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文件

安全信息

M5255

Sigma-Aldrich

霉酚酸

≥98%

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别名:
6-（1,3-二氢-7-羟基-5-甲氧基-4-甲基-1-氧代异苯并呋喃-6-基）-4-甲基-4-己酸, 6-（4-羟基-6-甲氧基-7-甲基-3-氧代-5-酞酰）-4-甲基-4-己烯酸, NSC 129185
经验公式（希尔记法）:
C17H20O6
CAS号:
24280-93-1
分子量:
320.34
Beilstein:
1295848
EC 号:
246-119-3
MDL编号:
MFCD00036814
UNSPSC代码:
12352106
PubChem化学物质编号:
24896987
NACRES:
NA.77

生物来源

Penicillium brevicompactum

质量水平

300

检测方案

≥98%

颜色

white to yellow-white

mp

<143.0 °C

溶解性

methanol: 49.00-51.00 mg/mL, clear, colorless to faintly yellow

作用机制

enzyme | inhibits

创始人

Novartis

储存温度

2-8°C

SMILES字符串

COc1c(C)c2COC(=O)c2c(O)c1C\C=C(/C)CCC(O)=O

InChI

1S/C17H20O6/c1-9(5-7-13(18)19)4-6-11-15(20)14-12(8-23-17(14)21)10(2)16(11)22-3/h4,20H,5-8H2,1-3H3,(H,18,19)/b9-4+

InChI key

HPNSFSBZBAHARI-RUDMXATFSA-N

基因信息

human ... IMPDH1(3614) , IMPDH2(3615)

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应用

霉酚酸 (MPA) 由 青霉 (Penicillum brevi-compactum) 产生 ，是一种选择性的肌苷一磷酸脱氢酶抑制剂，从而抑制 T、B 淋巴细胞的 DNA 合成。在人淋巴和单核细胞系中，它还被证明可作为免疫抑制剂，以及单核细胞分化和凋亡的诱导剂。作为选择剂，MPA 用于表达大肠杆菌黄嘌呤-鸟嘌呤磷酸核糖转移酶基因的转染动物细胞，推荐使用 25μg/mL。

生化/生理作用

作用方式：本品通过抑制细胞因子诱导的一氧化氮生成，抑制嘌呤核苷酸的早期生物合成，并作为 IMP 脱氢酶的特异性抑制剂发挥作用。

特点和优势

该化合物由 Novartis 开发。要浏览其他制药公司开发的化合物列表批准的药物/候选药物的列表，请 点击这里 。

注意

供应后，本品应在 2-8°C 干燥条件下储存，适当储存时可保持稳定 5 年。

制备说明

麦考酚酸可溶于 50 mg/mL 甲醇，产生无色至淡黄色溶液，以及氯仿、二氯甲烷、乙醇和 1 N 氢氧化钠溶液。复溶后，建议通过 0.22 μm 过滤器灭菌m 孔径过滤器，分装，-20°C 冷冻。

警示用语：

Danger

危险分类

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Muta. 2 - Repr. 1B - STOT RE 1 Oral

靶器官

Immune system

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

法规信息

监管及禁止进口产品

分析证书(COA)

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