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3,4,5-trimethoxy-benzoic acid 2,2'-piperazine-1,4-diyl-diethyl ester is a complex organic compound with the molecular formula C20H28N2O6. It is a derivative of benzoic acid, featuring three methoxy groups at the 3, 4, and 5 positions, and is esterified with the 1,4-diyl group of piperazine, which is further esterified with two ethyl groups. 3,4,5-trimethoxy-benzoic acid 2,2'-piperazine-1,4-diyl-diethyl ester is known for its potential applications in pharmaceutical research, particularly in the development of drugs targeting the central nervous system. Its structure allows for interactions with various receptors, making it a subject of interest for scientists exploring new therapeutic avenues. The compound's specific properties and mechanisms of action are under investigation, and it is not approved for medical use but serves as a valuable tool in the discovery of new medications.

1064-86-4

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1064-86-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1064-86-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,6 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1064-86:
(6*1)+(5*0)+(4*6)+(3*4)+(2*8)+(1*6)=64
64 % 10 = 4
So 1064-86-4 is a valid CAS Registry Number.

1064-86-4Downstream Products

1064-86-4Relevant academic research and scientific papers

Dilazep analogues for the study of equilibrative nucleoside transporters 1 and 2 (ENT1 and ENT2)

Playa, Hilaire,Lewis, Timothy A.,Ting, Amal,Suh, Byung-Chul,Muoz, Benito,Matuza, Robert,Passer, Brent J.,Schreiber, Stuart L.,Buolamwini, John K.

, p. 5801 - 5804 (2015/01/08)

As ENT inhibitors including dilazep have shown efficacy improving oHSV1 targeted oncolytic cancer therapy, a series of dilazep analogues was synthesized and biologically evaluated to examine both ENT1 and ENT2 inhibition. The central diamine core, alkyl chains, ester linkage and substituents on the phenyl ring were all varied. Compounds were screened against ENT1 and ENT2 using a radio-ligand cell-based assay. Dilazep and analogues with minor structural changes are potent and selective ENT1 inhibitors. No selective ENT2 inhibitors were found, although some analogues were more potent against ENT2 than the parent dilazep.

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