Page last updated: 2024-12-08

1,3-diphenyl-2-aminopropane hydrochloride

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

1,3-diphenyl-2-aminopropane hydrochloride, also known as **phenylpropanolamine hydrochloride (PPA)**, is a sympathomimetic amine that was previously used as a decongestant and appetite suppressant. However, it was withdrawn from the market due to safety concerns, particularly its association with an increased risk of stroke.

While PPA is no longer used clinically, it remains **important for research** for several reasons:

* **Pharmacological studies:** PPA serves as a model compound for studying the pharmacology of sympathomimetic amines. Researchers can investigate its interactions with various receptors, enzymes, and transporters to gain insights into the mechanisms of action of these drugs.
* **Drug discovery and development:** PPA can be used as a starting point for developing new drugs with improved therapeutic profiles. By modifying its structure, researchers can create analogs with different pharmacological properties, potentially leading to the development of safer and more effective drugs.
* **Toxicology research:** Understanding the toxicity of PPA is crucial for understanding the risks associated with other sympathomimetic amines. Researchers can study its effects on various organs and systems to identify potential hazards and develop strategies for mitigating them.
* **Forensic toxicology:** PPA can be detected in biological samples, and its presence can indicate drug use or abuse. Researchers in forensic toxicology use this information to identify potential causes of death or impairment.

Overall, 1,3-diphenyl-2-aminopropane hydrochloride continues to hold research value despite its withdrawal from clinical use. Its study provides insights into the pharmacology, toxicology, and potential therapeutic applications of sympathomimetic amines.

Cross-References

ID SourceID
PubMed CID202208
CHEMBL ID1726221
MeSH IDM0322165

Synonyms (21)

Synonym
MLS000719165
smr000291433
1,3-diphenyl-2-aminopropane hydrochloride
1,3-diphenyl-2-propylamine
alpha-benzylphenethylamine hydrochloride
benzeneethanamine, alpha-(phenylmethyl)-, hydrochloride
phenethylamine, alpha-benzyl-, hydrochloride
1,3-diphenylpropan-2-amine hydrochloride
7763-96-4
F2150-0005
(1-benzyl-2-phenylethyl)amine hydrochloride
1-benzyl-2-phenyl-ethylamine hydrochloride
AKOS005170071
DTXSID30228290
CHEMBL1726221
VU0298728-2
1,3-diphenylpropan-2-amine;hydrochloride
1,3-diphenylpropan-2-aminehydrochloride
Y13622
AS-83320
CS-0071058
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (14)

Assay IDTitleYearJournalArticle
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID651635Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID504812Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign2010Endocrinology, Jul, Volume: 151, Issue:7
A small molecule inverse agonist for the human thyroid-stimulating hormone receptor.
AID504810Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign2010Endocrinology, Jul, Volume: 151, Issue:7
A small molecule inverse agonist for the human thyroid-stimulating hormone receptor.
AID1794808Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL).2014Journal of biomolecular screening, Jul, Volume: 19, Issue:6
A High-Throughput Assay to Identify Inhibitors of the Apicoplast DNA Polymerase from Plasmodium falciparum.
AID1794808Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL).
[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's0 (0.00)18.2507
2000's1 (14.29)29.6817
2010's4 (57.14)24.3611
2020's2 (28.57)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.22

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 Index12.22 (24.57)
Research Supply Index2.08 (2.92)
Research Growth Index4.30 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.22)

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%
Other7 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]