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147622-60-4

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147622-60-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147622-60-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,6,2 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 147622-60:
(8*1)+(7*4)+(6*7)+(5*6)+(4*2)+(3*2)+(2*6)+(1*0)=134
134 % 10 = 4
So 147622-60-4 is a valid CAS Registry Number.

147622-60-4Relevant articles and documents

Synthesis of 4,7,9-Trihydroxy[1]benzofuro[3,2-d]pyrimidine-6-carboxamide: Evaluation of Cytotoxicity and Inhibition of Protein Kinase C (Ca Pkc1)

Hung, Dao Viet,Vu, Tran Khac

, (2021/08/12)

The protein kinase Pkc1 of Candida albicans (CaPkc1), one of the key proteins involved in MAPK pathway, is described as a regulator of cell wall integrity during growth, morphogenesis, and response to cell wall stress. The (-)-cercosporamide is an antifun

Elaboration of simplified vinca alkaloids and phomopsin hybrids

Ngo, Quoc Anh,Roussi, Fanny,Thoret, Sylviane,Gueritte, Francoise

experimental part, p. 284 - 294 (2010/12/19)

Nine simplified vinca alkaloids and phomospin A hybrids, in which vindoline moiety has been replaced by a simpler scaffold, have been elaborated to evaluate their activity on the inhibition of tubulin polymerization. This article deals with the synthesis of various simplified vinca alkaloids, using a stereoselective coupling of catharantine with reactive aromatic compounds and methanol as well as their subsequent condensation with a large peptide chain mimicking those of phomopsin A. Biological evaluation and molecular modeling studies are also reported.

A Formal Synthesis of Aflatoxin B2

Weeratunga, Gamini,Horne, Stephen,Rodrigo, Russell

, p. 721 - 722 (2007/10/02)

A brief synthesis of a ring A differentiated tetrahydrofurobenzofuran intermediate previously converted into Aflatoxin B2 is described.

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