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Medicinal Plants Classification Biosynthesis and ... - Index of

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194<br />

Jorge Castro-Garza, Delia E. Cruz-Vega <strong>and</strong> Ma. Teresa González-Garza<br />

Celahin C <strong>and</strong> salasol A isolated from the root <strong>of</strong> Microtropis japonica exhibited in vitro<br />

anti-tuberculosis activity, both with an MIC value <strong>of</strong> 15.0 mg/ml against M. tuberculosis<br />

H37Rv [Chou et al, 2008]. Ursolic acid, squalene <strong>and</strong> farnesol isolated from Chamaedora<br />

tepejilote hexane extract produced a M. tuberculosis growth inhibition <strong>of</strong> 99% at a<br />

concentration <strong>of</strong> 100 µg/mL [Jimenez et al, 2005].<br />

Alkaloids <strong>and</strong> lactones also show anti-mycobacterial activity: Anti-TB bioassay-directed<br />

fractionation led to the isolation <strong>of</strong> carbazole alkaloids, as well as the gamma-lactone<br />

derivative <strong>of</strong> oleic acid, from the CH2Cl2 extract <strong>of</strong> the stem bark <strong>of</strong> Micromelum hirsutum.<br />

The lactone derivative <strong>of</strong> oleic acid, (-)- Z-9-octadecene-4-olide showed potent in vitro anti-<br />

TB activity against H37Rv (MIC: 1.5 µg/mL), <strong>and</strong> exhibited activity against the Erdman<br />

strain <strong>of</strong> M. tuberculosis in a J774 mouse macrophage model (EC90: 5.6 µg/mL). The<br />

carbazoles include the new micromeline <strong>and</strong> known alkaloids: lansine, 3-formylcarbazole,<br />

<strong>and</strong> 3-formyl-6-methoxycarbazole, had anti-TB MIC values between 14.3 <strong>and</strong> 42.3 µg/mL<br />

[Ma et al, 2005].<br />

Constituents from the roots <strong>of</strong> Engelhardia roxburghiana, Engelhardione, 3methoxyjuglone,<br />

<strong>and</strong> (-)-4-hydroxy-1-tetralone showed antitubercular activities with MIC<br />

values <strong>of</strong> 3.125, 3.125, <strong>and</strong> 6.25 microg/mL against three different strains <strong>of</strong> M. tuberculosis,<br />

<strong>and</strong> with MIC values <strong>of</strong> 0.2, 0.2, <strong>and</strong> 4.0 µg/mL against M. tuberculosis H37Rv [Lin et al,<br />

2005].<br />

Antitubercular bioassay-guided fractionation <strong>of</strong> the n-hexane <strong>and</strong> CH2Cl2-soluble<br />

extracts <strong>of</strong> above-ground biomass <strong>and</strong> roots <strong>of</strong> Valeriana laxiflora led to the isolation <strong>of</strong> a<br />

new lignan (+)-1-hydroxy-2,6-bis- epi-pinoresinol, along with eleven known including<br />

compounds, betulin, betulinic acid, 5,7-dihydroxy-3,6,4'-trimethoxyflavone, 23hydroxyursolic<br />

acid, oleanolic acid, tricin, <strong>and</strong> ursolic acid. In a microplate alamar blue assay<br />

against Mycobacterium tuberculosis, compounds exhibited MICs <strong>of</strong> 15.5 - 127 µg/mL [Gu et<br />

al, 2004].<br />

Kanokmedhakul et al [2003], isolated from the mushroom Scleroderma citrinum the<br />

compound 4,4'-dimethoxyvulpinic acid <strong>and</strong> two <strong>of</strong> its derivatives, the dibromo derivative 5<br />

<strong>and</strong> acetate derivative 6; all <strong>of</strong> them exhibited inhibitory activity towards M. tuberculosis.<br />

Limmatvapirat et al, [2004] isolated from the aerial parts <strong>of</strong> Abrus precatorius, a known<br />

is<strong>of</strong>lavanquinone, the abruquinone B which exhibited antitubercular activity.<br />

From the hexane-soluble fraction <strong>of</strong> an ethanol extract from leaves <strong>and</strong> stems <strong>of</strong><br />

Stemodia foliosa (Scrophulariaceae), the new stearic acid 4-[(n-pentoxy)phenethyl] ester was<br />

isolated <strong>and</strong> exhibited antibacterial properties at 10 µg/mL concentration by using disc<br />

diffusion method against the fast-acid bacterium M. fortuitum. [Dantas da Silva et al, 2002].<br />

Cantrell et al [2001] presented a review about reports, up to that year, on plant-derived<br />

terpenoids showing moderate to high activity in in vitro bioassays against M. tuberculosis. In<br />

that review, mono-, sesqui-, di- <strong>and</strong> triterpenes, <strong>and</strong> sterols, their structural analogs <strong>and</strong><br />

semisynthetic derivatives are discussed, with particular emphasis on the structural features<br />

essential for anti-mycobacterial activity.<br />

There are some well known <strong>and</strong> characterized compounds from plants extracts that<br />

present relevant activity anti-TB; Luteolin isolated from methanol extracts <strong>of</strong> Ficus<br />

chlamydocarpa (FCR) <strong>and</strong> Ficus cordata showed activity against M. tuberculosis exhibiting a<br />

MIC <strong>of</strong> 4.88 µg/ml (Kuete, 2008). Norditerpenoid 12-demethylmulticauline from Salvia

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