CAS
|
339-72-0
|
中文名称
|
L-环丝氨酸
|
英文名称
|
L-Cycloserine
|
别名
|
Levcycloserine;Levcicloserina;Levcycloserinum;(-)-Cycloserine;(S)-Cycloserine;环丝氨酸;(S)-4-Amino-3-isoxazolidone
|
纯度
|
≥98%
|
分子式
|
C3H6N2O2
|
分子量
|
102.09
|
外观(性状)
|
White to off-white Solid
|
储存条件
|
Powder : 2-8℃, 2 years; In solvent(母液): -20℃, 1 month; -80℃, 6 months
|
溶解性
|
Soluble in Water/DMSO ≥5mg/mL
|
MDL
|
MFCD00064324
|
EC
|
EINECS 206-427-0
|
SMILES
|
O=C1NOC[C@@H]1N
|
描述
|
L-cycloserine不可逆地抑制GABA 5'-磷酸吡哆醛氨基转移酶。还可以抑制3-酮二氢鞘氨醇合成酶。(L-cycloserine irreversibly inhibits GABA 5'-phosphate pyridoxal aminotransferase. Also inhibits 3-ketodihydrosphingosine synthase.)
|
靶点
|
3-ketodihydrosphingosine synthetase,GABA pyridoxal 5′-phosphate-dependent aminitransferase
|
通路
|
Others
|
生物活性
|
L-Cycloserine (Levcycloserine, Levcicloserina, Levcycloserinum, (-)-Cycloserine, (S)-Cycloserine) is a potent inhibitor of the sphingolipid pathway via inhibiting 3-ketodihydrosphingosine synthetase.[1-3]
|
In Vitro
|
L-Cycloserine is a potent inhibitor of the first en zyme of the sphingolipid pathway, 3-ketodihydrosphin-gosine (3KDS) synthase (serine palmitoyltransferase) and causes an irreversible inhibition of 3KDS synthase derived from a bacterial source (Bacteroides levii) and from brain and heart microsomes in vitro[3].
|
In Vivo
|
Long-term administration of a low dosage of L-cycloserine subcutaneously to mice results in a significant reduction in the level of brain cerebrosides with little effect on other sphingolipids[3].
|
数据来源文献
|
[1] Williams RD, et al. J Lipid Res. 1987, 28(12):1478-81.
[2] Sundaram KS, et al. Antimicrob Agents Chemother. 1984, 26(2):211-3.
[3] Sundaram KS, et al. Neurochem Res. 1989, 14(3):245-8.
|
规格
|
5mg 10mg 20mg
|
单位
|
瓶
|