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(1-((3-hydroxy-1,4-dioxo-1,4-dihydronaphthalen-2-yl)methyl)cyclohexyl)methyl octanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1207286-36-9

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1207286-36-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1207286-36-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,7,2,8 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1207286-36:
(9*1)+(8*2)+(7*0)+(6*7)+(5*2)+(4*8)+(3*6)+(2*3)+(1*6)=139
139 % 10 = 9
So 1207286-36-9 is a valid CAS Registry Number.

1207286-36-9Downstream Products

1207286-36-9Relevant academic research and scientific papers

Transforming rhinacanthin analogues from potent anticancer agents into potent antimalarial agents

Kongkathip, Ngampong,Pradidphol, Narathip,Hasitapan, Komkrit,Grigg, Ronald,Kao, Wei-Chun,Hunte, Carola,Fisher, Nicholas,Warman, Ashley J.,Biagini, Giancarlo A.,Kongsaeree, Palangpon,Chuawong, Pitak,Kongkathip, Boonsong

experimental part, p. 1211 - 1221 (2010/08/07)

Twenty-six novel naphthoquinone aliphatic esters were synthesized by esterification of 1,4-naphthoquinone alcohols with various aliphatic acids. The 1,4-naphthoquinone alcohols were prepared from 1-hydroxy-2-naphthoic acid in nine steps with excellent yields. Twenty-four of the novel synthetic naphthoquinone esters showed significant antimalarial activity with IC 50 values in the range of 0.03-16.63 μM. The length of the aliphatic chain and the presence of C-2′ substituents on the propyl chain affected the activity. Interestingly, compounds 31 and 37 showed very good antimalarial activity and were not toxic to normal Vero cells, and the PTI values of 31 (> 1990.38) and 37 (1825.94) are excellent. Both 31 and 37 showed potent inhibition against P. falciparum 3D7 cyt bc1 and no inhibition on rat cyt bc1. They showed IC50 values in the nanomolar range, providing full inhibition of cyt bc1 with one molecule inhibitor bound per cyt bc1 monomer at the Qo site.

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