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1.
Cancers (Basel) ; 10(1)2017 Dec 21.
Article in English | MEDLINE | ID: mdl-29267206

ABSTRACT

Mitogen-activated protein kinases (MAP kinases) are a family of kinases that regulates a range of biological processes implicated in the response to growth factors like latelet-derived growth factor (PDGF), epidermal growth factor (EGF), vascular endothelial growth factor (VEGF), and stress, such as ultraviolet irradiation, heat shock, and osmotic shock. The MAP kinase family consists of four major subfamilies of related proteins (extracellular regulated kinases 1/2 (ERK1/2), c-Jun N-terminal kinase (JNK), p38, and extracellular regulated kinase 5 (ERK5)) and regulates numerous cellular activities, such as apoptosis, gene expression, mitosis, differentiation, and immune responses. The deregulation of these kinases is shown to be involved in human diseases, such as cancer, immune diseases, inflammation, and neurodegenerative disorders. The awareness of the therapeutic potential of the inhibition of MAP kinases led to a thorough search for small-molecule inhibitors. Here, we discuss some of the most well-known MAP kinase inhibitors and their use in cancer research.

2.
Zootaxa ; 3609: 223-30, 2013 Jan 29.
Article in English | MEDLINE | ID: mdl-24699584

ABSTRACT

Thirty-eight species of Nepticulidae are known from the Yucatán Peninsula and adjacent areas (mainland Mexico and Be-lize). This paper describes two new species: Stigmella maya Remeikis & Stonis, sp. nov. (a leaf-miner of Karwinskia hum-boldtiana, Rhamnaceae), and Acalyptris yucatani Remeikis & Stonis, sp. nov. (a leaf-miner of Schinus sp., Anacardiaceae). S. maya is among the smallest Lepidoptera in the world. In its male genitalia S. maya resembles a sizeable group of undescribed species occurring in the Andes (Patagonia: Argentina). The adults of both new species are illustrated with photographs of adults, genitalia and leaf-mines.


Subject(s)
Moths/anatomy & histology , Moths/classification , Animals , Female , Genitalia, Male/anatomy & histology , Male , Mexico
3.
Zootaxa ; 3737: 101-17, 2013 Nov 19.
Article in English | MEDLINE | ID: mdl-25112742

ABSTRACT

This paper describes four new species: Acalyptris basicornis Remeikis & Stonis, sp. nov., A. peteni Diskus & Stonis, sp. nov., A. caribbicus Diskus & Stonis, sp. nov. (host-plant: Lantana involucrata L., Verbenaceae), and A. statuarius Diskus & Stonis, sp. nov. Another species, Stigmella pruinosa Puplesis & Robinson, is re-described, with new distribution records in Guatemala and with the first documentation of leaf-mines on Guazuma ulmifolia Lam. (Malvaceae). All five species are illustrated with photographs of the leaf-mines, adults, and genitalia.


Subject(s)
Moths , Animal Distribution , Animals , Belize , Body Size , Genitalia , Guatemala
4.
Chem Biodivers ; 6(9): 1388-403, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19774595

ABSTRACT

The four possible isomers of tetradeca-4,8-dien-1-yl acetate and corresponding alcohols were synthesized stereoselectively by synthetic routes employing Wittig coupling reaction for the preparation of (Z,E)- and (Z,Z)-isomers, and alkylation of terminal alkynes for the preparation of (E,E)- and (E,Z)-isomers as the key steps. Synthetic products were characterized by 13C- and 1H-NMR spectroscopy as well as mass-spectrometric methods. All four isomers gave distinctive mass spectra where m/z 81 fragments clearly dominated. Elution order, followed by retention index presented in parenthesis, of tetradeca-4,8-dien-1-ols was determined as (Z,Z) (2082.1), (Z,E) (2082.8), (E,E) (2083.1), and (E,Z) (2083.2) from unpolar SPB-1 column, and as (E,E) (2210.2), (Z,E) (2222.1), (E,Z) (2223.4), and (Z,Z) (2224.7) from polar DB-WAX column. The isomers of tetradeca-4,8-dien-1-yl acetates eluted in the order of (Z,Z) (2176.1), (Z,E) (2178.4), (E,Z) (2185.9), and (E,E) (2186.4) from SPB-1, and (Z,E) (2124.3), (E,E) (2157.7), (Z,Z) (2128.9), and (E,Z) (2135.9) from DB-WAX columns. Field-screening tests for attractiveness of tetradeca-4,8-dien-1-yl acetates revealed that (4Z,8E)-tetradeca-4,8-dien-1-yl acetate significantly attracted Phyllonorycter coryli and Chrysoesthia drurella males. (4E,8E)-Tetradeca-4,8-dien-1-yl acetate was the most efficient attractant for Ph. esperella and Ph. saportella males, and (4E,8Z)-tetradeca-4,8-dien-1-yl acetate was attractive to Ph. cerasicolella males.


Subject(s)
Fatty Alcohols/chemical synthesis , Lepidoptera/chemistry , Sex Attractants/chemical synthesis , Animals , Fatty Alcohols/chemistry , Fatty Alcohols/pharmacology , Gas Chromatography-Mass Spectrometry , Male , Sex Attractants/chemistry , Sex Attractants/pharmacology , Stereoisomerism
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