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1H-Isoindole-1,3(2H)-dione, 2-[2-(6-amino-9H-purin-9-yl)ethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21708-28-1

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21708-28-1 Usage

Molar mass

326.32 g/mol
The mass of one mole of the compound is 326.32 grams.

Structure

Derivative of isoindole-1,3(2H)-dione
The compound is based on the isoindole-1,3(2H)-dione structure, with modifications to its chemical structure.
4. Contains a purine ring
The compound has a purine ring, which is a heterocyclic aromatic organic compound and a key component of nucleotides.
5. Heterocyclic compound
The compound consists of one or more rings with atoms of different elements, in this case, carbon, nitrogen, and oxygen.
6. Potential biological activity
The compound may have biological effects, which could be useful in pharmaceutical research and development.
7. Applications in pharmaceutical research and development
Due to its complex structure and potential biological activity, the compound could be studied for potential use in drug development.
8. Specific properties and potential uses depend on further research and testing
The exact properties and applications of the compound are not yet known and require additional investigation to be determined.

Check Digit Verification of cas no

The CAS Registry Mumber 21708-28-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,7,0 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 21708-28:
(7*2)+(6*1)+(5*7)+(4*0)+(3*8)+(2*2)+(1*8)=91
91 % 10 = 1
So 21708-28-1 is a valid CAS Registry Number.

21708-28-1Downstream Products

21708-28-1Relevant academic research and scientific papers

Synthesis and study of a new adenine-acridine tandem, inhibitor of exonuclease III

Belmont, Philippe,Demeunynck, Martine,Constant, Jean-Francois,Lhomme, Jean

, p. 293 - 295 (2000)

A new heterodimer adenine-chain-acridine containing a mixed amido-guanidinium linker chain was synthesized. To achieve the synthesis a new method of introduction of aminoalkyl chain at position 9 of adenine was designed. The heterodimer interacts specifically with the abasic sites in DNA and inhibits the major base excision repair enzyme in Escherichia coli, Exonuclease III. (C) 2000 Elsevier Science Ltd. All rights reserved.

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