| Identification | Back Directory | [Name]
RO 65-6570 HYDROCHLORIDE | [CAS]
228246-34-2 | [Synonyms]
RO 65-6570 HYDROCHLORIDE
Ro 65-6570 Hydrochloride >=98% (HPLC) | [Molecular Formula]
C25H26ClN3O | [MDL Number]
MFCD31697736 | [MOL File]
228246-34-2.mol | [Molecular Weight]
419.95 |
| Chemical Properties | Back Directory | [storage temp. ]
2-8°C | [solubility ]
DMSO: 2mg/mL, clear | [form ]
powder | [color ]
white to beige | [InChIKey]
CTPVGIUCSWWLNA-UHFFFAOYSA-N | [SMILES]
O=C1NCN(C2=CC=CC=C2)C13CCN(C4CC5=C6C4=CC=CC6=CC=C5)CC3.Cl |
| Hazard Information | Back Directory | [Uses]
GRT2932Q is a nonpeptidic opioid receptor-like 1 (ORL1)
agonist[1]. | [Biochem/physiol Actions]
Ro 65-6570 is a nonpeptidic, high-affinity (Ki = 0.52 against 0.1 nM OFQ for binding human ORL1) nociceptin/orphanin FQ (N/OFQ) receptor ORL-1 (KOR-3, NOP) agonist (EC50 = 40 nM by GTPγS binding assay; IC50 = 0.28 nM against 1 μM forskolin-stimulated cellular cAMP accumulation) with good selectivity over opioid receptors μ, k, δ (Ki = 5.9, 26, 250 nM against 1.5 nM naloxone, 3 nM naloxone, 0.3 nM [Ile5,6]-deltorphin II for binding respective receptors), dopamine and serotonin receptors (Ki = 520 nM/D2, 1210 nM/D3,350 nM/D4.4; Ki ≥1 μM for 5HT 1Dα, 2A, 2C, 6, 7). Ro 65-6570 elicits ORL1-dependent anxiolytic-like effects in rats in vivo (0.32-3.2 mg/kg i.p.; elevated plus maze) without affecting spontaneous locomotion. Unlike OFQ, Ro 65-6570 does not affect cocaine-induced conditioned place preference (CPP) in rats. | [References]
[1] Faulhammer
D, et al. Biostable aptamers with antagonistic properties to the neuropeptide
nociceptin/orphanin FQ. RNA. 2004 Mar;10(3):516-27. DOI:10.1261/rna.5186504 |
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