IKP-104
IKP-104 is a microtubule/tubulin inhibitor (IC50 = 1.31 μM). IKP-104 arrests cells in mitosis and the M phase by inhibiting microtubule polymerization and inducing cytoskeletal microtubule depolymerization. IKP-104 inhibits the growth of mouse and human tumor cell lines. IKP-104 exhibits anti-tumor effects in mouse ascites tumors and lung cancer models. IKP-104 is useful in the research of cancers such as leukemia, lung cancer and melanoma.
商品は「研究用試薬」です。人や動物の医療用・臨床診断用・食品用の製品ではありません。
研究用途以外に使用した場合、当社は一切の責任を負いかねます。
- CAS 番号: 114231-14-0
- 分子式: C26H21ClFNO3
- 分子量:449.90
-
保管条件:
Please store the product under the recommended conditions in the Certificate of Analysis.
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
-
生物活性
-
化学情報
- プロトコル
- 純度とドキュメンテーション
- 参考文献
-
Help & FAQs
生物活性
製品説明
体外実験
IKP-104 (0-25 μM) inhibits the tau-induced polymerization of unfractionated tubulin and isotypically pure αβII and αβIV, has no effect of αβIII[1].
IKP-104 (1.5 μM) forces a large proportion of the preformed microtubules into aggregates (unfractionated tubulin and αβIII) and the spirals (αβII isotype), has no effect on the morphology of microtubules formed from αβIV[1].
KP-104 (0-40 μM, 0-40 min) increases the absorbance, changes formation of aggregates and morphology of pre-existing microtubules[1].
KP-104 shows cell cytotoxicity against L1210, B16, Lewis, K562, HeLa cells, with IC50s of 0.0025, 5.2, 0.0017, 0.0012, 0.015 μg/mL[2].
KP-104 (3.6 μg/mL, 0-48 h) increases the proportion of round-shaped cells, arrests cells in M phase and the mitotic phase by inhibition of polymerization and induction of depolymerization of cytoskeletal microtubules in B16 cells[2][3].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
-
Cell Line:B16 cells
-
Concentration:3.6 μg/mL
-
Incubation Time:0, 1, 3, 6, 9, 12, 24 and 48 h
-
Result:Increased the proportion of round-shaped cells, arrested cells in G1-M phase, and induced polyploid and multinuclear.
Accumulated mitotic cells, and the Ml.
Caused the fine reticular microtubule network of prophase cells to disappear, resulting in a single mitotic spindle during metaphase, shortened the centromere microtubules during anaphase and telophase, and the early interphase microtubule network to re-form after cell division.
Depolymerized spindle microtubules in mitotic cells, but no changes in the microtubule network were observed in interphase cells after 20 minutes of exposure.
Caused the microtubule network of interphase cells to gradually disappear after 2 h of treatment, weak fluorescence appears in the cytoplasm of mitotic and interphase cells, accompanied by a small amount of microtubule fragments.
Resulted the induction of bundles of varying sizes composed of numerous wavy protofilaments at 2 and 24 h.
体内実験
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
-
Animal Model:CDF1 murine ascetic tumor (L1210, 1x105) model[2]
-
Dosage:0.5 mg/kg, 1 mg/kg, 5 mg/kg
-
Administration:i.p., once a day, 5 days
-
Result:Showed antitumor activity, at doses of 1.0 and 5.0 mg/kg showed effects com-parable to those of 5-Fluorouracil (HY-90006) at 10.0 and 20.0 mg/kg andvindesine at 0.3 mg/kg.
-
Animal Model:C57BL/6 murine Lewis (1x105) lung carcinoma model[2]
-
Dosage:1 mg/kg, 5 mg/kg
-
Administration:s.c., once a day, 9 days
-
Result:Showed antitumor activity.
化学情報
-
CAS 番号 114231-14-0
-
分子量 449.90
-
分子式 C26H21ClFNO3
-
SMILES
O=C1C(C)=C(C2=CC=C(F)C=C2)N(C3=CC(OC)=CC(OC)=C3Cl)C(C4=CC=CC=C4)=C1
-
輸送条件
Room temperature in continental US; may vary elsewhere.
-
保管条件
Please store the product under the recommended conditions in the Certificate of Analysis.
純度とドキュメンテーション
参考文献
[1]. Khan IA, et al. Differential interaction of tubulin isotypes with the antimitotic compound IKP-104. Biochemistry. 2000 Aug 1;39(30):9001-9. [Content Brief]
[2]. Mizuhashi F, et al. Antitumor activities of IKP-104, a 4(1H)-pyrizinone derivative, on cultured and implanted tumors. Jpn J Cancer Res. 1990 Dec;81(12):1300-6. [Content Brief]
[3]. Mizuhashi F, et al. Effects of the tumor inhibitor IKP-104, a 4(1H)-pyridinone derivative, on cytoskeletal microtubules of cultured tumor cells. Jpn J Cancer Res. 1991 Dec;82(12):1442-7. [Content Brief]
[4]. Mizuhashi F, et al. Interaction of the tumor inhibitor IKP-104, a 4(1H)-pyridinone derivative, with microtubule proteins. Jpn J Cancer Res. 1992 Feb;83(2):211-8. [Content Brief]
Calculators
濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)
IKP-104 関連分類
HY-W854934 関連分類
Powered by Bioz