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(3R,10R)-3,4,5,5a,6,7,8,9-Octahydro-2,2,5aβ,9β-tetramethyl-2H-3β,9aβ-methano-1-benzoxepine-5α,6β,10-triol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59812-41-8

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59812-41-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59812-41-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,8,1 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 59812-41:
(7*5)+(6*9)+(5*8)+(4*1)+(3*2)+(2*4)+(1*1)=148
148 % 10 = 8
So 59812-41-8 is a valid CAS Registry Number.

59812-41-8Downstream Products

59812-41-8Relevant academic research and scientific papers

Natural β-Dihydroagarofuran-Type Sesquiterpenoids as Cognition-Enhancing and Neuroprotective Agents from Medicinal Plants of the Genus Celastrus

Ning, Ruonan,Lei, Yun,Liu, Shuangzhu,Wang, Huan,Zhang, Rujun,Wang, Wei,Zhu, Yingdong,Zhang, Haiyan,Zhao, Weimin

, p. 2175 - 2186 (2015)

Alzheimers disease (AD) is an irreversible, multifaceted, and progressive neurodegenerative disorder. Over the past 30 years, the search for anti-AD drugs has been primarily based on the cholinergic deficiency hypothesis and/or the β-amyloid (Aβ) cascade hypothesis. In this study, we report the identification of 16 new and 38 known β-dihydroagarofuran-type sesquiterpenoids from Celastrus flagellaris and Celastrus angulatus. The β-dihydroagarofuran-type sesquiterpenoids 58, 59, 61, and 63 significantly attenuated scopolamine-induced prolonged escape latency and increased number of errors compared with the control group. At 10 μM, 21 of the 62 tested β-dihydroagarofuran-type sesquiterpenoids rescued Aβ25-35-induced SH-SY5Y cells from viability reduction, which increased the cell viability from 64.6% for the model to more than 74.0%. The majority of the β-dihydroagarofuran-type sesquiterpenoids with ester groups exhibited stronger activity than those with free hydroxy groups or without substituents at the same positions. These results identified a new chemical skeleton as drug lead for the investigation of novel therapeutic agents against AD.

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