Thozalinone
CAS No. 655-05-0
Thozalinone( —— )
Catalog No. M27185 CAS No. 655-05-0
Thozalinone is a psychostimulant agent inducing the release of norepinephrine and dopamine.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 28 | In Stock |
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| 10MG | 34 | In Stock |
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| 25MG | 61 | In Stock |
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| 50MG | 88 | In Stock |
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| 100MG | 133 | In Stock |
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| 200MG | 198 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameThozalinone
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NoteResearch use only, not for human use.
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Brief DescriptionThozalinone is a psychostimulant agent inducing the release of norepinephrine and dopamine.
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DescriptionThozalinone is a psychostimulant agent inducing the release of norepinephrine and dopamine.(In Vivo):In ICR male mice, Thozalinone (100 mg/kg, ip) test (SI) appear to provide the best prediction for the PS-inducing potencies among DL-DOPA, apomorphine, and amphetamine.
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In Vitro——
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In Vivo——
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Synonyms——
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PathwayOthers
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TargetOther Targets
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number655-05-0
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Formula Weight204.229
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Molecular FormulaC11H12N2O2
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Purity>98% (HPLC)
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Solubility——
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SMILESCN(C)C1=NC(=O)C(O1)c1ccccc1
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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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MI-3454
MI-3454 is an orally active, selective and potent inhibitor of Menin-MLL1 interaction that inhibits the proliferation and induces differentiation of acute leukemia cells with MLL1 translocation or NPM1 mutation.
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NSC 694623
NSC 694623 is a potent histone acetyltransferase (HAT) inhibitor with an IC50 of 15.9 μM against recombinant HAT p300/CBP-associated factor (PCAF) and exhibits anti-proliferative activity against certain cancer cells, making it useful for anti-cancer research.
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MS177
MS177 is an effective and fast-acting EZH2 degrader. MS177 is a PROTAC that consists of a CRBN ligand, linker, and a potent enzymatic EZH2 inhibitor C24 (C24 IC50): 12?nM). MS177 effectively depletes both canonical EZH2–PRC2 and noncanonical EZH2–cMyc complexes. MS177 induces leukaemia cell growth inhibition, apoptosis and cell cycle progression arrest.
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