Name | monocerin |
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Synonyms |
(+)-monocerin,hydrochloride
phenylmethyl-(2S,3aR,7aS)-octahydroindole-2-carboxylate hydrochloride 2,3,3a,4,5,6,7,7a-octahydro-1H-indole-2-carboxylic acid (phenylmethyl) ester hydrochloride (phenylmethyl) 2,3,3a,4,5,6,7,7a-octahydro-1H-indole-2-carboxylate hydrochloride (2S,3aR,9bR)-7,8-dimethoxy-6-hydroxy-2-propyl-2,3,3a,9b-tetrahydro-5H-furo[3,2-c][2]benzopyran-5-one benzyl-2S,3aR,7aS-octahydroindole carboxylate hydrochloride (2S,3aR,7aS)-benzyl octahydro-1H-indole-2-carboxylate hydrochloride benzyl (2S,3aR,7aS)-2,3,3a,4,5,6,7,7a-octahydro-1H-indole-2-carboxylate (2S,3aR,9bR)-2,3,3a,9b-tetrahydro-6-hydroxy-7,8-dimethoxy-2-propyl-5H-furo(3,2-c)(2)benzopyran-5-one |
Description | Monocerin is an isocoumarin derivative. Monocerin is isolated from Microdochium bolleyi, an endophytic fungus from Fagonia cretica. Monocerin shows good antifungal, antibacterial, and antialgal activities against Microbotryum violaceum, Escherichia coli, Bacillus megaterium, and Chlorella fusca[1]. |
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Related Catalog | |
References |
Density | 1.235 g/cm3 |
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Boiling Point | 506.7ºC at 760 mmHg |
Molecular Formula | C16H20O6 |
Molecular Weight | 308.32600 |
Flash Point | 187.5ºC |
Exact Mass | 308.12600 |
PSA | 74.22000 |
LogP | 2.57850 |
Index of Refraction | 1.539 |
Risk Phrases | R36/37/38 |
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Safety Phrases | 26-36/37/39 |