55353-32-7 Usage
Uses
Used in Medicinal Chemistry:
(11R)-11-C-(6-Amino-9H-purin-9-yl)-2,6:8,11-dianhydro-10-O-methyl-7-deoxy-α-L-ido-D-lyxo-5-undecoulo-5,9-pyranosonic acid methyl ester is used as a compound with potential biological activity for the development of new medications. Its unique structure and purine base may allow it to interact with biological systems in ways that could be harnessed for therapeutic purposes.
Used in Drug Development:
In the pharmaceutical industry, (11R)-11-C-(6-Amino-9H-purin-9-yl)-2,6:8,11-dianhydro-10-O-methyl-7-deoxy-α-L-ido-D-lyxo-5-undecoulo-5,9-pyranosonic acid methyl ester is utilized as a starting material or intermediate in the synthesis of novel drugs. Its complex structure and potential for modification make it a valuable asset in the creation of new pharmaceutical agents.
Used in Organic Chemistry Research:
(11R)-11-C-(6-Amino-9H-purin-9-yl)-2,6:8,11-dianhydro-10-O-methyl-7-deoxy-α-L-ido-D-lyxo-5-undecoulo-5,9-pyranosonic acid methyl ester serves as a subject of study in organic chemistry, where its synthesis, properties, and reactions are investigated. Understanding the behavior of (11R)-11-C-(6-Amino-9H-purin-9-yl)-2,6:8,11-dianhydro-10-O-methyl-7-deoxy-α-L-ido-D-lyxo-5-undecoulo-5,9-pyranosonic acid methyl ester can lead to advancements in synthetic methods and the discovery of new chemical entities.
Used in Pharmaceutical Research:
In the field of pharmaceuticals, (11R)-11-C-(6-Amino-9H-purin-9-yl)-2,6:8,11-dianhydro-10-O-methyl-7-deoxy-α-L-ido-D-lyxo-5-undecoulo-5,9-pyranosonic acid methyl ester is employed as a target for research aimed at uncovering its potential applications in medicine. This may include exploring its interactions with biological targets, assessing its pharmacological properties, and determining its safety and efficacy as a drug candidate.
Check Digit Verification of cas no
The CAS Registry Mumber 55353-32-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,3,5 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 55353-32:
(7*5)+(6*5)+(5*3)+(4*5)+(3*3)+(2*3)+(1*2)=117
117 % 10 = 7
So 55353-32-7 is a valid CAS Registry Number.
InChI:InChI=1/C18H23N5O9/c1-28-12-10-6(30-16(12)23-5-22-8-14(19)20-4-21-15(8)23)3-7-18(27,32-10)13(25)9(24)11(31-7)17(26)29-2/h4-7,9-13,16,24-25,27H,3H2,1-2H3,(H2,19,20,21)/t6-,7-,9-,10+,11+,12-,13+,16-,18-/m1/s1
55353-32-7Relevant academic research and scientific papers
Elucidation of the Herbicidin Tailoring Pathway Offers Insights into Its Structural Diversity
Pan, Hai-Xue,Chen, Zhang,Zeng, Tianfang,Jin, Wen-Bing,Geng, Yujie,Lin, Geng-Min,Zhao, Juan,Li, Wei-Tao,Xiong, Zijun,Huang, Sheng-Xiong,Zhai, Xin,Liu, Hung-Wen,Tang, Gong-Li
, p. 1374 - 1378 (2019/02/26)
The biosynthetic gene clusters for herbicidins (hbc) and aureonuclemycin (anm) were identified in Streptomyces sp. KIB-027 and Streptomyces aureus, respectively. The roles of genes possibly involved in post-core-assembly steps in herbicidin biosynthesis i
The first synthesis of herbicidin B. stereoselective construction of the tricyclic undecose moiety by a conformational restriction strategy using steric repulsion between adjacent bulky silyl protecting groups on a pyranose ring
Ichikawa, Satoshi,Shuto, Satoshi,Matsuda, Akira
, p. 10270 - 10280 (2007/10/03)
The first total synthesis of the nucleoside antibiotic herbicidin B (1b) was achieved, where a novel aldol-type C-glycosidation reaction promoted by samarium diiodide (SmI2) was used as a key step. Treatment of methyl 3,4-O-(1,1,3,3-tetraisopro
