ≥95%
Packaging: 5mg
Price: $49
Updated: 2024/03/01

Cayman Chemical

Product number: 25324
Product name: AC1903
Purity: ≥95%
Packaging: 10mg
Price: $87
Updated: 2024/03/01

Tocris

Product number: 6766
Product name: AC1903
Purity: ≥98%(HPLC)
Packaging: 25
Price: $275
Updated: 2021/12/16

Biorbyt Ltd

Product number: orb546177
Product name: AC1903
Purity: >98%
Packaging: 10mg
Price: $190.4
Updated: 2021/12/16

ChemScene

Product number: CS-0081483
Product name: AC1903
Purity: 98.64%
Packaging: 25mg
Price: $240
Updated: 2021/12/16

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1-benzyl-N-(furan-2-ylmethyl)benzimidazol-2-amine Chemical Properties,Usage,Production

Description

AC1903 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.

Uses

AC1903 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.

in vivo

AC1903 (intraperitoneal injection; 50 mg/kg; twice per day; 7 days) significantly suppresses proteinuria as well as reduces pseudocyst formation and podocyte loss in an AT1 receptor transgenic rat model of kidney disease^[1].AC1903 (intraperitoneal injection; 50 mg/kg; twice per day; initiated on day 7 and treated for 1 week until day 14) initiatation on day 7 exhibits significant suppression of proteinuria with preserved podocyte numbers. Besides, AC1903 does not affect the mean arterial pressure (MAP) and exhibits no effect on body weight, blood urea nitrogen, or creatinine in Dahl S rats^[1].

Animal Model:	Hypertension-induced focal segmental glomerulosclerosis (FSGS) model in Dahl salt-sensitive rats^[1]
Dosage:	50 mg/kg
Administration:	Intraperitoneal injection; 50 mg/kg; twice per day; 7 days
Result:	Inhibited the progression of proteinuric kidney disease by preserving podocytes.

Animal Model:	6-week-old Dahl S rats received 2% NaCl for 1 week with severe, progressive proteinuric disease^[1]
Dosage:	50 mg/kg
Administration:	Intraperitoneal injection; 50 mg/kg; twice per day; initiated on day 7 and treated for 1 week until day 14
Result:	Decreased 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.

storage

Store at -20°C

References

[1] YIMING ZHOU. A small-molecule inhibitor of TRPC5 ion channels suppresses progressive kidney disease in animal models[J]. Science, 2017, 358 6368. DOI:10.1126/science.aal4178

1-benzyl-N-(furan-2-ylmethyl)benzimidazol-2-amine Preparation Products And Raw materials

Raw materials

Preparation Products

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831234-13-0, 1-benzyl-N-(furan-2-ylmethyl)benzimidazol-2-amineRelated Search:

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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

AC1903, 10 mM in DMSO

1-Benzyl-N-(2-furylmethyl)-1H-benzimidazol-2-amine

AC1903 ，S0977

831234-13-0