IQUIMEFA   05518
INSTITUTO QUIMICA Y METABOLISMO DEL FARMACO
Unidad Ejecutora - UE
artículos
Título:
Hybanthus parviflorus (Violaceae): Insecticidal activity of a South American plant
Autor/es:
A.M. BROUSSALIS, S. CLEMENTE, G.E. FERRARO
Revista:
CROP PROTECTION
Editorial:
ELSEVIER SCI LTD
Referencias:
Lugar: Londres; Año: 2010 p. 953 - 956
ISSN:
0261-2194
Resumen:
Hybanthus parviflorus is a perennial shrub, widely distributed in the tropical and subtropical regions of
America, and is known as violetilla in Argentina. Previous phytochemical studies of this species led us to
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
America, and is known as violetilla in Argentina. Previous phytochemical studies of this species led us to
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
America, and is known as violetilla in Argentina. Previous phytochemical studies of this species led us to
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
America, and is known as violetilla in Argentina. Previous phytochemical studies of this species led us to
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
America, and is known as violetilla in Argentina. Previous phytochemical studies of this species led us to
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
America, and is known as violetilla in Argentina. Previous phytochemical studies of this species led us to
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
America, and is known as violetilla in Argentina. Previous phytochemical studies of this species led us to
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
florus is a perennial shrub, widely distributed in the tropical and subtropical regions of
America, and is known as violetilla in Argentina. Previous phytochemical studies of this species led us to
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined against
violetilla in Argentina. Previous phytochemical studies of this species led us to
the isolation and determination of the primary structure of a novel macrocyclic polypeptide, the
cyclotide hypa A. Here the insecticidal activities of extracts of H. parviflorus were determined againstH. parviflorus were determined against
Ceratitis capitata Wied., the Mediterranean fruit fly or Medfly. Mortality in the different life stages of
Medfly, total mortality and modifications of the insects physiology caused by 50% EtOH and CH2Cl2
Medfly, total mortality and modifications of the insects physiology caused by 50% EtOH and CH2Cl2
Medfly, total mortality and modifications of the insects physiology caused by 50% EtOH and CH2Cl2
Medfly, total mortality and modifications of the insects physiology caused by 50% EtOH and CH2Cl2
Medfly, total mortality and modifications of the insects physiology caused by 50% EtOH and CH2Cl2
Medfly, total mortality and modifications of the insects physiology caused by 50% EtOH and CH2Cl2
Medfly, total mortality and modifications of the insects physiology caused by 50% EtOH and CH2Cl2
Wied., the Mediterranean fruit fly or Medfly. Mortality in the different life stages of
Medfly, total mortality and modifications of the insects physiology caused by 50% EtOH and CH2Cl2fly, total mortality and modifications of the insects physiology caused by 50% EtOH and CH2Cl2
extracts of H. parviflorus were evaluated. In addition, we determined the occurrence of ursolic acid,H. parviflorus were evaluated. In addition, we determined the occurrence of ursolic acid,
b-sitosterol and the polyphenols quercetin, quercetin-3-methyl ether, apigenin, luteolin, kaempferol,
rutin, caffeic acid and chlorogenic acid. The promising insecticidal activity of 50% EtOH extracts of
rutin, caffeic acid and chlorogenic acid. The promising insecticidal activity of 50% EtOH extracts of
rutin, caffeic acid and chlorogenic acid. The promising insecticidal activity of 50% EtOH extracts of
rutin, caffeic acid and chlorogenic acid. The promising insecticidal activity of 50% EtOH extracts of
rutin, caffeic acid and chlorogenic acid. The promising insecticidal activity of 50% EtOH extracts of
rutin, caffeic acid and chlorogenic acid. The promising insecticidal activity of 50% EtOH extracts of
rutin, caffeic acid and chlorogenic acid. The promising insecticidal activity of 50% EtOH extracts of
-sitosterol and the polyphenols quercetin, quercetin-3-methyl ether, apigenin, luteolin, kaempferol,
rutin, caffeic acid and chlorogenic acid. The promising insecticidal activity of 50% EtOH extracts of
H. parviflorus and its purified fractions was related to the presence of cyclotides. The insecticidal activity
of CH2Cl2 extracts could be related to the presence of polyphenols, ursolic acid and b-sitosterol.
of CH2Cl2 extracts could be related to the presence of polyphenols, ursolic acid and b-sitosterol.
of CH2Cl2 extracts could be related to the presence of polyphenols, ursolic acid and b-sitosterol.
of CH2Cl2 extracts could be related to the presence of polyphenols, ursolic acid and b-sitosterol.
of CH2Cl2 extracts could be related to the presence of polyphenols, ursolic acid and b-sitosterol.
of CH2Cl2 extracts could be related to the presence of polyphenols, ursolic acid and b-sitosterol.
of CH2Cl2 extracts could be related to the presence of polyphenols, ursolic acid and b-sitosterol.
florus and its purified fractions was related to the presence of cyclotides. The insecticidal activity
of CH2Cl2 extracts could be related to the presence of polyphenols, ursolic acid and b-sitosterol.2Cl2 extracts could be related to the presence of polyphenols, ursolic acid and b-sitosterol.