U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C26H37N3O4
Molecular Weight 455.5897
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MOXILUBANT

SMILES

COC1=C(OCCCCCOC2=CC=C(C=C2)C(N)=N)C=CC(=C1)C(=O)N(C(C)C)C(C)C

InChI

InChIKey=VAYJLOGCWOXMAS-UHFFFAOYSA-N
InChI=1S/C26H37N3O4/c1-18(2)29(19(3)4)26(30)21-11-14-23(24(17-21)31-5)33-16-8-6-7-15-32-22-12-9-20(10-13-22)25(27)28/h9-14,17-19H,6-8,15-16H2,1-5H3,(H3,27,28)

HIDE SMILES / InChI

Molecular Formula C26H37N3O4
Molecular Weight 455.5897
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Moxilubant is an orally active leukotriene B4 antagonist patented by Ciba-Geigy A.-G. and studied for psoriasis, rheumatoid arthritis, and chronic obstructive pulmonary disease treatment. Moxilubant inhibits LTB4 signaling with a potency of 2–4 nM. In a phase 1 study in 10 healthy volunteers, Moxilubant was administered orally once or twice daily for 7 days at doses ranging from 100 to 500 mg. At dose levels of 150 mg and above, LTB4 pathway inhibition reached at least 75%. At doses of 300 mg and above, pathway inhibition reached 100%. A Phase 2 study was conducted in 24 patients with COPD treated with 240 mg/day Moxilubant for 4 weeks. In this study, there were no changes in sputum cell counts or biomarkers or in spirometry measures, even though plasma levels of Moxilubant were sufficient to significantly reduce pathway signaling.

Approval Year

PubMed

PubMed

TitleDatePubMed
Recent advances in clinical development of leukotriene B4 pathway drugs.
2017 Oct
Patents

Patents

Sample Use Guides

300 mg
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:05:34 UTC 2023
Edited
by admin
on Fri Dec 15 18:05:34 UTC 2023
Record UNII
2F3QKD3W17
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MOXILUBANT
INN  
INN  
Official Name English
4-((5-(P-AMIDINOPHENOXY)PENTYL)OXY)-N,N-DIISOPROPYL-3-METHOXYBENZAMIDE
Common Name English
moxilubant [INN]
Common Name English
Code System Code Type Description
SMS_ID
100000080599
Created by admin on Fri Dec 15 18:05:34 UTC 2023 , Edited by admin on Fri Dec 15 18:05:34 UTC 2023
PRIMARY
INN
7676
Created by admin on Fri Dec 15 18:05:34 UTC 2023 , Edited by admin on Fri Dec 15 18:05:34 UTC 2023
PRIMARY
PUBCHEM
9955657
Created by admin on Fri Dec 15 18:05:34 UTC 2023 , Edited by admin on Fri Dec 15 18:05:34 UTC 2023
PRIMARY
EVMPD
SUB09087MIG
Created by admin on Fri Dec 15 18:05:34 UTC 2023 , Edited by admin on Fri Dec 15 18:05:34 UTC 2023
PRIMARY
EPA CompTox
DTXSID90163552
Created by admin on Fri Dec 15 18:05:34 UTC 2023 , Edited by admin on Fri Dec 15 18:05:34 UTC 2023
PRIMARY
NCI_THESAURUS
C166570
Created by admin on Fri Dec 15 18:05:34 UTC 2023 , Edited by admin on Fri Dec 15 18:05:34 UTC 2023
PRIMARY
ChEMBL
CHEMBL89326
Created by admin on Fri Dec 15 18:05:34 UTC 2023 , Edited by admin on Fri Dec 15 18:05:34 UTC 2023
PRIMARY
CAS
146978-48-5
Created by admin on Fri Dec 15 18:05:34 UTC 2023 , Edited by admin on Fri Dec 15 18:05:34 UTC 2023
PRIMARY
FDA UNII
2F3QKD3W17
Created by admin on Fri Dec 15 18:05:34 UTC 2023 , Edited by admin on Fri Dec 15 18:05:34 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY