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Erinacine B Erinacin B is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

156101-10-9

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156101-10-9 Usage

Uses

Erinacin B can be used to enhance neurite outgrowth

Check Digit Verification of cas no

The CAS Registry Mumber 156101-10-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,1,0 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 156101-10:
(8*1)+(7*5)+(6*6)+(5*1)+(4*0)+(3*1)+(2*1)+(1*0)=89
89 % 10 = 9
So 156101-10-9 is a valid CAS Registry Number.

156101-10-9Upstream product

156101-10-9Downstream Products

156101-10-9Relevant academic research and scientific papers

Erinacines A, B and C, strong stimulators of nerve growth factor (NGF)-synthesis, from the mycelia of Hericium erinaceum

Kawagishi, Hirokazu,Shimada, Atsushi,Shirai, Ryoko,Okamoto, Kenji,Ojima, Fumihiro,Sakamoto, Hideki,Ishiguro, Yukio,Furukawa, Shoei

, p. 1569 - 1572 (1994)

The structures of novel diterpenoids, erinacines A, B, and C, isolated from the cultured mycelia of Hericium erinaceum were determined by interpretation of the spectral data, and chemical and enzymatic reactions. These compounds showed potent stimulating activity of nerve growth factor (NGF)-synthesis

Isolation of erinacine P, a new parental metabolite of cyathane- xylosides, from Hericium erinaceum and its biomimetic conversion into erinacines A and B

Kenmoku, Hiromichi,Sassa, Takeshi,Kato, Nobuo

, p. 4389 - 4393 (2000)

A new cyathane-xyloside, erinacine P, was isolated from mycelia of basidiomycetous Hericium erinaceum YB4-6237 in a shaken culture. Since its aglycon closely resembles typical cyathane diterpenoids such as cyathins and cyathatriols in its substitution pattern, this glycoside seems to be an important metabolite in the biosynthesis of erinacines and striatins. In fact, according to our biogenesis studies, erinacine P can be successfully converted chemically into erinacine B and, further, to erinacine A under mild conditions. (C) 2000 Elsevier Science Ltd.

Enantioselective total synthesis of (-)-erinacine B

Watanabe, Hideaki,Takano, Masashi,Umino, Akinori,Ito, Toshiya,Ishikawa, Hiroyuki,Nakada, Masahisa

, p. 359 - 362 (2007/10/03)

(Chemical Equation Presented) The first enantioselective total synthesis of (-)-erinacine B has been achieved. Our approach features convergent construction of the 5-6-7 tricyclic cyathane core system via chiral building blocks prepared using asymmetric c

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