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7-(6-benzyloxy-9-{5-[bis(4-methoxyphenyl)phenylmethoxymethyl]-4-hydroxytetrahydrofuran-2-yl}-9H-purin-2-ylamino)-6H-benzo[f][1,3]dioxolo[4',5':4,5]benzo[1,2,3-cd]indol-5-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1211798-17-2

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1211798-17-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1211798-17-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,1,7,9 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1211798-17:
(9*1)+(8*2)+(7*1)+(6*1)+(5*7)+(4*9)+(3*8)+(2*1)+(1*7)=142
142 % 10 = 2
So 1211798-17-2 is a valid CAS Registry Number.

1211798-17-2Relevant academic research and scientific papers

DNA adducts of aristolochic acid II: Total synthesis and site-specific mutagenesis studies in mammalian cells

Attaluri, Sivaprasad,Bonala, Radha R.,Yang, In-Young,Lukin, Mark A.,Wen, Yujing,Grollman, Arthur P.,Moriya, Masaaki,Iden, Charles R.,Johnson, Francis

experimental part, p. 339 - 352 (2011/01/03)

Aristolochic acids I and II (AA-I, AA-II) are found in all Aristolochia species. Ingestion of these acids either in the form of herbal remedies or as contaminated wheat flour causes a dose-dependent chronic kidney failure characterized by renal tubulointerstitial fibrosis. In ~50% of these cases, the condition is accompanied by an upper urinary tract malignancy. The disease is now termed aristolochic acid nephropathy (AAN). AA-I is largely responsible for the nephrotoxicity while both AA-I and AA-II are genotoxic. DNA adducts derived from AA-I and AA-II have been isolated from renal tissues of patients suffering from AAN. We describe the total synthesis, de novo, of the dA and dG adducts derived from AA-II, their incorporation site-specifically into DNA oligomers and the splicing of these modified oligomers into a plasmid construct followed by transfection into mouse embryonic fibroblasts. Analysis of the plasmid progeny revealed that both adducts blocked replication but were still partly processed by DNA polymerase(s). Although the majority of coding events involved insertion of correct nucleotides, substantial misincorporation of bases also was noted. The dA adduct is significantly more mutagenic than the dG adduct; both adducts give rise, almost exclusively, to misincorporation of dA, which leads to AL-II-dA→T and AL-II-dG→T transversions. The Author(s) 2009. Published by Oxford University Press.

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