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10β-benzenesulfonyl-9-epi-dihydroartemisinin is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

458535-73-4

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458535-73-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 458535-73-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,8,5,3 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 458535-73:
(8*4)+(7*5)+(6*8)+(5*5)+(4*3)+(3*5)+(2*7)+(1*3)=184
184 % 10 = 4
So 458535-73-4 is a valid CAS Registry Number.

458535-73-4Downstream Products

458535-73-4Relevant academic research and scientific papers

Synthesis and antiangiogenic activity of thioacetal artemisinin derivatives

Oh, Sangtae,Jeong, In Howa,Ahn, Chan Mug,Shin, Woon-Seob,Lee, Seokjoon

, p. 3783 - 3790 (2004)

Various thioacetal artemisinin derivatives can inhibit the angiogenesis and might be angiogenesis inhibitors. In particular, 10α- phenylthiodihydroartemisinins (5), 10β-benzenesulfonyl-9-epi- dihydroartemisinin (11) and 10α-mercaptodihydroartemisinin (13)

Synthesis and biological evaluation of extraordinarily potent C-10 carba artemisinin dimers against P. falciparum malaria parasites and HL-60 cancer cells

Chadwick, James,Mercer, Amy E.,Park, B. Kevin,Cosstick, Richard,O'Neill, Paul M.

experimental part, p. 1325 - 1338 (2009/08/15)

A series of artemisinin dimers incorporating a metabolically stable C-10 carba-linkage have been prepared, several of which show remarkable in vitro antimalarial activity (as low as 30 pM) versus Plasmodium falciparum and in vitro anticancer activity in t

Growth inhibition activity of thioacetal artemisinin derivatives against human umbilical vein endothelial cells

Oh, Sangtae,Jeong, In Howa,Shin, Woon-Seob,Lee, Seokjoon

, p. 3665 - 3668 (2007/10/03)

Thioacetal artemisinin derivatives, in particular, 10α -phenylthiodihydroartemisinins (5), 10β -benzenesulfonyl-9-epi-dihydroartemisinin (9) and 10α -mercaptodihydroartemisinin (11), exhibit good growth inhibition activity against HUVEC proliferation at t

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