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Synthesis of squalamine analogues on the basis of lupane triterpenoids

Gulnara Vladimirovna Giniyatullina 1
Gulnara Vladimirovna Giniyatullina
Oxana Borisovna Flekhter 1
Oxana Borisovna Flekhter
Genrikh Alexandrovich Tolstikov 1
Genrikh Alexandrovich Tolstikov
Published 2009-01-19
CommunicationVolume 19, Issue 1, 32-33
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Giniyatullina G. V., Flekhter O. B., Tolstikov G. A. Synthesis of squalamine analogues on the basis of lupane triterpenoids // Mendeleev Communications. 2009. Vol. 19. No. 1. pp. 32-33.
GOST all authors (up to 50) Copy
Giniyatullina G. V., Flekhter O. B., Tolstikov G. A. Synthesis of squalamine analogues on the basis of lupane triterpenoids // Mendeleev Communications. 2009. Vol. 19. No. 1. pp. 32-33.
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TY - JOUR
DO - 10.1016/j.mencom.2009.01.013
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2009.01.013
TI - Synthesis of squalamine analogues on the basis of lupane triterpenoids
T2 - Mendeleev Communications
AU - Giniyatullina, Gulnara Vladimirovna
AU - Flekhter, Oxana Borisovna
AU - Tolstikov, Genrikh Alexandrovich
PY - 2009
DA - 2009/01/19
PB - Mendeleev Communications
SP - 32-33
IS - 1
VL - 19
ER -
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@article{2009_Giniyatullina,
author = {Gulnara Vladimirovna Giniyatullina and Oxana Borisovna Flekhter and Genrikh Alexandrovich Tolstikov},
title = {Synthesis of squalamine analogues on the basis of lupane triterpenoids},
journal = {Mendeleev Communications},
year = {2009},
volume = {19},
publisher = {Mendeleev Communications},
month = {Jan},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2009.01.013},
number = {1},
pages = {32--33},
doi = {10.1016/j.mencom.2009.01.013}
}
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Giniyatullina, Gulnara Vladimirovna, et al. “Synthesis of squalamine analogues on the basis of lupane triterpenoids.” Mendeleev Communications, vol. 19, no. 1, Jan. 2009, pp. 32-33. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2009.01.013.

Keywords

betulin
polyamine
squalamine
steroids
synthesis
triterpenoids

Abstract

The first synthesis of a family of betulin-based triterpene–polyamine conjugates, which are structurally related to the potential antibiotic squalamine, is demonstrated.

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