Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H7BrN4O2.C4H11NO |
| Molecular Weight | 348.196 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)(N)CO.CN1C2=C(N=C(Br)N2)C(=O)N(C)C1=O
InChI
InChIKey=ATOTUUBRFJHZQG-UHFFFAOYSA-N
InChI=1S/C7H7BrN4O2.C4H11NO/c1-11-4-3(9-6(8)10-4)5(13)12(2)7(11)14;1-4(2,5)3-6/h1-2H3,(H,9,10);6H,3,5H2,1-2H3
| Molecular Formula | C4H11NO |
| Molecular Weight | 89.1362 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C7H7BrN4O2 |
| Molecular Weight | 259.06 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL318 Sources: https://www.ncbi.nlm.nih.gov/pubmed/8410976 |
10.2 µM [Ki] |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Palliative | DIUREX Approved UseUnknown |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
3685.6 ng/mL |
25 mg single, oral dose: 25 mg route of administration: Oral experiment type: SINGLE co-administered: ACETAMINOPHEN |
BROMOTHEOPHYLLINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: FASTED |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
46210.49 ng × h/mL |
25 mg single, oral dose: 25 mg route of administration: Oral experiment type: SINGLE co-administered: ACETAMINOPHEN |
BROMOTHEOPHYLLINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: FASTED |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
21.35 h |
25 mg single, oral dose: 25 mg route of administration: Oral experiment type: SINGLE co-administered: ACETAMINOPHEN |
BROMOTHEOPHYLLINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE food status: FASTED |
Doses
| Dose | Population | Adverse events |
|---|---|---|
25 mg 1 times / day multiple, oral Dose: 25 mg, 1 times / day Route: oral Route: multiple Dose: 25 mg, 1 times / day Sources: |
unhealthy, 26 years |
Disc. AE: Fixed drug eruption... AEs leading to discontinuation/dose reduction: Fixed drug eruption Sources: |
900 mg 1 times / day multiple, oral Highest studied dose Dose: 900 mg, 1 times / day Route: oral Route: multiple Dose: 900 mg, 1 times / day Sources: |
unhealthy, 44-78 years Health Status: unhealthy Age Group: 44-78 years Sex: M+F Sources: |
Disc. AE: Diarrhea... AEs leading to discontinuation/dose reduction: Diarrhea (mild, 1 patient) Sources: |
600 mg 1 times / day multiple, oral Dose: 600 mg, 1 times / day Route: oral Route: multiple Dose: 600 mg, 1 times / day Sources: |
unhealthy, 44-78 years Health Status: unhealthy Age Group: 44-78 years Sex: M+F Sources: |
Disc. AE: Nausea, Vomiting... AEs leading to discontinuation/dose reduction: Nausea (severe, 4 patients) Sources: Vomiting (severe, 4 patients) Skin rash (1 patient) |
AEs
| AE | Significance | Dose | Population |
|---|---|---|---|
| Fixed drug eruption | Disc. AE | 25 mg 1 times / day multiple, oral Dose: 25 mg, 1 times / day Route: oral Route: multiple Dose: 25 mg, 1 times / day Sources: |
unhealthy, 26 years |
| Diarrhea | mild, 1 patient Disc. AE |
900 mg 1 times / day multiple, oral Highest studied dose Dose: 900 mg, 1 times / day Route: oral Route: multiple Dose: 900 mg, 1 times / day Sources: |
unhealthy, 44-78 years Health Status: unhealthy Age Group: 44-78 years Sex: M+F Sources: |
| Skin rash | 1 patient Disc. AE |
600 mg 1 times / day multiple, oral Dose: 600 mg, 1 times / day Route: oral Route: multiple Dose: 600 mg, 1 times / day Sources: |
unhealthy, 44-78 years Health Status: unhealthy Age Group: 44-78 years Sex: M+F Sources: |
| Nausea | severe, 4 patients Disc. AE |
600 mg 1 times / day multiple, oral Dose: 600 mg, 1 times / day Route: oral Route: multiple Dose: 600 mg, 1 times / day Sources: |
unhealthy, 44-78 years Health Status: unhealthy Age Group: 44-78 years Sex: M+F Sources: |
| Vomiting | severe, 4 patients Disc. AE |
600 mg 1 times / day multiple, oral Dose: 600 mg, 1 times / day Route: oral Route: multiple Dose: 600 mg, 1 times / day Sources: |
unhealthy, 44-78 years Health Status: unhealthy Age Group: 44-78 years Sex: M+F Sources: |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Erythema multiforme secondary to dimenhydrinate in a patient with previous similar reactions to pamabrom. | 2014-03 |
|
| Fixed drug eruption caused by pamabrom. | 2009-10 |
|
| A study of diuretic action of pamabrom (2-amino-2-methyl-propanol-1-8-bromotheophylline) in cardiac failure. | 1953-08 |
Patents
Sample Use Guides
Adults: Take one (1) capsule after breakfast with a full glass of water. Dose may be repeated after six (6) hours, not to exceed four (4) capsules per day. Start taking 5 or 6 days before onset of period and continue until desired relief is obtained or end of period. Drink 6 to 8 glasses of water daily.
Route of Administration:
Oral
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:47:51 GMT 2025
by
admin
on
Mon Mar 31 17:47:51 GMT 2025
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| Record UNII |
UA8U0KJM72
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| Record Status |
Validated (UNII)
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LIVERTOX |
734
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NCI_THESAURUS |
C448
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CFR |
21 CFR 310.201
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DTXSID80209397
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C81076
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C069987
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54365
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DBSALT002688
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UA8U0KJM72
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606-04-2
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100000079715
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Pamabrom
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SUB14745MIG
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UA8U0KJM72
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210-103-4
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2047
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CHEMBL316160
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m8371
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11806
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ACTIVE MOIETY |