Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C15H22N2O3 |
| Molecular Weight | 278.3468 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCOC1=CC(CC2CNC(=O)N2)=CC=C1OC
InChI
InChIKey=PDMUULPVBYQBBK-UHFFFAOYSA-N
InChI=1S/C15H22N2O3/c1-3-4-7-20-14-9-11(5-6-13(14)19-2)8-12-10-16-15(18)17-12/h5-6,9,12H,3-4,7-8,10H2,1-2H3,(H2,16,17,18)
| Molecular Formula | C15H22N2O3 |
| Molecular Weight | 278.3468 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
RO-20-1724 is a potent inhibitor of Phosphodiesterase 4 (PDE4) originally developed by Roche. It showed some promise as a potential treatment for psoriasis, but it was discontinued when it could not match the efficacy of existing treatments. RO-20-1724 was also investigated as a potential treatment for asthma and septic shock.
CNS Activity
Sources: https://www.ncbi.nlm.nih.gov/pubmed/24637417
Curator's Comment: referenced study was conducted in rat
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL2093863 Sources: https://www.ncbi.nlm.nih.gov/pubmed/1393276 |
4.73 µM [IC50] |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | Unknown Approved UseUnknown |
|||
| Primary | Unknown Approved UseUnknown |
|||
| Primary | Unknown Approved UseUnknown |
Overview
| CYP3A4 | CYP2C9 | CYP2D6 | hERG |
|---|---|---|---|
OverviewOther
| Other Inhibitor | Other Substrate | Other Inducer |
|---|---|---|
Drug as perpetrator
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
| inconclusive [IC50 25.93 uM] | ||||
| no [IC50 >10 uM] | ||||
| no [IC50 >10 uM] | ||||
| no [IC50 >10 uM] | ||||
| no [IC50 >10 uM] | ||||
| no [IC50 >10 uM] | ||||
| no [IC50 >10 uM] | ||||
| no [IC50 >10 uM] | ||||
| no |
Tox targets
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
PubMed
| Title | Date | PubMed |
|---|---|---|
| Exposure of human seminal vesicle tissue to phosphodiesterase (PDE) inhibitors antagonizes the contraction induced by norepinephrine and increases production of cyclic nucleotides. | 2010-12 |
|
| Acute stress impairs hippocampal mossy fiber-CA3 long-term potentiation by enhancing cAMP-specific phosphodiesterase 4 activity. | 2010-06 |
|
| Decreased expression and activity of cAMP phosphodiesterases in cardiac hypertrophy and its impact on beta-adrenergic cAMP signals. | 2009-10-09 |
|
| Regulation of renovascular adenosine 3',5'-cyclic monophosphate in spontaneously hypertensive rats. | 2009-08 |
|
| Endothelin downregulates SERCA2 gene and protein expression in adult rat ventricular myocytes: regulation by pertussis toxin-sensitive Gi protein and cAMP. | 2009-03 |
|
| Intravenously administered phosphodiesterase 4 inhibitors dilate retinal blood vessels in rats. | 2009-01-05 |
|
| Adrenomedullin-induced relaxation of rat brain pericytes is related to the reduced phosphorylation of myosin light chain through the cAMP/PKA signaling pathway. | 2009-01-02 |
|
| Selective phosphodiesterase inhibitors: a promising target for cognition enhancement. | 2009-01 |
|
| Impact of anti-inflammatory agents on the gene expression profile of stimulated human neutrophils: unraveling endogenous resolution pathways. | 2009 |
|
| Antipsychotic-like properties of phosphodiesterase 4 inhibitors: evaluation of 4-(3-butoxy-4-methoxybenzyl)-2-imidazolidinone (RO-20-1724) with auditory event-related potentials and prepulse inhibition of startle. | 2008-07 |
|
| Inhibition of phosphodiesterase has an additive effect on estrogen's ability to inhibit collagen synthesis in vascular smooth muscle cells. | 2008-05-06 |
|
| Effect of cyclic AMP on barrier function of human lymphatic microvascular tubes. | 2008-05 |
|
| Numerous distinct PKA-, or EPAC-based, signalling complexes allow selective phosphodiesterase 3 and phosphodiesterase 4 coordination of cell adhesion. | 2007-12 |
|
| Autoregulation in PC12 cells via P2Y receptors: Evidence for non-exocytotic nucleotide release from neuroendocrine cells. | 2007-09 |
|
| Differential regulation of synaptic transmission by adrenergic agonists via protein kinase A and protein kinase C in layer V pyramidal neurons of rat cerebral cortex. | 2007-06-08 |
|
| Dual regulation of the ATP-sensitive potassium channel by caffeine. | 2007-06 |
|
| The effect of oxidative stress on macrophages and lung epithelial cells: the role of phosphodiesterases 1 and 4. | 2007-01-10 |
|
| Ca(2+)-dependent K(+) currents and spike-frequency adaptation in medial entorhinal cortex layer II stellate cells. | 2007 |
|
| Chronic ethanol feeding suppresses beta-adrenergic receptor-stimulated lipolysis in adipocytes isolated from epididymal fat. | 2006-09 |
|
| Inhibition of PGI2 signaling by miconazole in vascular smooth muscle cells. | 2006-07 |
|
| Characteristics of taurine release in slices from adult and developing mouse brain stem. | 2006-07 |
|
| Role of PDE3B in insulin-induced glucose uptake, GLUT-4 translocation and lipogenesis in primary rat adipocytes. | 2006-03 |
|
| Phosphodiesterase IV and neutral endopeptidase in airways from developing and allergen sensitized rabbits. | 2006 |
|
| Effects of various selective phosphodiesterase inhibitors on carbachol-induced contraction and cyclic nucleotide contents in the guinea pig gall bladder. | 2005-07 |
|
| Role of the adenosine 3',5'-cyclic monophosphate (cAMP) in enhancing the efficacy of siRNA-mediated gene silencing in neuroblastoma cells. | 2005-06-09 |
|
| Identification and characterization of PDE4A11, a novel, widely expressed long isoform encoded by the human PDE4A cAMP phosphodiesterase gene. | 2005-06 |
|
| Inhibition of mast cell histamine release by specific phosphodiesterase inhibitors. | 2005-04 |
|
| NSAIDs increase GM-CSF release by human synoviocytes: comparison with nitric oxide-donating derivatives. | 2005-01-31 |
|
| Autoinhibition of transmitter release from PC12 cells and sympathetic neurons through a P2Y receptor-mediated inhibition of voltage-gated Ca2+ channels. | 2004-12 |
|
| Phosphodiesterase type IV inhibitors prevent ischemia-reperfusion-induced gastric injury in rats. | 2004-07 |
|
| Phosphodiesterase-linked inhibition of nonmicturition activity in the isolated bladder. | 2004-06 |
|
| The effect of selective phosphodiesterase inhibitors, alone and in combination, on a murine model of allergic asthma. | 2004-05-05 |
|
| Sensitivity of proteasome to its inhibitors increases during cAMP-induced differentiation of neuroblastoma cells in culture and causes decreased viability. | 2004-02-10 |
|
| Group II metabotropic glutamate receptor modulation of excitatory transmission in rat subthalamic nucleus. | 2003-12-01 |
|
| Effects of phosphodiesterase inhibitors on spontaneous nuclear maturation and cAMP concentrations in bovine oocytes. | 2003-12 |
|
| Role of cyclic nucleotide phosphodiesterase isoforms in cAMP compartmentation following beta2-adrenergic stimulation of ICa,L in frog ventricular myocytes. | 2003-08-15 |
|
| The human D2 dopamine receptor synergizes with the A2A adenosine receptor to stimulate adenylyl cyclase in PC12 cells. | 2003-07 |
|
| Type IV phosphodiesterase inhibition improves cardiac contractility in endotoxemic rats. | 2003-03-28 |
|
| 5-HT7 receptor-mediated relaxation of the oviduct in nonpregnant proestrus pigs. | 2003-02-14 |
|
| Norepinephrine induces slow calcium signalling in murine brown preadipocytes through the beta-adrenoceptor/cAMP/protein kinase A pathway. | 2003-02 |
|
| Lipopolysaccharide-induced acute renal failure in conscious rats: effects of specific phosphodiesterase type 3 and 4 inhibition. | 2002-10 |
|
| Subtype-specific roles of cAMP phosphodiesterases in regulation of atrial natriuretic peptide release. | 2002-09-20 |
|
| Inducible expression of the gap junction protein connexin43 decreases the neoplastic potential of HT-1080 human fibrosarcoma cells in vitro and in vivo. | 2002-09 |
|
| Regulation of glypican-1, syndecan-1 and syndecan-4 mRNAs expression by follicle-stimulating hormone, cAMP increase and calcium influx during rat Sertoli cell development. | 2002-07 |
|
| Phosphodiesterase type 4 inhibitors, but not glucocorticoids, are more potent in suppression of cytokine secretion by mononuclear cells from atopic than nonatopic donors. | 1998-11 |
|
| Beta-adrenergic regulation of renin expression in differentiated U-937 monocytic cells. | 1997-06-15 |
|
| Expression, purification, and characterization of human cAMP-specific phosphodiesterase (PDE4) subtypes A, B, C, and D. | 1997-05-19 |
|
| Differential modulation of cytokine production by drugs: implications for therapy in heart failure. | 1996-12 |
|
| Dipyridamole enhances interleukin-1beta-stimulated nitric oxide production by cultured rat vascular smooth muscle cells. | 1996-02-05 |
|
| Inhibition of ornithine decarboxylase and S-adenosylmethionine decarboxylase activities of S49 lymphoma cells by agents increasing cyclic AMP. | 1981 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/383851
In a clinical trial for the treatment of psoriasis, a 1% RO-20-1724 cream was applied 4 times a day for 4 weeks to affected areas. RO-20-1724 was not as effective as intensive occlusive treatment of psoriatic lesions with 0.025% triamcinolone acetonide
Route of Administration:
Topical
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/7521256
Curator's Comment: referenced study was conducted in rat
Aortic vascular smooth muscle (VSM) cells were harvested from enzymatically dissociated rat thoracic aorta. Cells were stimulated by incubation with interleukin-lp (IL-10) at different concentrations for varying periods of time up to 48 h, with and without RO-20-1724. Nitric Oxide Synthase activity was assessed by measurement of nitrite production. RO-20-1724 had no detectable effect on nitrite levels in the absence of IL-lp but enhanced the production of nitrite in response to IL-Il in a dose-dependent manner.
| Substance Class |
Chemical
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TARGET -> INHIBITOR |
IC50
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ACTIVE MOIETY |
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