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Details

Stereochemistry ACHIRAL
Molecular Formula C16H17N3OS
Molecular Weight 299.391
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of E-3040

SMILES

CNC1=NC2=C(S1)C(C)=C(O)C(C)=C2CC3=CN=CC=C3

InChI

InChIKey=IONAQTGMWFXHIX-UHFFFAOYSA-N
InChI=1S/C16H17N3OS/c1-9-12(7-11-5-4-6-18-8-11)13-15(10(2)14(9)20)21-16(17-3)19-13/h4-6,8,20H,7H2,1-3H3,(H,17,19)

HIDE SMILES / InChI

Molecular Formula C16H17N3OS
Molecular Weight 299.391
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Interactions of urate transporter URAT1 in human kidney with uricosuric drugs.
2011-02
Construction of triple-transfected cells [organic anion-transporting polypeptide (OATP) 1B1/multidrug resistance-associated protein (MRP) 2/MRP3 and OATP1B1/MRP2/MRP4] for analysis of the sinusoidal function of MRP3 and MRP4.
2009-10
Role of breast cancer resistance protein (Bcrp1/Abcg2) in the extrusion of glucuronide and sulfate conjugates from enterocytes to intestinal lumen.
2005-03
Impaired renal excretion of 6-hydroxy-5,7-dimethyl-2-methylamino-4-(3-pyridylmethyl) benzothiazole (E3040) sulfate in breast cancer resistance protein (BCRP1/ABCG2) knockout mice.
2004-09
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 23:42:14 GMT 2025
Edited
by admin
on Mon Mar 31 23:42:14 GMT 2025
Record UNII
T4AB9WQ98U
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
E-3040
Code English
E 3040
Preferred Name English
6-HYDROXY-5,7-DIMETHYL-2-METHYLAMINO-4-(3-PYRIDYLMETHYL)BENZOTHIAZOLE
Common Name English
5,7-DIMETHYL-2-(METHYLAMINO)-4-(3-PYRIDINYLMETHYL)-6-BENZOTHIAZOLOL
Systematic Name English
6-BENZOTHIAZOLOL, 5,7-DIMETHYL-2-(METHYLAMINO)-4-(3-PYRIDINYLMETHYL)-
Systematic Name English
E3040
Code English
Code System Code Type Description
CHEBI
4732
Created by admin on Mon Mar 31 23:42:14 GMT 2025 , Edited by admin on Mon Mar 31 23:42:14 GMT 2025
PRIMARY
PUBCHEM
443292
Created by admin on Mon Mar 31 23:42:14 GMT 2025 , Edited by admin on Mon Mar 31 23:42:14 GMT 2025
PRIMARY
FDA UNII
T4AB9WQ98U
Created by admin on Mon Mar 31 23:42:14 GMT 2025 , Edited by admin on Mon Mar 31 23:42:14 GMT 2025
PRIMARY
EPA CompTox
DTXSID80162877
Created by admin on Mon Mar 31 23:42:14 GMT 2025 , Edited by admin on Mon Mar 31 23:42:14 GMT 2025
PRIMARY
CAS
145096-30-6
Created by admin on Mon Mar 31 23:42:14 GMT 2025 , Edited by admin on Mon Mar 31 23:42:14 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY