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Olcegepant

SKU: orb1309304

Description

Olcegepant (BIBN-4096) is a potent and highly selective small-molecule antagonist of the human CGRP1 receptor, exhibiting sub-nanomolar affinity (Ki = 14.4 pM). It is widely used in migraine research to investigate CGRP receptor function in both in vitro binding assays and in vivo animal models of neurogenic inflammation and vasodilation.

Research Area

Neuroscience, Pharmacology & Drug Discovery

Images & Validation

Key Properties

CAS Number204697-65-4
MW869.65
Purity98.16% (May vary between batches)
FormulaC38H47Br2N9O5
SMILESO=C1N(CC=2C(N1)=CC=CC2)C3CCN(C(N[C@H](CC4=CC(Br)=C(O)C(Br)=C4)C(N[C@H](C(=O)N5CCN(CC5)C=6C=CN=CC6)CCCCN)=O)=O)CC3
TargetCGRP Receptor
SolubilityDMSO:23.81 mg/mL (27.38 mM);10% DMSO+40% PEG300+5% Tween 80+45% Saline:2 mg/mL (2.3 mM)

Bioactivity

Target IC50
CGRP (human):14.4 pM (ki)|CGRP1:0.03 nM
In Vivo
Pre-treatment with Olcegepant (900 μg/kg) inhibits capsaicin-induced Fos expression in the spinal trigeminal nucleus by 57%, without altering phosphorylated extracellular signal-regulated kinase expression in the trigeminal ganglion. Olcegepant (1-30 μg/kg, i.v.) suppresses CGRP effects on facial blood flow in marmosets and significantly reduces mechanical allodynia in CCI-ION rats (0.3-0.9 mg/kg, i.v.). Additionally, Olcegepant (0.6 mg/kg, i.v.) decreases c-Fos immunolabeled cells and ATF3 transcript upregulation, but not interleukin-6, in the trigeminal ganglion of CCI-ION rats .
In Vitro
Olcegepant exhibits exceptional efficacy at primate CGRP receptors, demonstrating a high affinity (Ki) of 14.4±6.3 (n=4) pM for human CGRP receptors, surpassing that of the endogenous ligand CGRP and demonstrating a 150-fold greater affinity than the peptidic antagonist CGRP8-37. It competitively antagonizes CGRP-induced concentration-dependent relaxation, effectively reversing CGRP-mediated vasodilation in human cerebral vessels and inhibiting neurogenic vasodilation in a surrogate animal model for migraine pathophysiology. This suggests that Olcegepant, acting as a CGRP receptor antagonist, may be a potential novel abortive treatment for migraines. Its competitive antagonism has also been confirmed in SK-N-MC cells, with its effects observed in isolated human cerebral, coronary, and omental arteries using sensitive myograph techniques.

Storage & Handling

Storage-20°C
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

BIBN 4096, BIBN 4096BS, BIBN4096, BIBN-4096, Calcitonin gene-related peptide receptor, CGRP1, CGRPReceptor, CGRP Receptor, Olcegepant, inhibit, Inhibitor, hCGRP

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Quality Guarantee

Quality Guarantee

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Key Properties

No computed properties available.

Protocol Information

Available Sizes

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1 mg
$ 80.00
5 mg
$ 140.00
10 mg
$ 180.00
1 ml x 10 mM (in DMSO)
$ 240.00
25 mg
$ 280.00
100 mg
$ 560.00
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