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product name MHY1485


Description: MHY1485 is a potent mTOR activator that inhibits autophagy with suppression of fusion between autophagosomes and lysosomes. In Ac2F rat hepatocytes, MHY1485 treatment suppresses the basal autophagic flux, and it also shows inhibitory effect under cell starvation which is an inducer of autophagy. The effects of MHY1485 dose-and time- dependently cause accumulation of LC3II and enlargement of the autophagosomes. Ovaries of juvenile mice cultured with MHY1485 for 4 days increases ovarian explant weights and follicle development.

ReferencesPLoS One. 2012;7(8):e43418; PLoS One. 2015; 10(2): e0117769.   



Molecular Weight (MW)

387.39
Formula

C17H21N7O4
CAS No.

326914-06-1
Storage

-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)

DMSO: 33 mg/mL (85.2 mM)
Water: <1 mg/mL
Ethanol: <1 mg/mL
Solubility (In vivo)

 
Synonyms

 

other peoduct :References PubMed ID::http://www.ncbi.nlm.nih.gov/pubmed/19396176

In Vitro

In Vitro activity: MHY1485 suppresses the basal autophagic flux. MHY1485 causes the accumulation of LC3II and enlargement of the autophagosomes in a dose- and time- dependent manner. MHY1485 increases phospho-mTOR levels and phosphorylation of downstream S6K1 and rpS6 proteins without affecting total mTOR content, total S6K1 and rpS6 levels. Short-term treatment of ovaries with MHY1485 followed by allo-transplantation promoted secondary follicle growth. Treatment with MHY1485 and subsequent grafting allowed the derivation of mature oocytes and healthy offspring.


Kinase Assay:


Cell Assay:

In Vivo  
Animal model  
Formulation & Dosage  
References PLoS One. 2012;7(8):e43418; PLoS One. 2015; 10(2): e0117769.   

XMD8-92

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Author: Sodium channel

Share this post on:

product name MHY1485


Description: MHY1485 is a potent mTOR activator that inhibits autophagy with suppression of fusion between autophagosomes and lysosomes. In Ac2F rat hepatocytes, MHY1485 treatment suppresses the basal autophagic flux, and it also shows inhibitory effect under cell starvation which is an inducer of autophagy. The effects of MHY1485 dose-and time- dependently cause accumulation of LC3II and enlargement of the autophagosomes. Ovaries of juvenile mice cultured with MHY1485 for 4 days increases ovarian explant weights and follicle development.

ReferencesPLoS One. 2012;7(8):e43418; PLoS One. 2015; 10(2): e0117769.   



Molecular Weight (MW)

387.39
Formula

C17H21N7O4
CAS No.

326914-06-1
Storage

-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)

DMSO: 33 mg/mL (85.2 mM)
Water: <1 mg/mL
Ethanol: <1 mg/mL
Solubility (In vivo)

 
Synonyms

 

other peoduct :References PubMed ID::http://www.ncbi.nlm.nih.gov/pubmed/19396176

In Vitro

In Vitro activity: MHY1485 suppresses the basal autophagic flux. MHY1485 causes the accumulation of LC3II and enlargement of the autophagosomes in a dose- and time- dependent manner. MHY1485 increases phospho-mTOR levels and phosphorylation of downstream S6K1 and rpS6 proteins without affecting total mTOR content, total S6K1 and rpS6 levels. Short-term treatment of ovaries with MHY1485 followed by allo-transplantation promoted secondary follicle growth. Treatment with MHY1485 and subsequent grafting allowed the derivation of mature oocytes and healthy offspring.


Kinase Assay:


Cell Assay:

In Vivo  
Animal model  
Formulation & Dosage  
References PLoS One. 2012;7(8):e43418; PLoS One. 2015; 10(2): e0117769.   

XMD8-92

Share this post on:

Author: Sodium channel