1. Apoptosis Stem Cell/Wnt MAPK/ERK Pathway
  2. Apoptosis ERK
  3. FR900359

FR900359 is a depsipeptide selective inhibitor of q/11/14 in mammalia, can inhibits ERK pathway. FR900359 suppresses the proliferation of melanoma cells and decreases of blood pressure. FR900359 also protected against airway hyperreactivity in murine models of allergen sensitization in Ovalbumin, low endotoxin (HY-W250978A)-induced sensitization model of asthma. FR900359 can be used for cancer and cardiovascular disease research.

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。

FR900359

FR900359 構造式

CAS 番号 : 107530-18-7

容量 価格(税別) 在庫状況 数量
250 μg $450 在庫あり
500 μg $720 在庫あり

* アイテムを追加する前、数量をご選択ください

This product is a controlled substance and not for sale in your territory.

カスタマーレビュー

Based on 4 publication(s) in Google Scholar

Top Publications Citing Use of Products

ERK アイソフォーム固有の製品をすべて表示:

  • 生物活性

  • 純度とドキュメンテーション

  • 参考文献

  • カスタマーレビュー

製品説明

FR900359 is a depsipeptide selective inhibitor of q/11/14 in mammalia, can inhibits ERK pathway. FR900359 suppresses the proliferation of melanoma cells and decreases of blood pressure. FR900359 also protected against airway hyperreactivity in murine models of allergen sensitization in Ovalbumin, low endotoxin (HY-W250978A)-induced sensitization model of asthma. FR900359 can be used for cancer and cardiovascular disease research[1][2][3][4].

体外実験

FR900359 (1.0 μM, 1 hours) inhibits Gαq, Gα11 and Gα /14, but not Gα16 or any other mammalian Gα isoform in HEK293 cells[1].
FR900359 (0-10 μM, 24 hours) effectively reduces growth of B16 cells and suppressed cell proliferation and inhibits migration in a concentration-dependent manner[1].
FR900359 (10 nM, 72 hours) induces G1 cell cycle arrest in melanoma cells with Gq tone and forces melanoma cells (B16 cells) into differentiation [1].
FR900359 (1.0 μM, 5 min) interdicts the activation of extracellular signal-regulated kinases 1 and 2 (ERK1/2) that be largely Gq-mediated28[1].
FR900359 (1 μM, 24 hours) significantly induces more 92.1 cells undergoing apoptosis compared to untreated [3].
FR900359 (30 nM, 60 min) induces dose-dependent relaxation of murine, porcine, and human airways ex vivo[4].

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

Cell Proliferation Assay[1]

Cell Line: B16 cells
Concentration: 0-10 μM
Incubation Time: 24 hours
Result: Effectively reduced growth of B16 cells in a concentration-dependent manner and suppressed cell proliferation and migration.

Cell Differentiation Assay[1]

Cell Line: B16 cells
Concentration: 10 nM
Incubation Time: 72 hours
Result: Induced G1 cell cycle arrest in melanoma cells with Gq tone.
Treated cells appeared flattened, rather dark, and packed with melanin vesicles, attributes consistent with the adoption of a more differentiated state.
Made melanocyte differentiation marker gp100 was upregulated considerably on FR treatment.

Western Blot Analysis[1]

Cell Line: HEK293 cells
Concentration: 1.0 μM
Incubation Time: 5 min
Result: FR interdicts Gq-dependent ERK1/2 activation

Apoptosis Analysis[3]

Cell Line: 92.1 cells
Concentration: 1.0 μM
Incubation Time: 24 hours
Result: Significantly induced more 92.1 cells undergoing apoptosis compared to untreated cells
体内実験

FR900359 (0.2 or 1 mg/ml, 12 μL per mouse, i.v.) strongly reduces vascular tone in mouse tail artery[1].
FR900359 (0.1 mg/ml, 2.5 mg/mouse, intratracheally) abolishes airway hyperreactivity after Ovalbumin (HY-W250978)-induced sensitization in mice[4].

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

Animal Model: Isometric force measurements in mouse tail artery [1]
Dosage: 1.0 μM
Administration: Washed
Result: Strongly reduced vascular tone
Animal Model: Ovalbumins–induced sensitization model of asthma. [4]
Dosage: 0.1 mg/ml, 2.5 mg per mouse
Administration: Intratracheally
Result: Abolished airway hyperreactivity after ovalbumin-induced sensitization in mice
分子量

1002.16

分子式

C49H75N7O15

CAS 番号
Appearance

Solid

Color

Light yellow to brown

SMILES

CC(C)[C@@H](O)[C@H](NC(CC)=O)C(O[C@@H]([C@H](NC([C@H](C)N(C)C([C@H](C)NC(C(N(C)C([C@@H](CC1=CC=CC=C1)O2)=O)=C)=O)=O)=O)C(N(C)[C@@H]([C@H](OC)C)C(O[C@H](C(C)C)[C@H](NC(C)=O)C2=O)=O)=O)C(C)C)=O

Structure Classification
Initial Source
輸送条件

Room temperature in continental US; may vary elsewhere.

保管条件
Powder -20°C 3 years
In solvent -80°C 6 months
  -20°C 1 month
純度とドキュメンテーション

純度: 99.90%

参考文献
  • No file chosen (Maximum size is: 1024 Kb)
  • If you have published this work, please enter the PubMed ID.
  • Your name will appear on the site.
  • Molarity Calculator

  • Dilution Calculator

The molarity calculator equation

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

質量   濃度   体積   分子量 *
= × ×

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

一般には略語で表示されます:C1V1 = C2V2

濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)
× = ×
C1   V1   C2   V2
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.

最近チェックした製品:

オンラインお問い合わせ

Your information is safe with us. * Required Fields.

製品名

 

カスタマ需要量 *

お名前 *

 

タイトル

メールアドレス *

 

電話番号 *

デパートメント

 

組纖名 *

市区町村

都道府県

国或いは地域 *

     

必ず会社名を記載ください。個人への返信は行いません。

備考

バルクお問い合わせ

Inquiry Information

製品名:
FR900359
製品番号:
HY-117037
数量:
MCE 日本正規代理店: