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Lasalocid Sodium

Lasalocid Sodium is the salt form of Lasalocid, a carboxylic polyether ionophore. The compound has anticancer properties and antibacterial activity. Lasalocid is isolated from Streptomyces lasaliensis, first reported in 1951. It is also known as a...

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Leoidin

Leoidin is a metabolite of the lichen, Lecanora gangleoides, first published in 1986 and recently reported as an inhibitor ofprotein synthesis in Pseudomonas aeruginosa. Leoidin is bacteriostatic, targeting PheRS. Leoidin is a weak inhibitor of human...

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Lepimectin A4

Lepimectin A4 is a the major analog of a complex of semi-synthetic milbemycins synthesised from 15-hydroxy-5-ketomilbemycin A3/A4 by coupling to methoxyiminophenylacetic acid and then reducing with sodium borohydride.Commercially, Lepimectin is a mixture...

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Levodropropizine

Levodropropizine has anti-allergic properties and inhibits the histamine receptor. It acts as a peripheral antitussive agent. Mechanism of Action Levodropropizine has affinity for H1-histaminic and alpha-adrenergic receptors. Levodropropizine has a...

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Levofloxacin Hydrochloride

Levofloxacin HCl is the hydrochloride salt of Levofloxacin.  It is a broad-spectrum fluoroquinolone antibiotic and the optical S-(-) isomer of Ofloxacin. The compound is a DNA gyrase inhibitor, and has been shown to inhibit topoisomerase IV. ...

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Limonin

Limonin is a highly oxygenated terpenoid which forms the core structure of the citrus limonoid metabolites found mostly in the seeds, fruits and peel tissues of citrus. Limonin was first isolated over 175 years ago. In Australia, Limonin was isolated...

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Lupeol

Lupeol is a pentacyclic lupane triterpene produced by various fruits, vegetables and other plants, first isolated in 1898 and published in 1907. Lupeol is reported to have very diverse biological effects, including anti-inflammatory, anti-diabetic,...

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Manumycin A

Manumycin A was isolated by Zeeck and colleagues at the University of Gottingen, Germany published in 1987. Manumycin A is a potent and selective inhibitor of Ras farnesyl transferase. Manumycin A induces apoptosis and inhibits angiogenesis, and has...

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Mer-NF5003E

Mer-NF5003E is a sesquiterpenoid mycotoxin isolated from Stachybotrys strains, first published in 1994 as an avianmyeloblastosis virus (AMV) protease inhibitor. Mer-NF5003E is inactive against HIV due to host cell toxicity. An analogue, MerNF5003B has...

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Mer-NF5003F

Mer-NF5003F is a sesquiterpenoid mycotoxin isolated from Stachybotrys strains, first published in 1994 as an avianmyeloblastosis virus (AMV) protease inhibitor. Mer-NF5003F is inactive against HIV due to host cell toxicity. An analog, MerNF5003B has been...

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Meropenem Vaborbactam (1:1 mixture)

Meropenem Vaborbactam (1:1 mixture) is a mixture of Meropenem (a carbapenem antibiotic) and Vaborbactam (a cyclic, boronic acid-based, non-suicidal, reversible beta-lactamase inhibitor). It is active against the bacteria causing complicated urinary tract...

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Methyl Betulinate

Methyl Betulinate is the methyl ester of Betulinic Acid, a pentacyclic lupane terpene isolated as a constituent of various tree species, including birch. In Australia, Methyl Betulinate was isolated from Akania bidwillii (syn. Akania lucens) by Ritchie...

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