物质信息

ID:205

Dihydroergotamine

名称和标识
商标名
DihydergotDirgotarlOrstanormVerladynEndophlebanMorenaDiergoD.H.E.DHE-45ErgontD.H.E. 45DergotamineIkaranMigranalTonopresAgitAngionormDET MSErgomimetErgotonin
别名
9,10-dihydro-ergotamineDihydroergotamine monomethanesulfonateDihidroergotamina [INN-Spanish]Dihydroergotaminum [INN-Latin]Dihydroergotamine mesylateDihydroergotamine methanesulfonateDihydroergotamine
IUPAC标准名
(2R,4R,7R)-N-[(1S,2S,4R,7S)-7-benzyl-2-hydroxy-4-methyl-5,8-dioxo-3-oxa-6,9-diazatricyclo[7.3.0.0^{2,6}]dodecan-4-yl]-6-methyl-6,11-diazatetracyclo[7.6.1.0^{2,7}.0^{12,16}]hexadeca-1(16),9,12,14-tetraene-4-carboxamide
IUPAC传统名
dihydroergotamine
数据登录号
PubChem CID
PubChem SID
CAS号
化合物性质
理化性质
疏水性(logP)
2
描述信息
Drug Groups
approved
Description
A 9,10alpha-dihydro derivative of ergotamine. It is used as a vasoconstrictor, specifically for the therapy of migraine disorders. [PubChem]
Indication
For the acute treatment of migraine headaches with or without aura and the acute treatment of cluster headache episodes.
Pharmacology
Dihydroergotamine is indicated for the acute treatment of migraine headaches with or without aura and the acute treatment of cluster headache episodes. Dihydroergotamine binds with high affinity to 5-HT1Da and 5-HT1Db receptors. It also binds with high affinity to serotonin 5-HT1A, 5-HT2A, and 5-HT2C receptors, noradrenaline a2A, a2B and a receptors, and dopamine D2L and D3 receptors. The therapeutic activity of Dihydroergotamine in migraine is generally attributed to the agonist effect at 5-HT1D receptors.
Toxicity
Side effects include abdominal pain, abnormal speech, coma, confusion, convulsions, hallucinations, increase and/or decrease in blood pressure, nausea, numbness, tingling, pain, and a bluish color of your fingersand toes, slowed breathing, vomiting
Affected Organisms
Humans and other mammals
Biotransformation
Hepatic
Absorption
Interpatient variable and may be dependent on the administration technique
Half Life
9 hours
Protein Binding
93% (to plasma proteins)
Elimination
The major excretory route of dihydroergotamine is via the bile in the feces.
Only 6%-7% of unchanged dihydroergotamine is excreted in the urine after intramuscular injection.
Distribution
* 800 L
Clearance
* 1.5 L/min
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