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Solanum Type

Antifungal activity has been demonstrated mainly in two groups of plant steroids, glycoalkaloids of the Solanum type and saponins. Members of both groups are comprised of a steroidal aglycone... [Pg.286]

Solanum steroid alkaloids have been isolated so far from nearly 350 species of the plant families Solanaceae and Liliaceae, in which they generally occur as glycosides. All of the 75 known steroidal alkamines of the Solanum type,... [Pg.82]

Kowalaksi SP. Bamberg J, Tringey WM, Steffens JC. Inheritance of polyphenol oxidase in type A glandular trichomes of Solanum berthaultii. JHered 1990 81 475-478. [Pg.194]

The structural features of the solanum alkaloids are based on two primary skeletal configurations solanidane, with or without glycoside functionalities, as featured by the toxic and teratogenic steroidal alkaloids a-chaconine and a-solanine with the indolizidine type E-F ring (Figure 2.7a) and the spirosolane... [Pg.32]

Heibges, A., Salamini, F., Gebhardt, C. (2003). Funetional eomparison of homologous members of three groups of Kunitz-type enzyme inhibitors from potato tubers Solanum tuberosum L.). Mol Gen. Genomics, 269,535-541. [Pg.120]

Kunitz-type Solanales Potato Solanum Sola 12... [Pg.337]

Birk serine PIPs (BBPIPs) [137-141] Hordeum (barley) lipid transfer proteins (LTPs) that inhibit malt cysteine endopeptidases [169] and Solanum (potato) Kunitz Pi-type cysteine Pis [185-188] (Table 5). [Pg.592]

Solanum (potato) Kunitz PEPs inhibit the aspartic protease cathepsin D as well as trypsin [125-134] and potato cysteine protease inhibitor (PCPI) inhibits a variety of cysteine proteases [185-188]. The crystal structures of soybean trypsin inhibitor (STI) [362, 368] and of Erythrina trypsin inhibitor (ETI) [350] have been determined. The structure of this type of plant Kunitz serine PIP involves a [3-barrel formed by 6 loop-linked antiparallel [3-strands with a lid formed by 6 further loop-linked antiparallel [3-strands. The scissile bond is located within a loop that extends out from the surface of the [3-barrel [350, 362, 368]. [Pg.603]

Torvanol A and torvoside H isolated from Solanum torvum (76) showed antiviral activity (herpes simplex virus type 1) in vitro. The IC50 values were threefold less compared with the reference compound, acyclovir. [Pg.68]

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Solanum

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