Substance
ID:184312
Names and Identifiers
IUPAC Traditional name
(+)-cycloserine
IUPAC name
(4S)-4-amino-1,2-oxazolidin-3-one
Synonyms
环丝氨酸(S)-4-Amino-3-isoxazolidoneL-Cycloserine
Registration numbers
EC Number
CAS Number
Beilstein Number
MDL Number
PubChem SID
Properties
Physical Property
Solubility
H2O: soluble50 mg/mg protein
Safety Information
RTECS
NY2976000
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Storage Temperature
-20°C
German water hazard class
2
Molecule Details
包装
10, 25, 100 mg in poly bottle
250 mg in poly tube
Biochem/physiol Actions
Blocks sphingosine biosynthesis by inhibition of ketosphinganine synthetase. Cytotoxicity toward neuroblastoma and medulloblastoma cells mediated by suppression of ganglioside synthesis.1
L-cycloserine is a potent inhibitor of serine palmitoyltransferase, the first step of sphingolipid synthesis.
10, 25, 100 mg in poly bottle
250 mg in poly tube
Biochem/physiol Actions
Blocks sphingosine biosynthesis by inhibition of ketosphinganine synthetase. Cytotoxicity toward neuroblastoma and medulloblastoma cells mediated by suppression of ganglioside synthesis.1
L-cycloserine is a potent inhibitor of serine palmitoyltransferase, the first step of sphingolipid synthesis.
Molecular Spectra
No Data Available
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References
No Data Available
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