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"9-[2-(1,3-benzodioxol-5-ylmethylidene)hydrazinyl]-1,2,3,4-tetrahydroacridine" is a complex organic compound with a molecular formula of C22H20N2O2. It is characterized by a tetrahydroacridine core, which is a tricyclic structure derived from acridine, a polycyclic aromatic compound. The molecule features a hydrazinyl group attached to the 9-position of the tetrahydroacridine, and a benzodioxole ring that is alkylated with a methylene group, forming a methyleneidene bridge between the benzodioxole and the hydrazinyl group. This chemical structure may be of interest in medicinal chemistry due to the potential biological activities of such compounds, particularly in the development of drugs targeting the central nervous system. The specific properties and applications of 9-[2-(1,3-benzodioxol-5-ylmethylidene)hydrazinyl]-1,2,3,4-tetrahydroacridine would depend on its pharmacological profile, which is not detailed in this summary.

91074-35-0

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91074-35-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91074-35-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,0,7 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 91074-35:
(7*9)+(6*1)+(5*0)+(4*7)+(3*4)+(2*3)+(1*5)=120
120 % 10 = 0
So 91074-35-0 is a valid CAS Registry Number.

91074-35-0Downstream Products

91074-35-0Relevant academic research and scientific papers

Design, synthesis, and structure-activity relationship studies of 4-quinolinyl- and 9-acrydinylhydrazones as potent antimalarial agents

Fattorusso, Caterina,Campiani, Giuseppe,Kukreja, Gagan,Persico, Marco,Butini, Stefania,Romano, Maria Pia,Altarelli, Maria,Ros, Sindu,Brindisi, Margherita,Savini, Luisa,Novellino, Ettore,Nacci, Vito,Fattorusso, Ernesto,Parapini, Silvia,Basilico, Nicoletta,Taramelli, Donatella,Yardley, Vanessa,Croft, Simon,Borriello, Marianna,Gemma, Sandra

, p. 1333 - 1343 (2008/09/20)

Malaria is a major health problem in poverty-stricken regions where new antiparasitic drugs are urgently required at an affordable price. We report herein the design, synthesis, and biological investigation of novel antimalarial agents with low potential to develop resistance and structurally based on a highly conjugated scaffold. Starting from a new hit, the designed modifications were performed hypothesizing a specific interaction with free heme and generation of radical intermediates. This approach provided antimalarials with improved potency against chloroquine-resistant plasmodia over known drugs. A number of structure-activity relationship (SAR) trends were identified and among the analogues synthesized, the pyrrolidinylmethylarylidene and the imidazole derivatives 5r, 5t, and 8b were found as the most potent antimalarial agents of the new series. The mechanism of action of the novel compounds was investigated and their in vivo activity was assessed.

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