Page last updated: 2024-12-11

retinamide

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

Description

retinamide: metabolite of tretinoin [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID5370221
SCHEMBL ID60864
MeSH IDM0153729

Synonyms (22)

Synonym
ro 4-3930
retinoyl amid
all-trans-retinamide
vitamin a amide
vitamin a-saeureamid [german]
retinamide
retinamide, all-trans-
retinoyl amide
all-trans-vitamin a amide
(2e,4e,6e,8e)-3,7-dimethyl-9-(2,6,6-trimethylcyclohexen-1-yl)nona-2,4,6,8-tetraenamide
20638-84-0
bqc43t81dz ,
vitamin a-saeureamid
unii-bqc43t81dz
vitamin a amide, all-trans
SCHEMBL60864
15-aminoretinal #
3,7-dimethyl-9-(2,6,6-trimethylcyclohexen-1-yl)nona-2,4,6,8-tetraenamide
J-013485
Q27274815
DTXSID001318373
(2e,4e,6e,8e)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)nona-2,4,6,8-tetraenamide

Research Excerpts

Treatment

ExcerptReferenceRelevance
"Retinamide treatment resulted in increased ratios of deamidated verses transamidated levels of Bcl-xL in U87 cells."( Retinamide-induced apoptosis in glioblastomas is associated with down-regulation of Bcl-xL and Bcl-2 proteins.
Higashikubo, R; Jiang, Z; Lytle, RA; Rich, KM; Zheng, X, 2005
)
2.49

Toxicity

ExcerptReferenceRelevance
" The results of cytotoxicity and flow cytometry data showed that the compounds had a moderate to strong effect against MCF-7 and HepG2 cells and were less toxic to HEK293 cells."( Novel all trans-retinoic Acid derivatives: cytotoxicity, inhibition of cell cycle progression and induction of apoptosis in human cancer cell lines.
Al-Khedhairy, AA; Al-Oqail, MM; Al-Sheddi, ES; Farshori, NN; Musarrat, J; Saquib, Q; Siddiqui, MA, 2015
)
0.42

Pharmacokinetics

ExcerptReferenceRelevance
" This method was applied to determine the pharmacokinetic parameters."( Quantitative determination and pharmacokinetics of retinamido-ester in rat plasma by liquid chromatography-atmospheric pressure chemical ionization-tandem mass spectrometry.
Cao, L; Di, B; Ding, L; Hang, TJ; Liu, WY; Ma, PC; Sun, D; Wang, Y; Yang, Q; Yu, P; Zheng, F, 2008
)
0.35

Dosage Studied

ExcerptRelevanceReference
" Group A received oral retinamide at a dosage of 20mg/kg, every day for eight weeks."( [Treatment of oral leukoplakia with retinamide].
Liu, X; Shen, S; Sun, Z, 1996
)
0.88
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (41)

TimeframeStudies, This Drug (%)All Drugs %
pre-19904 (9.76)18.7374
1990's12 (29.27)18.2507
2000's14 (34.15)29.6817
2010's9 (21.95)24.3611
2020's2 (4.88)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 21.48

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 moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index21.48 (24.57)
Research Supply Index3.99 (2.92)
Research Growth Index4.88 (4.65)
Search Engine Demand Index21.17 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (21.48)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials11 (26.19%)5.53%
Reviews1 (2.38%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other30 (71.43%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Clinical Trials (6)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Phase II Trial of Intravenous Fenretinide (N-(4-hydroxyphenyl) Retinamide, 4-HPR) Emulsion for Patients With Relapsed/Refractory Peripheral T-cell Lymphomas (PTCL) [NCT02495415]Phase 2140 participants (Anticipated)Interventional2016-12-31Recruiting
"A Phase I Study of Intravenous (Emulsion) Fenretinide (4-HPR, NSC 374551) in Children With Recurrent or Resistant Acute Lymphoblastic Leukemia (ALL), Acute Myelogenous Leukemia (AML), and Non-Hodgkin's Lymphoma (NHL) IND #70,058" [NCT01187810]Phase 13 participants (Actual)Interventional2010-08-31Terminated(stopped due to drug supply)
A Phase 1a/1b Trial in Relapsed/Refractory T-cell Non-Hodgkin Lymphoma to Determine the Safety Profile, Pharmacology, and Maximum Tolerated Dose of ST-001, a Fenretinide Phospholipid Suspension (12.5 mg/mL) for Intravenous Infusion [NCT04234048]Phase 146 participants (Anticipated)Interventional2023-12-18Recruiting
Phase I/II Trial of Fenretinide/LXS Oral Powder (NSC 374551) Plus Ketoconazole in Recurrent Ovarian Cancer and Primary Peritoneal Carcinoma [NCT01535157]Phase 1/Phase 212 participants (Actual)Interventional2012-02-29Terminated(stopped due to drug combination not providing any efficacy. Will use this data in opening new trial)
A Single Arm, Phase II Study to Determine the Safety and Efficacy of 4-HPRN-(4-Hydroxyphenyl) Retinamide for Treating Oral Intraepithelial Neoplasia [NCT00003223]Phase 25 participants (Actual)Interventional1997-12-31Terminated(stopped due to Closed due to poor accrual.)
Phase II Clinical Trial of N-(4-hydroxyphenyl) Retinamide (4-HPR) and Tamoxifen in Breast Neoplasia, Administration During the Period Between the Diagnostic Core Biopsy and Definitive Surgery [NCT00003099]Phase 252 participants (Actual)Interventional1996-05-31Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]