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N-trans-Sinapoyltyramine
CAS No. 200125-11-7
N-trans-Sinapoyltyramine( —— )
Catalog No. M23901 CAS No. 200125-11-7
N-trans-Sinapoyltyramine exhibited strong and selective cytotoxicity on the HeLa human cancer cell line with IC50 values of 9.77 ± 1.25 Μm.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 599 | In Stock |
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| 5MG | 589 | In Stock |
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| 10MG | 838 | In Stock |
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| 25MG | 1264 | In Stock |
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| 50MG | 1655 | 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 NameN-trans-Sinapoyltyramine
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NoteResearch use only, not for human use.
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Brief DescriptionN-trans-Sinapoyltyramine exhibited strong and selective cytotoxicity on the HeLa human cancer cell line with IC50 values of 9.77 ± 1.25 Μm.
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DescriptionN-trans-Sinapoyltyramine exhibited strong and selective cytotoxicity on the HeLa human cancer cell line with IC50 values of 9.77 ± 1.25 Μm.
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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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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number200125-11-7
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Formula Weight343.37
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Molecular FormulaC19H21NO5
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Purity>98% (HPLC)
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Solubility——
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SMILESCOc1cc(/C=C/C(NCCc(cc2)ccc2O)=O)cc(OC)c1O
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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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Diphenylterazine
Diphenylterazine is a bioluminescence compound.Diphenylterazine alone yields very little background with excellent signal-to-background ratios. Furthermore, Diphenylterazine elicits minimal cell toxicity at millimolar concentrations. Diphenylterazine injections into untransfected BALB/c mice do not yield any background emission.
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Parethoxycaine hydro...
Parethoxycaine hydrochloride is an anesthetic.
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Orexin A (human, rat...
Orexin A human, rat, mouse, a 33 amino acid excitatory neuropeptide, orchestrates diverse central and peripheral processes. Orexin A human, rat, mouse has been used to study its effect on the functioning of porcine pancreatic islets. It has also been used as an orexin receptor 1 (OX1R) antagonist to study the effect of orexin systems in the effect of etonogestrel on respiratory response to prolonged metabolic acidosis.
