tricoumaroyl spermidine
CAS No. 131086-78-7
tricoumaroyl spermidine( N1,N5,N10-(Z)-tri-p-coumaroylspermidine )
Catalog No. M23469 CAS No. 131086-78-7
Tricoumaroyl spermidine was discovered as unique tea (Camellia sinensis) flower metabolites.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 203 | In Stock |
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| 5MG | 294 | In Stock |
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| 10MG | 446 | In Stock |
|
| 25MG | 712 | In Stock |
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| 50MG | 1008 | In Stock |
|
| 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 Nametricoumaroyl spermidine
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NoteResearch use only, not for human use.
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Brief DescriptionTricoumaroyl spermidine was discovered as unique tea (Camellia sinensis) flower metabolites.
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DescriptionTricoumaroyl spermidine was discovered as unique tea (Camellia sinensis) flower metabolites.
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In Vitro——
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In Vivo——
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SynonymsN1,N5,N10-(Z)-tri-p-coumaroylspermidine
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PathwayEndocrinology/Hormones
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Target5-HT Receptor
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Recptor5-HT
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Research Area——
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Indication——
Chemical Information
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CAS Number131086-78-7
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Formula Weight583.67
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Molecular FormulaC34H37N3O6
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Purity>98% (HPLC)
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Solubility——
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SMILESOc1ccc(/C=C/C(NCCCCN(CCCNC(/C=C/c(cc2)ccc2O)=O)C(/C=C/c(cc2)ccc2O)=O)=O)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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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.
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DSP-6952 hydrobromid...
DSP-6952 is a novel potent, selective, orally active 5-HT4 receptor partial agonist with Ki of 50-100 nM for human 5-HT4a/4b/4c.
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Pindolol
Pindolol is a nonselective β-blocker with partial beta-adrenergic receptor agonist activity, also functions as a 5-HT1A receptor weak partial agonist / antagonist (Ki=33nM).
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