推荐产品
质量水平
描述
RTECS - JX3890000
方案
≥95% (TLC)
表单
solid
制造商/商品名称
Calbiochem®
储存条件
OK to freeze
颜色
white
溶解性
DMSO: 25 mg/mL
运输
ambient
储存温度
−20°C
SMILES字符串
N[C@]([C@@H](O)[C@H](O)C\C=C\CCCCCCC(=O)CCCCCC)(CO)C(=O)O
InChI
1S/C21H39NO6/c1-2-3-4-10-13-17(24)14-11-8-6-5-7-9-12-15-18(25)19(26)21(22,16-23)20(27)28/h9,12,18-19,23,25-26H,2-8,10-11,13-16,22H2,1H3,(H,27,28)/b12-9+/t18-,19+,21+/m1/s1
InChI key
ZZIKIHCNFWXKDY-GNTQXERDSA-N
一般描述
一种有效的免疫抑制剂。比环孢菌素A显示出10至100倍更强的免疫抑制活性。可有效抑制丝氨酸棕榈酰转移酶（SPT；Ki = 280 pM），从而阻断了神经酰胺的合成。破坏黑色素瘤细胞的基质粘附。在IL-2依赖性鼠细胞毒性T淋巴细胞CTLL-2中抑制细胞增殖并诱导凋亡。
生化/生理作用
产物不与ATP竞争。
可逆：否
细胞渗透性：否
靶标Ki：针对丝氨酸棕榈酰转移酶为280 pM
首要靶标
丝氨酸棕榈酰转移酶
丝氨酸棕榈酰转移酶
警告
毒性：有害（C）
重悬
溶解后，等分并冷冻保存（-20°C）。储备溶液在-20°C下可稳定保存至多3个月。
其他说明
Hanada, K., et al. 2000.生物化学。Pharmacol.59, 1211.
Chen, J.K., et al. 1999.Chem. Biol. 6, 221.
Hidari, K.I.P.J., et al. 1996.J. Biol. Chem. 271, 14636.
Nakamura, S., et al. 1996.J. Biol. Chem. 271, 1255.
Mikaye, Y., et al. 1995.Biochem.Biophys.Res. Commun.211, 396.
Fujita, T., et al. 1994.J. Antibiot.47, 208.
Chen, J.K., et al. 1999.Chem. Biol. 6, 221.
Hidari, K.I.P.J., et al. 1996.J. Biol. Chem. 271, 14636.
Nakamura, S., et al. 1996.J. Biol. Chem. 271, 1255.
Mikaye, Y., et al. 1995.Biochem.Biophys.Res. Commun.211, 396.
Fujita, T., et al. 1994.J. Antibiot.47, 208.
法律信息
CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany
警示用语：
Danger
危险声明
危险分类
Acute Tox. 3 Oral
储存分类代码
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
J K Chen et al.
Chemistry & biology, 6(4), 221-235 (1999-04-01)
Myriocin is a natural product that potently induces apoptosis of a murine cytotoxic T lymphocyte cell line (CTLL-2) and inhibits a serine palmitoyltransferase (SPT) activity that has been detected in cell extracts and is thought to initiate sphingolipid biosynthesis. Because
K Hanada et al.
Biochemical pharmacology, 59(10), 1211-1216 (2000-03-29)
In the present study, we demonstrate a model cell system for evaluating the specificity of inhibitors of serine palmitoyltransferase (SPT), the enzyme that catalyzes the first step of sphingolipid biosynthesis. The LY-B strain is a Chinese hamster ovary (CHO) cell
Song Yu et al.
Foods (Basel, Switzerland), 12(13) (2023-07-14)
Human health is seriously threatened by mycotoxin contamination, yet health risk assessments are typically based on just one mycotoxin, potentially excluding the additive or competitive interactions between co-occurring mycotoxins. In this investigation, we evaluated the individual or combined toxicological effects
T Fujita et al.
The Journal of antibiotics, 47(2), 208-215 (1994-02-01)
A potent immunosuppressive activity was found in the culture broth of the fungus Isaria sinclairii (ATCC 24400). The metabolite, ISP-I ((2S,3R,4R)-(E)-2-amino-3,4-dihydroxy-2- hydroxymethyl-14-oxoeicos-6-enoic acid, myriocin = thermozymocidin) suppressed the proliferation of lymphocytes in mouse allogeneic mixed lymphocyte reaction, but had no
Song Yu et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 136, 111080-111080 (2020-01-01)
Fumonisin B1 (FB1) is a mycotoxin, produced by Fusarium verticillioides and Fusarium proliferatum, and a common fungal contaminant of maize worldwide. Its potential health hazard as a natural toxin is well documented in human and domestic animals. However, the molecular
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