الصفحة الرئيسية>>Signaling Pathways>> Chromatin/Epigenetics>> Sirtuin>>SIRT2-IN-9

SIRT2-IN-9

رقم الكتالوجGC66026

SIRT2-IN-9 (المركب 12) هو مثبط انتقائي لـ SRIT2 بقيمة IC50 1.3 μ ؛ M. يمنع SIRT2-IN-9 النشاط التكاثري لخلايا سرطان الثدي MCF-7. يمكن استخدام SIRT2-IN-9 في أبحاث السرطان.

Products are for research use only. Not for human use. We do not sell to patients.

SIRT2-IN-9 التركيب الكيميائي

Cas No.: 522650-91-5

الحجم السعر المخزون الكميّة
10mg
117٫40
متوفر
25mg
243٫00
متوفر
50mg
392٫80
متوفر
100mg
631٫80
متوفر

Tel:(909) 407-4943 Email: sales@glpbio.com

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents

SIRT2-IN-9 (compound 12) is a selective inhibitor of SRIT2 with an IC50 value of 1.3 μM. SIRT2-IN-9 inhibits proliferative activity of MCF-7 breast cancer cells. SIRT2-IN-9 can be used for the research of cancer[1].

SIRT2-IN-9 (1-100 μM; 15 min) dose-dependently inhibits SRIT2 with an IC50 value of 1.3 μM, and inhibits SRIT1 and SRIT3 with IC50s ??300 μM[1].
SIRT2-IN-9 (0-50 μM; 72 h) affects cell viability of MCF-7 cells[1].
SIRT2-IN-9 (0-50 μM; 6 h) affects acetylation of α-tubulin protein[1].

Cell Proliferation Assay[1]

Cell Line: MCF-7 breast cancer cell line
Concentration: 0-50 μM
Incubation Time: 72 hours
Result: Dose-dependently inhibited cell proliferation of MCF-7 breast cancer cells.

Western Blot Analysis[1]

Cell Line: MCF-7 breast cancer cell line
Concentration: 6.25, 12.5, 25 and 50 μM
Incubation Time: 6 hours
Result: Dose-dependently increased acetylation of α-tubulin protein.

مراجعات

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