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7beta,25-Dihydroxycholesterol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64907-21-7

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64907-21-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64907-21-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,9,0 and 7 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 64907-21:
(7*6)+(6*4)+(5*9)+(4*0)+(3*7)+(2*2)+(1*1)=137
137 % 10 = 7
So 64907-21-7 is a valid CAS Registry Number.

64907-21-7Upstream product

64907-21-7Downstream Products

64907-21-7Relevant academic research and scientific papers

Fluoro analogs of bioactive oxy-sterols: Synthesis of an EBI2 agonist with enhanced metabolic stability

Deng, Xiaohu,Sun, Siquan,Wu, Jiejun,Kuei, Chester,Joseph, Victory,Liu, Changlu,Mani, Neelakandha S.

, p. 4888 - 4891 (2016/10/05)

Synthesis of several 7-hydroxy oxysterols and their potential roles as signaling molecules in the innate and adaptive immune responses is discussed. Discovery of a new, fluorinated, synthetic analog of the 7α,25-dihydroxycholesterol—the endogenous ligand of GPR 183 (EBI2), a G-protein coupled receptor highly expressed upon Epstein–Barr virus infection is described. Fluoro oxysterol 12 showed good metabolic stability while maintaining excellent EBI2 agonist activity.

Structure-activity relationships of oxysterol-derived pharmacological chaperones for Niemann-Pick type C1 protein

Ohgane, Kenji,Karaki, Fumika,Noguchi-Yachide, Tomomi,Dodo, Kosuke,Hashimoto, Yuichi

, p. 3480 - 3485 (2014/07/22)

Niemann-Pick disease type C is a fatal neurodegenerative disease, and its major cause is mutations in NPC1 gene. This gene encodes NPC1 protein, a late endosomal polytopic membrane protein required for intracellular cholesterol trafficking. One prevalent mutation (I1061T) has been shown to cause a folding defect, which results in failure of endosomal localization of the protein, leading to loss-of-function phenotype. We have previously demonstrated that several oxysterols and their derivatives act as pharmacological chaperones; binding of these compounds to NPC1I1061T mutant protein corrects the localization/maturation defect of the mutant protein. Here, we disclose detailed structure-activity relationships of oxysterol derivatives as pharmacological chaperones for NPC1I1061T mutant.

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