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1427030-83-8

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1427030-83-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1427030-83-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,7,0,3 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1427030-83:
(9*1)+(8*4)+(7*2)+(6*7)+(5*0)+(4*3)+(3*0)+(2*8)+(1*3)=128
128 % 10 = 8
So 1427030-83-8 is a valid CAS Registry Number.

1427030-83-8Upstream product

1427030-83-8Downstream Products

1427030-83-8Relevant articles and documents

Fungal metabolites of xanthohumol with potent antiproliferative activity on human cancer cell lines in vitro

Tronina, Tomasz,Bartmańska, Agnieszka,Filip-Psurska, Beata,Wietrzyk, Joanna,Pop?oński, Jaros?aw,Huszcza, Ewa

, p. 2001 - 2006 (2013)

Xanthohumol (1) and xanthohumol D (2) were isolated from spent hops. Isoxanthohumol (3) was obtained from xanthohumol by isomerisation in alkaline solution. Six metabolites were obtained as a result of transformation of xanthohumol (1) by selected fungal cultures. Their structures were established on the basis of their spectral data. One of them: 2″- (2′′′-hydroxyisopropyl)-dihydrofurano-[4″,5″: 3′,4′]-4′,2-dihydroxy-6′-methoxy-α, β-dihydrochalcone (6) has not been previously reported in the literature. The antioxidant properties of hops flavonoids and xanthohumol derivatives were investigated using the 2,2′-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging method. The effects of these compounds on proliferation of MCF-7, PC-3 and HT-29 human cancer cell lines were determined by the SRB assay. With the exception of one metabolite, all tested compounds showed antiproliferative activity against the tested human cancer lines. α,β- Dihydroxanthohumol (4), obtained through the biotransformation of xanthohumol, showed higher antiproliferative activity against MCF-7 human breast carcinoma cell line than cisplatin, a widely used anticancer therapeutic agent, and a comparably high activity against PC-3 human prostate cancer cell line.

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