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ONO 3307
RN given refers to parent cpd; structure given in first source
Also Known As:
4-sulfamoylphenyl 4-guanidinobenzoate methanesulfonate; 4-sulfamoylphenyl 4-guanidinobenzoate monomethanesulfonate; ONO-3307
Networked:
8
relevant articles (
7
outcomes,
2
trials/studies)
Relationship Network
Bio-Agent Context: Research Results
Organic Chemicals: 133
Amidines: 14
Guanidines: 29
ONO 3307: 8
Related Diseases
1.
Pancreatitis
03/01/1993 - "
The survival rates were improved dose dependently when ONO-3307 was administered 1 h before and after induction of pancreatitis.
"
03/01/1993 - "
ONO-3307 showed favorable effects on the initial stage of severe acute pancreatitis when given in divided doses to maintain the effective serum levels.
"
01/01/1992 - "
ONO 3307 showed a significant protective effect against this hepatic injury in acute pancreatitis, the dose of 5 mg/kg.h showing a more potent effect than the dose of 2 mg/kg.h.
"
09/01/1992 - "
These results suggest that impaired hepatic energy metabolism is closely related to increased hepatic lysosomal and mitochondrial fragility and that some proteases, which are derived from pancreatitis and are susceptible to inhibition by ONO 3307, seem to play an important pathological role in this liver injury induced by pancreatitis.
"
09/01/1992 - "
Decreased BKBR and hepatic EC as well as increased hepatic lysosomal and mitochondrial fragility were observed in rats with this type of acute pancreatitis, and both PGE2 and ONO 3307 had a significant protective effect against hepatic injury in these rats, especially ONO 3307.
"
2.
Wounds and Injuries (Trauma)
05/01/1992 - "
The administration of ONO 3307 plus allopurinol almost completely prevented the pancreatic injuries induced by PBDO with ischemia.
"
06/01/1995 - "
To evaluate the protective effects of combined prophylaxis with 4-sulfamoylphenyl, 4-guanidinobenzoate methanesulfonate (E3123), potent new protease inhibitor, and superoxide dismutase (SOD), a free radical scavenger, against the multifactor-related pancreatic injuries that occur in acute pancreatitis.
"
3.
Disseminated Intravascular Coagulation
10/01/1990 - "
Protective effects of ONO-3307, a new synthetic protease inhibitor against experimental disseminated intravascular coagulation in rats.
"
12/01/1989 - "
To examine the effects of ONO-3307 on disseminated intravascular coagulation (DIC), we developed an experimental thrombosis model.
"
10/01/1990 - "
The effects of ONO-3307 (4-sulfamoylphenyl 4-guanidinobenzoate methanesulfonate), a new synthetic protease inhibitor, on endotoxin-induced experimental disseminated intravascular coagulation (DIC) were studied in rats.
"
4.
Thrombosis (Thrombus)
12/01/1989 - "
To examine the effects of ONO-3307 on disseminated intravascular coagulation (DIC), we developed an experimental thrombosis model.
"
12/01/1989 - "
These results indicate that ONO-3307 exhibits a wide range of inhibitory effects on various proteases, and ONO-3307 may be useful for the treatment of protease-mediated diseases such as thrombosis and DIC.
"
12/01/1989 - "
The effect of ONO-3307 (4-sulfamoyl phenyl-4-guanidinobenzoate methanesulfonate), a new protease inhibitor, was studied on various proteases in vitro and in an experimental thrombosis model in vivo.
"
12/01/1989 - "
Inhibitory effects of ONO-3307 on various proteases and tissue thromboplastin in vitro and on experimental thrombosis in vivo.
"
5.
Ischemia
05/01/1992 - "
The administration of ONO 3307 plus allopurinol almost completely prevented the pancreatic injuries induced by PBDO with ischemia.
"
05/01/1992 - "
The protective effect of a new potent protease inhibitor, ONO 3307, in combination with a xanthine oxidase inhibitor, allopurinol, was tested in pancreatico-biliary duct obstruction (PBDO) with temporary pancreatic ischemia in rats.
"
Related Drugs and Biologics
1.
Protease Inhibitors (Protease Inhibitor)
2.
Ceruletide
3.
Dinoprostone (PGE2)
4.
NAD (NADH)
5.
Malate Dehydrogenase (Dehydrogenase, Malate)
6.
Ketones
7.
Hexosaminidases (Hexosaminidase)
8.
Glucuronidase
9.
Enzymes
10.
Cathepsin B
Related Therapies and Procedures
1.
Therapeutics