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(R)-(-)-IBUPROFEN

(R)-(-)-IBUPROFEN

CAS: 51146-57-7

Molecular Formula: C13H18O2

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(R)-(-)-IBUPROFEN - Names and Identifiers

Name (R)-(-)-IBUPROFEN
Synonyms l-Ibuprofen
levibuprofen
(R)-IBUPROFEN
(-)-Ibuprophen
(R)-(-)-IBUPROFEN
(R)-2-(4-Isobutylphenyl)propanoic acid
(R)-(-)-2-(4-ISOBUTYLPHENYL)-PROPIONIC ACID
Benzeneacetic acid, α-methyl-4-(2-methylpropyl)-, (R)-
Benzeneacetic acid, α-methyl-4-(2-methylpropyl)-, (αR)-
CAS 51146-57-7

(R)-(-)-IBUPROFEN - Physico-chemical Properties

Molecular FormulaC13H18O2
Molar Mass206.28
Density1.0176 (rough estimate)
Melting Point41-42°C
Boling Point305.14°C (rough estimate)
Water Solubility369.3mg/L(25 ºC)
Solubility Soluble in methanol, 0.1 M NaOH, dichloromethane, and ethyl acetate.
AppearanceShape White crystalline powder, color Colourless to Pale Beige Oil
pKa4.41±0.10(Predicted)
Storage ConditionSealed in dry,2-8°C
Refractive Index1.5290 (estimate)
MDLMFCD00069290
Physical and Chemical PropertiesBioactive (R)-(-)-Ibuprofen is a Ibuprofen R-type isomer, which has no effect on COX and can inhibit the activation of NF-κB. (R)-(-)-Ibuprofen has anti-inflammatory and analgesic effects.
UseUse Ibuprofen is a non-steroidal anti-inflammatory drug (NSAID); the activity is mainly present in the (S)-isomer.

(R)-(-)-IBUPROFEN - Risk and Safety

Safety Description24/25 - Avoid contact with skin and eyes.
HS Code29155090

(R)-(-)-IBUPROFEN - Introduction

(R)-Ibuprofen are ibuprofen low-activity enantiomers.
Last Update:2022-10-16 17:30:56

(R)-(-)-IBUPROFEN - Nature

Solubility Chloroform (Slightly), Ethanol (Slightly), Methanol (Slightly)
Last Update:2024-04-10 22:29:15

(R)-(-)-IBUPROFEN - Uses and synthesis methods

Target

NF-κ B

in vitro studies

(R)-(-)-Ibuprofen is the R enantiomer of Ibuprofen, with no inhibitory effect on COX, but is involved in pathways of lipid metabolism and is incorporated into triglycerides along with endogenous fatty acids. (R)-(-)-Ibuprofen (1 μM) significantly reduces NF-κ B activation and completely prevents NF-κ B induction at 10 μM. (R)-(-)-Ibuprofen inhibits NF-κ B luciferase activity with an IC 50 of 121.8 μM, weaker than that of S( )-ibuprofen (IC 50 , 61.7 μM). Furthermore, (R)-(-)-Ibuprofen (10 mM) has no effect on HSF.

Last Update:2024-04-10 22:29:15
(R)-(-)-IBUPROFEN
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(R)-(-)-IBUPROFEN
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