Page last updated: 2024-08-02 16:57:52

kmup 1

Description

KMUP 1: a potassium channel opener and stimulator of the NO/sGC/cGMP pathway; structure in first source [MeSH]

Cross-References

ID SourceID
PubMed CID10453764
SCHEMBL ID458792
MeSH IDM0404950

Synonyms (18)

Synonym
kmup1 cpd
kmup 1
kmup-1
81996-46-5
1h-purine-2,6-dione, 7-(2-(4-(2-chlorophenyl)-1-piperazinyl)ethyl)-3,7-dihydro-1,3-dimethyl-
7-(2-(4-(2-chlorophenyl)piperazinyl)ethyl)-1,3-dimethylxanthine
1x0h7wec5d ,
unii-1x0h7wec5d
SCHEMBL458792
DTXSID80440203
7-[2-[4-(2-chlorophenyl)piperazin-1-yl]ethyl]-1,3-dimethylpurine-2,6-dione
gtpl8896
(7-[2-[4-(2-chlorophenyl)piperazinyl]ethyl]-1,3-dimethylxanthine)
AKOS033007292
1254041-13-8
NIDVDYQCGWISJZ-UHFFFAOYSA-N
Q15634084
Z104874704

Bioassays (3)

Assay IDTitleYearJournalArticle
AID1345993Rat alpha1B-adrenoceptor (Adrenoceptors)2007The Prostate, Sep-15, Volume: 67, Issue:13
ISSN: 0270-4137
cGMP-enhancing- and alpha1A/alpha1D-adrenoceptor blockade-derived inhibition of Rho-kinase by KMUP-1 provides optimal prostate relaxation and epithelial cell anti-proliferation efficacy.
AID1345857Rat alpha1A-adrenoceptor (Adrenoceptors)2007The Prostate, Sep-15, Volume: 67, Issue:13
ISSN: 0270-4137
cGMP-enhancing- and alpha1A/alpha1D-adrenoceptor blockade-derived inhibition of Rho-kinase by KMUP-1 provides optimal prostate relaxation and epithelial cell anti-proliferation efficacy.
AID1345920Rat alpha1D-adrenoceptor (Adrenoceptors)2007The Prostate, Sep-15, Volume: 67, Issue:13
ISSN: 0270-4137
cGMP-enhancing- and alpha1A/alpha1D-adrenoceptor blockade-derived inhibition of Rho-kinase by KMUP-1 provides optimal prostate relaxation and epithelial cell anti-proliferation efficacy.

Research

Studies (36)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's7 (19.44)29.6817
2010's28 (77.78)24.3611
2020's1 (2.78)2.80

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other39 (100.00%)84.16%
SubstanceStudiesClassesRolesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
chlorinehalide anion;
monoatomic chlorine
cofactor;
Escherichia coli metabolite;
human metabolite
2011201113.0low000010
nitratesmonovalent inorganic anion;
nitrogen oxoanion;
reactive nitrogen species
2006200618.0low000100
nitritesmonovalent inorganic anion;
nitrogen oxoanion;
reactive nitrogen species
human metabolite2006201613.0low000110
xanthinexanthineSaccharomyces cerevisiae metabolite2001201416.5low000110
1h-(1,2,4)oxadiazolo(4,3-a)quinoxalin-1-oneoxadiazoloquinoxalineEC 4.6.1.2 (guanylate cyclase) inhibitor2001200123.0low000100
4-aminopyridineaminopyridine;
aromatic amine
avicide;
orphan drug;
potassium channel blocker
2005200519.0low000100
theophyllinedimethylxanthineadenosine receptor antagonist;
anti-asthmatic drug;
anti-inflammatory agent;
bronchodilator agent;
drug metabolite;
EC 3.1.4.* (phosphoric diester hydrolase) inhibitor;
fungal metabolite;
human blood serum metabolite;
immunomodulator;
muscle relaxant;
vasodilator agent
201620168.0low000010
chelerythrinebenzophenanthridine alkaloid;
organic cation
antibacterial agent;
antineoplastic agent;
EC 2.7.11.13 (protein kinase C) inhibitor
2011201113.0low000010
doxazosinaromatic amine;
benzodioxine;
monocarboxylic acid amide;
N-acylpiperazine;
N-arylpiperazine;
quinazolines
alpha-adrenergic antagonist;
antihyperplasia drug;
antihypertensive agent;
antineoplastic agent;
vasodilator agent
2009200915.0low000100
glyburidemonochlorobenzenes;
N-sulfonylurea
anti-arrhythmia drug;
EC 2.7.1.33 (pantothenate kinase) inhibitor;
EC 3.6.3.49 (channel-conductance-controlling ATPase) inhibitor;
hypoglycemic agent
2001200123.0low000100
isoproterenolcatechols;
secondary alcohol;
secondary amino compound
beta-adrenergic agonist;
bronchodilator agent;
cardiotonic drug;
sympathomimetic agent
2010201014.0low000100
pinacidilpyridines2012201212.0low000010
methylene blueorganic chloride saltacid-base indicator;
antidepressant;
antimalarial;
antimicrobial agent;
antioxidant;
cardioprotective agent;
EC 1.4.3.4 (monoamine oxidase) inhibitor;
EC 3.1.1.8 (cholinesterase) inhibitor;
EC 4.6.1.2 (guanylate cyclase) inhibitor;
fluorochrome;
histological dye;
neuroprotective agent;
physical tracer
2001200123.0low000100
quinoxalinesmancude organic heterobicyclic parent;
naphthyridine;
ortho-fused heteroarene
2001200123.0low000100
monocrotalinepyrrolizidine alkaloid2010201412.0low000110
barium chloridebarium salt;
inorganic chloride
potassium channel blocker2011201113.0low000010
ng-nitroarginine methyl esteralpha-amino acid ester;
L-arginine derivative;
methyl ester;
N-nitro compound
EC 1.14.13.39 (nitric oxide synthase) inhibitor2001201217.5low000110
simvastatindelta-lactone;
fatty acid ester;
hexahydronaphthalenes;
statin (semi-synthetic)
EC 1.1.1.34/EC 1.1.1.88 (hydroxymethylglutaryl-CoA reductase) inhibitor;
EC 3.4.24.83 (anthrax lethal factor endopeptidase) inhibitor;
ferroptosis inducer;
geroprotector;
prodrug
201420169.0low000020
atorvastatinaromatic amide;
dihydroxy monocarboxylic acid;
monofluorobenzenes;
pyrroles;
statin (synthetic)
environmental contaminant;
xenobiotic
201620168.0low000010
cromakalim2001200123.0low000100
clarithromycinmacrolide antibioticantibacterial drug;
environmental contaminant;
protein synthesis inhibitor;
xenobiotic
2014201410.0low000010
tamsulosin5-(2-{[2-(2-ethoxyphenoxy)ethyl]amino}propyl)-2-methoxybenzenesulfonamidealpha-adrenergic antagonist;
antineoplastic agent
2007200717.0low000100
mevalonic acid3,5-dihydroxy-3-methylpentanoic acid201520159.0low000010
y 27632aromatic amide201520159.0low000010
oxadiazoles2001200123.0low000100
7-(2-(4-(4-nitrobenzene)piperazinyl)ethyl)-1,3-dimethylxanthine2006200618.0medium000100
endothelin-1201420159.5low000020
piperidines2001202011.6high00011250
ascorbic acidascorbic acid;
vitamin C
coenzyme;
cofactor;
flour treatment agent;
food antioxidant;
food colour retention agent;
geroprotector;
plant metabolite;
skin lightening agent
201520159.0low000010
cyclic gmp3',5'-cyclic purine nucleotide;
guanyl ribonucleotide
Escherichia coli metabolite;
human metabolite;
mouse metabolite;
plant metabolite;
Saccharomyces cerevisiae metabolite
2001202013.2medium000560
sildenafil citratecitrate saltEC 3.1.4.35 (3',5'-cyclic-GMP phosphodiesterase) inhibitor;
vasodilator agent
2002201514.5low000220
ConditionIndicatedStudiesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
Adenoma, Prostatic02014201410.0low000020
Age-Related Osteoporosis02013201311.0low000010
Airway Remodeling02012201212.0low000010
Allergic Reaction02012201212.0low000010
Allodynia02014201410.0low000010
Alloxan Diabetes0201720186.5low000020
Alveolitis, Fibrosing02014201410.0low000010
Angiospasm, Intracranial02012201212.0low000010
Anoxemia0201520159.0low000010
Body Weight0201420169.0low000020
Cancer of Pituitary0201520159.0low000010
Cancer of Prostate02009200915.0low000100
Cardiac Hypertrophy02010201014.0low000100
Cardiomegaly02010201014.0low000100
Chronic Disease02010201014.0low000100
Chronic Illness02010201014.0low000100
Chronic Kidney Failure0202020204.0low000010
Cirrhosis02010201710.5low000110
Diabetic Glomerulosclerosis0201720177.0low000010
Diabetic Nephropathies0201720177.0low000010
Disease Models, Animal02010202010.0low000150
Experimental Lung Inflammation02012201411.0low000020
Fatty Liver0201620168.0low000010
Fibrosis02010201710.5low000110
Heart Disease, Ischemic0201920195.0low000010
Hemorrhage, Subarachnoid02012201212.0low000010
Hyperlipoproteinemia0201520159.0low000010
Hyperlipoproteinemias0201520159.0low000010
Hypersensitivity02012201212.0low000010
Hypertension, Pulmonary02010201511.8low000220
Hypertrophy0201520159.0low000010
Hypertrophy, Left Ventricular02012201212.0low000010
Hypertrophy, Right Ventricular02010201412.0low000110
Hypoxia0201520159.0low000010
Inflammation02006201414.0low000110
Innate Inflammatory Response02006201414.0low000110
Kidney Failure, Chronic0202020204.0low000010
Left Ventricular Hypertrophy02012201212.0low000010
Liver Steatosis0201620168.0low000010
Muscle Contraction02007201513.3low000210
Muscle Relaxation02002200421.0low000200
Myocardial Ischemia0201920195.0low000010
Nerve Pain02014201410.0low000010
Neuralgia02014201410.0low000010
Osteoporosis02013201311.0low000010
Peripheral Nerve Injuries02012201212.0low000010
Peripheral Nerve Injury02012201212.0low000010
Pituitary Neoplasms0201520159.0low000010
Pneumonia02012201411.0low000020
Prostatic Hyperplasia02014201410.0low000020
Prostatic Neoplasms02009200915.0low000100
Pulmonary Fibrosis02014201410.0low000010
Pulmonary Hypertension02010201511.8low000220
Subarachnoid Hemorrhage02012201212.0low000010
Vascular Calcification0202020204.0low000010
Vascular Diseases0201820186.0low000010
Vasospasm, Intracranial02012201212.0low000010

Safety/Toxicity (2)

ArticleYear
Xanthine-derived KMUP-1 reverses glucotoxicity-activated Kv channels through the cAMP/PKA signaling pathway in rat pancreatic β cells.
Chemico-biological interactions, , Jan-05, Volume: 279
2018
KMUP-1 attenuates serum deprivation-induced neurotoxicity in SH-SY5Y cells: roles of PKG, PI3K/Akt and Bcl-2/Bax pathways.
Toxicology, , Jan-31, Volume: 268, Issue:1-2
2010

Long-term Use (2)

ArticleYear
Theophylline-Based KMUP-1 Improves Steatohepatitis via MMP-9/IL-10 and Lipolysis via HSL/p-HSL in Obese Mice.
International journal of molecular sciences, , Aug-17, Volume: 17, Issue:8
2016
Endothelial nitric oxide synthase-enhancing G-protein coupled receptor antagonist inhibits pulmonary artery hypertension by endothelin-1-dependent and endothelin-1-independent pathways in a monocrotaline model.
The Kaohsiung journal of medical sciences, , Volume: 30, Issue:6
2014