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2-[1-(2-cyclopropylphenoxy)ethyl]-4,5-dihydro-1H-imidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1197813-07-2

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1197813-07-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1197813-07-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,7,8,1 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1197813-07:
(9*1)+(8*1)+(7*9)+(6*7)+(5*8)+(4*1)+(3*3)+(2*0)+(1*7)=182
182 % 10 = 2
So 1197813-07-2 is a valid CAS Registry Number.

1197813-07-2Downstream Products

1197813-07-2Relevant academic research and scientific papers

Synergic stimulation of serotonin 5-HT1A receptor and α2-adrenoceptors for neuropathic pain relief: Preclinical effects of 2-substituted imidazoline derivatives

Di Cesare Mannelli, Lorenzo,Ghelardini, Carla,Micheli, Laura,Del Bello, Fabio,Giannella, Mario,Piergentili, Alessandro,Pigini, Maria,Quaglia, Wilma

, p. 128 - 133 (2017)

Neuropathic pain affects millions of people causing disability and impairing quality of life. Commonly used analgesics are generally characterized by limited therapeutic outcomes. The serotonin 5‐HT1A receptor and the α2 adrenergic receptors are involved in central nociceptive mechanisms with a pivotal role in the inhibitory descending pain pathway. Since their stimulation may modulate the nervous signaling altered by neuropathies, the purpose of the present research is the study of the combined activation of 5‐HT1A and α2 receptors by rationally designed imidazoline ligands ((S)-(-)-1 and 2–5) in a rat model of neuropathic pain (chronic constriction injury - CCI). On day 14 after nerve damage, the acute administration per os (p.o.) of low doses of (S)-(-)-1 (0.1–1?mg/kg) was able to significantly increase the pain threshold to mechanical noxious stimuli for more than 1?h. (S)-(-)-1 efficacy was confirmed by the decrease of spontaneous pain evaluated as hind limb weight bearing alterations. The clinically-used compound gabapentin (100?mg/kg p.o.) induced a pain relieving effect similar to (S)-(-)-1 administered at 100 fold lower dose. In the same model, the selected analogues, compounds 2–5 (1?mg/kg p.o.) were effective 30?min after administration. In particular, 5 fully reverted the CCI-induced hypersensitivity. The pain relieving activity of 5 was significantly prevented by the selective 5-HT1A receptor antagonist WAY 100635 (1?mg/kg intraperitoneally, i.p.) and, at a lesser extent, by the α2 antagonist yohimbine (3?mg/kg i.p.). A novel pharmacodynamic approach to the treatment of neuropathic pain is presented.

Might adrenergic α2C-agonists/α2A- antagonists become novel therapeutic tools for pain treatment with morphine?

Cardinaletti, Claudia,Mattioli, Laura,Ghelfi, Francesca,Del Bello, Fabio,Giannella, Mario,Bruzzone, Ariana,Paris, Hervé,Perfumi, Marina,Piergentili, Alessandro,Quaglia, Wilma,Pigini, Maria

experimental part, p. 7319 - 7322 (2010/09/07)

The imidazoline nucleus linked in position 2 via an oxyethylene bridge to a phenyl ring carrying an ortho substituent of moderate steric bulk provided α2-adrenergic (AR) ligands endowed with significant α2C- agonism/α2A-antagonism. S

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