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M1633

Sigma-Aldrich

4-Methylumbelliferyl β-D-galactopyranoside

fluorogenic, ≥99% (TLC), powder

Sinónimos:

MUG, MUGA

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About This Item

Fórmula empírica (notación de Hill):
C16H18O8
Número de CAS:
6160-78-7
Peso molecular:
338.31
Beilstein/REAXYS Number:
94673
EC Number:
228-185-5
MDL number:
MFCD00036773
UNSPSC Code:
12352204
PubChem Substance ID:
24896676
NACRES:
NA.32

product name

4-Methylumbelliferyl β-D-galactopyranoside, ≥99% (TLC)

assay

≥99% (TLC)

form

powder

solubility

pyridine: 10 mg/mL, clear, colorless to faintly yellow

storage temp.

−20°C

SMILES string

CC1=CC(=O)Oc2cc(O[C@@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)ccc12

InChI

1S/C16H18O8/c1-7-4-12(18)23-10-5-8(2-3-9(7)10)22-16-15(21)14(20)13(19)11(6-17)24-16/h2-5,11,13-17,19-21H,6H2,1H3/t11-,13+,14+,15-,16-/m1/s1

InChI key

YUDPTGPSBJVHCN-DZQJYWQESA-N

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General description

4-Methylumbelliferyl β-D-galactopyranoside (MUG) is a UV-absorbing dye that serves as a fluorescent substrate for β-galactosidase in a planar yeast estrogen screen (pYES) for the detection of estrogen active compounds.

Application

4-Methylumbelliferyl β-D-galactopyranoside has been used as a substrate in β-galactosidase activity assay.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Mucopolysaccharidoses (MPS) are genetic disorders that affect up to 1 in 25,000 births. They are caused by dysfunctions of lysosomal hydrolases that degrade glycosaminoglycans (GAGs) which accumulate in cells, damaging their proper functioning. There are 7 types of MPS, distinguished
Yousuke Takaoka et al.
Nature communications, 9(1), 3654-3654 (2018-09-09)
The phytohormone 7-iso-(+)-jasmonoyl-L-isoleucine (JA-Ile) mediates plant defense responses against herbivore and pathogen attack, and thus increases plant resistance against foreign invaders. However, JA-Ile also causes growth inhibition; and therefore JA-Ile is not a practical chemical regulator of plant defense responses.
Mithila Ferdous et al.
Journal of clinical microbiology, 53(11), 3530-3538 (2015-08-28)
The ability of Escherichia coli O157:H7 to induce cellular damage leading to disease in humans is related to numerous virulence factors, most notably the stx gene, encoding Shiga toxin (Stx) and carried by a bacteriophage. Loss of the Stx-encoding bacteriophage
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Amanda R Luu et al.
The Journal of biological chemistry, 295(39), 13556-13569 (2020-07-31)
Mutations in the galactosidase β 1 (GLB1) gene cause lysosomal β-galactosidase (β-Gal) deficiency and clinical onset of the neurodegenerative lysosomal storage disease, GM1 gangliosidosis. β-Gal and neuraminidase 1 (NEU1) form a multienzyme complex in lysosomes along with the molecular chaperone
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