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Uridine Triphosphate (UTP)

Uridine 5'-(tetrahydrogen triphosphate). A uracil nucleotide containing three phosphate groups esterified to the sugar moiety.
Also Known As:
UTP; Magnesium UTP; Magnesium Uridine Triphosphate; Mg-UTP; Mg UTP; Triphosphate, Magnesium Uridine; Triphosphate, Uridine; UTP, Magnesium; Uridine 5'-(tetrahydrogen triphosphate)
Networked: 345 relevant articles (11 outcomes, 21 trials/studies)

Relationship Network

Bio-Agent Context: Research Results

Experts

1. Mazzon, Emanuela: 7 articles (02/2010 - 02/2005)
2. Bramanti, Placido: 7 articles (02/2010 - 02/2005)
3. Cuzzocrea, Salvatore: 7 articles (02/2010 - 02/2005)
4. Genovese, Tiziana: 7 articles (02/2010 - 02/2005)
5. Jacobson, Kenneth A: 6 articles (05/2014 - 04/2005)
6. Shainberg, Asher: 6 articles (12/2013 - 04/2005)
7. Di Paola, Rosanna: 6 articles (02/2010 - 09/2007)
8. Hochhauser, Edith: 5 articles (12/2013 - 10/2006)
9. Yitzhaki, Smadar: 5 articles (04/2009 - 04/2005)
10. Esposito, Emanuela: 5 articles (09/2008 - 09/2007)

Related Diseases

1. Cystic Fibrosis (Mucoviscidosis)
2. Infection
3. Carcinoma (Carcinomatosis)
05/01/1998 - "For this purpose, we used the human carcinoma cell line A431, which has a varied resting [Ca2+]i. We found that the amplitude of the Ca2+ response evoked by Ca2+ readdition did not correlate with the amplitude of the preceding UTP-evoked Ca2+ release, but did positively correlate with the initial [Ca2+]i. An inspection of the two patterns of response seen in this study (the large biphasic and small plateau-shaped Ca2+ responses) revealed that there is an accelerating rise in [Ca2+]i during the biphasic response. "
01/02/2001 - "Using the patch-clamp technique, here we describe the plasma membrane Ca2+ channels in human carcinoma A431 cells, which can be activated by extracellular UTP, by depletion of intracellular Ca2+ stores after exposure to the Ca2+-pump inhibitor thapsigargin, or by loading the cells with Ca2+ chelator 1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetate. "
09/01/2000 - "For detection of apoptotic cells, apoptotic incidences (AIs) were examined by the terminal deoxynucleotidyl transferase-mediated deoxy-uridine triphosphate biotin nick end labeling method, on gastric carcinoma lesions based on the endoscopic findings before administration in the biopsy and resected tissues. "
03/01/1986 - "In TA3 mammary carcinoma cells in suspension culture, D-glucosamine X HCl (GlcN) induced a diversion of uridylate from UTP into UDP-N-acetylhexosamines, reducing the intracellular pool of UTP and eliciting an increased rate of de novo uridylate synthesis. "
04/01/1993 - "At the maximum tolerated doses, the antitumor activity in mice bearing advanced colon carcinoma can be summarized as follows: (a) FdUrd is significantly more active than FUra; (b) for both drugs the weekly for 3 weeks i.v. push schedule is superior to the c.i. or i.v. push daily for 4 days schedules; (c) pretreatment with PALA enhances the antitumor activity of FdUrd and FUra and resulted in 95 and 13% complete responses, respectively; (d) long-term survivors with FUra could only be achieved in the presence of PALA; in mice bearing leukemia 1210 cells, FdUrd or FUra with or without PALA exhibited no significant antitumor activity when PALA was administered in a single dose 24 h prior to fluoropyrimidine treatment; and (e) in C-26 and L1210, PALA reduced the pools of CTP and UTP equally, to about 10% of controls with significant difference in their rates of recovery."
4. Leukemia
01/01/2010 - "This study is aimed to determine the role of calcium signaling evoked by the calcium-mobilizing agonist uridine-5'-triphosphate (UTP) and by the specific inhibitor of the endoplasmic reticulum calcium reuptake thapsigargin on caspase activation in human leukemia cell line HL-60. "
04/01/1993 - "At the maximum tolerated doses, the antitumor activity in mice bearing advanced colon carcinoma can be summarized as follows: (a) FdUrd is significantly more active than FUra; (b) for both drugs the weekly for 3 weeks i.v. push schedule is superior to the c.i. or i.v. push daily for 4 days schedules; (c) pretreatment with PALA enhances the antitumor activity of FdUrd and FUra and resulted in 95 and 13% complete responses, respectively; (d) long-term survivors with FUra could only be achieved in the presence of PALA; in mice bearing leukemia 1210 cells, FdUrd or FUra with or without PALA exhibited no significant antitumor activity when PALA was administered in a single dose 24 h prior to fluoropyrimidine treatment; and (e) in C-26 and L1210, PALA reduced the pools of CTP and UTP equally, to about 10% of controls with significant difference in their rates of recovery."
09/01/2000 - "Here, we investigated the signaling pathway leading to SPP production by the G protein-coupled P2Y(2) receptor and its functional implication in human leukemia (HL-60) cells, which do not respond to extracellular SPP. P2Y(2) receptor activation by UTP or ATP resulted in rapid and transient production of SPP, which was insensitive to pertussis toxin and blocked by the sphingosine kinase inhibitor, DL-threo-dihydrosphingosine. "
12/15/1990 - "At 250 microM TDHO methyl ester, analysis of cell extracts by high-performance liquid chromatography showed that after 4 h carbamyl aspartate had accumulated from undetectable levels to 760 microM, whereas UTP decreased from 580 to 110 microM and CTP from 350 to 86 microM, indicating inhibition of dihydroorotase in growing leukemia cells. "
5. Chronic Bronchitis

Related Drugs and Biologics

1. Adenosine Triphosphate (ATP)
2. DNA Nucleotidylexotransferase (Terminal Deoxynucleotidyl Transferase)
3. Uridine
4. Cytidine Triphosphate (CTP)
5. NSC 224131 (PALA)
6. batimastat (BB 94)
7. Uridine Diphosphate (UDP)
8. Uridine Triphosphate (UTP)
9. Adenosine Diphosphate (ADP)
10. Calcium

Related Therapies and Procedures

1. Nebulizers and Vaporizers (Inhaler)
2. Transplantation (Transplant Recipients)
3. Microelectrodes
4. Drug Therapy (Chemotherapy)
5. Ligation