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Key Documents

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I3132

Supelco

Indoprofen

analytical standard

Sinónimos:

α-Methyl-p-(1-oxo-2-isoindolinyl)benzeneacetic acid

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About This Item

Fórmula empírica (notación de Hill):
C17H15NO3
Número de CAS:
31842-01-0
Peso molecular:
281.31
EC Number:
250-833-0
MDL number:
MFCD00057144
UNSPSC Code:
41116107
PubChem Substance ID:
329815369
NACRES:
NA.24

grade

analytical standard

Quality Level

200

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

forensics and toxicology
pharmaceutical (small molecule)
veterinary

format

neat

SMILES string

CC(C(O)=O)c1ccc(cc1)N2Cc3ccccc3C2=O

InChI

1S/C17H15NO3/c1-11(17(20)21)12-6-8-14(9-7-12)18-10-13-4-2-3-5-15(13)16(18)19/h2-9,11H,10H2,1H3,(H,20,21)

InChI key

RJMIEHBSYVWVIN-UHFFFAOYSA-N

Gene Information

human ... IL8RA(3577) , PTGS1(5742) , PTGS2(5743)

Application

Indoprofen is a non-steroidal drug, which can show a range of pharmacological properties such as analgesic and anti-inflammatory activities. Its mode of action involves the inhibition of prostaglandin synthesis.
Indoprofen may be used as an analytical reference standard for the quantification of the analyte in biological samples and pharmaceutical formulations using different chromatography techniques.
Indoprofen is a non-steroidal drug, which can show a range of pharmacological properties such as analgesic and anti-inflammatory activities.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms

Skull and crossbonesHealth hazard
GHS06,GHS08

signalword

Danger

hcodes

H301,H351

Hazard Classifications

Acute Tox. 3 Oral - Carc. 2

Storage Class

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

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

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Certificados de análisis (COA)

Lot/Batch Number
127F0834V
127F0834
127F0834

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M Rosin et al.
Journal of clinical periodontology, 32(6), 617-621 (2005-05-11)
The pharmacodynamic properties of ibuprofen are related nearly exclusively to the S(+)enantiomer (dexibuprofen). This study investigated the effect of a 1.5% dexibuprofen mouth rinse in an experimentally induced gingivitis. The trial was a randomized, double-blinded, placebo-controlled, two-period and two-sequence parallel
Mitchell R Lunn et al.
Chemistry & biology, 11(11), 1489-1493 (2004-11-24)
Most patients with the pediatric neurodegenerative disease spinal muscular atrophy have a homozygous deletion of the survival motor neuron 1 (SMN1) gene, but retain one or more copies of the closely related SMN2 gene. The SMN2 gene encodes the same
D Siebler et al.
Arzneimittel-Forschung, 39(6), 659-660 (1989-06-01)
Binding of Racemic Indoprofen and its Enantiomers to Human Serum Albumin. The binding to 2% and 4% human serum albumin (HSA) of (+/-)-indoprofen, (-)-indoprofen, and (+)-indoprofen was examined applying a modified ultrafiltration process. The binding properties to HSA were characterized
B Lund et al.
British journal of clinical pharmacology, 22(6), 721-724 (1986-12-01)
Multiple dosing four times daily for 7 days of indoprofen 200 mg, a non-steroidal anti-inflammatory drug with a short half-life (t1/2), revealed drug accumulation in eight elderly subjects. This indicates a substantially longer t1/2 (11 h) than that reported in
Da-Qing Jin et al.
Pharmacology, biochemistry, and behavior, 89(3), 404-411 (2008-02-26)
Non-steroidal anti-inflammatory drugs (NSAIDs) have been proposed as a therapeutics to reduce the risk of Alzheimer's disease (AD). The present study shows that the peripheral administration of dexibuprofen (S(+)-isomer ibuprofen), which causes less gastric damage and has better anti-inflammatory effects
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Chromatograms

application for HPLC

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