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  • Product Name: Hymeglusin
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  • Purity: 98.0%
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29066-42-0

29066-42-0 structure
29066-42-0 structure
  • Name: hymeglusin
  • Chemical Name: Hymeglusin
  • CAS Number: 29066-42-0
  • Molecular Formula: C18H28O5
  • Molecular Weight: 324.412
  • Catalog: Research Areas Cancer
  • Create Date: 2017-12-11 00:29:16
  • Modify Date: 2024-01-09 10:05:31
  • Hymeglusin, as a fungal β-lactone antibiotic, is a HMG-CoA synthase inhibitor (IC50 = 0.12 μM). Hymeglusin covalently modifies the active Cys129 residue of the enzyme[2][3].

Name Hymeglusin
Synonyms (2E,4E,7R)-11-[(2R,3R)-3-(Hydroxymethyl)-4-oxo-2-oxetanyl]-3,5,7-trimethyl-2,4-undecadienoic acid
2,4-Undecadienoic acid, 11-[(2R,3R)-3-(hydroxymethyl)-4-oxo-2-oxetanyl]-3,5,7-trimethyl-, (2E,4E,7R)-
hymeglusin
Description Hymeglusin, as a fungal β-lactone antibiotic, is a HMG-CoA synthase inhibitor (IC50 = 0.12 μM). Hymeglusin covalently modifies the active Cys129 residue of the enzyme[2][3].
Related Catalog
Target

IC50: 1.2 μM (HMG-CoA)[2][3]

In Vitro Hymeglusin inhibits dengue type 2 (DEN-2) New Guinea C (NGC) live virus replication in K562 cells. The therapeutic index (CC50/IC50) of Hymeglusin is 11. The EC50 of Hymeglusin in K562 cells is 4.5 μM[1].
In Vivo At a dose of 25 mg/kg, hymeglusin inhibits cholesterol biosynthesis in rats by 45 %[2].
References

[1]. Rothwell C, et al. Cholesterol biosynthesis modulation regulates dengue viral replication. Virology. 2009 Jun 20;389(1-2):18-19.

[2]. Greenspan MD, et al. Inhibition of hydroxymethylglutaryl-coenzyme A synthase by L-659,699. Proc Natl Acad Sci U S A. 1987 Nov;84(21):7488-92.

[3]. Tomoda H, et al. Binding site for fungal beta-lactone hymeglusin on cytosolic 3-hydroxy-3-methylglutaryl coenzyme A synthase. Biochim Biophys Acta. 2004 Feb 27;1636(1):22-8.

Density 1.1±0.1 g/cm3
Boiling Point 516.6±15.0 °C at 760 mmHg
Molecular Formula C18H28O5
Molecular Weight 324.412
Flash Point 181.3±13.9 °C
Exact Mass 324.193665
PSA 83.83000
LogP 2.59
Vapour Pressure 0.0±3.0 mmHg at 25°C
Index of Refraction 1.510

CHEMICAL IDENTIFICATION

RTECS NUMBER :
YQ1170000
CHEMICAL NAME :
2,4-Undecadienoic acid, 11-(3-(hydroxymethyl)-4-oxo-2-oxetanyl)-3,5,7-trimeth yl-, (2R-(2-alpha(2E,4E,7R*),3-beta))-
CAS REGISTRY NUMBER :
29066-42-0
LAST UPDATED :
199406
DATA ITEMS CITED :
2
MOLECULAR FORMULA :
C18-H28-O5
MOLECULAR WEIGHT :
324.46

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD - Lethal dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
>500 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JANTAJ Journal of Antibiotics. (Japan Antibiotics Research Assoc., 2-20-8 Kamiosaki, Shinagawa-ku, Tokyo, 141, Japan) V.2-5, 1948-52; V.21- 1968- Volume(issue)/page/year: 41,247,1988
TYPE OF TEST :
LD - Lethal dose
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
>100 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JANTAJ Journal of Antibiotics. (Japan Antibiotics Research Assoc., 2-20-8 Kamiosaki, Shinagawa-ku, Tokyo, 141, Japan) V.2-5, 1948-52; V.21- 1968- Volume(issue)/page/year: 41,247,1988
RIDADR NONH for all modes of transport
RTECS YQ1170000
Precursor  2

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