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6754-20-7

6754-20-7 structure
6754-20-7 structure
  • Name: (-)-Polygodial
  • Chemical Name: polygodial
  • CAS Number: 6754-20-7
  • Molecular Formula: C15H22O2
  • Molecular Weight: 234.334
  • Catalog: Signaling Pathways Anti-infection Fungal
  • Create Date: 2018-07-04 18:11:42
  • Modify Date: 2024-01-02 18:58:37
  • Polygodial (Poligodial) is an antifungal potentiator[1]. Polygodial is a sesquiterpene with anti-hyperalgesic properties[2].

Name polygodial
Synonyms (1R,4aS,8aS)-5,5,8a-trimethyl-1,4,4a,5,6,7,8,8a-octahydronaphthalene-1,2-dicarbaldehyde
UNII:A00RAV0W57
Podofilox
Wartec
Condylox
Podophyllotoxin 7
1,2-Naphthalenedicarboxaldehyde, 1,4,4a,5,6,7,8,8a-octahydro-5,5,8a-trimethyl-, (1R,4aS,8aS)-
Condyline
[1R-(1a,4ab,8aa)]-1,4,4a,5,6,7,8,8a-Octahydro-5,5,8a-trimethyl-1,2-naphthalenedicarboxaldehyde
S-Isopropylisothiourea hydrobromide
Polygodial
Warticon
(1R,4aS,8aS)-5,5,8a-Trimethyl-1,4,4a,5,6,7,8,8a-octahydro-1,2-naphthalenedicarbaldehyde
Podophyllinic acid lactone
Description Polygodial (Poligodial) is an antifungal potentiator[1]. Polygodial is a sesquiterpene with anti-hyperalgesic properties[2].
Related Catalog
In Vitro Polygodial exhibits fungicidal activity against Saccharomyces cerevisiae, Candida albicans, and other fungal pathogens in standardized susceptibility tests (NCCLS). Polygodial (12.5 μg/mL, 3 hours) induces significant shrinkage compared to controls in Saccharomyces cerevisiae cells with the minimum fungicidal concentration (MFC) for 106 CFU/mL in RPMI 1640 medium[3]. Cell Viability Assay[3] Cell Line: S. cerevisiae cells Concentration: 12.5 μg/mL Incubation Time: 3 hours Result: Treated cells exhibited significant shrinkage compared to controls, and the organization of subcellular organelles appears either disrupted or compacted.
In Vivo Polygodial is a sesquiterpene isolated from the barks of Drymis winteri (Winteraceae). Polygodial (0.5 to 10 mg/kg; 0.5 h; given by i.p. route to mice) induces significant, dose-related and almost complete inhibition of Acetic acid, Kaolin and Zymosan-induced abdominal constrictions. The calculated mean ID50 values are 0.8, 2.1 and 2.6 mg/kg and maximal inhibitions of 90.0±3.0, 98.0±1.0 and 97.0±2.0 %, against Acetic acid, Kaolin and Zymosan, respectively. Polygodial is about 14- to 27-fold more potent than the hydroalcoholic extract (HE) at the ID50 level[2]. Animal Model: Non-fasted male Swiss mice (20-30 g) or male Wistar rats (150-180 g)[2] Dosage: 0.1 to 10 mg/kg Administration: Injected i.p. 0.5 h before the injection of irritant substances Result: Produced significant inhibition of Acetic acid, Kaolin and Zymosan-induced writhing in mice.
References

[1]. I Kubo, et al. Polygodial, an antifungal potentiator. J Nat Prod. Jan-Feb 1988;51(1):22-9.

[2]. G L Mendes, et al. Anti-hyperalgesic properties of the extract and of the main sesquiterpene polygodial isolated from the barks of Drymis winteri (Winteraceae). Life Sci. 1998;63(5):369-81.

[3]. C S Lunde, et al. Effect of polygodial on the mitochondrial ATPase of Saccharomyces cerevisiae. Antimicrob Agents Chemother. 2000 Jul;44(7):1943-53.

Density 1.1±0.1 g/cm3
Boiling Point 330.7±35.0 °C at 760 mmHg
Molecular Formula C15H22O2
Molecular Weight 234.334
Flash Point 124.0±22.9 °C
Exact Mass 234.161987
PSA 34.14000
LogP 3.84
Vapour Pressure 0.0±0.7 mmHg at 25°C
Index of Refraction 1.570
Storage condition 20°C
Hazard Codes Xn
Risk Phrases 52/53
RIDADR NONH for all modes of transport
RTECS QJ2850000