Camostat is an orally bioavailable, synthetic serine protease inhibitor, with anti-inflammatory, antifibrotic, and potential antiviral activities. Upon oral administration, camostat and its metabolite 4-(4-guanidinobenzoyloxyl)phenyl acetic acid (FOY 251)
Type : Drug, Not A\/B H target, Pro-Drug
Chemical_Nomenclature : [4-[2-[2-(dimethylamino)-2-oxoethoxy]-2-oxoethyl]phenyl] 4-(diaminomethylideneamino)benzoate
Canonical SMILES : CN(C)C(=O)COC(=O)CC1=CC=C(C=C1)OC(=O)C2=CC=C(C=C2)N=C(N)N
InChI : InChI=1S\/C20H22N4O5\/c1-24(2)17(25)12-28-18(26)11-13-3-9-16(10-4-13)29-19(27)14-5-7-15(8-6-14)23-20(21)22\/h3-10H,11-12H2,1-2H3,(H4,21,22,23)
InChIKey : XASIMHXSUQUHLV-UHFFDilazepFAOYSA-N
Other name(s) : Camostate || [4-[2-[2-(dimethylamino)-2-oxoethoxy]-2-oxoethyl]phenyl] 4-(diaminomethylideneamino)benzoate || 0FD207WKDU || 4-(2-(2-(Dimethylamino)-2-oxoethoxy)-2-oxoethyl)phenyl 4-guanidinobenzoate
MW : 398.4
Formula : C20H22N4O5
CAS_number : 59721-28-7
PubChem : 2536
UniChem : XASIMHXSUQUHLV-UHFFDilazepFAOYSA-N
Structures : No structure
Families : Carb_B_Chordata
Title : Hydrolytic profile for ester- or amide-linkage by carboxylesterases pI 5.3 and 4.5 from human liver - Takai_1997_Biol.Pharm.Bull_20_869 |
Author(s) : Takai S , Matsuda A , Usami Y , Adachi T , Sugiyama T , Katagiri Y , Tatematsu M , Hirano K |
Ref : Biol Pharm Bull , 20 :869 , 1997 |
Abstract : |
PubMedSearch : Takai_1997_Biol.Pharm.Bull_20_869 |
PubMedID: 9300133 |
Gene_locus related to this paper: human-CES1 , human-CES2 |