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Merck
CN

M0883

Sigma-Aldrich

4-Methylumbelliferyl acetate

esterase substrate

别名:

MU-Ac

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About This Item

经验公式(希尔记法):
C12H10O4
CAS号:
分子量:
218.21
Beilstein:
189667
EC 号:
MDL编号:
UNSPSC代码:
12352204
PubChem化学物质编号:
NACRES:
NA.32

质量水平

方案

≥98% (TLC)

表单

powder

mp

149-150 °C (lit.)

溶解性

chloroform: 100 mg/mL, clear, colorless

荧光

λex 312 nm in methanol
λex 360 nm; λem 499 nm (Reaction product)

储存温度

−20°C

SMILES字符串

CC(=O)Oc1ccc2C(C)=CC(=O)Oc2c1

InChI

1S/C12H10O4/c1-7-5-12(14)16-11-6-9(15-8(2)13)3-4-10(7)11/h3-6H,1-2H3

InChI key

HXVZGASCDAGAPS-UHFFFAOYSA-N

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象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Latent blue and red fluorophores based on the trimethyl lock.
Luke D Lavis et al.
Chembiochem : a European journal of chemical biology, 7(8), 1151-1154 (2006-06-07)
Abha Kathuria et al.
Bioorganic & medicinal chemistry, 17(4), 1550-1556 (2009-02-03)
Calreticulin Transacetylase (CRTAase) catalyzes the transfer of acetyl groups from polyphenolic acetates (PAs) to the receptor proteins and modulates their biological activities. CRTAase was conveniently assayed by the irreversible inhibition of cytosolic glutathione S-transferase (GST) by the model acetoxycoumarin, 7,8-diacetoxy-4-methylcoumarin
M L Graber et al.
The American journal of physiology, 250(1 Pt 2), F159-F168 (1986-01-01)
Intracellular pH (pHi) of turtle bladder mucosal cells was studied by the trapped fluorescent indicator technique. Bladders efficiently accumulated and converted 4-methylumbelliferyl acetate to its pH-sensitive derivative 4-methylumbelliferone (4MU). Excited at the pH-indifferent wavelength 334 nm, bladders fluoresced a uniform
H A Berman et al.
Biochemistry, 29(47), 10640-10649 (1990-11-27)
This paper examines covalent reactivity of AchE with respect to cationic and uncharged methylphosphonates and substrates in the absence and presence of cationic ligands selective for the active center and the peripheral anionic site. The organophosphorus inhibitors are enantiomeric alkyl
H G Raj et al.
Bioorganic & medicinal chemistry, 9(5), 1085-1089 (2001-05-30)
Our earlier work established a convenient assay procedure for acetoxycoumarin (AC): protein transacetylase (TA) by indirectly quantifying the activity of glutathione (GSH)-S-transferase (GST), the extent of inhibition of GST under the conditions of the assay represented TA activity. In this

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