Page last updated: 2024-12-11

(n,n-bis(2-chloroethyl))-2-aminoethyl-3-((acridin-9-yl)amino)propionate

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

Description

The compound you've described, **(n,n-bis(2-chloroethyl))-2-aminoethyl-3-((acridin-9-yl)amino)propionate**, is a complex molecule with a unique structure and potential for research. It contains several functional groups that could contribute to its activity.

Here's a breakdown of the molecule and its potential implications:

* **Structure:** This compound is a derivative of the acridine molecule. It has a long, flexible alkyl chain containing a nitrogen mustard group (bis(2-chloroethyl)amino). The acridine moiety is known to intercalate into DNA, while the nitrogen mustard group is a potent alkylating agent.
* **Potential for Research:** The combination of these functional groups suggests this compound could be investigated for its potential as an anti-cancer agent. Here's how:
* **DNA Intercalation:** The acridine moiety can bind to DNA, potentially interfering with replication and transcription.
* **DNA Alkylation:** The nitrogen mustard group can react with DNA, leading to cross-linking and damage. This damage can trigger cell death or inhibit cell division, ultimately preventing tumor growth.

**Why is it Important for Research?**

While the specific compound you mentioned might not have been extensively studied, understanding its structure provides valuable insights into its potential applications. This molecule belongs to a class of compounds that are being explored for their potential in cancer therapy. Research in this area is crucial for developing new treatments for cancer and improving the efficacy and safety of current therapies.

**Important Note:** Research with this compound should be conducted in a controlled laboratory setting with proper safety precautions. Nitrogen mustards are potent chemicals that can be hazardous to human health.

**Additional Research:**

To learn more about this specific compound or similar molecules, you can consult scientific databases like PubChem or search for research publications on nitrogen mustard derivatives and acridine-based anti-cancer drugs.

(N,N-bis(2-chloroethyl))-2-aminoethyl-3-((acridin-9-yl)amino)propionate: an alkylating agent; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID6433104
CHEMBL ID2111082
SCHEMBL ID685675
MeSH IDM0493011

Synonyms (20)

Synonym
2-[bis(2-chloroethyl)amino]ethyl 3-(acridin-9-ylamino)propanoate
s 303
unii-25571657uw
amustaline
pic 1
(n,n-bis(2-chloroethyl))-2-aminoethyl-3-((acridin-9-yl)amino)propionate
25571657uw ,
220180-88-1
beta-alanine, n-9-acridinyl-, 2-(bis(2-chloroethyl)amino)ethyl ester
SCHEMBL685675
.beta.-alanine, n-9-acridinyl-, 2-(bis(2-chloroethyl)amino)ethyl ester
s-303
2-(bis(2-chloroethyl)amino)ethyl 3-(acridin-9-ylamino)propanoate
CHEMBL2111082
DTXSID20176473
beta-alanine, n-9-acridinyl-, 2-[bis(2-chloroethyl)amino]ethyl ester
878189-87-8
Q27253910
220180-88-1 (free base)
-alanine, n-9-acridinyl-, 2-[bis(2-chloroethyl)amino]ethyl ester

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" The adverse event profile was similar between groups; however, patients who received S-303 RBCs were significantly more likely to develop constipation and less likely to suffer supraventricular extrasystoles."( Therapeutic efficacy and safety of red blood cells treated with a chemical process (S-303) for pathogen inactivation: a Phase III clinical trial in cardiac surgery patients.
Benjamin, RJ; Conlan, MG; Corash, L; Lin, JS; McCullough, J; Mintz, PD; Rizzo, RJ; Snyder, E; Spotnitz, WD; Wages, D; Wood, L, 2005
)
0.33

Pharmacokinetics

ExcerptReferenceRelevance
"As part of a preclinical safety evaluation program, intravenous toxicity, safety pharmacology, toxicokinetic, and pharmacokinetic studies were conducted in rats and dogs with S-303 RBCs and S-300."( Preclinical pharmacokinetic and toxicology assessment of red blood cells prepared with S-303 pathogen inactivation treatment.
Ciaravino, V; Corash, L; Mufti, N; North, A, 2011
)
0.37
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (15)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (13.33)29.6817
2010's9 (60.00)24.3611
2020's4 (26.67)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 11.86

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 Index11.86 (24.57)
Research Supply Index3.00 (2.92)
Research Growth Index4.86 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (11.86)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials4 (26.67%)5.53%
Reviews1 (6.67%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other10 (66.67%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]