ChemicalBook--->CAS DataBase List--->293762-45-5

293762-45-5

293762-45-5 Structure

293762-45-5 Structure
IdentificationBack Directory
[Name]

RO 90-7501
[CAS]

293762-45-5
[Synonyms]

RO90-7501; RO 907501
2'-(4-aMinophenyl)-1H,3'H-2,5'-bibenzo[d]iMidazol-6-aMine
[Molecular Formula]

C20H16N6
[MDL Number]

MFCD07784512
[MOL File]

293762-45-5.mol
[Molecular Weight]

340.388
Chemical PropertiesBack Directory
[storage temp. ]

Store at +4°C
[solubility ]

DMSO: ~20mg/mL
[form ]

solid
[color ]

brown
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36/37
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

Ro 90-7501 exhibits antibacterial activity. In addition, it also promote both toll-like receptor 3 (TLR3) and RIG-I-like receptor (RLR) ligand-induced IFN-β gene expression and antiviral response.
[Definition]

ChEBI: 2-[2-(4-aminophenyl)-3H-benzimidazol-5-yl]-3H-benzimidazol-5-amine is a member of benzimidazoles.
[Biological Activity]

Inhibitor of amyloid β 42 (A β 42) fibril assembly; reduces A β 42-induced toxicity (EC 50 = 2 μ M).
[in vivo]

Ro 90-7501 (5 μg/g; intraperitoneal injection; daily; for 21 days; female BALB/c nude mice) treatment significantly delays tumor growth and significantly decreases tumor volume[1].

Animal Model:Female BALB/c nude mice (8-week-old) with HeLa cells under irradiation[1]
Dosage:5 μg/g
Administration:Intraperitoneal injection; daily; for 21 days
Result:Tumor growth was significantly delayed in the combination group. Tumor volume was also significantly decreased in the irradiation group.
[IC 50]

Amyloid β42; ATM; Protein phosphatase 5; Apoptosis
[storage]

Store at +4°C
Spectrum DetailBack Directory
[Spectrum Detail]

RO 90-7501(293762-45-5)1HNMR
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