Page last updated: 2024-11-07

cyclohexylaminoglutethimide

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

cyclohexylaminoglutethimide: structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID126253
CHEMBL ID70901
SCHEMBL ID3290521
MeSH IDM0233882

Synonyms (23)

Synonym
2,6-piperidinedione, 3-(4-aminophenyl)-3-cyclohexyl-
3-cyclohexyl-3-(4-aminophenyl)-2,6-piperidinedione
3-(4-aminophenyl)-3-cyclohexyl-2,6-piperidinedione
115883-22-2
cyclohexylaminoglutethimide
chag
nphchexpipone
CHEMBL70901 ,
3-(4-aminophenyl)-3-cyclohexylpiperidine-2,6-dione
3-(4-amino-phenyl)-3-cyclohexyl-piperidine-2,6-dione
bdbm50006551
(+)3-(4-amino-phenyl)-3-cyclohexyl-piperidine-2,6-dione
(-)3-(4-amino-phenyl)-3-cyclohexyl-piperidine-2,6-dione
137548-41-5
(+-)-3-(4-aminophenyl)-3-cyclohexyl-2,6-piperidinedione
2,6-piperidinedione, 3-(4-aminophenyl)-3-cyclohexyl-, (+-)-
AKOS015891370
SCHEMBL3290521
3-(4-aminophenyl)-3-cyclohexyl-2,6-piperidinedione #
3-cyclo-hexyl-3-( 4-aminophenyl)-2,6-piperidinedione
DTXSID20921829
3-(4-aminophenyl)-3-cyclohexyl-6-hydroxy-4,5-dihydropyridin-2(3h)-one
PD067346
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Protein Targets (3)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
AromataseHomo sapiens (human)IC50 (µMol)1.68330.00001.290410.0000AID38923
Thromboxane-A synthase Homo sapiens (human)IC50 (µMol)0.15000.00091.230410.0000AID154268
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (25)

Processvia Protein(s)Taxonomy
C21-steroid hormone biosynthetic processCholesterol side-chain cleavage enzyme, mitochondrial Bos taurus (cattle)
cholesterol metabolic processCholesterol side-chain cleavage enzyme, mitochondrial Bos taurus (cattle)
vitamin D metabolic processCholesterol side-chain cleavage enzyme, mitochondrial Bos taurus (cattle)
negative regulation of chronic inflammatory responseAromataseHomo sapiens (human)
steroid biosynthetic processAromataseHomo sapiens (human)
estrogen biosynthetic processAromataseHomo sapiens (human)
androgen catabolic processAromataseHomo sapiens (human)
syncytium formationAromataseHomo sapiens (human)
negative regulation of macrophage chemotaxisAromataseHomo sapiens (human)
sterol metabolic processAromataseHomo sapiens (human)
female genitalia developmentAromataseHomo sapiens (human)
mammary gland developmentAromataseHomo sapiens (human)
uterus developmentAromataseHomo sapiens (human)
prostate gland growthAromataseHomo sapiens (human)
testosterone biosynthetic processAromataseHomo sapiens (human)
positive regulation of estradiol secretionAromataseHomo sapiens (human)
female gonad developmentAromataseHomo sapiens (human)
response to estradiolAromataseHomo sapiens (human)
prostaglandin biosynthetic processThromboxane-A synthase Homo sapiens (human)
icosanoid metabolic processThromboxane-A synthase Homo sapiens (human)
cyclooxygenase pathwayThromboxane-A synthase Homo sapiens (human)
intracellular chloride ion homeostasisThromboxane-A synthase Homo sapiens (human)
response to ethanolThromboxane-A synthase Homo sapiens (human)
positive regulation of vasoconstrictionThromboxane-A synthase Homo sapiens (human)
response to fatty acidThromboxane-A synthase Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (13)

Processvia Protein(s)Taxonomy
iron ion bindingCholesterol side-chain cleavage enzyme, mitochondrial Bos taurus (cattle)
cholesterol monooxygenase (side-chain-cleaving) activityCholesterol side-chain cleavage enzyme, mitochondrial Bos taurus (cattle)
heme bindingCholesterol side-chain cleavage enzyme, mitochondrial Bos taurus (cattle)
iron ion bindingAromataseHomo sapiens (human)
steroid hydroxylase activityAromataseHomo sapiens (human)
electron transfer activityAromataseHomo sapiens (human)
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygenAromataseHomo sapiens (human)
oxygen bindingAromataseHomo sapiens (human)
heme bindingAromataseHomo sapiens (human)
aromatase activityAromataseHomo sapiens (human)
monooxygenase activityThromboxane-A synthase Homo sapiens (human)
thromboxane-A synthase activityThromboxane-A synthase Homo sapiens (human)
iron ion bindingThromboxane-A synthase Homo sapiens (human)
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygenThromboxane-A synthase Homo sapiens (human)
heme bindingThromboxane-A synthase Homo sapiens (human)
12-hydroxyheptadecatrienoic acid synthase activityThromboxane-A synthase Homo sapiens (human)
hydroperoxy icosatetraenoate dehydratase activityThromboxane-A synthase Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (6)

Processvia Protein(s)Taxonomy
mitochondrionCholesterol side-chain cleavage enzyme, mitochondrial Bos taurus (cattle)
mitochondrial inner membraneCholesterol side-chain cleavage enzyme, mitochondrial Bos taurus (cattle)
endoplasmic reticulumAromataseHomo sapiens (human)
endoplasmic reticulum membraneAromataseHomo sapiens (human)
membraneAromataseHomo sapiens (human)
endoplasmic reticulumAromataseHomo sapiens (human)
endoplasmic reticulumThromboxane-A synthase Homo sapiens (human)
endoplasmic reticulum membraneThromboxane-A synthase Homo sapiens (human)
cytosolThromboxane-A synthase Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (6)

Assay IDTitleYearJournalArticle
AID56617Inhibition of bovine adrenal desmolase (IC50) relative to aminoglutethimide1992Journal of medicinal chemistry, Jun-12, Volume: 35, Issue:12
Synthesis and aromatase inhibition of 3-cycloalkyl-substituted 3-(4-aminophenyl)piperidine-2,6-diones.
AID39058Inhibition of cytochrome P450 Aromatase (IC50) relative to aminoglutethimide1992Journal of medicinal chemistry, Jun-12, Volume: 35, Issue:12
Synthesis and aromatase inhibition of 3-cycloalkyl-substituted 3-(4-aminophenyl)piperidine-2,6-diones.
AID38923Concentration inhibiting Aromatase1992Journal of medicinal chemistry, Jun-12, Volume: 35, Issue:12
Synthesis and aromatase inhibition of 3-cycloalkyl-substituted 3-(4-aminophenyl)piperidine-2,6-diones.
AID56616Inhibition of bovine adrenal desmolase at 25 uM1992Journal of medicinal chemistry, Jun-12, Volume: 35, Issue:12
Synthesis and aromatase inhibition of 3-cycloalkyl-substituted 3-(4-aminophenyl)piperidine-2,6-diones.
AID56611Inhibition of bovine adrenal desmolase1992Journal of medicinal chemistry, Jun-12, Volume: 35, Issue:12
Synthesis and aromatase inhibition of 3-cycloalkyl-substituted 3-(4-aminophenyl)piperidine-2,6-diones.
AID154268Inhibition of thromboxane synthase P450 TXA22000Journal of medicinal chemistry, Nov-16, Volume: 43, Issue:23
Synthesis and evaluation of 17-aliphatic heterocycle-substituted steroidal inhibitors of 17alpha-hydroxylase/C17-20-lyase (P450 17).
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (7)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's4 (57.14)18.2507
2000's1 (14.29)29.6817
2010's2 (28.57)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.13

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index12.13 (24.57)
Research Supply Index2.20 (2.92)
Research Growth Index4.32 (4.65)
Search Engine Demand Index10.37 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.13)

All Compounds (24.57)

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%
Other8 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]