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Dive into the research topics where Mariano Castillo is active.

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Featured researches published by Mariano Castillo.


Phytochemistry | 1993

Mono and sesquiterpenoids from Satureja gilliesii

Cecilia Labbé; Mariano Castillo

Abstract Two new isomeric monoterpene peroxides along with (+)-T-cadinol and (−)-cadin-4-en-1-o1 were isolated from the leaves of Satureja gilliesii (Lamiaceae). Significant toxicity toward Artemia salina (brine shrimp bioassay) was observed for the cadinane sesquiterpenoids.


Phytochemistry | 1979

Alkaloids of Lycopodium magellanicum

Luis A. Loyola; Glauco Morales; Mariano Castillo

Abstract Six alkaloids have been isolated from Lycopodium magellanicum . These include the known alkaloids lycopodine, acetyldihydrolycopodine, lycodine, N -methyllycodine, acetylfawcettine and a new alkaloid, 5-dehydro-magellanine. The chemical correlation of magellanine and paniculatine and the establishment of their absolute configuration are described.


Phytochemistry | 1980

Tropane alkaloids from Schizanthus hookeri

Aurelio San Martin; Juana Rovirosa; Vicente Gambaro; Mariano Castillo

Abstract Tropine, a pair of diastereoisomeric hygrolines and two new tropane alkaloids; 3α-senecioyloxytropan-6β-ol and 6β-angeloyloxytropan-3α-ol, were isolated from roots of Schizanthus hookeri .


Phytochemistry | 1987

Tropane alkaloids from Schizanthus grahamii

Aurelio San-Martín; Cecilia Labbé; Orlando Muñoz; Mariano Castillo; Matías Reina; Gabriel De La Fuente; Antonio Lobos González

Abstract Three new tropanol dimers of mesaconic and itaconic acids and 3α-senecioyloxytropane, together with other known alkaloids, were isolated from Schizanthus grahamii . The structures of the new compounds were established by spectroscopic and chemical transformations including 2-D long-range 13 C- 1 H correlations.


Phytochemistry | 1987

Neo-clerodane diterpenoids and other constituents from Baccharis species

Francesca Faini; Patricio Rivera; Manuel Mahú; Mariano Castillo

Abstract A new neo -clerodane dilactone, desoxyarticulin, and dihydrotucumanoic acid, together with other known compounds, were isolated from Baccharis pedicellata and Baccharis marginalis . The structures of the new compounds were elucidated by spectroscopic methods.


Phytochemistry | 1985

Neo-clerodane diterpenoids from Baccharis incarum

Arturo Givovich; Aurelio San-Martín; Mariano Castillo

Abstract A new neo-clerodane diterpenoid was isolated from the aerial parts of Baccharis incarum together with the previously known diterpenoids bacchalineol and barticulidiol.


Phytochemistry | 1983

Angeloyl, tigloyl and senecioyloxytropane alkaloids from Schizanthus hookerii

Vicente Gambaro; Cecilia Labbé; Mariano Castillo

Abstract 6β-Angeloyloxytropan-3α-ol, 3α-senecioyloxytropan-6β-ol and 6β-tigloyloxytropan-3α-ol, tropine and two diasteromeric hygrolines were isolated from Schizanthus hookerii .


Phytochemistry | 1994

Rearranged isopimarenes and other diterpenoids from Satureja gilliesii

Cecilia Labbé; Mariano Castillo; Francesca Fainia; Josep Coll

Abstract Seven new diterpenoids, a labdane, three isopimarenes and three rearranged isopimarenes, have been isolated from the flowering tops of Satureja gilliesii . Their structures are based on their spectroscopic properties and, in the case of one compound, confirmed by crystal structure analysis. A new 18(4→3)abeoisopimarene nucleus is proposed for three of the compounds. The compounds were tested for toxicity (brine shrimp bioassay) and antifeedant activity ( Spodoptera littoralis , disc choice). The results of this study suggest the existence of chemical races of S. gilliesii .


Phytochemistry | 1986

Neo-clerodane diterpenoids from Baccharis rhomboidalis

Aurelio San-Martín; Juana Rovirosa; Cecilia Labbé; Arturo Givovich; Manuel Mahú; Mariano Castillo

Abstract Three new neo-clerodane diterpenoids were isolated together with other known clerodanes from Baccharis rhomboidalis . Their structures were established by spectroscopic methods.


Phytochemistry | 1984

(25R)-isonuatigenin, an unusual steroidal sapogenin from Vestia lycioides

Francesca Faini; René Torres; Mariano Castillo

Abstract (25 R )-Isonuatigenin, a 5 -spirosten-3β,25-diol, was isolated from aerial parts of Vestia lycioides . Its structure was elucidated mainly by 1 H NMR and 13 C NMR spectroscopy. A mixture of (25 R )-nuatigenin and (25 S )-isonuatigenin was also characterized. This is the first report on the natural occurrence of the two (25 R )-isomers.

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Glauco Morales

University of Antofagasta

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Luis A. Loyola

University of Antofagasta

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