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68899

Supelco

Ibuprofen acyl-β-D-glucuronide

analytical standard

Synonym(s):

Ibuprofen glucuronide

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About This Item

Empirical Formula (Hill Notation):
C19H26O8
CAS Number:
115075-59-7
Molecular Weight:
382.40
MDL number:
MFCD00871942
UNSPSC Code:
41116107
PubChem Substance ID:
329761208
NACRES:
NA.24

grade

analytical standard

Quality Level

100

Assay

≥92% (HPLC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

forensics and toxicology
pharmaceutical (small molecule)

format

neat

storage temp.

−20°C

SMILES string

CC(C)Cc1ccc(cc1)C(C)C(=O)O[C@@H]2O[C@@H]([C@@H](O)[C@H](O)[C@H]2O)C(O)=O

InChI

1S/C19H26O8/c1-9(2)8-11-4-6-12(7-5-11)10(3)18(25)27-19-15(22)13(20)14(21)16(26-19)17(23)24/h4-7,9-10,13-16,19-22H,8H2,1-3H3,(H,23,24)/t10?,13-,14-,15+,16-,19-/m0/s1

InChI key

ABOLXXZAJIAUGR-JPMMFUSZSA-N

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL7362
BCCL8709
BCCG2533
BCCC9070
BCCB5816

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M Castillo et al.
Clinical pharmacology and therapeutics, 57(6), 636-644 (1995-06-01)
Ibuprofen is an over-the-counter nonsteroidal anti-inflammatory drug with a low incidence of severe adverse reactions. It is metabolized by oxidation to carboxyibuprofen and hydroxyibuprofen and by conjugation to an acyl glucuronide. In vitro studies have indicated that ibuprofen glucuronide is
Masahiro Iwaki et al.
Biological & pharmaceutical bulletin, 40(6), 926-931 (2017-06-02)
Combination therapy of non-steroidal anti-inflammatory drugs (NSAIDs) and methotrexate (MTX) sometimes triggers adverse effects, such as liver injury, renal failure, gastrointestinal disorders, and myelosuppression, owing to the reduction of MTX clearance. Previous reports have suggested that NSAIDs inhibit renal MTX
Robert W Smith et al.
Journal of chromatography. A, 1278, 76-81 (2013-01-23)
The incorporation of a chip-based high field asymmetric waveform ion mobility spectrometry (FAIMS) separation in the ultra (high)-performance liquid chromatography-high resolution mass spectrometry (UHPLC-HRMS) determination of the (R/S) ibuprofen 1-β-O-acyl glucuronide metabolite in urine is reported. UHPLC-FAIMS-HRMS reduced matrix chemical
Stephen J Vanderhoeven et al.
Journal of pharmaceutical and biomedical analysis, 41(3), 1002-1006 (2006-02-18)
The products arising from the intra-molecular acyl migration reactions of drug ester glucuronides can be reactive towards cellular proteins and have been proposed to cause toxic side effects. The relative reactivity of a range of drug and model glucuronides have
Atsushi Kawase et al.
The Journal of pharmacology and experimental therapeutics, 356(2), 366-374 (2015-12-15)
Combined administration of methotrexate (MTX) and nonsteroidal anti-inflammatory drugs (NSAIDs) can result in a decreased systemic clearance of MTX. To date, inhibition of renal uptake via organic anion transporters and efflux via multidrug resistance-associated protein (MRPs) by NSAIDs has been
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