MMU

General

Type : Natural,Urea derivative

Chemical_Nomenclature : 1,3-bis[(4-methoxyphenyl)methyl]urea

Canonical SMILES : COC1=CC=C(C=C1)CNC(=O)NCC2=CC=C(C=C2)OC

InChI : InChI=1S\/C17H20N2O3\/c1-21-15-7-3-13(4-8-15)11-18-17(20)19-12-14-5-9-16(22-2)10-6-14\/h3-10H,11-12H2,1-2H3,(H2,18,19,20)

InChIKey : PPSSZWOYSHYRJP-UHFFFAOYSA-N

Other name(s) : 1,3-bis(4-methoxybenzyl)urea,1,3-bis[(4-methoxyphenyl)methyl]urea,N,N'-bis(4-methoxybenzyl)urea,ST50667790,NSC108740


MW : 300.35

Formula : C17H20N2O3

CAS_number : 93731-94-3

PubChem : 268493

UniChem : PPSSZWOYSHYRJP-UHFFFAOYSA-N

IUPHAR :

Wikipedia :

Target

Families : MMU ligand of proteins in family: Epoxide_hydrolase

Stucture :

Protein :

References (3)

Title : Occurrence of urea-based soluble epoxide hydrolase inhibitors from the plants in the order Brassicales - Kitamura_2017_PLoS.One_12_e0176571
Author(s) : Kitamura S , Morisseau C , Harris TR , Inceoglu B , Hammock BD
Ref : PLoS ONE , 12 :e0176571 , 2017
Abstract : Kitamura_2017_PLoS.One_12_e0176571
ESTHER : Kitamura_2017_PLoS.One_12_e0176571
PubMedSearch : Kitamura_2017_PLoS.One_12_e0176571
PubMedID: 28472063

Title : Potent natural soluble epoxide hydrolase inhibitors from Pentadiplandra brazzeana baillon: synthesis, quantification, and measurement of biological activities in vitro and in vivo - Kitamura_2015_PLoS.One_10_e0117438
Author(s) : Kitamura S , Morisseau C , Inceoglu B , Kamita SG , De Nicola GR , Nyegue M , Hammock BD
Ref : PLoS ONE , 10 :e0117438 , 2015
Abstract : Kitamura_2015_PLoS.One_10_e0117438
ESTHER : Kitamura_2015_PLoS.One_10_e0117438
PubMedSearch : Kitamura_2015_PLoS.One_10_e0117438
PubMedID: 25659109

Title : Urea derivatives from Pentadiplandra brazzeana - Tsopmo_1999_J.Nat.Prod_62_1435
Author(s) : Tsopmo A , Ngnokam D , Ngamga D , Ayafor JF , Sterner O
Ref : Journal of Natural Products , 62 :1435 , 1999
Abstract : Tsopmo_1999_J.Nat.Prod_62_1435
ESTHER : Tsopmo_1999_J.Nat.Prod_62_1435
PubMedSearch : Tsopmo_1999_J.Nat.Prod_62_1435
PubMedID: 10543911