N-p-trans-Coumaroyltyramine
CAS No. 36417-86-4
N-p-trans-Coumaroyltyramine( —— )
Catalog No. M24324 CAS No. 36417-86-4
N-p-trans-Coumaroyltyramine is a natural product, is an acetylcholinesterase (AChE) inhibitor with an an IC50 of 122 μM. N-p-trans-Coumaroyltyramine exhibits anti-trypanosomal activity with an IC50 of 13.3 μM for T. brucei rhodesiense.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 177 | In Stock |
|
| 10MG | 290 | In Stock |
|
| 25MG | 485 | In Stock |
|
| 50MG | 695 | In Stock |
|
| 100MG | 945 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameN-p-trans-Coumaroyltyramine
-
NoteResearch use only, not for human use.
-
Brief DescriptionN-p-trans-Coumaroyltyramine is a natural product, is an acetylcholinesterase (AChE) inhibitor with an an IC50 of 122 μM. N-p-trans-Coumaroyltyramine exhibits anti-trypanosomal activity with an IC50 of 13.3 μM for T. brucei rhodesiense.
-
DescriptionN-p-trans-Coumaroyltyramine is a natural product, is an acetylcholinesterase (AChE) inhibitor with an an IC50 of 122 μM. N-p-trans-Coumaroyltyramine exhibits anti-trypanosomal activity with an IC50 of 13.3 μM for T. brucei rhodesiense.
-
In Vitro——
-
In Vivo——
-
Synonyms——
-
PathwayEndocrinology/Hormones
-
TargetAChR
-
RecptorAChE
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number36417-86-4
-
Formula Weight283.33
-
Molecular FormulaC17H17NO3
-
Purity>98% (HPLC)
-
SolubilityDMSO:10 mM
-
SMILESO=C(NCCC1=CC=C(O)C=C1)/C=C/C2=CC=C(O)C=C2
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Inhibitory effect of trans-N-p-coumaroyl tryamine from the twigs of Celtis chinensis on the acetylcholinesterase.Arch. Pharm. Res.,2003, 26(9):735-8.
molnova catalog
related products
-
Decamethonium bromid...
Decamethonium Bromide is a nicotinic AChR partial agonist and neuromuscular blocking agent.
-
G007-LK
G007-LK is a selective inhibitor of TNKS1 and TNKS2, with IC50s of 46 nM and 25 nM, respectively.
-
Hypaphorine
Hypaphorine is an indole-3-acetic acid antagonist which specifically compete with indole-3-acetic acid in binding to the indole-3-acetic acid-binding site in plant peroxidases.
Cart
sales@molnova.com