(R)-Duloxetine
(R)-Duloxetine ((R)-LY248686) is a neuronal voltage-gated sodium channel blocker with analgesic activity. (R)-Duloxetine blocks Na+ currents with higher affinity for the inactivated state than for the resting state. (R)-Duloxetine alleviates postoperative mechanical allodynia and hyperalgesia. (R)-Duloxetine exerts its effects through a local peripheral mechanism of action. (R)-Duloxetine can be used for research on postoperative (post-incisional) pain.
For research use only. We do not sell to patients.
- CAS No.: 116539-60-7
- Formula: C18H19NOS
- Molecular Weight:297.41
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Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Description
Cellular Effect
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Cell Line
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Type | Value | Description | References |
|---|---|---|---|---|
| GH3 | IC50 |
33.78 μM
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Resting-state block of voltage-gated Na+ currents in rat pituitary GH3 cells measured by whole-cell patch-clamp assay with Na+ currents evoked by a test pulse to +50 mV from a holding potential of −140 mV.
Resting-state block of voltage-gated Na+ currents in rat pituitary GH3 cells measured by whole-cell patch-clamp assay with Na+ currents evoked by a test pulse to +50 mV from a holding potential of −140 mV.
|
26646348 |
| GH3 | IC50 |
5.82 μM
|
Inactivated-state block of voltage-gated Na+ currents in rat pituitary GH3 cells measured by whole-cell patch-clamp assay with a 10-second conditioning pulse to −70 mV applied prior to the test pulse to promote channel inactivation.
Inactivated-state block of voltage-gated Na+ currents in rat pituitary GH3 cells measured by whole-cell patch-clamp assay with a 10-second conditioning pulse to −70 mV applied prior to the test pulse to promote channel inactivation.
|
26646348 |
In Vitro
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
In Vivo
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Sprague-Dawley (male; weight 250-300 g; skin incision plus extension model on dorsothoracic skin)[1]
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Dosage:2 mg (ipsilateral s.c.); 10 mg (i.p.); 10 mg (contralateral s.c.)
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Administration:s.c. (ipsilateral to incision; single injection; 1 hour prior to surgery); i.p. (single injection; 1 hour prior to surgery); s.c. (contralateral to incision; single injection; 1 hour prior to surgery)
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Result:Reduced 4 g von Frey allodynia 5-day AUC to 11% of control at 0.5 cm, 27% of control at 1.0 cm, 41% of control at 2.0 cm, and 46% of control at the contralateral site following 2 mg ipsilateral subcutaneous administration.
Reduced 15 g von Frey hyperalgesia 5-day AUC to 1% of control at 0.5 cm, 11% of control at 1.0 cm, and 65% of control at the contralateral site following 2 mg ipsilateral subcutaneous administration.
Produced analgesic effects on allodynia from time 0 through 5 days at all ipsilateral sites, with contralateral allodynia relief lasting 1 day post-injection after 2 mg ipsilateral subcutaneous administration.
Produced antihyperalgesic effects persisting for 5 days at ipsilateral sites, with responses below baseline at 0.5-1 cm from day 0 to day 3 after 2 mg ipsilateral subcutaneous administration.
Reduced 4 g allodynia 5-day AUC to 31% of control at 0.5 cm, 37% of control at 1.0 cm, 54% of control at 2.0 cm, and 72% of control at the contralateral site following 10 mg intraperitoneal administration.
Reduced 15 g hyperalgesia 5-day AUC to 35% of control at 0.5 cm, 40% of control at 1.0 cm, 48% of control at 2.0 cm, and 52% of control at the contralateral site following 10 mg intraperitoneal administration.
Produced immediate systemic allodynia reduction post-injection following 10 mg intraperitoneal administration.
Produced minimal analgesic effects on allodynia and hyperalgesia at the ipsilateral incision side, with 4 g allodynia AUC values at 89%-105% of control and 15 g hyperalgesia AUC values at 84%-92% of control across 0.5-2.0 cm ipsilateral sites following 10 mg contralateral subcutaneous administration.
Chemical Information
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CAS No. 116539-60-7
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Molecular Weight 297.41
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Formula C18H19NOS
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SMILES
CNCC[C@@H](OC1=CC=CC2=C1C=CC=C2)C3=CC=CS3
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Synonyms
(R)-LY248686
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Keywords
- (R)-Duloxetine
- 116539-60-7
- (R)-LY248686
- Sodium Channel
- local peripheral mechanism of action
- analgesic activity
- rat GH3 cells
- Na+ currents
- neuronal voltage-gated sodium channel blocker
- voltage-gated Na+ channels
- rat postoperative pain model
- postoperative mechanical allodynia
- postincisional pain
- hyperalgesia
- Inhibitor
- inhibitor
- inhibit