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ent-16β-hydroxybeyeran-19-oic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30217-45-9

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30217-45-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30217-45-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,2,1 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 30217-45:
(7*3)+(6*0)+(5*2)+(4*1)+(3*7)+(2*4)+(1*5)=69
69 % 10 = 9
So 30217-45-9 is a valid CAS Registry Number.

30217-45-9Downstream Products

30217-45-9Relevant academic research and scientific papers

Chemistry and structure of diterpene compounds of the kaurane series: IV. Acylation of reduction products of the isosteviol keto group

Al'fonsov,Bakaleinik,Gubaidullin,Kataev,Kovylyaeva,Konovalov,Litvinov,Strobykina,Andreeva,Korochkina

, p. 1144 - 1148 (2001)

Acetylation with acetic anhydride of (4α,8β,13β)-16-hydroxy-13-methyl-17-norkaurane-18-carboxylic acid and its methyl ester, obtained by reduction of isosteviol and (4α,8β,13β)-18-methoxycarbonyl-13-methyl-16-oxo-17-norkaurane, respectively, gives rise to

Diversity-Oriented Library Synthesis from Steviol and Isosteviol-Derived Scaffolds

Georg, Gunda I.,Holth, Trinh A. D.,Hutt, Oliver E.,Walters, Michael A.

, (2020/03/10)

The readily available natural product stevioside provides a unique diterpene core structure that can be explored for small molecule library development by diversity-oriented synthesis and functional group transformations. Validation arrays were prepared from steviol, isosteviol, and related analogues, derived from stevioside, to produce over 90 compounds. These compounds were submitted to the NIH Molecular Libraries Small Molecule Repository for screening in the Molecular Libraries Screening Center Network. Micromolar hits were identified in multiple high-throughput assays for several library members. A cheminformatics analysis of the compounds was performed that verified the expected diversity and complexity of this set of compounds. The screening results indicate that scaffolds-derived natural products can provide screening hits against multiple target proteins.

Design and synthesis of an α-mannosyl terpenoid as selective inhibitor of P-selectin

Ikeda, Tsuyoshi,Kajimoto, Tetsuya,Kondo, Hirosato,Wong, Chi-Huey

, p. 2485 - 2490 (2007/10/03)

In an effort to develop the structural and functional mimics of the tetrasaccharide sialyl Lewis x as selective inhibitors of P-selectin, we have designed a mannosyl terpenoid derivative that selectively inhibits P-selectin within an IC50 value of 60 μM, but exhibits no inhibition activity against E- and L-selectins.

THE BIOTRANSFORMATION OF SOME ENT-BEYERAN-19-OIC ACIDS BY GIBBERELLA FUJIKUROI

Ali, Mohammad Shaiq,Hanson, James R.,Oliveira, Bras H. de

, p. 507 - 510 (2007/10/02)

The biotransformation of isostevic acid (ent-beyeran-19-oic acid), ent-16β-hydroxybeyeran-19-oic acid, and ent-16β-hydroxy-16α-methylbeyeran-19-oic acid by Gibberella fujikuroi has been shown to give ring A desoxybeyergibberellin abalogues of GA9, GA12 and GA25.The ent-16β-hydroxybeyeran-19-oic acid also gave some hydroxylated beyeranes and the 7β-hydroxybeyeranolide. Key words: Gibberella fujikuroi; diterpenoid; beyeran-19-oic acids; gibberellins; biotransformation.

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