Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C31H41N5O5.CH4O3S |
Molecular Weight | 659.793 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 7 / 7 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CS(O)(=O)=O.[H][C@@]12CCCN1C(=O)[C@H](C(C)C)N3C(=O)[C@](NC(=O)[C@H]4CN(C)[C@]5([H])CC6=CNC7=C6C(=CC=C7)[C@@]5([H])C4)(O[C@@]23O)C(C)C
InChI
InChIKey=UOOWRCRLTSXSAV-GSZJWLEYSA-N
InChI=1S/C31H41N5O5.CH4O3S/c1-16(2)26-28(38)35-11-7-10-24(35)31(40)36(26)29(39)30(41-31,17(3)4)33-27(37)19-12-21-20-8-6-9-22-25(20)18(14-32-22)13-23(21)34(5)15-19;1-5(2,3)4/h6,8-9,14,16-17,19,21,23-24,26,32,40H,7,10-13,15H2,1-5H3,(H,33,37);1H3,(H,2,3,4)/t19-,21-,23-,24+,26+,30-,31+;/m1./s1
Molecular Formula | C31H41N5O5 |
Molecular Weight | 563.6877 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 7 / 7 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Molecular Formula | CH4O3S |
Molecular Weight | 96.106 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
DescriptionSources: https://www.drugs.com/cdi/hydergine.htmlCurator's Comment: description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/2869188 | https://www.ncbi.nlm.nih.gov/pubmed/4205319 | https://www.ncbi.nlm.nih.gov/pubmed/14350151 | https://www.ncbi.nlm.nih.gov/pubmed/17941060
Sources: https://www.drugs.com/cdi/hydergine.html
Curator's Comment: description was created based on several sources, including
https://www.ncbi.nlm.nih.gov/pubmed/2869188 | https://www.ncbi.nlm.nih.gov/pubmed/4205319 | https://www.ncbi.nlm.nih.gov/pubmed/14350151 | https://www.ncbi.nlm.nih.gov/pubmed/17941060
Dihydroergocornine is an ergot alkaloid, one of the three components of ergoloid (trade name Hydergine). Dihydroergocornine (as the component of Ergoloid mesylates) has been used to treat dementia and age-related cognitive impairment (such as in Alzheimer disease), as well as to aid in recovery after stroke. There is no specific evidence which clearly establishes the mechanism by which Hydergine® (ergoloid mesylates) preparations produce mental effects, nor is there conclusive evidence that the drug particularly affects cerebral arteriosclerosis or cerebrovascular insufficiency. Hydergine may stimulates dopaminergic and serotonergic receptors and blocks alpha-adrenoreceptors.
CNS Activity
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL217 Sources: https://www.ncbi.nlm.nih.gov/pubmed/2869188 |
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Target ID: CHEMBL265 Sources: https://www.ncbi.nlm.nih.gov/pubmed/2869188 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Primary | Hydergine Approved UseUnknown Launch Date1977 |
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Sources: https://www.drugs.com/pro/hydergine.html |
Primary | Hydergine Approved UseUnknown Launch Date1977 |
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Primary | Hydergine Approved UseUnknown Launch Date1977 |
Cmax
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
0.04 μg/L EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17941060/ |
27 mg single, oral dose: 27 mg route of administration: Oral experiment type: SINGLE co-administered: |
DIHYDROERGOCRISTINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
0.04 μg/L EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17941060/ |
27 mg single, oral dose: 27 mg route of administration: Oral experiment type: SINGLE co-administered: |
DIHYDROERGOCRYPTINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
0.04 μg/L EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17941060/ |
27 mg single, oral dose: 27 mg route of administration: Oral experiment type: SINGLE co-administered: |
DIHYDROERGOCORNINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
0.98 μg/L EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17941060/ |
27 mg single, oral dose: 27 mg route of administration: Oral experiment type: SINGLE co-administered: |
HYDROXY-DIHYDROERGOCORNIN plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
0.53 μg/L EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17941060/ |
27 mg single, oral dose: 27 mg route of administration: Oral experiment type: SINGLE co-administered: |
HYDROXY-DIHYDROERGOCRYPTINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
|
0.3 μg/L EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/17941060/ |
27 mg single, oral dose: 27 mg route of administration: Oral experiment type: SINGLE co-administered: |
HYDROXY-DIHYDROERGOCRISTINE plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
PubMed
Title | Date | PubMed |
---|---|---|
The treatment of minocycline-induced brainstem vertigo by the combined administration of piracetam and ergotoxin. | 1989 |
|
Bioavailability and pharmacokinetic profile of dihydroergotoxine from a tablet and from an oral solution formulation. | 2001 Jan |
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Placebo adverse events in headache trials: headache as an adverse event of placebo. | 2003 Sep |
|
Contractile responses to ergotamine and dihydroergotamine in the perfused middle cerebral artery of rat. | 2007 Apr |
|
Identification and human pharmacokinetics of dihydroergotoxine metabolites in man: preliminary results. | 2008 Jan |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.drugs.com/pro/hydergine.html
1 mg of ergoloid mesylates three times daily.
1 mg of ergoloid mesylates contains: dihydroergocornine mesylate 0.333 mg, dihydroergocristine mesylate 0.333 mg, and dihydroergocryptine (dihydro-alpha-ergocryptine and dihydro-beta-ergocryptine in the proportion of 2:1) mesylate 0.333 mg,
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/17941060
Biotransformation assays were performed in incubates of rat liver microsomes. Dihydroergotoxine alkaloids in CH3CN–H2O (1:1, v/v) were individually added (30 mm, final concentration) to cold Sorensen buffer 0.1 m pH 7.4 containing the liver enzyme preparation (5mgprot/ml), MgCl2 (10mm), glucose 6-phosphate (10mm), NADP (0.5mm) and glucose 6-phosphate dehydrogenase (1 U/ml) in a total volume of 500 ml. Blank and control incubates were performed similarly, except by adding the buffer solution instead of the drug and NADPH regenerating system, respectively. After incubation at 378C for 30 min, the reactions were terminated by the addition of 50 ml NaOH 0.1m, and vortex-mixing (30 s) with 4ml of diethyl ether. After 15 min at -80C, the upper organic layers were separated and concentrated under a gentle N2 stream.
Substance Class |
Chemical
Created
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admin
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Edited
Fri Dec 15 15:46:29 GMT 2023
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Fri Dec 15 15:46:29 GMT 2023
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Record UNII |
42RX8KPW29
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Record Status |
Validated (UNII)
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Record Version |
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NCI_THESAURUS |
C29713
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NCI_THESAURUS |
C66884
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168870
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42RX8KPW29
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34502
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249-539-5
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ACTIVE MOIETY |