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Details

Stereochemistry ACHIRAL
Molecular Formula C16H23N3O4.CH4O3S
Molecular Weight 417.477
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GABEXATE MESYLATE

SMILES

CS(O)(=O)=O.CCOC(=O)C1=CC=C(OC(=O)CCCCCNC(N)=N)C=C1

InChI

InChIKey=DNTNDFLIKUKKOC-UHFFFAOYSA-N
InChI=1S/C16H23N3O4.CH4O3S/c1-2-22-15(21)12-7-9-13(10-8-12)23-14(20)6-4-3-5-11-19-16(17)18;1-5(2,3)4/h7-10H,2-6,11H2,1H3,(H4,17,18,19);1H3,(H,2,3,4)

HIDE SMILES / InChI

Molecular Formula C16H23N3O4
Molecular Weight 321.3715
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula CH4O3S
Molecular Weight 96.106
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Gabexate is a synthetic protease inhibitor, was shown to be effective in treating patients with sepsis-associated disseminated intravascular coagulation in which tumor necrosis factor-alpha (TNF-alpha) plays a critical role. Gabexate mesylate is a drug marketed only in Italy and Japan and it is considered an essential drug in the treatment of acute pancreatitis. Gabexate is marketed under the brand name REMINARON among others in Japan. It relieves inflammatory symptoms in the pancreas by inhibiting various enzymes. It also improves organ disorders and bleeding tendency caused by blood clots in blood vessels by inhibiting blood coagulation. It is usually used to treat acute pancreatitis with deviation of proteolytic enzymes (such as trypsin, kallikrein and plasmin), acute exacerbation of chronic recurrent pancreatitis, acute pancreatitis after surgery and disseminated intravascular coagulation.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
REMINARON

Approved Use

This medicine relieves inflammatory symptoms in the pancreas by inhibiting various enzymes. It also improves organ disorders and bleeding tendency caused by blood clots in blood vessels by inhibiting blood coagulation. It is usually used to treat acute pancreatitis with deviation of proteolytic enzymes (such as trypsin, kallikrein and plasmin), acute exacerbation of chronic recurrent pancreatitis, acute pancreatitis after surgery and disseminated intravascular coagulation.
Primary
REMINARON

Approved Use

This medicine relieves inflammatory symptoms in the pancreas by inhibiting various enzymes. It also improves organ disorders and bleeding tendency caused by blood clots in blood vessels by inhibiting blood coagulation. It is usually used to treat acute pancreatitis with deviation of proteolytic enzymes (such as trypsin, kallikrein and plasmin), acute exacerbation of chronic recurrent pancreatitis, acute pancreatitis after surgery and disseminated intravascular coagulation.
PubMed

PubMed

TitleDatePubMed
Selective inhibition of human mast cell tryptase by gabexate mesylate, an antiproteinase drug.
2001 Feb 1
Continuous regional arterial infusion therapy with gabexate mesilate for severe acute pancreatitis.
2008 Nov 7
Patents

Sample Use Guides

Prevention of post-endoscopic retrograde cholangiopancreatography pancreatitis: continuous intravenous infusion (600 mg)
Route of Administration: Intravenous
The LPS-induced increase in TNF-a production by human monocytes was significantly inhibited by gabexate mesilate at a concentration of 1.0 x10(-3) M.
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:28:45 UTC 2023
Edited
by admin
on Fri Dec 15 15:28:45 UTC 2023
Record UNII
E3Q07L0649
Record Status Validated (UNII)
Record Version
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Name Type Language
GABEXATE MESYLATE
Common Name English
GABEXATE MESILATE [JAN]
Common Name English
GABEXATE METHANESULFONATE
MI  
Common Name English
BENZOIC ACID, 4-((6-((AMINOIMINOMETHYL)AMINO)-1-OXOHEXYL)OXY)-, ETHYL ESTER, METHANESULFONATE (1:1)
Common Name English
GABEXATE METHANESULFONATE [MI]
Common Name English
Gabexate mesilate [WHO-DD]
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID0045591
Created by admin on Fri Dec 15 15:28:45 UTC 2023 , Edited by admin on Fri Dec 15 15:28:45 UTC 2023
PRIMARY
CAS
56974-61-9
Created by admin on Fri Dec 15 15:28:45 UTC 2023 , Edited by admin on Fri Dec 15 15:28:45 UTC 2023
PRIMARY
MERCK INDEX
m5620
Created by admin on Fri Dec 15 15:28:45 UTC 2023 , Edited by admin on Fri Dec 15 15:28:45 UTC 2023
PRIMARY Merck Index
ChEMBL
CHEMBL87563
Created by admin on Fri Dec 15 15:28:45 UTC 2023 , Edited by admin on Fri Dec 15 15:28:45 UTC 2023
PRIMARY
EVMPD
SUB02295MIG
Created by admin on Fri Dec 15 15:28:45 UTC 2023 , Edited by admin on Fri Dec 15 15:28:45 UTC 2023
PRIMARY
DRUG BANK
DBSALT002364
Created by admin on Fri Dec 15 15:28:45 UTC 2023 , Edited by admin on Fri Dec 15 15:28:45 UTC 2023
PRIMARY
PUBCHEM
6604561
Created by admin on Fri Dec 15 15:28:45 UTC 2023 , Edited by admin on Fri Dec 15 15:28:45 UTC 2023
PRIMARY
FDA UNII
E3Q07L0649
Created by admin on Fri Dec 15 15:28:45 UTC 2023 , Edited by admin on Fri Dec 15 15:28:45 UTC 2023
PRIMARY
SMS_ID
100000087255
Created by admin on Fri Dec 15 15:28:45 UTC 2023 , Edited by admin on Fri Dec 15 15:28:45 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
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ACTIVE MOIETY