| Identification | Back Directory | [Name]
GOITRINE | [CAS]
1072-93-1 | [Synonyms]
GOITRINE
R-GOITRIN
D-Goitrin
Epigotrin
Epigoitrin
BA-51-090278
R、Sepigoitrin
Goitrine
Epigoitrin
Epigoitrin/(R,S)-goitrin
5-VINYL-2-THIOOXAZOLIDONE
(-)5-VINYL-2-OXAZOLIDINETHIONE
(R)-5-Vinyl-2-oxazolidinethione
(5R)-5-Vinyloxazolidine-2-thione
(5R)-5β-Vinyloxazolidine-2-thione
(R)-5-Ethenyl-2-oxazolidinethione
2-Oxazolidinethione, 5-ethenyl-, (5R)-
Goitrine, 98%, from Isatis indigotica Fortune | [Molecular Formula]
C5H7NOS | [MDL Number]
MFCD01709801 | [MOL File]
1072-93-1.mol | [Molecular Weight]
129.18 |
| Chemical Properties | Back Directory | [Melting point ]
47.5°C | [Boiling point ]
150.6±43.0 °C(Predicted) | [density ]
1.170 (estimate) | [refractive index ]
1.5480 (estimate) | [storage temp. ]
Amber Vial, -20°C Freezer | [solubility ]
DMSO (Slightly), Methanol (Slightly) | [form ]
solid | [pka]
13.34±0.40(Predicted) | [color ]
White to Off-White | [InChI]
InChI=1S/C5H7NOS/c1-2-4-3-6-5(8)7-4/h2,4H,1,3H2,(H,6,8)/t4-/m1/s1 | [InChIKey]
UZQVYLOFLQICCT-SCSAIBSYSA-N | [SMILES]
O1[C@H](C=C)CNC1=S |
| Safety Data | Back Directory | [Safety Statements ]
24/25 | [HS Code ]
29349990 | [Toxicity]
mouse,LD50,unreported,1260mg/kg (1260mg/kg),Journal of Agricultural and Food Chemistry. Vol. 17, Pg. 483, 1969. |
| Hazard Information | Back Directory | [Chemical Properties]
Derived from the root of Isatis indigotica Fort. | [Uses]
Goitrine is a cyclic thiocarbamate that is seen reducing production of thyroid hormones. | [Definition]
ChEBI:(R)-goitrin is a 5-ethenyl-1,3-oxazolidine-2-thione that has R-configuration. It is a constituent of a traditional Chinese herbal medicine, Radix isatidis. It has a role as an antiviral agent and a plant metabolite. It is an enantiomer of a (S)-goitrin. | [Biological Activity]
Epigoitrin is a sulfur containing alkaloid isolated from Isatis indigotica (Ban Lan Gen) th at exhibits antiviralanticancerand antithyroid activities. Epigoitrin significantly decreases the susceptibility of restraint mice to H1N1 influenza virus. Epigoitrin and goitrin appear to show virucidal effect on influenza virus A (H1N1) in vitro and in ovo. | [in vivo]
Epigoitrin (88-176 mg/kg/d; oral administration; once daily; for 7 consecutive days) reduces the susceptibility of mice to influenza virus in a restraint - stress - induced H1N1 virus - infected mouse model, manifested as reduced mortality, attenuated inflammation, and decreased viral replication in the lungs[1].
Epigoitrin (50-100 mg/kg; added to the feed; for 12 weeks) reduces fat deposition, improves glucose tolerance and insulin sensitivity, and increases energy expenditure in a high-fat diet-induced obese mouse model[3]. | Animal Model: | Five-week-old male C57BL/6J mice were fed a high-fat diet to establish an obesity model[3].
| | Dosage: | 50 mg/kg, 100 mg/kg | | Administration: | Added to the feed, continuously administered for 12 weeks | | Result: | Reduced fat deposition in HFD mice.
Reduced adipocyte hypertrophy.
Alleviated hepatic steatosis, as shown by reduced liver lipid droplets and lower liver and serum TG and TC levels.
Had no effect on food intake. |
| Animal Model: | Specific-pathogen-free male Kunming mice (4 weeks of age; 12-15 g) loaded with restraint stress[1] | | Dosage: | 88 mg/kg, 176 mg/kg | | Administration: | Oral administration, once daily, for 7 days | | Result: | Increased the survival rate, prolonged the mean day to death, and reduced the morbidity sign.
Significantly decreased the virus titer in the lungs, reduced the infiltration of inflammatory cells in the lungs, and lowered the levels of TNF-α and IL-1β in bronchoalveolar lavage fluid.
Increased the protein expressions of MAVS, IFN-β, and IFITM3 in the lung tissue, and decreased the protein level of MFN2 and virus nucleoprotein (NP) in stressed mice.
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| [target]
Influenza virus | [storage]
4°C, protect from light |
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| Company Name: |
China Langchem Inc.
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| Telephone: |
0086-21-58956006 |
| Website: |
www.chemicalbook.com/ShowSupplierProductsList19141/0_EN.htm |
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