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Anpirtoline hydrochloride
CAS No. 99201-87-3
Anpirtoline hydrochloride( —— )
Catalog No. M33830 CAS No. 99201-87-3
Anpirtoline hydrochloride (D-16949 hydrochloride) is a novel and potent 5-HT1B receptor agonist and 5-HT3 receptor antagonist with anti-injurious, analgesic, and antidepressant activity, and is used in the study of movement disorders.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 73 | In Stock |
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| 5MG | 107 | In Stock |
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| 10MG | 170 | In Stock |
|
| 25MG | 273 | In Stock |
|
| 50MG | 417 | In Stock |
|
| 100MG | 588 | In Stock |
|
| 500MG | 1215 | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameAnpirtoline hydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionAnpirtoline hydrochloride (D-16949 hydrochloride) is a novel and potent 5-HT1B receptor agonist and 5-HT3 receptor antagonist with anti-injurious, analgesic, and antidepressant activity, and is used in the study of movement disorders.
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DescriptionAnpirtoline hydrochloride is a hydrochloride of anpirtoline. Anpirtoline is a agonist of 5-HT1B.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayGPCR/G Protein
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Target5-HT Receptor
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Recptor5-HT Receptor
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Research Area——
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Indication——
Chemical Information
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CAS Number99201-87-3
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Formula Weight265.2
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Molecular FormulaC10H14Cl2N2S
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Purity>98% (HPLC)
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Solubility——
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SMILESCl.ClC=1N=C(SC2CCNCC2)C=CC1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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Tegaserod
Tegaserod is an orally available 5-HT4R agonist and 5-HT2B receptor antagonist with inhibitory effects on various 5-hydroxytryptamine receptors. Tegaserod has antitumor activity and is used in the treatment of irritable bowel syndrome (IBS).
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Adatanserin
Adatanserin (WY 50324) is a mixed 5-HT1A receptor partial agonist and a 5-HT2A and 5-HT2C receptor antagonist with potential neuroprotective activity for the study of coke oven and depression.
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Seganserin
Seganserin, a non-selective 5-hydroxytryptamine 2-HT receptor antagonist, reversed the inhibitory effects of fluoxetine and quipazine on luteinizing hormone-induced hyperphagia, depression and nociception, and reversed the antidepressant and analgesic effects induced by fluoxetine and quipazine.
