Name | (-)-Chrodrimanin B |
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Synonyms |
(-)-Chrodrimanin B
chrodrimanin B (1R,2R,7aR,8S,9aR,13aS,13bS)-5,8-Dihydroxy-2,7a,10,10,13a-pentamethyl-4,11-dioxo-1,7a,8,9,9a,10,11,13a,13b,14-decahydro-2H,4H-benzo[a]pyrano[3,4-j]xanthen-1-yl acetate 2H,4H-Benzo[a]pyrano[3,4-j]xanthene-4,11(7aH)-dione, 1-(acetyloxy)-1,8,9,9a,10,13a,13b,14-octahydro-5,8-dihydroxy-2,7a,10,10,13a-pentamethyl-, (1R,2R,7aR,8S,9aR,13aS,13bS)- |
Description | Chrodrimanin B, a metabolite of a fungal, is a potent, non-open-channel-blocking antagonist on B. mori GABAR RDL with an IC50 of 1.13 nM. Chrodrimanin B attenuates the peak current amplitude of the GABA response of RDL with an IC50 of 1.66 nM. Chrodrimanin B, a meroterpenoid, shows insecticidal activity[1]. |
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Related Catalog | |
In Vitro | Chrodrimanin B exhibits much weaker blocking action on human α1β2γ2 GABAR compared to RDL (IC50=1.48 μM)[1]. Chrodrimanin B shows competitive actions at low concentrations and non-competitive actions at higher concentrations on B. mori GABAR RDL[1]. |
References |
Density | 1.4±0.1 g/cm3 |
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Boiling Point | 663.7±55.0 °C at 760 mmHg |
Molecular Formula | C27H32O8 |
Molecular Weight | 484.538 |
Flash Point | 221.1±25.0 °C |
Exact Mass | 484.209717 |
LogP | 2.97 |
Vapour Pressure | 0.0±2.1 mmHg at 25°C |
Index of Refraction | 1.614 |