Aminopurvalanol A

Modify Date: 2024-01-04 12:12:35

Aminopurvalanol A Structure
Aminopurvalanol A structure
Common Name Aminopurvalanol A
CAS Number 220792-57-4 Molecular Weight 403.90900
Density 1.4g/cm3 Boiling Point 639ºC at 760mmHg
Molecular Formula C19H26ClN7O Melting Point N/A
MSDS N/A Flash Point 340.2ºC

 Use of Aminopurvalanol A


Aminopurvalanol A is a potent, selective, and cell permeable inhibitor of Cyclins/Cdk complexes. Aminopurvalanol A preferentially targets the G2/M-phase transition inhibiting cancer cell differentiation. Aminopurvalanol A causes the inhibition of sperm fertilizing ability via the inhibition of physiological capacitation-dependent actin polymerization[1][2].

 Names

Name Aminopurvalanol A,(2R)-2-[[6-[(3-Amino-5-chlorophenyl)amino]-9-(1-methylethyl)-9H-purin-2-yl]amino]-3-methyl-1-butanol
Synonym More Synonyms

 Aminopurvalanol A Biological Activity

Description Aminopurvalanol A is a potent, selective, and cell permeable inhibitor of Cyclins/Cdk complexes. Aminopurvalanol A preferentially targets the G2/M-phase transition inhibiting cancer cell differentiation. Aminopurvalanol A causes the inhibition of sperm fertilizing ability via the inhibition of physiological capacitation-dependent actin polymerization[1][2].
Related Catalog
Target

Cyclins/Cdk[1]

In Vitro Aminopurvalanol A (5 and 40 μM; 8 hours) inhibits cell growth primarily by arresting the cells in the G2 phase of the cell cycle and, at higher concentration, triggering apoptosis[2]. Cell Cycle Analysis[2] Cell Line: Human U937 leukemic cells Concentration: 5 and 40 μM Incubation Time: 8 hours Result: Increased the number of cells with a 4N DNA content as early as 8 h after the beginning of treatment at 5 μM. 40 μM led to cellular fragmentation and cells with an irregular DNA distribution, characteristic of apoptotic cell populations. Apoptosis Analysis[2] Cell Line: Human U937 leukemic cells Concentration: 5 and 40 μM Incubation Time: 8 hours Result: 40 μM Aminopurvalanol A led to apoptosis rather than after the beginning of treatment at 5 μM.
References

[1]. Bernabò N, et al. Aminopurvalanol A, a Potent, Selective, and Cell Permeable Inhibitor of Cyclins/Cdk Complexes, Causes the Reduction of in Vitro Fertilizing Ability of Boar Spermatozoa, by Negatively Affecting the Capacitation-Dependent Actin Polymerization. Front Physiol. 2017;8:1097.

[2]. Rosania GR, et al. A cyclin-dependent kinase inhibitor inducing cancer cell differentiation: biochemical identification using Xenopus egg extracts. Proc Natl Acad Sci U S A. 1999;96(9):4797-4802.

 Chemical & Physical Properties

Density 1.4g/cm3
Boiling Point 639ºC at 760mmHg
Molecular Formula C19H26ClN7O
Molecular Weight 403.90900
Flash Point 340.2ºC
Exact Mass 403.18900
PSA 113.91000
LogP 4.54240
Vapour Pressure 3.34E-17mmHg at 25°C
Index of Refraction 1.678

 Synonyms

ng-97
aminopurvalanol a
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