Details
Stereochemistry | ACHIRAL |
Molecular Formula | C16H15FO |
Molecular Weight | 242.2881 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC(\C=C\C2=CC=C(F)C=C2)=CC(C)=C1O
InChI
InChIKey=HJGJDFXTHQBVNV-ONEGZZNKSA-N
InChI=1S/C16H15FO/c1-11-9-14(10-12(2)16(11)18)4-3-13-5-7-15(17)8-6-13/h3-10,18H,1-2H3/b4-3+
Molecular Formula | C16H15FO |
Molecular Weight | 242.2881 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
The effects of a 5-lipoxygenase inhibitor on antigen-induced mediator release, late-phase bronchoconstriction and cellular infiltrates in primates. | 1991 |
|
BI-L-239, a 5-lipoxygenase inhibitor, blocks inhaled antigen-induced airway hyperresponsiveness in conscious guinea pigs. | 1991 Sep |
Sample Use Guides
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/8473681
In vitro enofelast (BI-L-239) inhibited 5-lipoxygenase product generation from human lung mast cells, alveolar macrophages, and peripheral blood leukocytes with a concentration that would provide 50% inhibition values of 28 to 340 nmol/L.
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 16:13:48 GMT 2023
by
admin
on
Sat Dec 16 16:13:48 GMT 2023
|
Record UNII |
3T93TS0430
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C29712
Created by
admin on Sat Dec 16 16:13:48 GMT 2023 , Edited by admin on Sat Dec 16 16:13:48 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
6439222
Created by
admin on Sat Dec 16 16:13:48 GMT 2023 , Edited by admin on Sat Dec 16 16:13:48 GMT 2023
|
PRIMARY | |||
|
127035-60-3
Created by
admin on Sat Dec 16 16:13:48 GMT 2023 , Edited by admin on Sat Dec 16 16:13:48 GMT 2023
|
PRIMARY | |||
|
C74134
Created by
admin on Sat Dec 16 16:13:48 GMT 2023 , Edited by admin on Sat Dec 16 16:13:48 GMT 2023
|
PRIMARY | |||
|
CHEMBL57358
Created by
admin on Sat Dec 16 16:13:48 GMT 2023 , Edited by admin on Sat Dec 16 16:13:48 GMT 2023
|
PRIMARY | |||
|
DD-20
Created by
admin on Sat Dec 16 16:13:48 GMT 2023 , Edited by admin on Sat Dec 16 16:13:48 GMT 2023
|
PRIMARY | |||
|
SUB06538MIG
Created by
admin on Sat Dec 16 16:13:48 GMT 2023 , Edited by admin on Sat Dec 16 16:13:48 GMT 2023
|
PRIMARY | |||
|
6962
Created by
admin on Sat Dec 16 16:13:48 GMT 2023 , Edited by admin on Sat Dec 16 16:13:48 GMT 2023
|
PRIMARY | |||
|
C067524
Created by
admin on Sat Dec 16 16:13:48 GMT 2023 , Edited by admin on Sat Dec 16 16:13:48 GMT 2023
|
PRIMARY | |||
|
100000080253
Created by
admin on Sat Dec 16 16:13:48 GMT 2023 , Edited by admin on Sat Dec 16 16:13:48 GMT 2023
|
PRIMARY | |||
|
3T93TS0430
Created by
admin on Sat Dec 16 16:13:48 GMT 2023 , Edited by admin on Sat Dec 16 16:13:48 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
ACTIVE MOIETY |