Cardiogenol C

Modify Date: 2024-01-02 07:22:49

Cardiogenol C Structure
Cardiogenol C structure
Common Name Cardiogenol C
CAS Number 671225-39-1 Molecular Weight 296.753
Density 1.305g/cm3 Boiling Point 520.3ºC at 760 mmHg
Molecular Formula C13H16N4O2 Melting Point N/A
MSDS Chinese USA Flash Point 268.5ºC
Symbol GHS07
GHS07
Signal Word Warning

 Use of Cardiogenol C


Cardiogenol C is a potent cell-permeable pyrimidine inducer which prompts the differentiation of ESCs into cardiomyocytes (EC50=100 nM)[1]. Cardiogenol C also acts cardiomyogenic on already lineage-committed progenitor cell types with a limited degree of plasticity. Cardiogenol C is a useful cardiomyogenic agent and can be used as a tool to improve cardiac repair by cell transplantation therapy in animal models[2].

 Names

Name Cardiogenol C hydrochloride
Synonym More Synonyms

 Cardiogenol C Biological Activity

Description Cardiogenol C is a potent cell-permeable pyrimidine inducer which prompts the differentiation of ESCs into cardiomyocytes (EC50=100 nM)[1]. Cardiogenol C also acts cardiomyogenic on already lineage-committed progenitor cell types with a limited degree of plasticity. Cardiogenol C is a useful cardiomyogenic agent and can be used as a tool to improve cardiac repair by cell transplantation therapy in animal models[2].
Related Catalog
Target

EC50: 100 nM (differentiation of ESCs into cardiomyocytes)[1]

In Vitro Cardiogenol C (1 μM; 7 days) has a cardiomyogenic effect on P19 cells, it significantly increases atrial natriuretic factor (ANF, nppa) in P19 cells when it compares to untreated control cells[1]. Cardiogenol C (0.01-100 μM; 7 days) significantly increases ANF expression. In addition, another frequently used cardiac marker gene (NKX2-5) is also significantly increased by this small molecule in C2C12 cells[2]. Cardiogenol C (0.001-100 μM; 7 days) increases cardiac Nav1.5 sodium channel protein expression as dose-dependent manner in C2C12 cells[2]. Cardiogenol C (0.01-100 μM; 7 days) does not effect cell growth even at 10 μM. In addition, Cardiogenol C either solves in water or DMSO generates a similar effect. The highest concentration, 100 μM has significant cellular toxicity on C2C12 cells[2]. RT-PCR[2] Cell Line: C2C12 cells Concentration: 0.01 μM; 0.1 μM; 1 μM; 3 μM; 10 μM; 30 μM; 100 μM Incubation Time: 7 days Result: Increases ANF and NKX2.5 mRNA level as a dose-dependent manner. Western Blot Analysis[2] Cell Line: C2C12 cells Concentration: 0.001 μM; 0.01 μM; 0.1 μM; 1 μM; 10 μM Incubation Time: 7 days Result: Increased cardiac Nav1.5 sodium channel protein levels. Cell Proliferation Assay[2] Cell Line: C2C12 cells Concentration: 0.01 μM; 0.1 μM; 1 μM Incubation Time: 7 days Result: Did not exert toxic effects on C2C12 cells at 0.01-10 μM treatment.
References

[1]. Wu X, et al. Small molecules that induce cardiomyogenesis in embryonic stem cells.J Am Chem Soc. 2004 Feb 18;126(6):1590-1.

[2]. Mike AK, et al. Small molecule cardiogenol C upregulates cardiac markers and induces cardiac functional properties in lineage-committed progenitor cells. Cell Physiol Biochem. 2014;33(1):205-21.

 Chemical & Physical Properties

Density 1.305g/cm3
Boiling Point 520.3ºC at 760 mmHg
Molecular Formula C13H16N4O2
Molecular Weight 296.753
Flash Point 268.5ºC
Exact Mass 296.104004
PSA 79.30000
LogP 2.58100
Index of Refraction 1.667
Storage condition -20℃

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305 + P351 + P338
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xi
Risk Phrases 36/37/38
Safety Phrases 26-36
RIDADR NONH for all modes of transport

 Articles1

More Articles
Small molecules that induce cardiomyogenesis in embryonic stem cells.

J. Am. Chem. Soc. 126 , 1590-1591, (2004)

A phenotypic cell-based screen of a large combinatorial chemical library led to the identification of a class of diaminopyrimidine compounds (cardiogenol A-D) which can selectively and efficiently ind...

 Synonyms

Ethanol, 2-[[2-[(4-methoxyphenyl)amino]-4-pyrimidinyl]amino]-, hydrochloride (1:1)
2-({2-[(4-Methoxyphenyl)amino]pyrimidin-4-yl}amino)ethanol hydrochloride (1:1)
2-({2-[(4-Methoxyphenyl)amino]-4-pyrimidinyl}amino)ethanol hydrochloride (1:1)
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