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Methiothepin mesylate
CAS No. 74611-28-2
Methiothepin mesylate( —— )
Catalog No. M15847 CAS No. 74611-28-2
Metitepine (INN), also commonly known as methiothepin, is a drug that acts as an antagonist at various serotonin and dopamine receptors.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 29 | In Stock |
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| 10MG | 48 | In Stock |
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| 100MG | Get Quote | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameMethiothepin mesylate
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NoteResearch use only, not for human use.
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Brief DescriptionMetitepine (INN), also commonly known as methiothepin, is a drug that acts as an antagonist at various serotonin and dopamine receptors.
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DescriptionMetitepine (INN), also commonly known as methiothepin, is a drug that acts as an antagonist at various serotonin and dopamine receptors. It is used as an antipsychotic.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayEndocrinology/Hormones
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Target5-HT Receptor
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Recptor5-HT| Dopamine
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Research AreaNeurological Disease
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Indication——
Chemical Information
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CAS Number74611-28-2
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Formula Weight452.65
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Molecular FormulaC21H28N2O3S3
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Purity>98% (HPLC)
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SolubilityDMSO: 10 mM
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SMILESCS(O)(=O)=O.CSC1=CC2=C(SC3=CC=CC=C3CC2N2CCN(C)CC2)C=C1
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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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Granisetron hydrochl...
Granisetron Hcl(BRL 43694A) is a serotonin 5-HT3 receptor antagonist used as an antiemetic to treat nausea and vomiting following chemotherapy.
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Ro 67-7476
Ro 67-7476 is a positive allosteric modulator of mGlu1 receptors. No activity at human mGlu1 receptors. Potentiates glutamate-induced calcium release with EC 50 of 60.1 nM.
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PRX-07034
PRX-07034 is a selective antagonist of 5-HT6 receptor. It has cognition and memory-enhancing properties and potently decreases food intake and body weight in rodents.?PRX-07034 is both a potent (Ki = 4-8 nM) and highly selective 5-HT(6) receptor antagonist (≥100-fold selectivity for the 5-HT(6) receptor compared to 68 other GPCRs, ion channels, and transporters, except D(3) (Ki = 71 nM) and 5-HT(1B) (Ki = 260 nM) receptors.
