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1-benzoyl-2,3-dihydro-1H-indol-5-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

108013-44-1

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108013-44-1 Usage

Chemical class

Indole class of organic compounds

Structure

A benzene ring attached to an indole ring

Functional groups

Carbonyl group (benzoyl group) and amine group

Derivative

An amine derivative of indole

Indole

A heterocyclic aromatic compound

Applications

Used in the synthesis of various pharmaceuticals and agrochemicals

Biological activities

Possesses potential biological activities

Interest

Subject of interest in medicinal and organic chemistry research

Check Digit Verification of cas no

The CAS Registry Mumber 108013-44-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,0,1 and 3 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 108013-44:
(8*1)+(7*0)+(6*8)+(5*0)+(4*1)+(3*3)+(2*4)+(1*4)=81
81 % 10 = 1
So 108013-44-1 is a valid CAS Registry Number.

108013-44-1Relevant academic research and scientific papers

Synthesis, structure-activity relationships and biological evaluation of 7-phenyl-pyrroloquinolinone 3-amide derivatives as potent antimitotic agents

Carta, Davide,Bortolozzi, Roberta,Sturlese, Mattia,Salmaso, Veronica,Hamel, Ernest,Basso, Giuseppe,Calderan, Laura,Quintieri, Luigi,Moro, Stefano,Viola, Giampietro,Ferlin, Maria Grazia

, p. 643 - 660 (2017)

A small library of 7-pyrrolo[3,2-f]quinolinones was obtained by introducing benzoyl, sulfonyl and carbamoyl side chains at the 3-N position, and their cytotoxicity against a panel of leukemic and solid tumor cell lines was evaluated. Most of them showed high antiproliferative activity with GI50s ranging from micro-to sub-nanomolar values, and these values correlated well with the inhibitory activities of the compounds against tubulin polymerization. Based on a recently proposed colchicine bind site inhibitors (CBSIs) pharmacophore, the interactions of the novel 7-PPyQs at the colchicine domain were rationalized. The most active compounds (4a and 4b) did not induce significant cell death in normal human lymphocytes, suggesting that the compounds may be selective against cancer cells. In particular, 4a was a potent inducer of apoptosis in both the HeLa and Jurkat cell lines. On the other hand, the sulfonyl derivative 4b exhibited a lower potency in comparison with 4a. With both compounds, induction of apoptosis was associated with dissipation of the mitochondrial transmembrane potential and production of reactive oxygen species, suggesting that cells treated with the compounds followed the intrinsic pathway of apoptosis.

Indole derivatives or salts thereof as well as preparation method and application of indole derivatives or salts thereof

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Paragraph 0149; 0154-0155; 0188; 0193-0194, (2019/02/06)

The invention belongs to the technical field of chemical medicine, and relates to an Hh (Hedgehog) signal pathway Smoothed (SMO) receptor small molecule inhibitor, in particular to indole derivativesor salts thereof with Smoothed inhibitory activity, which are shown in chemical general formula (I) in the description, as well as a preparation method and pharmaceutical composition of the indole derivatives or salts thereof. Tests on inhibitory activity of Hh signal pathways show that most compounds have better inhibitory activity on the Hh signal pathways. The invention further discloses the application of the compounds to preparation of medicines for treating diseases associated with Hh, wherein the diseases are BCC (basal cell carcinoma), MB (medullblastoma), SCLC (small cell lung cancer), medulloblastoma, rhabdomyosarcoma, or a combination of the diseases.

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