Details
Stereochemistry | ACHIRAL |
Molecular Formula | C7H4O7 |
Molecular Weight | 200.1025 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C1=CC(=O)C(O)=C(O1)C(O)=O
InChI
InChIKey=ZEGRKMXCOCRTCS-UHFFFAOYSA-N
InChI=1S/C7H4O7/c8-2-1-3(6(10)11)14-5(4(2)9)7(12)13/h1,9H,(H,10,11)(H,12,13)
Molecular Formula | C7H4O7 |
Molecular Weight | 200.1025 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Poppy acid occurs in opium (Papaver somniferum) and other Papaver species. Meconic acid has been described as a mild narcotic, but it has little or no physiological action, and is not now used medicinally. Its chemical reactions are of importance in toxicology as a valuable indication of the presence of opium.
CNS Activity
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL2094129 Sources: https://www.ncbi.nlm.nih.gov/pubmed/10768488 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Unknown Approved UseUnknown |
PubMed
Title | Date | PubMed |
---|---|---|
Liquid chromatographic-atmospheric pressure chemical ionization mass spectrometric analysis of opiates and metabolites in rat urine after inhalation of opium. | 2003 Jun 5 |
|
The monoethyl ester of meconic acid is an active site inhibitor of HCV NS5B RNA-dependent RNA polymerase. | 2004 Jun 21 |
|
HCV NS5b RNA-dependent RNA polymerase inhibitors: from alpha,gamma-diketoacids to 4,5-dihydroxypyrimidine- or 3-methyl-5-hydroxypyrimidinonecarboxylic acids. Design and synthesis. | 2004 Oct 21 |
|
Inhibitors of foot and mouth disease virus targeting a novel pocket of the RNA-dependent RNA polymerase. | 2010 Dec 21 |
Patents
Sample Use Guides
Dogs: Meconic acid, taken in a dose of from eight to ten grains, produces no sensible effect upon young and week dogs.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/10768488
Effects of comenic and meconic acids on cultured dorsal root ganglion cells were investigated by the whole-cell patch clamp technique. The acids decreased effective charge transfer in the activation gating system of TTX-resistant (slow) sodium channels in a dose-dependent manner. The effects were described by Hill's equation. The dissociation constant and Hill coefficient values were K(D) = 100 nM and X = 0.5 (for comenic acid) and K(D) = 10 nM and X = 0.34 (for meconic acid).
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 04:19:05 GMT 2023
by
admin
on
Sat Dec 16 04:19:05 GMT 2023
|
Record UNII |
V502I79516
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
m7123
Created by
admin on Sat Dec 16 04:19:05 GMT 2023 , Edited by admin on Sat Dec 16 04:19:05 GMT 2023
|
PRIMARY | Merck Index | ||
|
V502I79516
Created by
admin on Sat Dec 16 04:19:05 GMT 2023 , Edited by admin on Sat Dec 16 04:19:05 GMT 2023
|
PRIMARY | |||
|
207-848-2
Created by
admin on Sat Dec 16 04:19:05 GMT 2023 , Edited by admin on Sat Dec 16 04:19:05 GMT 2023
|
PRIMARY | |||
|
DTXSID2060096
Created by
admin on Sat Dec 16 04:19:05 GMT 2023 , Edited by admin on Sat Dec 16 04:19:05 GMT 2023
|
PRIMARY | |||
|
10347
Created by
admin on Sat Dec 16 04:19:05 GMT 2023 , Edited by admin on Sat Dec 16 04:19:05 GMT 2023
|
PRIMARY | |||
|
805
Created by
admin on Sat Dec 16 04:19:05 GMT 2023 , Edited by admin on Sat Dec 16 04:19:05 GMT 2023
|
PRIMARY | |||
|
497-59-6
Created by
admin on Sat Dec 16 04:19:05 GMT 2023 , Edited by admin on Sat Dec 16 04:19:05 GMT 2023
|
PRIMARY | |||
|
MECONIC ACID
Created by
admin on Sat Dec 16 04:19:05 GMT 2023 , Edited by admin on Sat Dec 16 04:19:05 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
SOLVATE->ANHYDROUS | |||
|
SOLVATE->ANHYDROUS |