InChI key
XWNJZPKETIWTTF-RIHGSVRJSA-N
InChI
1S/C17H37N7O4.3ClH/c18-7-5-9-21-8-3-4-10-22-15(27)16(28)24-14(26)12-13(25)6-1-2-11-23-17(19)20;;;/h13,16,21,25,28H,1-12,18H2,(H,22,27)(H,24,26)(H4,19,20,23);3*1H/t13-,16-;;;/m0.../s1
biological source
Bacillus laterosporus
assay
>95% (HPLC and TLC)
storage condition
desiccated
solubility
H2O: soluble, acetone: insoluble, ethanol: insoluble, ethyl acetate: insoluble, methanol: soluble
antibiotic activity spectrum
neoplastics
shipped in
wet ice
storage temp.
−20°C
Application
Spergualin trihydrochloride was used to compare the 15-deoxyspergualin, a derivative of spergualin by thin layer chromatography.1
Biochem/physiol Actions
Spergualin is an antibiotic isolated from Bacillus laterosporus that has antibacterial, antitumor, and strong immunosuppressive properties. Spergualin exhibits antitumor activity against transplantable leukemias in mice such as lymphatic leukemia L1210, monocytic leukemia P388, mastocytoma P815, or thymoma EL-4. Spergualin was found effective in inhibiting skin graft rejection, preventing GVHD (Graft-Versus-Host-Disease) in mice recipients of allogeneic bone marrow and spleen cells, and modulating other immunologic diseases.
Spergualin is an antibiotic that posses antibacterial, antitumor, and strong immunosuppressive properties.
Preparation Note
Spergulain is very soluble in water and methanol. It is slighly or not soluble in ethanol, ethyl acetate, acetone cyclohexane, and other organic solvents. Spergualin solutions are unstable at acidic pH (pH <2) and at highly alkaline pH (pH >9). The powder is highly hygroscopic.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Christopher G Evans et al.
Bioorganic & medicinal chemistry letters, 21(9), 2587-2590 (2011-03-23)
Spergualin is a natural product that exhibits immunosuppressive, anti-tumor and anti-bacterial activities. Its derivatives, such as 15-deoxyspergualin (15-DSG), have been clinically approved for acute allograft rejection. However, the reported syntheses are cumbersome (>10 steps) and they suffer from low overall
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