Details
Stereochemistry | EPIMERIC |
Molecular Formula | C17H24NO3.Br |
Molecular Weight | 370.281 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 3 / 4 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[Br-].C[N+]1(C)[C@H]2CC[C@@H]1C[C@@H](C2)OC(=O)C(O)C3=CC=CC=C3
InChI
InChIKey=FUFVKLQESJNNAN-RIMUKSHESA-M
InChI=1S/C17H24NO3.BrH/c1-18(2)13-8-9-14(18)11-15(10-13)21-17(20)16(19)12-6-4-3-5-7-12;/h3-7,13-16,19H,8-11H2,1-2H3;1H/q+1;/p-1/t13-,14+,15+,16?;
Molecular Formula | C17H23NO3 |
Molecular Weight | 289.3694 |
Charge | 0 |
Count |
|
Stereochemistry | MIXED |
Additional Stereochemistry | No |
Defined Stereocenters | 3 / 4 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Molecular Formula | BrH |
Molecular Weight | 80.912 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
DescriptionSources: https://www.drugs.com/pro/hydromet.html
Sources: https://www.drugs.com/pro/hydromet.html
Homatropine methylbromide or Methylhomatropine bromide is a quaternary ammonium salt of methylhomatropine. It is a peripherally acting anticholinergic medication that inhibits muscarinic acetylcholine receptors and thus the parasympathetic nervous system. Certain preparations of drugs such as hydrocodone are mixed with a small, sub-therapeutic amount of homatropine methylbromide to discourage intentional overdose.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL2094109 Sources: https://www.ncbi.nlm.nih.gov/pubmed/6135619 |
350.0 nM [Ki] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Sources: http://www.ndrugs.com/?s=paratropina |
Primary | PARATROPINA Approved UseFor spasmodic pains & disorders of the GIT eg irritable colon, mucous colitis, colicky pains, peptic ulcer, pylorospasm, cardiospasm, flatulence, nausea, vomiting & hyperacidity |
Sample Use Guides
In Vivo Use Guide
Sources: http://www.paratropina.com.ar/como-se-toma.php
Oral administration: 40 drops of paratropin should be dissolved in a glass of water and administered orally.
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/6135619
The brains from SD rats were removed following decapitation, dissected free of membranes, and the cerebella discarded. Tissues were then homogenized with a Brinkmann Polytron in 20 vol of ice cold Tris-HCl buffer (50 mM, pH 7.7). The homogenates were centrifuged at 40000 × g for 10 min at 4°C and the pellets resuspended in the buffer at a concentration of 50 mg wet weight/ml. Radioligand displacement binding studies were performed using 0.06 nM of [3H]QNB and 0.2-0.4 mg protein. The Kd value for [3H]QNB was previously determined in our laboratory to be 0.1 nM. Analysis of the results was performed as described above. Methylhomatropine displaces radioligand with Ki of 350 nM.
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 17:10:54 GMT 2023
by
admin
on
Fri Dec 15 17:10:54 GMT 2023
|
Record UNII |
68JRS2HC1C
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Brand Name | English | ||
|
Common Name | English | ||
|
Brand Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C29704
Created by
admin on Fri Dec 15 17:10:54 GMT 2023 , Edited by admin on Fri Dec 15 17:10:54 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
C61784
Created by
admin on Fri Dec 15 17:10:54 GMT 2023 , Edited by admin on Fri Dec 15 17:10:54 GMT 2023
|
PRIMARY | |||
|
C056244
Created by
admin on Fri Dec 15 17:10:54 GMT 2023 , Edited by admin on Fri Dec 15 17:10:54 GMT 2023
|
PRIMARY | |||
|
68JRS2HC1C
Created by
admin on Fri Dec 15 17:10:54 GMT 2023 , Edited by admin on Fri Dec 15 17:10:54 GMT 2023
|
PRIMARY | |||
|
DB00725
Created by
admin on Fri Dec 15 17:10:54 GMT 2023 , Edited by admin on Fri Dec 15 17:10:54 GMT 2023
|
PRIMARY | |||
|
SUB08048MIG
Created by
admin on Fri Dec 15 17:10:54 GMT 2023 , Edited by admin on Fri Dec 15 17:10:54 GMT 2023
|
PRIMARY | |||
|
757048
Created by
admin on Fri Dec 15 17:10:54 GMT 2023 , Edited by admin on Fri Dec 15 17:10:54 GMT 2023
|
PRIMARY | |||
|
CHEMBL1201235
Created by
admin on Fri Dec 15 17:10:54 GMT 2023 , Edited by admin on Fri Dec 15 17:10:54 GMT 2023
|
PRIMARY | |||
|
100000083964
Created by
admin on Fri Dec 15 17:10:54 GMT 2023 , Edited by admin on Fri Dec 15 17:10:54 GMT 2023
|
PRIMARY | |||
|
DTXSID4023127
Created by
admin on Fri Dec 15 17:10:54 GMT 2023 , Edited by admin on Fri Dec 15 17:10:54 GMT 2023
|
PRIMARY | |||
|
HOMATROPINE METHYLBROMIDE
Created by
admin on Fri Dec 15 17:10:54 GMT 2023 , Edited by admin on Fri Dec 15 17:10:54 GMT 2023
|
PRIMARY | Description: A white, crystalline powder; odourless. Solubility: Very soluble in water; freely soluble in ethanol (~750 g/l) TS; practically insoluble in ether R and acetone R. Category: Mydriatic. Storage: Homatropine methylbromide should be kept in a tightly closed container, protected from light. Additional information: Homatropine methylbromide darkens on exposure to light. Requirement: Homatropine methylbromide contains not less than 98.5% and not more than the equivalent of 101.0% of C17H24BrNO3, calculated with reference to the dried substance. | ||
|
1311000
Created by
admin on Fri Dec 15 17:10:54 GMT 2023 , Edited by admin on Fri Dec 15 17:10:54 GMT 2023
|
PRIMARY | |||
|
34399
Created by
admin on Fri Dec 15 17:10:54 GMT 2023 , Edited by admin on Fri Dec 15 17:10:54 GMT 2023
|
PRIMARY | |||
|
68JRS2HC1C
Created by
admin on Fri Dec 15 17:10:54 GMT 2023 , Edited by admin on Fri Dec 15 17:10:54 GMT 2023
|
PRIMARY | |||
|
80-49-9
Created by
admin on Fri Dec 15 17:10:54 GMT 2023 , Edited by admin on Fri Dec 15 17:10:54 GMT 2023
|
PRIMARY | |||
|
27085
Created by
admin on Fri Dec 15 17:10:54 GMT 2023 , Edited by admin on Fri Dec 15 17:10:54 GMT 2023
|
PRIMARY | RxNorm | ||
|
131
Created by
admin on Fri Dec 15 17:10:54 GMT 2023 , Edited by admin on Fri Dec 15 17:10:54 GMT 2023
|
PRIMARY | |||
|
Homatropine methylbromide
Created by
admin on Fri Dec 15 17:10:54 GMT 2023 , Edited by admin on Fri Dec 15 17:10:54 GMT 2023
|
PRIMARY | |||
|
201-284-0
Created by
admin on Fri Dec 15 17:10:54 GMT 2023 , Edited by admin on Fri Dec 15 17:10:54 GMT 2023
|
PRIMARY | |||
|
m6038
Created by
admin on Fri Dec 15 17:10:54 GMT 2023 , Edited by admin on Fri Dec 15 17:10:54 GMT 2023
|
PRIMARY | Merck Index | ||
|
50373
Created by
admin on Fri Dec 15 17:10:54 GMT 2023 , Edited by admin on Fri Dec 15 17:10:54 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
PARENT -> SALT/SOLVATE |
Related Record | Type | Details | ||
---|---|---|---|---|
|
IMPURITY -> PARENT |
|
||
|
IMPURITY -> PARENT |
|
||
|
IMPURITY -> PARENT |
|
Related Record | Type | Details | ||
---|---|---|---|---|
|
ACTIVE MOIETY |