Chlorodihydrocodide: Difference between revisions
CSV import |
CSV import |
||
| Line 1: | Line 1: | ||
''' | {{Short description|A semi-synthetic opioid analgesic}} | ||
{{Drugbox | |||
| verifiedfields = changed | |||
| verifiedrevid = 477002123 | |||
| image = Chlorodihydrocodide.svg | |||
| image_size = 200px | |||
| image_alt = Structural formula of Chlorodihydrocodide | |||
| IUPAC_name = (5_,6_)-7,8-didehydro-4,5-epoxy-3-methoxy-17-methylmorphinan-6-yl chloride | |||
}} | |||
'''Chlorodihydrocodide''' is a [[semi-synthetic opioid]] derived from [[codeine]]. It is primarily used for its [[analgesic]] properties in the management of moderate to severe pain. As a member of the [[opioid]] class, it acts on the [[central nervous system]] to produce pain relief, sedation, and euphoria. | |||
==Chemical Structure== | |||
[[File:Chlorodihydrocodide.svg|thumb|right|200px|Structural formula of Chlorodihydrocodide]] | |||
Chlorodihydrocodide is chemically related to [[morphine]] and [[codeine]], sharing the core [[morphinan]] structure. The presence of a chlorine atom distinguishes it from other opioids, potentially affecting its pharmacokinetics and pharmacodynamics. | |||
==Pharmacology== | ==Pharmacology== | ||
Chlorodihydrocodide exerts its effects by binding to the [[mu-opioid receptor]]s in the brain and spinal cord. This binding inhibits the transmission of [[pain]] signals and alters the perception of pain. The drug also affects the [[dopaminergic system]], contributing to its potential for [[addiction]]. | |||
===Metabolism=== | |||
The metabolism of chlorodihydrocodide occurs primarily in the [[liver]], where it is converted into various metabolites. These metabolites are then excreted through the [[kidneys]]. The metabolic pathway involves [[cytochrome P450]] enzymes, which are responsible for the [[biotransformation]] of many drugs. | |||
== | ==Medical Uses== | ||
Chlorodihydrocodide is indicated for the relief of moderate to severe pain where alternative treatments are inadequate. It is often used in a [[clinical setting]] under strict medical supervision due to its potential for [[abuse]] and [[dependence]]. | |||
==Side Effects== | ==Side Effects== | ||
Common side effects of chlorodihydrocodide include [[nausea]], [[vomiting]], [[constipation]], and [[drowsiness]]. More serious side effects can include [[respiratory depression]], [[hypotension]], and [[allergic reactions]]. | |||
== | ==Regulation== | ||
Due to its potential for abuse, chlorodihydrocodide is classified as a [[controlled substance]] in many countries. Its use is strictly regulated, and it is typically available only by [[prescription]]. | |||
== | ==Related pages== | ||
* [[Opioid]] | |||
* [[Codeine]] | |||
* [[Morphine]] | |||
* [[Analgesic]] | |||
* [[Addiction]] | |||
[[Category:Opioids]] | [[Category:Opioids]] | ||
[[Category:Analgesics]] | [[Category:Analgesics]] | ||
[[Category: | [[Category:Controlled substances]] | ||
Latest revision as of 06:47, 16 February 2025
A semi-synthetic opioid analgesic
| Chlorodihydrocodide | |
|---|---|
| INN | |
| Drug class | |
| Routes of administration | |
| Pregnancy category | |
| Bioavailability | |
| Metabolism | |
| Elimination half-life | |
| Excretion | |
| Legal status | |
| CAS Number | |
| PubChem | |
| DrugBank | |
| ChemSpider | |
| KEGG | |
Chlorodihydrocodide is a semi-synthetic opioid derived from codeine. It is primarily used for its analgesic properties in the management of moderate to severe pain. As a member of the opioid class, it acts on the central nervous system to produce pain relief, sedation, and euphoria.
Chemical Structure[edit]

Chlorodihydrocodide is chemically related to morphine and codeine, sharing the core morphinan structure. The presence of a chlorine atom distinguishes it from other opioids, potentially affecting its pharmacokinetics and pharmacodynamics.
Pharmacology[edit]
Chlorodihydrocodide exerts its effects by binding to the mu-opioid receptors in the brain and spinal cord. This binding inhibits the transmission of pain signals and alters the perception of pain. The drug also affects the dopaminergic system, contributing to its potential for addiction.
Metabolism[edit]
The metabolism of chlorodihydrocodide occurs primarily in the liver, where it is converted into various metabolites. These metabolites are then excreted through the kidneys. The metabolic pathway involves cytochrome P450 enzymes, which are responsible for the biotransformation of many drugs.
Medical Uses[edit]
Chlorodihydrocodide is indicated for the relief of moderate to severe pain where alternative treatments are inadequate. It is often used in a clinical setting under strict medical supervision due to its potential for abuse and dependence.
Side Effects[edit]
Common side effects of chlorodihydrocodide include nausea, vomiting, constipation, and drowsiness. More serious side effects can include respiratory depression, hypotension, and allergic reactions.
Regulation[edit]
Due to its potential for abuse, chlorodihydrocodide is classified as a controlled substance in many countries. Its use is strictly regulated, and it is typically available only by prescription.