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  4. Antitumor agent-51

Antitumor agent-51 对骨肉瘤细胞的生长和迁移具有有效的选择性抑制作用，对 MNNG/HOS 细胞的 IC50 为 21.9 nM。Antitumor agent-51 具有低毒性和相当大的生物利用度。

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Antitumor agent-51 Chemical Structure

Antitumor agent-51 Chemical Structure

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Antitumor agent-51 相关抗体

Top Publications Citing Use of Products

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Antitumor agent-51 possesses potent and selective inhibitory for osteosarcoma cell growth and migration with IC50 of 21.9 nM in MNNG/HOS cells. Antitumor agent-51 has a considerable bioavailability and a low toxicity[1].

IC50 & Target

IC50: 21.9 nM in MNNG/HOS cells[1]
体外研究
(In Vitro)

Antitumor agent-51 (compound R-8i) (0-20 μM; 72 hours) selectively inhibits MNNG/HOS OS cells proliferation with IC50=21.9 nM, and has much less inhibitory activity on two normal BMSC and GES1 cells (IC50>10 μM)[1].
Antitumor agent-51 (5 nM; 24 hours) induces a cell cycle arrest in MNNG/HOS cells with a 23% increase in G0/G1 phase, but no apparent cell apoptosis[1].
Antitumor agent-51 (5 and 20 nM; 24 hours) significantly suppresses the migration of MNNG/HOS cells[1].

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

Antitumor agent-51 相关抗体:

Cell Proliferation Assay

Cell Line: MNNG/HOS, MG63, SJSA-1, U2OS, 143B, SAOS-2, HOS, SW1353, GES1, and BMSC cells[1]
Concentration: 0-20 μM
Incubation Time: 72 hours
Result: Selectively inhibited MNNG/HOS cells proliferation with IC50=21.9 nM, and showed much less inhibitory activity on two normal BMSC and GES1 cells (IC50>10 μM).

Cell Cycle Analysis

Cell Line: MNNG/HOS cells[1]
Concentration: 5 nM
Incubation Time: 24 hours
Result: Induced a cell cycle arrest with a 23% increase in G0/G1 phase, but no apparent cell apoptosis.
体内研究
(In Vivo)

Antitumor agent-51 (12.5 or 62.5 mg/kg; i.p. or i.v., single) exhibits good intraperitoneal plasma exposures (AUC0-∞>6900 h ng/mL) and an acceptable bioavailability (52.1%) for the i.p. administration in male ICR mice[1].
Antitumor agent-51 (62.5 mg/kg; i.p., twice per day for 18 days) significantly suppresses MNNG/HOS tumor growth with tumor growth inhibition (TGI) of 52.9% and does not induce an obvious toxicity in nude mice[1].
Pharmacokinetic Parameters of Antitumor agent-51 in male ICR mice[1].

IV (12.5 mg/kg) IP (62.5 mg/kg)
T1/2 (h) 0.061 0.641
AUC0-inf (h·ng/mL) 3230 8406
Cmax (ng/mL) 20511
CL (mL/min/kg) 66.9
F (%) 52.1

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

Animal Model: Male ICR mice (30 g, n=3)[1]
Dosage: 12.5 or 62.5 mg/kg
Administration: i.p. or i.v., single (Pharmacokinetic Analysis)
Result: Showed good intraperitoneal plasma exposures (AUC0-∞ > 6900 h ng/mL) and an acceptable bioavailability (52.1%) for the i.p. administration.
Animal Model: Female BALB/c nude mice (3 months, human MNNG/HOS xenografts)[1]
Dosage: 62.5 mg/kg
Administration: i.p., twice per day for 18 days
Result: Significantly suppressed MNNG/HOS tumor growth with tumor growth inhibition (TGI) of 52.9% and did not induce an obvious toxicity.
分子量

435.54

Formula

C23H25N5O2S
运输条件

Room temperature in continental US; may vary elsewhere.
储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.
纯度 & 产品资料
参考文献

Antitumor agent-51 相关分类

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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

Keywords:

Antitumor agent-51Antitumor agent51Antitumor agent 51OthersOsteosarcomaThiazolidinoneICR miceBALB/c nude miceMNNG/HOSProliferationSelectivityInhibitorinhibitorinhibit

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