Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C10H15BrO |
| Molecular Weight | 231.13 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1(C)[C@@H]2CC[C@@]1(C)C(=O)[C@H]2Br
InChI
InChIKey=NJQADTYRAYFBJN-FWWHASMVSA-N
InChI=1S/C10H15BrO/c1-9(2)6-4-5-10(9,3)8(12)7(6)11/h6-7H,4-5H2,1-3H3/t6-,7+,10+/m1/s1
| Molecular Formula | C10H15BrO |
| Molecular Weight | 231.13 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 3 / 3 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
DescriptionCurator's Comment: description was created based on several sources, including
https://www.drugs.com/international/bromocamphor.html | https://www.ncbi.nlm.nih.gov/pubmed/21365113 | https://www.ncbi.nlm.nih.gov/pubmed/22357322 | https://www.rlsnet.ru/mnn_index_id_261.htm
Curator's Comment: description was created based on several sources, including
https://www.drugs.com/international/bromocamphor.html | https://www.ncbi.nlm.nih.gov/pubmed/21365113 | https://www.ncbi.nlm.nih.gov/pubmed/22357322 | https://www.rlsnet.ru/mnn_index_id_261.htm
3-Bromcamphor is camphor derivative, that used in Russia as a calming agent and an indirect anticoagulant in the form of tablets based on both left-hand-rotating and racemic isoforms of this compound. The use of racemic bromcamphor instead of the optically active forms is explained by the much (almost tenfold) lower cost at a comparable physiological activity of the former drug. Racemic bromcamphor has a lower melting point as
compared to that of the left-hand-rotating isomer (48 – 53°C versus 71 – 76°C, respectively) and is susceptible to fusion at room temperature
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.rlsnet.ru/tn_index_id_14474.htm
Adults: for 0.15-0.5 g. BidChildren: under the age of 2 years - 0.05 g, 3-6 years - 0.1 g, 7-9 years - 0.15 g, 10-15 years - 0.15-0.25 g. Bid
Route of Administration:
Oral
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:35:37 GMT 2025
by
admin
on
Mon Mar 31 18:35:37 GMT 2025
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| Record UNII |
E6SHQ2AT1P
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