Details
Stereochemistry | RACEMIC |
Molecular Formula | C17H27NO2 |
Molecular Weight | 277.4018 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)N[C@H](C)[C@@H](O)COC1=C2CCCC2=C(C)C=C1
InChI
InChIKey=VFIDUCMKNJIJTO-CJNGLKHVSA-N
InChI=1S/C17H27NO2/c1-11(2)18-13(4)16(19)10-20-17-9-8-12(3)14-6-5-7-15(14)17/h8-9,11,13,16,18-19H,5-7,10H2,1-4H3/t13-,16+/m1/s1
Molecular Formula | C17H27NO2 |
Molecular Weight | 277.4018 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 2 / 2 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/27602067https://www.ncbi.nlm.nih.gov/pubmed/15908513 | https://www.ncbi.nlm.nih.gov/pubmed/18652905 | https://www.ncbi.nlm.nih.gov/pubmed/2900871 | https://www.ncbi.nlm.nih.gov/pubmed/2570461 | https://www.ncbi.nlm.nih.gov/pubmed/19470879 | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1987085/ http://onlinelibrary.wiley.com/doi/10.1111/j.1365-2125.1988.tb03326.x/pdfCurator's Comment: The description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/28064316 | https://www.ncbi.nlm.nih.gov/pubmed/26762097 | https://www.ncbi.nlm.nih.gov/pubmed/3320184 | https://www.ncbi.nlm.nih.gov/pubmed/2908820
Sources: https://www.ncbi.nlm.nih.gov/pubmed/27602067https://www.ncbi.nlm.nih.gov/pubmed/15908513 | https://www.ncbi.nlm.nih.gov/pubmed/18652905 | https://www.ncbi.nlm.nih.gov/pubmed/2900871 | https://www.ncbi.nlm.nih.gov/pubmed/2570461 | https://www.ncbi.nlm.nih.gov/pubmed/19470879 | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1987085/ http://onlinelibrary.wiley.com/doi/10.1111/j.1365-2125.1988.tb03326.x/pdf
Curator's Comment: The description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/28064316 | https://www.ncbi.nlm.nih.gov/pubmed/26762097 | https://www.ncbi.nlm.nih.gov/pubmed/3320184 | https://www.ncbi.nlm.nih.gov/pubmed/2908820
ICI-118,551 is a selective subtype β2 adrenergic receptor (adrenoreceptor) antagonist. ICI-118,551 binds to the β2 subtype with at least 100 times greater affinity than to other subtypes of the beta adrenoceptor β1 or β3. Pharmacological experiments proved that the right shift of the norepinephrine dose-response curve by ICI-118,551 was mediated via a beta(2)-adrenoceptor/G(i/o) protein-dependent pathway enhancing NO production in the endothelium. These results were corroborated in beta-adrenoceptor and endothelial NO synthase knockout mice where ICI had no effect. ICI-118,551 increased vascular lumen diameter in lung sections and reduced pulmonary arterial pressure under normoxia and under hypoxia in the isolated perfused lung model. These effects were found to be physiologically relevant, because ICI-118,551 specifically decreased pulmonary but not systemic blood pressure in vivo. Thus, it has been suggested that ICI-118,551 is a pulmonary arterial-specific vasorelaxant and might be a potential novel therapeutic agent for the treatment of pulmonary arterial hypertension. It was also demonstrated that systemic topical administration of ICI 118,551 results in decreased intraocular pressure in both eyes of rabbits, indicating that at least part of the ocular hypotensive effect of topical ICI 118,551 is mediated through systemic absorption. However, ICI 118,551 did not lower blood pressure in hypertensive patients known to respond to therapy with atenolol or propranolol.
CNS Activity
Sources: https://www.ncbi.nlm.nih.gov/pubmed/3320184http://hyper.ahajournals.org/content/54/1/157.long | doi:10.1093/bja/ael238 | Retrieved from https://academic.oup.com/bja/article/97/5/617/321808/2-Adrenergic-antagonist-inhibits-cerebral-cortical
Curator's Comment: Known to be CNS penetrant in rats, guinea pig. Human data not available
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL210 Sources: https://www.ncbi.nlm.nih.gov/pubmed/23614528 |
1.2 nM [IC50] | ||
Target ID: CHEMBL213 Sources: https://www.ncbi.nlm.nih.gov/pubmed/23614528 |
240.0 nM [Kd] | ||
Target ID: CHEMBL1867 Sources: https://www.ncbi.nlm.nih.gov/pubmed/23582449 |
0.5 nM [IC50] | ||
Target ID: P07550|||Q53GA6|||Q9UCZ3 Gene ID: 154.0 Gene Symbol: ADRB2 Target Organism: Homo sapiens (Human) |
2.0 nM [Ki] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Unknown Approved UseUnknown |
|||
Primary | Unknown Approved UseUnknown |
|||
Primary | Unknown Approved UseUnknown |
|||
Primary | Unknown Approved UseUnknown |
|||
Primary | Unknown Approved UseUnknown |
Doses
Dose | Population | Adverse events |
---|---|---|
50 mg 3 times / day multiple, oral (unknown) Studied dose Dose: 50 mg, 3 times / day Route: oral Route: multiple Dose: 50 mg, 3 times / day Sources: |
unhealthy n = 10 Health Status: unhealthy Condition: schizophrenia Sex: M Food Status: UNKNOWN Population Size: 10 Sources: |
Other AEs: headache... |
AEs
AE | Significance | Dose | Population |
---|---|---|---|
headache | 2 patients | 50 mg 3 times / day multiple, oral (unknown) Studied dose Dose: 50 mg, 3 times / day Route: oral Route: multiple Dose: 50 mg, 3 times / day Sources: |
unhealthy n = 10 Health Status: unhealthy Condition: schizophrenia Sex: M Food Status: UNKNOWN Population Size: 10 Sources: |
PubMed
Title | Date | PubMed |
---|---|---|
The pharmacology of a beta 2-selective adrenoceptor antagonist (ICI 118,551). | 1983 May-Jun |
|
Human fat cell beta-adrenergic receptors: beta-agonist-dependent lipolytic responses and characterization of beta-adrenergic binding sites on human fat cell membranes with highly selective beta 1-antagonists. | 1988 May |
|
Beta 1- and beta 2-adrenergic receptor-mediated adenylate cyclase stimulation in nonfailing and failing human ventricular myocardium. | 1989 Mar |
|
Molecular characterization of the human beta 3-adrenergic receptor. | 1989 Sep 8 |
|
Beta-adrenoceptor subtypes and the opening of plasmalemmal K(+)-channels in trachealis muscle: electrophysiological and mechanical studies in guinea-pig tissue. | 1993 Aug |
|
Nicotine-induced NO-mediated increase in cortical cerebral blood flow is blocked by beta2-adrenoceptor antagonists in the anesthetized rats. | 2002 Mar 18 |
|
Functional characterization of the beta-adrenergic receptor subtypes expressed by CA1 pyramidal cells in the rat hippocampus. | 2005 Aug |
|
A cell-based assay to assess the persistence of action of agonists acting at recombinant human beta(2) adrenoceptors. | 2008 Nov-Dec |
|
beta(2)-adrenoceptor antagonist ICI 118,551 decreases pulmonary vascular tone in mice via a G(i/o) protein/nitric oxide-coupled pathway. | 2009 Jul |
|
[Changes in the receptor activity of β2-adrenoreceptors of human T-lymphocytes under the effect of β2-agonists]. | 2016 Nov-Dec |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2908820
50 mg t.i.d. for a week
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/28064316
Curator's Comment: https://www.ncbi.nlm.nih.gov/pubmed/26762097
Changes in the activity of beta2-adrenergic receptors of human T-lymphocytes under the effect of salbutamol (a short-acting beta2-agonist) have been evaluated with a new modified radioligand method utilizing [125I]cyanopindolol and a specific ligand ICI 118551. One hundred μL of water solution of [125I]cyanopindolol in PBS with a concentration of 1000 imp./min/μL, 0.16 μL of unlabelled ligand (ICI-118551) in various concentrations (or 10 μL water) and 100 μL of cell suspension with concentration 10 million cells/mL were incubated for 1 hour at 37°C with careful mixing on the shaker, rotating at 100 rpm in the 1.5mL centrifuge tubes (Eppendorf). The process was stopped by the addition of 400 μL of ice-cold water to each probe. Cells were centrifuged in the Microspin12 BioSan (Latvia) at 2000 g for 10 min, the supernatant was discarded, and the pellet was carefully suspended in 200 μL of ice-cold PBS and again centrifuged in the same conditions. The supernatant was discarded; the pellet was suspended carefully in 200 μL of ice-cold PBS and centrifuged at 10000 g for 2 min. The supernatant was discarded, and the pellet in the tubes was analyzed on a γcounter Wallac Wizard 1470 (PerkinElmer) measuring the amount of radioactive material in each probe.
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:25:25 GMT 2023
by
admin
on
Sat Dec 16 08:25:25 GMT 2023
|
Record UNII |
46OL1UC10R
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Code | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
DTXSID701033231
Created by
admin on Sat Dec 16 08:25:25 GMT 2023 , Edited by admin on Sat Dec 16 08:25:25 GMT 2023
|
PRIMARY | |||
|
C199137
Created by
admin on Sat Dec 16 08:25:25 GMT 2023 , Edited by admin on Sat Dec 16 08:25:25 GMT 2023
|
PRIMARY | |||
|
72795-26-7
Created by
admin on Sat Dec 16 08:25:25 GMT 2023 , Edited by admin on Sat Dec 16 08:25:25 GMT 2023
|
PRIMARY | |||
|
104824
Created by
admin on Sat Dec 16 08:25:25 GMT 2023 , Edited by admin on Sat Dec 16 08:25:25 GMT 2023
|
PRIMARY | |||
|
12274
Created by
admin on Sat Dec 16 08:25:25 GMT 2023 , Edited by admin on Sat Dec 16 08:25:25 GMT 2023
|
PRIMARY | |||
|
ICI-118,551
Created by
admin on Sat Dec 16 08:25:25 GMT 2023 , Edited by admin on Sat Dec 16 08:25:25 GMT 2023
|
PRIMARY | |||
|
46OL1UC10R
Created by
admin on Sat Dec 16 08:25:25 GMT 2023 , Edited by admin on Sat Dec 16 08:25:25 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
TARGET -> INHIBITOR |
IC50
|
||
|
SALT/SOLVATE -> PARENT |
|
||
|
TARGET -> INHIBITOR |
IC50
|
Related Record | Type | Details | ||
---|---|---|---|---|
|
ACTIVE MOIETY |
|