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Ivermectin B1 Mono-sugar Derivative is a compound derived from Ivermectin, an antiparasitic drug that is effective against a broad range of nematode and arthropod parasites. It is used to treat scabies and lice in humans and has shown in vitro inhibitory activity against SARS-CoV-2, the virus responsible for COVID-19.

71837-27-9

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71837-27-9 Usage

Uses

Used in Pharmaceutical Industry:
Ivermectin B1 Mono-sugar Derivative is used as an impurity in the production of Ivermectin, an antiparasitic drug. It is utilized for its potential therapeutic effects against parasitic infections and as an in vitro inhibitor of SARS-CoV-2, contributing to the development of treatments for COVID-19.
Used in Antiviral Applications:
Ivermectin B1 Mono-sugar Derivative is used as an in vitro inhibitor of SARS-CoV-2, the virus responsible for COVID-19. Its potential antiviral properties make it a candidate for further research and development in the context of COVID-19 treatment and prevention strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 71837-27-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,8,3 and 7 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 71837-27:
(7*7)+(6*1)+(5*8)+(4*3)+(3*7)+(2*2)+(1*7)=139
139 % 10 = 9
So 71837-27-9 is a valid CAS Registry Number.

71837-27-9Relevant academic research and scientific papers

USE OF AVERMECTIN DERIVATIVE FOR INCREASING BIOAVAILABILITY AND EFFICACY OF MACROCYLIC LACTONES

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Page/Page column 13, (2013/05/09)

The present invention relates to the use of avermectin derivative as a drug for the treatment of parasitic infections. The avermectin derivative is represented by the formula (I) wherein: (i) R1 is chosen from the group constituted of -CH(CH3)2, -CH(CH3)CH2CH3, or cyclohexyle, (ii) X represents -CH2-CH2-, or -CH=CH-, (iii) R2 is chosen from the group constituted of or -OH group, (iv) R3 is OH or NOH, (v) represents a single bond when R3 is OH, or a double bond when R3 is NOH, as an inhibitor of a membrane-bound protein which transports exogenous compounds out of target cells

The in vitro characterization of the iterative avermectin glycosyltransferase AveBI reveals reaction reversibility and sugar nucleotide flexibility

Zhang, Changsheng,Albermann, Christoph,Fu, Xun,Thorson, Jon S.

, p. 16420 - 16421 (2007/10/03)

The glycosyltransferase AveBI, which is involved in the biosynthesis of the macrolide antihelmintic avermectin (AVM), was characterized in vitro. AveBI was confirmed to catalyze two separate iterative additions of l-oleandrose, and the reversibility of AveBI-catalyzed reaction was also demonstrated. Investigation of sugar nucleotide specificity revealed 10 unique sugar nucleotide substrates which, in combination with five distinct aglycones, led to the production of 50 differentially glycosylated AVM variants. Copyright

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