Allobetulone rearrangement to l8αH,19βH-ursane triterpenoids with antiviral activity-Reference-Cited by-同舟云学术

Allobetulone rearrangement to l8αH,19βH-ursane triterpenoids with antiviral activity

Published:2020-12-08 Issue: Volume: Page:1-11
ISSN:1478-6419
Container-title:Natural Product Research
language:en
Short-container-title:Natural Product Research

Author:

Babaev Marat¹,Khusnutdinova Elmira¹^ORCID,Lobov Alexander¹^ORCID,Galimova Zarema¹,Petrova Anastasiya¹,Rybalova Tatyana²,Nguyen Ha Thi Thu³,Meyers Craig⁴,Prichard Mark⁵,Kazakova Oxana¹

Affiliation:

1. Ufa Institute of Chemistry UFRC RAS, Ufa, Russian Federation

2. N.N. Vorozhtzov, Novosibirsk Institute of Organic Chemistry SB RAS, Novosibirsk, Russian Federation

3. Institute of Chemistry, Vietnamese Academy of Science and Technology, Cau Giay Dist, Hanoi, Vietnam

4. Penn State College of Medicine, Hershey, PA, USA

5. University of Alabama at Birmingham, Birmingham, AL, USA

Funder

Russian Foundation for Basic Research

Federal program

National Institutes of Allergy and Infectious Diseases, National Institutes of Health, Department of Health and Human Services

Publisher

Informa UK Limited

Subject

Organic Chemistry,Plant Science,Biochemistry,Analytical Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/14786419.2020.1855159

Reference35 articles.

1. Pharmacological properties of the ubiquitous natural product betulin

2. Betulinic Acid: Recent Advances in Chemical Modifications, Effective Delivery, and Molecular Mechanisms of a Promising Anticancer Therapy

3. Betulin and its derivatives as novel compounds with different pharmacological effects

4. Spermine amides of selected triterpenoid acids: dynamic supramolecular system formation influences the cytotoxicity of the drugs

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