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13-(2-hydroxy-3-methylphenyl)-10,13-dihydrofuro[3,4-b]pyrido[3,2-f][1,7] phenanthrolin-12(9H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1620171-33-6

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1620171-33-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1620171-33-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,0,1,7 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1620171-33:
(9*1)+(8*6)+(7*2)+(6*0)+(5*1)+(4*7)+(3*1)+(2*3)+(1*3)=116
116 % 10 = 6
So 1620171-33-6 is a valid CAS Registry Number.

1620171-33-6Downstream Products

1620171-33-6Relevant academic research and scientific papers

Synthesis and biological evaluation of 4-aza-2,3- dihydropyridophenanthrolines as tubulin polymerization inhibitors

Kamal, Ahmed,Srinivasa Reddy,Polepalli, Sowjanya,Paidakula, Suresh,Srinivasulu, Vunnam,Ganga Reddy,Jain, Nishant,Shankaraiah, Nagula

, p. 3356 - 3360 (2014)

A series of novel 4-aza-2,3-dihydropyridophenanthrolines 12(a-t) were synthesized by a one-step three component condensation of 1,10-phenanthroline amine, tetronic acid and various aromatic aldehydes. These were evaluated for their antiproliferative activity against three human cancer cell lines (MIAPACA, MCF-7 and HeLa) using SRB assay. Majority of the tested compounds exhibited significant anticancer activity on these cell lines and interestingly compounds 12h and 12i were more potent than etoposide and podophyllotoxin against all three tested cancer cell lines with GI50 values in the range of 0.01-0.5 μM. Furthermore, these compounds showed significant inhibition of tubulin polymerization which is comparable to that of podophyllotoxin and disrupted microtubule network by accumulating tubulin in the soluble fraction. The flow cytometry analysis confirmed that the synthesized compounds led to cell cycle arrest at the G2/M phase. Moreover, the structure activity relationship studies in this series are also discussed.

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