Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C17H26N4O |
| Molecular Weight | 302.4145 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C(CNC[C@H]1CCC2=CC=CC=C2O1)CNC3=NCCCN3
InChI
InChIKey=QVSXOXCYXPQXMF-OAHLLOKOSA-N
InChI=1S/C17H26N4O/c1-2-6-16-14(5-1)7-8-15(22-16)13-18-9-3-10-19-17-20-11-4-12-21-17/h1-2,5-6,15,18H,3-4,7-13H2,(H2,19,20,21)/t15-/m1/s1
| Molecular Formula | C17H26N4O |
| Molecular Weight | 302.4145 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Alniditan is a non-indole migraine-abortive agent. It is a benzopyran derivative The action of sumatriptan is thought to be mediated by 5-hydroxytryptamine (5-HT)1D-type receptors. Alniditan did not attenuate substance P-induced inflammation, suggesting that the mediating receptors are located prejunctionally. In vitro alniditan exhibited less vasoconstrictive effects on the rat basilar artery than did sumatriptan, although at a very high concentration, alniditan caused intensive constriction, most likely through a mechanism independent from 5-HT receptor activation. Alniditan dose dependently attenuated the neurogenic inflammation and was more potent than sumatriptan. Adverse effects are: head pressure, paraesthesia, and hot flushes.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Agonistic properties of alniditan, sumatriptan and dihydroergotamine on human 5-HT1B and 5-HT1D receptors expressed in various mammalian cell lines. | 1998-04 |
|
| Alniditan, a new 5-hydroxytryptamine1D agonist and migraine-abortive agent: ligand-binding properties of human 5-hydroxytryptamine1D alpha, human 5-hydroxytryptamine1D beta, and calf 5-hydroxytryptamine1D receptors investigated with [3H]5-hydroxytryptamine and [3H]alniditan. | 1996-12 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/8933995
Single dose - 1.4 mg
Route of Administration:
Other
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:22:37 GMT 2025
by
admin
on
Mon Mar 31 18:22:37 GMT 2025
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| Record UNII |
B57Z82EOGE
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| Record Status |
Validated (UNII)
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| Record Version |
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Official Name | English | ||
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Preferred Name | English | ||
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Systematic Name | English | ||
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Common Name | English |
| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C47794
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66004
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7258
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152317-89-0
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C77255
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DTXSID20870005
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SUB05354MIG
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100000087464
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C100822
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CHEMBL88240
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B57Z82EOGE
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ALNIDITAN
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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TARGET -> AGONIST |
IC50
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TARGET -> AGONIST |
IC50
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SALT/SOLVATE -> PARENT |
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ACTIVE MOIETY |
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