Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C21H25BrN2O3 |
| Molecular Weight | 433.339 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC[C@@]12CCCN3CCC4=C([C@H]13)N(C5=C4C=CC(Br)=C5)[C@](O)(C2)C(=O)OC
InChI
InChIKey=WYIJGAVIVKPUGJ-GIVPXCGWSA-N
InChI=1S/C21H25BrN2O3/c1-3-20-8-4-9-23-10-7-15-14-6-5-13(22)11-16(14)24(17(15)18(20)23)21(26,12-20)19(25)27-2/h5-6,11,18,26H,3-4,7-10,12H2,1-2H3/t18-,20+,21+/m1/s1
| Molecular Formula | C21H25BrN2O3 |
| Molecular Weight | 433.339 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
DescriptionSources: http://www.ncbi.nlm.nih.gov/pubmed/8851150
Sources: http://www.ncbi.nlm.nih.gov/pubmed/8851150
Brovincamine also known as brovincamine fumarate (BV, Sabromin) was used in Japan mainly as an improver of cerebral circulation and metabolism, and also as an inhibitor of the aggregation of platelets through the cyclic AMP pathway in patients with normal tension glaucoma. Brovincamine exerts its action via calcium channels blockade. The current drug status is unknown.
Originator
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: Calcium channels Sources: http://www.ncbi.nlm.nih.gov/pubmed/4006317 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Primary | Unknown Approved UseUnknown |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
3 μg/mL/(mg dose/kg) EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/7169608/ |
0.5 mg/kg single, oral dose: 0.5 mg/kg route of administration: Oral experiment type: SINGLE co-administered: |
[3H]-11-BROMOVINCAMINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: FASTED |
|
1900 ng × eq/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/4085521/ |
40 mg single, oral dose: 40 mg route of administration: Oral experiment type: SINGLE co-administered: |
[3H]-11-BROMOVINCAMINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: FASTED |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
28 μg × h/mL/(mg dose/kg) EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/7169608/ |
0.5 mg/kg single, oral dose: 0.5 mg/kg route of administration: Oral experiment type: SINGLE co-administered: |
[3H]-11-BROMOVINCAMINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: FASTED |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
17 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/7169608/ |
0.5 mg/kg single, oral dose: 0.5 mg/kg route of administration: Oral experiment type: SINGLE co-administered: |
[3H]-11-BROMOVINCAMINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: FASTED |
|
11 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/4085521/ |
40 mg single, oral dose: 40 mg route of administration: Oral experiment type: SINGLE co-administered: |
[3H]-11-BROMOVINCAMINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: FASTED |
Funbound
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
3% EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/7169608/ |
0.5 mg/kg single, oral dose: 0.5 mg/kg route of administration: Oral experiment type: SINGLE co-administered: |
[3H]-11-BROMOVINCAMINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: FASTED |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Use of calcium channel blockers for glaucoma. | 2011-01 |
|
| Inhibitory action of brovincamine on catecholamine secretion from cultured bovine adrenal medullary cells: possible relation to its blocking action on Ca2+ channels. | 1991-06-21 |
|
| Effects of brovincamine on the stereological parameters of corticocerebral capillaries. | 1987-03-09 |
|
| Cardiovascular effects of brovincamine and possible mechanisms involved. | 1985-03-01 |
|
| Calcium antagonistic action involved in vasodilation by brovincamine. | 1984 |
|
| The metabolic fate of 11-bromo-[15-3H] vincamine in rats, dogs and humans. | 1982-12 |
|
| Determination of 11-bromovincamine in human plasma by high-performance liquid chromatography. | 1982-03-12 |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/10209728
20 mg three times daily.
Route of Administration:
Oral
In Vitro Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/6698382
Possible mode of vasodilative action of brovincamine was assessed in isolated cardiovascular preparations in comparison with verapamil and papaverine. Brovincamine (IC50: 1.2 x 10(-5)M) caused a dose-dependent relaxation of potassium (30 mM)-contracture in the rabbit pulmonary arterial segment. This relaxation was antagonized by increasing external Ca2+ concentration to 12.4 mM.
| Substance Class |
Chemical
Created
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AYN5T18K5R
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C29707
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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SALT/SOLVATE -> PARENT |
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TARGET -> INHIBITOR |
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| Related Record | Type | Details | ||
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ACTIVE MOIETY |
Vasodilator
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