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90101

Ampliflu™ Red

suitable for fluorescence, ≥98.0% (HPLC)

Synonym(s):

10-Acetyl-3,7-dihydroxyphenoxazine

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About This Item

Empirical Formula (Hill Notation):
C14H11NO4
CAS Number:
119171-73-2
Molecular Weight:
257.24
NACRES:
NA.32
PubChem Substance ID:
329769846
UNSPSC Code:
12352108
MDL number:
MFCD00467861
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Quality Level

100

assay

≥98.0% (HPLC)

form

powder

mol wt

257.24 g/mol

concentration

90-100 % (w/w) (Ampliflu Red)

color

slightly brown-red, white to slightly brown

solubility

water: slightly soluble at 20 °C

fluorescence

λex 571 nm; λem 585 nm in DMSO

suitability

suitable for fluorescence

storage temp.

2-8°C

SMILES string

CC(=O)N1c2ccc(O)cc2Oc3cc(O)ccc13

InChI

1S/C14H11NO4/c1-8(16)15-11-4-2-9(17)6-13(11)19-14-7-10(18)3-5-12(14)15/h2-7,17-18H,1H3

InChI key

PKYCWFICOKSIHZ-UHFFFAOYSA-N

Related Categories

Application

Ampliflu™ Red has been used to study mitochondrial abnormalities and oxidative stress related to Parkinson’s Disease. Ampliflu™ Red assay was suitable as an alternative indicator assay for detecting the inhibition of hTPO (human thyroid peroxidase) activity. Phospholipase D, an essential cellular process ingredient, used Ampliflu™ Red (10-Acetyl-3,7-dihydroxyphenoxazine) to determine its activity.Ampliflu™ Red is used for the following applications:
  • Quantification of inflammatory mediators
  • Determination of free and esterified cholesterol contents
  • Evaluation of compounds as substrates for GABA-AT compounds

Legal Information

Ampliflu is a trademark of Sigma-Aldrich Co. LLC

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN7829
BCCL4452
BCCM5952
BCCK0843
BCCH1284

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Barae Jomaa et al.
ALTEX, 32(3), 191-200 (2015-03-31)
A simple and rapid luminometric assay for the detection of chemical inhibitors of human thyroid peroxidase (hTPO) activity was developed and validated with 10 model compounds. hTPO was derived from the human thyroid follicular cell line Nthy-ori 3-1 and its
Maria Luisa Di Paolo et al.
Journal of enzyme inhibition and medicinal chemistry, 34(1), 740-752 (2019-03-05)
Fourteen polyamine analogues, asymmetric or symmetric substituted spermine (1-9) or methoctramine (10-14) analogues, were evaluated as potential inhibitors or substrates of two enzymes of the polyamine catabolic pathway, spermine oxidase (SMOX) and acetylpolyamine oxidase (PAOX). Compound 2 turned out to
Yu Ji et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 24(63), 16865-16872 (2018-08-29)
Cetyl-trimethylammonium bromide (CTAB) is a widely used cationic surfactant that is biodegradable in nature. CTAB biodegradation requires hydroxylation in the first step, which is rate-limiting and crucial for solubility in water. In this study, the OmniChange multi-site mutagenesis method was
Thais Soprani Ayala et al.
Scientific reports, 9(1), 11447-11447 (2019-08-09)
Macrophages may be a crucial aspect of diabetic complications associated with the inflammatory response. In this study, we examined how hyperglycaemia, a common aspect of diabetes, modulates bone marrow-derived macrophages (BMDMs) under an inflammatory stimulus. To perform this study, BMDMs
Kazuo Sugiyama et al.
PloS one, 9(4), e94460-e94460 (2014-04-11)
Most of experiments for HCV infection have been done using lytic infection systems, in which HCV-infected cells inevitably die. Here, to elucidate metabolic alteration in HCV-infected cells in a more stable condition, we established an HCV-persistently-infected cell line, designated as
View All Related Papers

Global Trade Item Number

SKUGTIN
90101-1EA-KC-F04061823359610
90101-0.515MG-F04061832533650
90101-1MG-KC-F04061823359627
90101-5MG-F04061835183944

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