16 Results for "

antimigraine activity

" in MedChemExpress (MCE) Product Catalog:
Products (16)

16 Results for "antimigraine activity" in MCE Product Catalog:

7
7 Publications Verification
Cat. No.: HY-B0121B
CAS No.: 103628-46-2
Synonyms: GR 43175 free base
Target:  

5-HT Receptor

Sumatriptan (GR 43175) is an orally active 5-HT1 receptor agonist with IC50s of 7.3 nm, 9.3nm and 17.8 nm for 5-HT1D, 5-HT1B and 5-HT1F receptors, respectively. Sumatriptan can be used for migraine headache research .
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7
7 Publications Verification
Cat. No.: HY-B0121
CAS No.: 103628-48-4
Synonyms: GR 43175 succinate
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

Sumatriptan succinate (GR 43175) is an orally active 5-HT1 receptor agonist with IC50s of 7.3 nm, 9.3nm and 17.8 nm for 5-HT1D, 5-HT1B and 5-HT1F receptors, respectively. Sumatriptan succinate can be used for migraine headache research .
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6
6 Cited Publications
Cat. No.: HY-B0358
CAS No.: 52468-60-7
Flunarizine is a potent dual Na +/Ca 2+ channel (T-type) blocker. Flunarizine is a D2 dopamine receptor antagonist. Flunarizine shows anticonvulsive and antimigraine activity, and peripheral vasodilator effects .
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6
6 Cited Publications
Cat. No.: HY-B0358A
CAS No.: 30484-77-6
Flunarizine dihydrochloride is a potent dual Na +/Ca 2+ channel (T-type) blocker. Flunarizine dihydrochloride is a D2 dopamine receptor antagonist. Flunarizine dihydrochloride shows anticonvulsive and antimigraine activity, and peripheral vasodilator effects .
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1
1 Cited Publications
Cat. No.: HY-A0010
CAS No.: 177834-92-3
Synonyms: Eletriptan HBr; UK-116044 hydrobromide
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

Eletriptan hydrobromide (Eletriptan HBr) is a 5-HT1B and 5-HT1D receptor agonist with antimigraine activity, with Ki of 0.92 nM and 3.14 nM, respectively .
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Cat. No.: HY-B0358AR
CAS No.: 30484-77-6
Flunarizine (dihydrochloride) (Standard) is the analytical standard of Flunarizine (dihydrochloride). This product is intended for research and analytical applications. Flunarizine dihydrochloride is a potent dual Na +/Ca 2+ channel (T-type) blocker. Flunarizine dihydrochloride is a D2 dopamine receptor antagonist. Flunarizine dihydrochloride shows anticonvulsive and antimigraine activity, and peripheral vasodilator effects .
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Cat. No.: HY-Z8176
CAS No.: 693765-11-6
Target:  

Sodium Channel

Research Areas:  

Neurological Disease

(Z)-Flunarizine is the (Z)-isomer of Flunarizine (HY-B0358). Flunarizine is a potent dual Na +/Ca 2+ channel (T-type) blocker. Flunarizine is a D2 dopamine receptor antagonist. Flunarizine shows anticonvulsive and antimigraine activity, and peripheral vasodilator effects .
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Cat. No.: HY-B0358AS
Flunarizine-d8 dihydrochloride is deuterated labeled Flunarizine dihydrochloride (HY-B0358A). Flunarizine dihydrochloride is a potent dual Na +/Ca 2+ channel (T-type) blocker. Flunarizine dihydrochloride is a D2 dopamine receptor antagonist. Flunarizine dihydrochloride shows anticonvulsive and antimigraine activity, and peripheral vasodilator effects .
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Cat. No.: HY-B0121BR
CAS No.: 103628-46-2
Synonyms: GR 43175 free base (Standard)
Research Areas:  

Neurological Disease

Sumatriptan (Standard) is the analytical standard of Sumatriptan. This product is intended for research and analytical applications. Sumatriptan (GR 43175) is an orally active 5-HT1 receptor agonist with IC50s of 7.3 nm, 9.3nm and 17.8 nm for 5-HT1D, 5-HT1B and 5-HT1F receptors, respectively. Sumatriptan can be used for migraine headache research .
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Cat. No.: HY-B0121R
CAS No.: 103628-48-4
Synonyms: GR 43175 succinate (Standard)
Research Areas:  

Neurological Disease

Sumatriptan (succinate) (Standard) is the analytical standard of Sumatriptan (succinate). This product is intended for research and analytical applications. Sumatriptan succinate (GR 43175) is an orally active 5-HT1 receptor agonist with Kis of 17 nM, 27 nM and 100 nM for 5-HT1D, 5-HT1B and 5-HT1A receptors, respectively. Sumatriptan succinate can be used for migraine headache research .
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Cat. No.: HY-19238
CAS No.: 165250-47-5
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

BMS-181885 is a selective 5-HT1 receptor agonist and a ligand for 5-HT1B/1D receptors. BMS-181885 exhibits anti-migraine activity. BMS-181885 can be used in the research of neurological diseases such as migraine .
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Cat. No.: HY-B0358R
CAS No.: 52468-60-7
Flunarizine (Standard) is the analytical standard of Flunarizine. This product is intended for research and analytical applications. Flunarizine is a potent dual Na +/Ca 2+ channel (T-type) blocker. Flunarizine is a D2 dopamine receptor antagonist. Flunarizine shows anticonvulsive and antimigraine activity, and peripheral vasodilator effects .
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Cat. No.: HY-103107A
CAS No.: 199673-74-0
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

LY334370 hydrochloride is a selective 5-HT1F receptor agonist with a Kd value of 0.446 nM. LY334370 hydrochlorid has anti-migraine activity .
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Cat. No.: HY-B0121A
CAS No.: 103628-62-2
Synonyms: GR 43175 hydrochloride
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

Sumatriptan hydrochloride (GR 43175) is an orally active 5-HT1 receptor agonist with IC50s of 7.3 nm, 9.3nm and 17.8 nm for 5-HT1D, 5-HT1B and 5-HT1F receptors, respectively. Sumatriptan hydrochloride can be used for migraine headache research .
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Cat. No.: HY-B0121BS2
Synonyms: GR 43175 free base-d5
Sumatriptan-d5 is deuterated labeled Sumatriptan (HY-B0121B). Sumatriptan (GR 43175) is an orally active 5-HT1 receptor agonist with IC50s of 7.3 nm, 9.3nm and 17.8 nm for 5-HT1D, 5-HT1B and 5-HT1F receptors, respectively. Sumatriptan can be used for migraine headache research .
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Cat. No.: HY-A0010R
CAS No.: 177834-92-3
Synonyms: Eletriptan HBr (Standard); UK-116044 hydrobromide (Standard)
Research Areas:  

Neurological Disease

Eletriptan hydrobromide (Standard) is an analytical standard for Eletriptan hydrobromide. This product is intended for research and analytical applications. Eletriptan hydrobromide (Eletriptan HBr) is a 5-HT1B and 5-HT1D receptor agonist with antimigraine activity, with Ki of 0.92 nM and 3.14 nM, respectively .
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