Art. -Nr.: HY-171047

Autophagy inducer 7

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Autophagy inducer 7 (Compound SSA) is an Autophagy and Apoptosis inducer. Autophagy inducer 7 activates autophagy by inhibiting Akt/mTOR signaling and the expression of downstream proteins. Autophagy inducer 7 suppresses DNA synthesis and causes a G0-G1 cell-cycle arrest. Autophagy inducer 7 inhibits tumor cell growth.

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Reinheit: 99.45%
CAS. Nr.: 944159-20-0
Formel: C₂₄H₂₇FN₂OS
Molecular Weight:410.55

Speicherung:

4°C, sealed storage, away from moisture and light

* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)

Autophagy inducer 7 Chemical Structure

CAS. Nr.: 944159-20-0

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Biologische Aktivität
- Beschreibung
- Cellular Effect
- In Vitro
Chemical Information
Lösungsmittel & Löslichkeit
- In Vitro
Reinheit & Dokumentation
Verweise
Help & FAQs
Classifications
Bioz

Biologische Aktivität

Beschreibung

Alle DNA/RNA Synthesis Isoform-spezifische Produkte anzeigen :

Alle Akt Isoform-spezifische Produkte anzeigen :

Alle mTOR Isoform-spezifische Produkte anzeigen :

Cellular Effect

Cell Line	Type	Value	Description	References
BJ	EC₅₀	>7.57 μM Compound: 1; SSA	Growth inhibition of human BJ cells after 72 hrs by CellTiter-Glo reagent based assay Growth inhibition of human BJ cells after 72 hrs by CellTiter-Glo reagent based assay	[PMID: 28935266]
HT-29	CC₅₀	0.65 μM Compound: 1; SSA	Growth inhibition of human HT-29 cells after 72 hrs by CellTiter-Glo reagent based assay Growth inhibition of human HT-29 cells after 72 hrs by CellTiter-Glo reagent based assay	[PMID: 28935266]
HT-29	CC₅₀	0.65 μM Compound: SSA	Growth inhibition of human HT-29 cells measured after 72 hrs by Celltiter-Glo reagent based assay Growth inhibition of human HT-29 cells measured after 72 hrs by Celltiter-Glo reagent based assay	[PMID: 29776741]
HT-29	IC₅₀	11.3 μM Compound: 36	Antiproliferative activity against human HT-29 cells after 72 hrs by MTT assay Antiproliferative activity against human HT-29 cells after 72 hrs by MTT assay	[PMID: 22940705]
MDA-MB-231	CC₅₀	2.67 μM Compound: 1; SSA	Growth inhibition of human MDA-MB-231 cells after 72 hrs by CellTiter-Glo reagent based assay Growth inhibition of human MDA-MB-231 cells after 72 hrs by CellTiter-Glo reagent based assay	[PMID: 28935266]
MDA-MB-231	CC₅₀	2.67 μM Compound: SSA	Growth inhibition of human MDA-MB-231 cells measured after 96 hrs by Celltiter-Glo reagent based assay Growth inhibition of human MDA-MB-231 cells measured after 96 hrs by Celltiter-Glo reagent based assay	[PMID: 29776741]
PC-3	CC₅₀	3.12 μM Compound: 1; SSA	Growth inhibition of human PC3 cells after 72 hrs by CellTiter-Glo reagent based assay Growth inhibition of human PC3 cells after 72 hrs by CellTiter-Glo reagent based assay	[PMID: 28935266]
PC-3	CC₅₀	3.12 μM Compound: SSA	Growth inhibition of human PC3 cells measured after 72 hrs by Celltiter-Glo reagent based assay Growth inhibition of human PC3 cells measured after 72 hrs by Celltiter-Glo reagent based assay	[PMID: 29776741]

In Vitro

Autophagy inducer 7 (72 h) inhibits the growth of human lung adenocarcinoma cell lines, with IC₅₀s of 1.95 μM (HOP-62), 4.72 μM (A549), 3.05μM (H1299)^[1].
Autophagy inducer 7 (0-10 μM, 24 h) induces apoptosis in HOP-62, A549, H1299 cells, but not significant as Sulindac sulfide (HY-B1786) and Staurosporine (HY-15141)^[1].
Autophagy inducer 7 (0-7.5 μM, 24 h) inhibits DNA synthesis in HOP-62, A549, H1299 cells, and increases the percentage of cells in the G0-G1 phase of the cell cycle^[1].
Autophagy inducer 7 (0-7.5 μM, 24 h) induces autophagy and increases autophagic flux by inhibiting Akt/mTOR/p70S6k signaling in A549 cells^[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Apoptosis Analysis^[1]

Cell Line:

HOP-62, A549, H1299 cells
Concentration:

2.5, 5, 7.5, 10 μM
Incubation Time:

24 h
Result:

Induced caspase3/7 activation dose-dependently.
Induced cleaved PARP expression at 10 μM.
Increased Annexin-V surface staining and PI labeling.

Cell Autophagy Assay^[1]

Cell Line:

HOP-62, A549, H1299 cells
Concentration:

2.5, 5, 7.5, 10 μM
Incubation Time:

24 h
Result:

Induced dose- and time-dependent cleavage of cytosolic LC3-I to autophagosome-associated LC3-II.
Decreased p62 expression.
Displayed a striking accumulation of vesicle-like structures within the cytoplasm.
Increased both the number and size of acidic vesicles within the cytoplasm.

Chemical Information

CAS. Nr. 944159-20-0
Appearance Solid
Molecular Weight 410.55
Formel C₂₄H₂₇FN₂OS
Color Light yellow to yellow
SMILES

CN(C)CCNC(CC1=C(C)/C(C2=CC=C(F)C=C21)=C/C3=CC=C(C=C3)SC)=O
Versand

Room temperature in continental US; may vary elsewhere.
Speicherung

4°C, sealed storage, away from moisture and light

* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)

Lösungsmittel & Löslichkeit

In Vitro:

DMSO : 50 mg/mL (121.79 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

View the Complete Stock Solution Preparation Table

Preparing Stock Solutions

View the Complete Stock Solution Preparation Table

Concentration Solvent Mass

1 mg

5 mg

10 mg

Concentration

Solvent

Mass

1 mM

2.4358 mL

12.1788 mL

24.3576 mL

5 mM

0.4872 mL

2.4358 mL

4.8715 mL

10 mM

0.2436 mL

1.2179 mL

2.4358 mL

Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.

Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Molaritätsrechner

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

Konzentration Konzentration

Volumen Volumen

Molecular Weight Molecular Weight

Verdünnungsrechner

Konzentration _{(Stammlösung)} × Volumen _{(Stammlösung)} = Konzentration _{(Ziellösung)} × Volumen _{(Ziellösung)}

Konzentration _{(Stammlösung)} Konzentration _{(Stammlösung)}

Volumen _{(Stammlösung)} Volumen _{(Stammlösung)}

Konzentration _{(Ziellösung)} Konzentration _{(Ziellösung)}

Volumen _{(Ziellösung)} Volumen _{(Ziellösung)}

Reinheit & Dokumentation

Select Batch:

Reinheit: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (273 KB)
SDS (252 KB)
- English - EN (252 KB)
- Français - FR (252 KB)
- Deutsch - DE (252 KB)
- Norwegian - NO (252 KB)
- Español - ES (252 KB)
- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Korean - KR (252 KB)
- Portuguese - PT (252 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

Verweise

[1]. 1. Gurpinar E, et al. A novel sulindac derivative inhibits lung adenocarcinoma cell growth through suppression of Akt/mTOR signaling and induction of autophagy. Mol Cancer Ther. 2013 May;12(5):663-74. [Content Brief]

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

Complete Stock Solution Preparation Table

Optional Solvent	Concentration Solvent Mass	1 mg	5 mg	10 mg	25 mg
DMSO	1 mM	2.4358 mL	12.1788 mL	24.3576 mL	60.8939 mL
	5 mM	0.4872 mL	2.4358 mL	4.8715 mL	12.1788 mL
	10 mM	0.2436 mL	1.2179 mL	2.4358 mL	6.0894 mL
	15 mM	0.1624 mL	0.8119 mL	1.6238 mL	4.0596 mL
	20 mM	0.1218 mL	0.6089 mL	1.2179 mL	3.0447 mL
	25 mM	0.0974 mL	0.4872 mL	0.9743 mL	2.4358 mL
	30 mM	0.0812 mL	0.4060 mL	0.8119 mL	2.0298 mL
	40 mM	0.0609 mL	0.3045 mL	0.6089 mL	1.5223 mL
	50 mM	0.0487 mL	0.2436 mL	0.4872 mL	1.2179 mL
	60 mM	0.0406 mL	0.2030 mL	0.4060 mL	1.0149 mL
	80 mM	0.0304 mL	0.1522 mL	0.3045 mL	0.7612 mL
	100 mM	0.0244 mL	0.1218 mL	0.2436 mL	0.6089 mL

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Autophagy inducer 7

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Alle DNA/RNA Synthesis Isoform-spezifische Produkte anzeigen

Alle Akt Isoform-spezifische Produkte anzeigen

Alle mTOR Isoform-spezifische Produkte anzeigen

Biologische Aktivität

Chemical Information

Lösungsmittel & Löslichkeit

Reinheit & Dokumentation

Verweise

Help & FAQs

Complete Stock Solution Preparation Table

Autophagy inducer 7 Related Classifications

HY-171047 Related Classifications