Powder: -20°C for 3 years | In solvent: -80°C for 1 year
PI-55 (6-(2-hydroxy-3-methylbenzylamino)purine) is a cytokinin receptor inhibitor that exhibits structural similarity to 6-benzylaminopurine (BAP). It competitively inhibits BAP binding on the specific Arabidopsis receptors CRE1/AHK4 and AHK3. Furthermore, PI-55 effectively suppresses cytokinins-induced haustorium formation and enhances parasite aggressiveness [1].
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
1 mg | In stock | $ 119.00 | |
5 mg | In stock | $ 297.00 | |
10 mg | In stock | $ 472.00 | |
25 mg | In stock | $ 777.00 | |
50 mg | In stock | $ 1,090.00 | |
100 mg | In stock | $ 1,460.00 | |
500 mg | In stock | $ 2,930.00 | |
1 mL * 10 mM (in DMSO) | In stock | $ 327.00 |
Description | PI-55 (6-(2-hydroxy-3-methylbenzylamino)purine) is a cytokinin receptor inhibitor that exhibits structural similarity to 6-benzylaminopurine (BAP). It competitively inhibits BAP binding on the specific Arabidopsis receptors CRE1/AHK4 and AHK3. Furthermore, PI-55 effectively suppresses cytokinins-induced haustorium formation and enhances parasite aggressiveness [1]. |
In vitro | High concentrations of PI-55 (10 μM and 100 μM) result in partial inhibition of early haustorial structure development, particularly in the presence of cytokinin. Further, PI-55 treatment, when combined with BAP, diminishes the virulence of P. ramosa compared to the application of BAP alone. This suggests the involvement of histidine kinase receptors analogous to CRE1/AHK4 and AHK3 in the signaling pathway that initiates early haustorial formation [1]. |
Synonyms | 6-(2-hydroxy-3-methylbenzylamino)purine |
Molecular Weight | 255.28 |
Formula | C13H13N5O |
CAS No. | 1122579-42-3 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 11.7 mg/mL (45.8 mM), Sonication and heating to 70℃ are recommended.
You can also refer to dose conversion for different animals. More
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PI-55 1122579-42-3 Others PI55 PI 55 6-(2-hydroxy-3-methylbenzylamino)purine inhibitor inhibit