1. GPCR/G Protein Neuronal Signaling
  2. Opioid Receptor
  3. SR-16435

SR-16435 is a nociceptin/orphanin FQ (NOP)/μ-opioid receptor partial agonist, with high binding affinity (NOP receptor Ki=7.49; μ-Opioid receptor Ki=2.70). SR-16435 can relieve pain.

For research use only. We do not sell to patients.

SR-16435 Chemical Structure

SR-16435 Chemical Structure

CAS No. : 857262-16-9

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Description

SR-16435 is a nociceptin/orphanin FQ (NOP)/μ-opioid receptor partial agonist, with high binding affinity (NOP receptor Ki=7.49; μ-Opioid receptor Ki=2.70). SR-16435 can relieve pain[1].

IC50 & Target[1]

NOP receptor

7.49 (Ki)

μ-opioid

2.70 (Ki)

κ-opioid

219.47 (Ki)

In Vivo

SR 16435 (10, 30 mg/kg; s.c.; single-dose) produces dose-dependent increase in tail-flick latency and induces antinociception[1].
SR 16435 (10, 30 mg/kg; s.c. once daily for 9 days) produces an increase in tail-lick latency across days, induces conditioned place preference, and decreases global activity[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: 20 to 25 g male ICR mice[1]
Dosage: 10, 30 mg/kg
Administration: s.c. for single-dose
Result: Produced dose-dependent increase in tail-flick latency and induced antinociception.
Animal Model: 20 to 25 g male ICR mice[1]
Dosage: 10, 30 mg/kg
Administration: s.c. once daily for 9 days
Result: Produced an increase in tail-lick latency across days, induced conditioned place preference, and decreased global activity.
Molecular Weight

338.49

Formula

C22H30N2O

CAS No.
SMILES

O=C1N(C2CCN(C3C4CCCC3CCC4)CC2)C5=C(C=CC=C5)C1

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
References
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SR-16435
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HY-122681
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