The Synthesis of Triterpene 2,6-Dideoxy-α-L-arabino-Hexopyranosides from L-Rhamnal and Their Pharmacological Properties

Bioorganicheskaya Khimiya

Volumn 23, Issue 10, 1997, Pages 830-831

  Baltina, L A ^a   Flekhter, O B ^a   Davydova, V A ^a   Ismagilova, A F ^a   Zarudii, F S ^a   Nasyrov, Kh M ^b   Gromakova, L S ^b   Tolstikov, G A ^a  

^a INSTITUTE OF ORGANIC CHEMISTRY   (Russian Federation)

^b BASHKIR STATE MEDICAL UNIVERSITY   (Russian Federation)

Author keywords

Antiulcerous activity; Hepatoprotectant activity; Reparative skin regeneration; Synthesis; Triterpene 2,6 dideoxy L arabino hexopyranosides

Indexed keywords

ANTIULCER AGENT; BROMIDE; CARBON TETRACHLORIDE; DRUG DERIVATIVE; GLYCOSIDE; ION EXCHANGE RESIN; LITHIUM BROMIDE; LITHIUM DERIVATIVE; RHAMNOSE; TRITERPENE;

ANIMAL; ARTICLE; DRUG EFFECT; LIVER; RAT; SKIN; SYNTHESIS;

ANIMALS; ANTI-ULCER AGENTS; BROMIDES; CARBON TETRACHLORIDE; GLYCOSIDES; ION EXCHANGE RESINS; LITHIUM COMPOUNDS; LIVER; RATS; RHAMNOSE; SKIN; TRITERPENES;

EID: 0347169910     PISSN: 01323423     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (18)

1. Baltina L.A., Flekhter O.B., Vasiljieva E.V. // Mendeleev Commun. 1996. P. 63-64.
2. Flekhter O.B., Baltina LA., Vasiljieva E.V., Tolstikov G.A. // Mendeleev Commun. 1997. P. 3-5.
3. Finney R.S., Tarnoky A.L. // J. Pharm. Pharmacol. 1960. V. 12. P. 49-58.
4. Sabesan S., Neira S. // J. Org. Chem. 1991. V. 56. P. 5468-5472.
5. Iselin B., Reichstem T. // Helv. Chim. Acta. 1944. V. 27. P. 1146-1149.
6. Lugemwa F.N., Huang F.-Y., Bently M.D., Mendel M.J., Alford A.R. // J. Agric. Food Chem. 1990. P. 493-496.