erucylphosphocholine: structure given in first source
ID Source | ID |
---|---|
PubMed CID | 6439461 |
CHEMBL ID | 229567 |
SCHEMBL ID | 4064798 |
MeSH ID | M0202269 |
Synonym |
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ethanaminium, 2-(((13-docosenyloxy)hydroxyphosphinyl)oxy)-n,n,n-trimethyl-, hydroxide, inner salt, (z)- |
erucylphosphocholine |
CHEMBL229567 |
[(z)-docos-13-enyl] 2-(trimethylazaniumyl)ethyl phosphate |
143317-74-2 |
SCHEMBL4064798 |
DTXSID601315365 |
Erucylphosphocholine is a promising anti-neoplastic drug for the treatment of malignant brain tumours.
Excerpt | Reference | Relevance |
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"Erucylphosphocholine (ErPC) is a promising candidate for the treatment of human brain tumors. " | ( Structure-activity relationships of alkylphosphocholine derivatives: antineoplastic action on brain tumor cell lines in vitro. Eibl, H; Erdlenbruch, B; Hammersen, K; Jendrossek, V; Krügener, R; Kugler, W; Lakomek, M, 2002) | 1.76 |
"Erucylphosphocholine (ErPC) is a promising anti-neoplastic drug for the treatment of malignant brain tumours. " | ( Erucylphosphocholine-induced apoptosis in glioma cells: involvement of death receptor signalling and caspase activation. Eibl, H; Erdlenbruch, B; Heinemann, D; Jünemann, A; Kugler, W; Lakomek, M, 2002) | 3.2 |
"Erucylphosphocholine (ErPC) is a promising antineoplastic drug for the treatment of malignant brain tumors. " | ( MAP kinase pathways involved in glioblastoma response to erucylphosphocholine. Eibl, H; Erdlenbruch, B; Jendrossek, V; Kugler, W; Lakomek, M; Otten, K, 2004) | 2.01 |
Excerpt | Reference | Relevance |
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"Erucylphosphocholine (ErPC) has been shown to exert strong antineoplastic effects against various brain tumor cell lines in vitro. " | ( Increased delivery of erucylphosphocholine to C6 gliomas by chemical opening of the blood-brain barrier using intracarotid pentylglycerol in rats. Eibl, H; Erdlenbruch, B; Jendrossek, V; Kugler, W; Lakomek, M, 2002) | 2.07 |
Excerpt | Reference | Relevance |
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" Adverse effects on the anterior and posterior segment were assessed by slit-lamp biomicroscopy and ophthalmoscopy." | ( Toxicity study of erucylphosphocholine in a rat model. Blatsios, G; Eibl, KH; May, CA; Rejdak, R; Schuettauf, F; Shinoda, K; Thaler, S; Welge-Lussen, U, 2005) | 0.66 |
Excerpt | Reference | Relevance |
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" Moreover, activity of the survival kinase PKB/Akt was downregulated upon treatment with ErPC/ErPC3 alone or in combination with ionizing radiation." | ( Increased cytotoxicity of ionizing radiation in combination with membrane-targeted apoptosis modulators involves downregulation of protein kinase B/Akt-mediated survival-signaling. Belka, C; Eibl, H; Faltin, H; Handrick, R; Jendrossek, V; Rübel, A, 2006) | 0.33 |
Excerpt | Reference | Relevance |
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"To develop a stable micellar formulation of vitamin K for oral delivery, because the commercial and clinically used formulation of vitamin K (Konakion® MM) destabilizes at gastric pH resulting in low bioavailability of this vitamin in neonates with cholestasis." | ( A Mixed Micelle Formulation for Oral Delivery of Vitamin K. Hennink, WE; Jaspers, TC; Sun, F; van Hasselt, PM; van Nostrum, CF, 2016) | 0.43 |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID288954 | Antifungal activity against Cryptococcus neoformans ATCC 90112 | 2007 | Bioorganic & medicinal chemistry, Aug-01, Volume: 15, Issue:15 | Synthesis, antifungal and antimicrobial activity of alkylphospholipids. |
AID633816 | Cytotoxicity against human KATO III cells after 24 hrs by FACS analysis | 2012 | European journal of medicinal chemistry, Jan, Volume: 47, Issue:1 | Synthesis and biological evaluation of cyclopentane-linked alkyl phosphocholines as potential anticancer agents that act by inhibiting Akt phosphorylation. |
AID633734 | Inhibition of Akt phosphorylation in insulin-stimulated human A549 cells at 10 uM treated 2 hrs before insulin stimulation measured after 30 mins by ELISA | 2012 | European journal of medicinal chemistry, Jan, Volume: 47, Issue:1 | Synthesis and biological evaluation of cyclopentane-linked alkyl phosphocholines as potential anticancer agents that act by inhibiting Akt phosphorylation. |
AID288968 | Antibacterial activity against Staphylococcus aureus ATCC 25923 after 24 hrs | 2007 | Bioorganic & medicinal chemistry, Aug-01, Volume: 15, Issue:15 | Synthesis, antifungal and antimicrobial activity of alkylphospholipids. |
AID633814 | Cytotoxicity against human A549 cells after 24 hrs by FACS analysis | 2012 | European journal of medicinal chemistry, Jan, Volume: 47, Issue:1 | Synthesis and biological evaluation of cyclopentane-linked alkyl phosphocholines as potential anticancer agents that act by inhibiting Akt phosphorylation. |
AID288970 | Antibacterial activity against vancomycin-resistant Enterococcus ATCC 51299 after 24 hrs | 2007 | Bioorganic & medicinal chemistry, Aug-01, Volume: 15, Issue:15 | Synthesis, antifungal and antimicrobial activity of alkylphospholipids. |
AID288964 | Toxicity assessed as haemolytic activity against human erythrocytes at 44 uM | 2007 | Bioorganic & medicinal chemistry, Aug-01, Volume: 15, Issue:15 | Synthesis, antifungal and antimicrobial activity of alkylphospholipids. |
AID288969 | Antibacterial activity against methicillin-resistant Staphylococcus aureus after 24 hrs | 2007 | Bioorganic & medicinal chemistry, Aug-01, Volume: 15, Issue:15 | Synthesis, antifungal and antimicrobial activity of alkylphospholipids. |
AID633813 | Inhibition of Akt phosphorylation in insulin-stimulated human A549 cells treated 2 hrs before insulin stimulation measured after 30 mins by ELISA | 2012 | European journal of medicinal chemistry, Jan, Volume: 47, Issue:1 | Synthesis and biological evaluation of cyclopentane-linked alkyl phosphocholines as potential anticancer agents that act by inhibiting Akt phosphorylation. |
AID633815 | Cytotoxicity against human MCF7 cells after 24 hrs by FACS analysis | 2012 | European journal of medicinal chemistry, Jan, Volume: 47, Issue:1 | Synthesis and biological evaluation of cyclopentane-linked alkyl phosphocholines as potential anticancer agents that act by inhibiting Akt phosphorylation. |
AID288965 | Toxicity assessed as haemolytic activity against human erythrocytes at 17.5 uM | 2007 | Bioorganic & medicinal chemistry, Aug-01, Volume: 15, Issue:15 | Synthesis, antifungal and antimicrobial activity of alkylphospholipids. |
AID288967 | Antibacterial activity against Escherichia coli ATCC 25922 after 24 hrs | 2007 | Bioorganic & medicinal chemistry, Aug-01, Volume: 15, Issue:15 | Synthesis, antifungal and antimicrobial activity of alkylphospholipids. |
AID288955 | Antifungal activity against Candida albicans ATCC 10231 | 2007 | Bioorganic & medicinal chemistry, Aug-01, Volume: 15, Issue:15 | Synthesis, antifungal and antimicrobial activity of alkylphospholipids. |
AID288963 | Toxicity assessed as haemolytic activity against human erythrocytes at 88 uM | 2007 | Bioorganic & medicinal chemistry, Aug-01, Volume: 15, Issue:15 | Synthesis, antifungal and antimicrobial activity of alkylphospholipids. |
AID288961 | Toxicity assessed as haemolytic activity against human erythrocytes at 350 uM | 2007 | Bioorganic & medicinal chemistry, Aug-01, Volume: 15, Issue:15 | Synthesis, antifungal and antimicrobial activity of alkylphospholipids. |
AID288966 | Toxicity assessed as haemolytic activity against human erythrocytes at 3.5 uM | 2007 | Bioorganic & medicinal chemistry, Aug-01, Volume: 15, Issue:15 | Synthesis, antifungal and antimicrobial activity of alkylphospholipids. |
AID288962 | Toxicity assessed as haemolytic activity against human erythrocytes at 175 uM | 2007 | Bioorganic & medicinal chemistry, Aug-01, Volume: 15, Issue:15 | Synthesis, antifungal and antimicrobial activity of alkylphospholipids. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 10 (25.64) | 18.2507 |
2000's | 19 (48.72) | 29.6817 |
2010's | 10 (25.64) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
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.
| This Compound (10.74) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 0 (0.00%) | 5.53% |
Reviews | 1 (2.38%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 41 (97.62%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |