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Merck

M5255

Sigma-Aldrich

霉酚酸

from Penicillium brevicompactum, ≥98% (HPLC), powder, IMP dehydrogenase inhibitor

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

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50 MG
$225.00
250 MG
$507.00

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预计发货时间2025年2月17日详情


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50 MG
$225.00
250 MG
$507.00

About This Item

经验公式(希尔记法):
C17H20O6
CAS号:
分子量:
320.34
Beilstein:
1295848
EC號碼:
MDL號碼:
分類程式碼代碼:
12352106
PubChem物質ID:
NACRES:
NA.77

$225.00


预计发货时间2025年2月17日详情


获取大包装报价

产品名称

霉酚酸, ≥98%

生物源

Penicillium brevicompactum

品質等級

化驗

≥98%

顏色

white to yellow-white

mp

<143.0 °C

溶解度

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

作用方式

enzyme | inhibits

起源

Novartis

儲存溫度

2-8°C

SMILES 字串

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 密鑰

HPNSFSBZBAHARI-RUDMXATFSA-N

基因資訊

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應用

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。

特點和優勢

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。

準備報告

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。

訊號詞

Danger

危險分類

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

標靶器官

Immune system

儲存類別代碼

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

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


历史批次信息供参考:

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