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BMVC
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
BMVC图片
CAS NO:627810-06-4
包装与价格:
包装价格(元)
5mg电议
10mg电议
25mg电议
50mg电议
100mg电议
200mg电议

产品介绍
BMVC 是一种有效的 G-四联体 (G4) 稳定剂和选择性的端粒酶 (telomerase) 抑制剂,IC50约为 0.2 μM。BMVC 抑制 Taq DNA 聚合酶,IC50约为 2.5 μ M。BMVC 提高了端粒G4结构的熔化温度,并加速了端粒长度的缩短。抗癌活性。
生物活性

BMVC is a potentG-quadruplex(G4)stabilizer and a selectivetelomeraseinhibitor with anIC50of ~0.2 μM. BMVC inhibits Taq DNA polymerase with anIC50of ~2.5 μM. BMVC increases the melting temperature ofG4structure of telomere and accelerates telomere length shortening. Anticancer activities[1][2].

IC50& Target

IC50: ~0.2 μM (Telomerase)[1]
G-quadruplex[1]
IC50: ~2.5 μM (Taq DNA polymerase)[1]

体外研究
(In Vitro)

BMVC (0.5 μM; 0-18 days; H1299 cells) treatment markedly increases the percentage of sub-G1-phase cells after 18 days[1].
BMVC (0.5 μM; 0-18 days; H1299 cells) long-term treatment leads to ceasing of cell growth and eventually cell death through apoptosis. The long-term BMVC treatment induces senescence program in H1299 cells[1].
In BMVC-treated cancer cells, hallmarks of senescence, including morphologic changes, detection of senescence-associated β-galactosidase activity, and decreasesd bromodeoxyuridine incorporation, are detected. The BMVC-induced senescence phenotype is accompanied by progressive telomere shortening and detection of the DNA damage foci, indicating that BMVC caused telomere uncapping after long-term treatments[1].
BMVC also suppresses the tumor-related properties of cancer cells, including cell migration, colony-forming ability, and anchorage-independent growth[1].

Cell Cycle Analysis[1]

Cell Line:H1299 cells
Concentration:0.5 μM
Incubation Time:0 day, 6 days, 12 days, 18 days
Result:The percentage of sub-G1-phase cells was markedly increased after 18 days.

Apoptosis Analysis[1]

Cell Line:H1299 cells
Concentration:0.5 μM
Incubation Time:0 day, 6 days, 12 days, 18 days
Result:Increased apoptotic cells.
体内研究
(In Vivo)

BMVC (1 mg/kg; intraperitoneal injection; every 3 day; BALB/cAnN.Cg-Foxn1nu/CrlNarl mice) treatment delays tumorigenic potential of cancer cells in vivo[1].

Animal Model:BALB/cAnN.Cg-Foxn1nu/CrlNarl mice injected with H1299 cells[1]
Dosage:1 mg/kg
Administration:Intraperitoneal injection; every 3 day
Result:The growth rates of tumors in animals were significantly slower than that of control animals. The tumor cells of the mice were indeed entering apoptosis.
分子量

657.33

性状

Solid

Formula

C28H25I2N3

CAS 号

627810-06-4

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder-20°C3 years
4°C2 years
In solvent-80°C6 months
-20°C1 month