N1,N10-Bis(p-coumaroyl)spermidine | CAS:114916-05-1

N1,N10-Bis(p-coumaroyl)spermidine

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Product Name	N1,N10-Bis(p-coumaroyl)spermidine
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CAS No.:	114916-05-1
Catalog No.:	CFN99248
Molecular Formula:	C₂₅H₃₁N₃O₄
Molecular Weight:	437.5 g/mol
Purity:	>=98%
Type of Compound:	Phenylpropanoids
Physical Desc.:	Powder
Source:	The herbs of Exochorda racemosa
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download:	COA MSDS SDF Manual
Similar structural:	Comparison (Web) (SDF)
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Size /Price /Stock	10 mM * 1 mL in DMSO / Inquiry
Other Packaging	*Packaging according to customer requirements(100uL/well, 200uL/well and more), and Container use Storage Tube With Screw Cap

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N1,N10-Bis(p-coumaroyl)spermidine Description

Source:	The herbs of Exochorda racemosa
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage:	Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C). Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
After receiving:	The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.

Structure Identification:

Phytochemistry, 1998, 47(3):375-387.

The biosynthesis of lunarine in seeds of Lunaria annua.[Reference: WebLink]

METHODS AND RESULTS:
Using an optimized precursor feeding system, the biosynthesis of the alkaloid lunarine in Lunaria annua seeds was investigated. The synthesis of radioactively labelled precursors for the application experiments is described. Lunarine was shown to be synthesized by stereo-selective phenol-oxidative coupling of N1,N10-Bis(p-coumaroyl)spermidine. p-Coumaric acid for the biosynthesis of this dimer is formed from L-phenylalanine via trans-cinnamic acid. The polyamine moiety of lunarine, spermidine, and its immediate precursor putrescine are preferentially synthesized from arginine.
CONCLUSIONS:
Enzyme studies with microsomes of Lunaria annua seeds indicated that a cytochrome P-450 enzyme might be responsible for the phenol-oxidative coupling of N1,N10-bis (p-coumaroyl)spermidine yielding the hexahydrodibenzofuran ring of lunarine.

Size /Price /Stock	10 mM * 100 uL in DMSO / Inquiry / In-stock 10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries	Phenylpropanoids Compound Library

	1 mg	5 mg	10 mg	20 mg	25 mg
1 mM	2.2857 mL	11.4286 mL	22.8571 mL	45.7143 mL	57.1429 mL
5 mM	0.4571 mL	2.2857 mL	4.5714 mL	9.1429 mL	11.4286 mL
10 mM	0.2286 mL	1.1429 mL	2.2857 mL	4.5714 mL	5.7143 mL
50 mM	0.0457 mL	0.2286 mL	0.4571 mL	0.9143 mL	1.1429 mL
100 mM	0.0229 mL	0.1143 mL	0.2286 mL	0.4571 mL	0.5714 mL

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CFN98494	N-p-trans-Coumaroyltyramine	36417-86-4	283.3	C₁₇H₁₇NO₃
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CFN99238	N-p-coumaroyl-N'-caffeoylputrescine	1138156-77-0	396.4	C₂₂H₂₄N₂O₅
CFN95637	N-trans-p-Coumaroyl-N'-trans-feruloyl-3-hydroxy-cadaverine	2584997-91-9	470.5	C₂₅H₃₀N₂O₇
CFN99248	N1,N10-Bis(p-coumaroyl)spermidine	114916-05-1	437.5	C₂₅H₃₁N₃O₄
CFN99316	3,4-Dihydroxycinnamamide	1202-41-1	179.2	C₉H₉NO₃