Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C17H12O8 |
| Molecular Weight | 344.2724 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCC1=C2OC(=CC(=O)C2=CC3=C1OC(=CC3=O)C(O)=O)C(O)=O
InChI
InChIKey=WEQNUNAIQXHGHB-UHFFFAOYSA-N
InChI=1S/C17H12O8/c1-2-3-7-14-8(10(18)5-12(24-14)16(20)21)4-9-11(19)6-13(17(22)23)25-15(7)9/h4-6H,2-3H2,1H3,(H,20,21)(H,22,23)
| Molecular Formula | C17H12O8 |
| Molecular Weight | 344.2724 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Probicromil is a Histamine H1 antagonist. It was taken to the clinic and found to be effective in exercise and antigen challenge. Probicromil inhibited Ascaris-induced bronchoconstriction and the increase in plasma histamine levels seen after Ascaris inhalation. Therapeutic efficacy in seasonal rhinitis was also demonstrated. Further clinical studies were halted because of a side-effect associated with the compound, namely a sensation of warmth (especially in the perineal region) experienced by some volunteers after inhalation.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:17:46 GMT 2025
by
admin
on
Mon Mar 31 18:17:46 GMT 2025
|
| Record UNII |
49BO3YUP40
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C29714
Created by
admin on Mon Mar 31 18:17:46 GMT 2025 , Edited by admin on Mon Mar 31 18:17:46 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
CHEMBL2110970
Created by
admin on Mon Mar 31 18:17:46 GMT 2025 , Edited by admin on Mon Mar 31 18:17:46 GMT 2025
|
PRIMARY | |||
|
58805-38-2
Created by
admin on Mon Mar 31 18:17:46 GMT 2025 , Edited by admin on Mon Mar 31 18:17:46 GMT 2025
|
PRIMARY | |||
|
C84108
Created by
admin on Mon Mar 31 18:17:46 GMT 2025 , Edited by admin on Mon Mar 31 18:17:46 GMT 2025
|
PRIMARY | |||
|
49BO3YUP40
Created by
admin on Mon Mar 31 18:17:46 GMT 2025 , Edited by admin on Mon Mar 31 18:17:46 GMT 2025
|
PRIMARY | |||
|
100000087667
Created by
admin on Mon Mar 31 18:17:46 GMT 2025 , Edited by admin on Mon Mar 31 18:17:46 GMT 2025
|
PRIMARY | |||
|
5098
Created by
admin on Mon Mar 31 18:17:46 GMT 2025 , Edited by admin on Mon Mar 31 18:17:46 GMT 2025
|
PRIMARY | |||
|
C040112
Created by
admin on Mon Mar 31 18:17:46 GMT 2025 , Edited by admin on Mon Mar 31 18:17:46 GMT 2025
|
PRIMARY | |||
|
71950
Created by
admin on Mon Mar 31 18:17:46 GMT 2025 , Edited by admin on Mon Mar 31 18:17:46 GMT 2025
|
PRIMARY | |||
|
DTXSID10866710
Created by
admin on Mon Mar 31 18:17:46 GMT 2025 , Edited by admin on Mon Mar 31 18:17:46 GMT 2025
|
PRIMARY | |||
|
SUB05396MIG
Created by
admin on Mon Mar 31 18:17:46 GMT 2025 , Edited by admin on Mon Mar 31 18:17:46 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
SALT/SOLVATE -> PARENT |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |