6-(Furfurylamino)purine | CAS:525-79-1

6-(Furfurylamino)purine

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Description:

6-Furfurylaminopurine may inhibit the initiation of the synthesis of virus coat protein. 6-Furfurylaminopurine can inhibit the increase in activity of peptidase after 4 days.

In vitro:

Biochem. J.,1966 Feb;98(2):401-4.

The Effect of 6-furfurylaminopurine on Senescence in Tobacco-Leaf Tissue After Harvest.[Reference: WebLink]

METHODS AND RESULTS:
1. The concentration of chlorophyll decreased and the concentration of alpha-amino nitrogen and the absolute and specific activity of peptidase increased in disks of tobacco leaf incubated on water in darkness at 25 degrees . 2. Although 6-(Furfurylamino)purine (kinetin) applied to the disks inhibited the increase in activity of peptidase after 4 days, this effect was too slow to account for the significant inhibition of increase in alpha-amino nitrogen after 24hr. 3. Treating with kinetin also delayed loss of chlorophyll and soluble protein, though not until 4 and 8 days respectively.
CONCLUSIONS:
4. The only significant effect of treating disks prepared from tobacco plants deficient in nitrogen with kinetin for 8 days was to inhibit the increase in alpha-amino nitrogen. 5. Adding kinetin (5mmum to 5mum) in vitro did not affect the activity of peptidase extracted from tobacco leaf.

Biochemie und physiologie der pflanzen, 1990,186(5-6):403-407.

Kinetin ( 6-(Furfurylamino)purine) Inhibits the Replication Cycle of Potato Virus X at a Distinct Event.[Reference: WebLink]

METHODS AND RESULTS:
The time course of inhibition of PYX (potato virus X) synthesis by Kinetin ( 6-(Furfurylamino)purine) was determined in synchronously infected disks from leaves of Nicotiana tabacum L. “Samsun”. Synchrony was obtained in one series of experiments by the differential temperature inoculation method. In a second series the synchrony of the first replication cycle was used. The results of both series demonstrate that kinetin (0.1 mM) inhibits an event of the replication cycle of PVX, which occurs later than the early event influenced by the reference substance 2-thioracil and earlier than the late event inhibited by the reference substance cycloheximide. It coincides with the event inhibited by the amino acid analogue ethionine.
CONCLUSIONS:
These data suggest that kinetin may inhibit the initiation of the synthesis of virus coat protein.

6-(Furfurylamino)purine Description

Source:
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.

Product Name	6-(Furfurylamino)purine
Price:	$30 / 20mg
CAS No.:	525-79-1
Catalog No.:	CFN70129
Molecular Formula:	C₁₀H₉N₅O
Molecular Weight:	215.2 g/mol
Purity:	>=98%
Type of Compound:	Alkaloids
Physical Desc.:	Powder
Source:
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download:	COA MSDS
Similar structural:	Comparison
Guestbook:

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

	1 mg	5 mg	10 mg	20 mg	25 mg
1 mM	4.6468 mL	23.2342 mL	46.4684 mL	92.9368 mL	116.171 mL
5 mM	0.9294 mL	4.6468 mL	9.2937 mL	18.5874 mL	23.2342 mL
10 mM	0.4647 mL	2.3234 mL	4.6468 mL	9.2937 mL	11.6171 mL
50 mM	0.0929 mL	0.4647 mL	0.9294 mL	1.8587 mL	2.3234 mL
100 mM	0.0465 mL	0.2323 mL	0.4647 mL	0.9294 mL	1.1617 mL

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