1. Cell Cycle/DNA Damage Cytoskeleton
  2. Microtubule/Tubulin
  3. Pironetin

Pironetin is an α/β unsaturated lactone isolated from Streptomyces species. Pironetin binds to α-tubulin and is a potent inhibitor of microtubule polymerization, and has cell cycle arrest and antitumor activity.

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。

Pironetin

Pironetin 構造式

CAS 番号 : 151519-02-7

容量 価格(税別) 在庫状況 数量
500 μg $474 在庫あり
1 mg $787 在庫あり
5 mg $2600 在庫あり
10 mg   お問い合わせ  
50 mg   お問い合わせ  

* 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 0 publication(s) in Google Scholar

Top Publications Citing Use of Products
  • 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

Pironetin is an α/β unsaturated lactone isolated from Streptomyces species. Pironetin binds to α-tubulin and is a potent inhibitor of microtubule polymerization, and has cell cycle arrest and antitumor activity[1][2].

IC50 & Target

Microtubule[1]

Cellular Effect
Cell Line Type Value Description References
A2780 GI50
22.2 1
Compound: 1
Inhibition of tubulin alpha in human A2780 cells assessed as cell growth inhibition after 48 hrs by MTT assay
Inhibition of tubulin alpha in human A2780 cells assessed as cell growth inhibition after 48 hrs by MTT assay
[PMID: 30693770]
A2780 IC50
0.0029 3
Compound: Pironetin
Cytotoxicity against compound-sensitive human A2780 cells after 24 hrs by MTT assay
Cytotoxicity against compound-sensitive human A2780 cells after 24 hrs by MTT assay
[PMID: 21396747]
A2780 IC50
0.0029 3
Compound: Pironetin
Cytotoxicity against compound-sensitive human A2780 cells after 24 hrs by MTT assay
Cytotoxicity against compound-sensitive human A2780 cells after 24 hrs by MTT assay
[PMID: 21396747]
A2780 IC50
0.0029 3
Compound: Pironetin
Cytotoxicity against compound-sensitive human A2780 cells after 24 hrs by MTT assay
Cytotoxicity against compound-sensitive human A2780 cells after 24 hrs by MTT assay
[PMID: 21396747]
A2780 IC50
0.008 3
Compound: pironetin
Cytotoxicity against human A2780 cells after 24 hrs by MTT assay
Cytotoxicity against human A2780 cells after 24 hrs by MTT assay
[PMID: 25426924]
A2780 IC50
0.008 3
Compound: pironetin
Cytotoxicity against human A2780 cells after 24 hrs by MTT assay
Cytotoxicity against human A2780 cells after 24 hrs by MTT assay
[PMID: 25426924]
A2780 IC50
0.008 3
Compound: pironetin
Cytotoxicity against human A2780 cells after 24 hrs by MTT assay
Cytotoxicity against human A2780 cells after 24 hrs by MTT assay
[PMID: 25426924]
A2780 ADR IC50
0.003 3
Compound: Pironetin
Cytotoxicity against compound-resistant human A2780AD cells after 24 hrs by MTT assay
Cytotoxicity against compound-resistant human A2780AD cells after 24 hrs by MTT assay
[PMID: 21396747]
A2780 GI50
22.2 1
Compound: 1
Inhibition of tubulin alpha in human A2780 cells assessed as cell growth inhibition after 48 hrs by MTT assay
Inhibition of tubulin alpha in human A2780 cells assessed as cell growth inhibition after 48 hrs by MTT assay
[PMID: 30693770]
A2780 ADR IC50
0.025 3
Compound: pironetin
Cytotoxicity against human A2780AD cells after 24 hrs by MTT assay
Cytotoxicity against human A2780AD cells after 24 hrs by MTT assay
[PMID: 25426924]
A2780 IC50
26 1
Compound: 1
Inhibition of tubulin alpha in human A2780 cells assessed as reduction in cell growth
Inhibition of tubulin alpha in human A2780 cells assessed as reduction in cell growth
[PMID: 30693770]
A2780 ADR IC50
0.003 3
Compound: Pironetin
Cytotoxicity against compound-resistant human A2780AD cells after 24 hrs by MTT assay
Cytotoxicity against compound-resistant human A2780AD cells after 24 hrs by MTT assay
[PMID: 21396747]
MDA-MB-231 GI50
4.6 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against human MDA-MB-231 cells assessed as reduction in growth after 4 days by HCS assay
Cytotoxicity against human MDA-MB-231 cells assessed as reduction in growth after 4 days by HCS assay
[PMID: 31130264]
A2780 ADR IC50
0.003 3
Compound: Pironetin
Cytotoxicity against compound-resistant human A2780AD cells after 24 hrs by MTT assay
Cytotoxicity against compound-resistant human A2780AD cells after 24 hrs by MTT assay
[PMID: 21396747]
A2780 ADR IC50
0.025 3
Compound: pironetin
Cytotoxicity against human A2780AD cells after 24 hrs by MTT assay
Cytotoxicity against human A2780AD cells after 24 hrs by MTT assay
[PMID: 25426924]
A2780 ADR IC50
0.025 3
Compound: pironetin
Cytotoxicity against human A2780AD cells after 24 hrs by MTT assay
Cytotoxicity against human A2780AD cells after 24 hrs by MTT assay
[PMID: 25426924]
MCF7 GI50
5 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against human MCF7 cells assessed as reduction in growth after 3 days by MTT assay
Cytotoxicity against human MCF7 cells assessed as reduction in growth after 3 days by MTT assay
[PMID: 31130264]
A549 GI50
7.5 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against human A549 cells assessed as reduction in growth after 4 days by HCS assay
Cytotoxicity against human A549 cells assessed as reduction in growth after 4 days by HCS assay
[PMID: 31130264]
DC3F GI50
9.5 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against hamster DC-3F cells assessed as reduction in growth after 4 days by HCS assay
Cytotoxicity against hamster DC-3F cells assessed as reduction in growth after 4 days by HCS assay
[PMID: 31130264]
HCT-15 IC50
<0.015 3
Compound: Pironetin
Cytotoxicity against human HCT15 cells after 48 hrs by sulforhodamine B assay
Cytotoxicity against human HCT15 cells after 48 hrs by sulforhodamine B assay
[PMID: 30601004]
A549 GI50
7.5 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against human A549 cells assessed as reduction in growth after 4 days by HCS assay
Cytotoxicity against human A549 cells assessed as reduction in growth after 4 days by HCS assay
[PMID: 31130264]
A549 GI50
7.5 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against human A549 cells assessed as reduction in growth after 4 days by HCS assay
Cytotoxicity against human A549 cells assessed as reduction in growth after 4 days by HCS assay
[PMID: 31130264]
DC3F GI50
9.5 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against hamster DC-3F cells assessed as reduction in growth after 4 days by HCS assay
Cytotoxicity against hamster DC-3F cells assessed as reduction in growth after 4 days by HCS assay
[PMID: 31130264]
EL4 GI50
15 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against C57BL/6 mouse EL4 cells assessed as reduction in growth after 3 days
Cytotoxicity against C57BL/6 mouse EL4 cells assessed as reduction in growth after 3 days
[PMID: 31130264]
EL4 GI50
15 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against C57BL/6 mouse EL4 cells assessed as reduction in growth after 3 days
Cytotoxicity against C57BL/6 mouse EL4 cells assessed as reduction in growth after 3 days
[PMID: 31130264]
T98G GI50
7.5 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against human T98G cells assessed as reduction in growth after 4 days by MTS assay
Cytotoxicity against human T98G cells assessed as reduction in growth after 4 days by MTS assay
[PMID: 31130264]
HCT-15 IC50
< 0.015 3
Compound: Pironetin
Cytotoxicity against human HCT15 cells after 48 hrs by sulforhodamine B assay
Cytotoxicity against human HCT15 cells after 48 hrs by sulforhodamine B assay
[PMID: 30601004]
HCT-15 IC50
< 0.015 3
Compound: Pironetin
Cytotoxicity against human HCT15 cells after 48 hrs by sulforhodamine B assay
Cytotoxicity against human HCT15 cells after 48 hrs by sulforhodamine B assay
[PMID: 30601004]
DC3F GI50
9.5 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against hamster DC-3F cells assessed as reduction in growth after 4 days by HCS assay
Cytotoxicity against hamster DC-3F cells assessed as reduction in growth after 4 days by HCS assay
[PMID: 31130264]
HEK293 IC50
0.017 3
Compound: pironetin
Cytotoxicity against human HEK293 cells after 3 days by MTT assay
Cytotoxicity against human HEK293 cells after 3 days by MTT assay
[PMID: 25426924]
HEK293 IC50
0.017 3
Compound: Pironetin
Cytotoxicity against HEK293 cells assessed as inhibition of cell growth after 72 hrs by MTT assay
Cytotoxicity against HEK293 cells assessed as inhibition of cell growth after 72 hrs by MTT assay
[PMID: 25240870]
HEK293 IC50
0.017 3
Compound: Pironetin
Cytotoxicity against HEK293 cells assessed as inhibition of cell growth after 72 hrs by MTT assay
Cytotoxicity against HEK293 cells assessed as inhibition of cell growth after 72 hrs by MTT assay
[PMID: 25240870]
HEK293 IC50
0.017 3
Compound: Pironetin
Cytotoxicity against HEK293 cells assessed as inhibition of cell growth after 72 hrs by MTT assay
Cytotoxicity against HEK293 cells assessed as inhibition of cell growth after 72 hrs by MTT assay
[PMID: 25240870]
HEK293 IC50
0.017 3
Compound: pironetin
Cytotoxicity against human HEK293 cells after 3 days by MTT assay
Cytotoxicity against human HEK293 cells after 3 days by MTT assay
[PMID: 25426924]
HeLa IC50
0.092 3
Compound: Pironetin
Cytotoxicity against human HeLa cells after 48 hrs by sulforhodamine B assay
Cytotoxicity against human HeLa cells after 48 hrs by sulforhodamine B assay
[PMID: 30601004]
HEK293 IC50
0.017 3
Compound: pironetin
Cytotoxicity against human HEK293 cells after 3 days by MTT assay
Cytotoxicity against human HEK293 cells after 3 days by MTT assay
[PMID: 25426924]
EL4 GI50
15 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against C57BL/6 mouse EL4 cells assessed as reduction in growth after 3 days
Cytotoxicity against C57BL/6 mouse EL4 cells assessed as reduction in growth after 3 days
[PMID: 31130264]
HL-60 GI50
20 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against human HL60 cells assessed as reduction in growth after 24 hrs by MTT assay
Cytotoxicity against human HL60 cells assessed as reduction in growth after 24 hrs by MTT assay
[PMID: 31130264]
HL-60 GI50
20 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against human HL60 cells assessed as reduction in growth after 24 hrs by MTT assay
Cytotoxicity against human HL60 cells assessed as reduction in growth after 24 hrs by MTT assay
[PMID: 31130264]
HT-29 IC50
0.0064 3
Compound: pironetin
Cytotoxicity against human HT-29 cells after 3 days by MTT assay
Cytotoxicity against human HT-29 cells after 3 days by MTT assay
[PMID: 25426924]
K562/Adr GI50
16 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against human K562/ADR cells assessed as reduction in growth after 4 days by MTT assay
Cytotoxicity against human K562/ADR cells assessed as reduction in growth after 4 days by MTT assay
[PMID: 31130264]
HeLa IC50
0.092 3
Compound: Pironetin
Cytotoxicity against human HeLa cells after 48 hrs by sulforhodamine B assay
Cytotoxicity against human HeLa cells after 48 hrs by sulforhodamine B assay
[PMID: 30601004]
HT-29 IC50
0.0064 3
Compound: Pironetin
Cytotoxicity against human HT-29 cells assessed as inhibition of cell growth after 72 hrs by MTT assay
Cytotoxicity against human HT-29 cells assessed as inhibition of cell growth after 72 hrs by MTT assay
[PMID: 25240870]
K562 GI50
17.3 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against human K562 cells assessed as reduction in growth after 4 days by MTT assay
Cytotoxicity against human K562 cells assessed as reduction in growth after 4 days by MTT assay
[PMID: 31130264]
K562 GI50
17.3 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against human K562 cells assessed as reduction in growth after 4 days by MTT assay
Cytotoxicity against human K562 cells assessed as reduction in growth after 4 days by MTT assay
[PMID: 31130264]
NCI-H69 GI50
17.5 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against human H69 cells assessed as reduction in growth after 7 days by MTT assay
Cytotoxicity against human H69 cells assessed as reduction in growth after 7 days by MTT assay
[PMID: 31130264]
K562/Adr GI50
16 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against human K562/ADR cells assessed as reduction in growth after 4 days by MTT assay
Cytotoxicity against human K562/ADR cells assessed as reduction in growth after 4 days by MTT assay
[PMID: 31130264]
HT-29 IC50
0.0064 3
Compound: Pironetin
Cytotoxicity against human HT-29 cells assessed as inhibition of cell growth after 72 hrs by MTT assay
Cytotoxicity against human HT-29 cells assessed as inhibition of cell growth after 72 hrs by MTT assay
[PMID: 25240870]
HL-60 GI50
20 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against human HL60 cells assessed as reduction in growth after 24 hrs by MTT assay
Cytotoxicity against human HL60 cells assessed as reduction in growth after 24 hrs by MTT assay
[PMID: 31130264]
MCF7 IC50
0.006 3
Compound: pironetin
Cytotoxicity against human MCF7 cells after 3 days by MTT assay
Cytotoxicity against human MCF7 cells after 3 days by MTT assay
[PMID: 25426924]
HT-29 IC50
0.0064 3
Compound: pironetin
Cytotoxicity against human HT-29 cells after 3 days by MTT assay
Cytotoxicity against human HT-29 cells after 3 days by MTT assay
[PMID: 25426924]
MCF7 IC50
0.006 3
Compound: Pironetin
Cytotoxicity against human MCF7 cells assessed as inhibition of cell growth after 72 hrs by MTT assay
Cytotoxicity against human MCF7 cells assessed as inhibition of cell growth after 72 hrs by MTT assay
[PMID: 25240870]
A2780 GI50
22.2 1
Compound: 1
Inhibition of tubulin alpha in human A2780 cells assessed as cell growth inhibition after 48 hrs by MTT assay
Inhibition of tubulin alpha in human A2780 cells assessed as cell growth inhibition after 48 hrs by MTT assay
[PMID: 30693770]
HT-29 IC50
0.0064 3
Compound: pironetin
Cytotoxicity against human HT-29 cells after 3 days by MTT assay
Cytotoxicity against human HT-29 cells after 3 days by MTT assay
[PMID: 25426924]
HeLa GI50
30 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against human HeLa cells assessed as reduction in growth
Cytotoxicity against human HeLa cells assessed as reduction in growth
[PMID: 31130264]
MCF7 IC50
0.015 3
Compound: Pironetin
Cytotoxicity against human MCF7 cells after 48 hrs by sulforhodamine B assay
Cytotoxicity against human MCF7 cells after 48 hrs by sulforhodamine B assay
[PMID: 30601004]
HT-29 IC50
0.0064 3
Compound: Pironetin
Cytotoxicity against human HT-29 cells assessed as inhibition of cell growth after 72 hrs by MTT assay
Cytotoxicity against human HT-29 cells assessed as inhibition of cell growth after 72 hrs by MTT assay
[PMID: 25240870]
HeLa IC50
0.092 3
Compound: Pironetin
Cytotoxicity against human HeLa cells after 48 hrs by sulforhodamine B assay
Cytotoxicity against human HeLa cells after 48 hrs by sulforhodamine B assay
[PMID: 30601004]
MCF7 GI50
5 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against human MCF7 cells assessed as reduction in growth after 3 days by MTT assay
Cytotoxicity against human MCF7 cells assessed as reduction in growth after 3 days by MTT assay
[PMID: 31130264]
K562 GI50
17.3 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against human K562 cells assessed as reduction in growth after 4 days by MTT assay
Cytotoxicity against human K562 cells assessed as reduction in growth after 4 days by MTT assay
[PMID: 31130264]
MDA-MB-231 GI50
4.6 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against human MDA-MB-231 cells assessed as reduction in growth after 4 days by HCS assay
Cytotoxicity against human MDA-MB-231 cells assessed as reduction in growth after 4 days by HCS assay
[PMID: 31130264]
A2780 IC50
26 1
Compound: 1
Inhibition of tubulin alpha in human A2780 cells assessed as reduction in cell growth
Inhibition of tubulin alpha in human A2780 cells assessed as reduction in cell growth
[PMID: 30693770]
K562/Adr GI50
16 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against human K562/ADR cells assessed as reduction in growth after 4 days by MTT assay
Cytotoxicity against human K562/ADR cells assessed as reduction in growth after 4 days by MTT assay
[PMID: 31130264]
NCI-H69 GI50
17.5 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against human H69 cells assessed as reduction in growth after 7 days by MTT assay
Cytotoxicity against human H69 cells assessed as reduction in growth after 7 days by MTT assay
[PMID: 31130264]
HeLa GI50
30 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against human HeLa cells assessed as reduction in growth
Cytotoxicity against human HeLa cells assessed as reduction in growth
[PMID: 31130264]
MCF7 GI50
5 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against human MCF7 cells assessed as reduction in growth after 3 days by MTT assay
Cytotoxicity against human MCF7 cells assessed as reduction in growth after 3 days by MTT assay
[PMID: 31130264]
P388 GI50
100 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against mouse P388 cells assessed as reduction in growth after 24 hrs by MTT assay
Cytotoxicity against mouse P388 cells assessed as reduction in growth after 24 hrs by MTT assay
[PMID: 31130264]
MCF7 IC50
0.006 3
Compound: pironetin
Cytotoxicity against human MCF7 cells after 3 days by MTT assay
Cytotoxicity against human MCF7 cells after 3 days by MTT assay
[PMID: 25426924]
MCF7 IC50
0.015 3
Compound: Pironetin
Cytotoxicity against human MCF7 cells after 48 hrs by sulforhodamine B assay
Cytotoxicity against human MCF7 cells after 48 hrs by sulforhodamine B assay
[PMID: 30601004]
T98G GI50
7.5 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against human T98G cells assessed as reduction in growth after 4 days by MTS assay
Cytotoxicity against human T98G cells assessed as reduction in growth after 4 days by MTS assay
[PMID: 31130264]
MCF7 IC50
0.006 3
Compound: Pironetin
Cytotoxicity against human MCF7 cells assessed as inhibition of cell growth after 72 hrs by MTT assay
Cytotoxicity against human MCF7 cells assessed as inhibition of cell growth after 72 hrs by MTT assay
[PMID: 25240870]
MCF7 IC50
0.006 3
Compound: Pironetin
Cytotoxicity against human MCF7 cells assessed as inhibition of cell growth after 72 hrs by MTT assay
Cytotoxicity against human MCF7 cells assessed as inhibition of cell growth after 72 hrs by MTT assay
[PMID: 25240870]
MCF7 IC50
0.006 3
Compound: pironetin
Cytotoxicity against human MCF7 cells after 3 days by MTT assay
Cytotoxicity against human MCF7 cells after 3 days by MTT assay
[PMID: 25426924]
P388 GI50
100 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against mouse P388 cells assessed as reduction in growth after 24 hrs by MTT assay
Cytotoxicity against mouse P388 cells assessed as reduction in growth after 24 hrs by MTT assay
[PMID: 31130264]
MCF7 IC50
0.015 3
Compound: Pironetin
Cytotoxicity against human MCF7 cells after 48 hrs by sulforhodamine B assay
Cytotoxicity against human MCF7 cells after 48 hrs by sulforhodamine B assay
[PMID: 30601004]
MDA-MB-231 GI50
4.6 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against human MDA-MB-231 cells assessed as reduction in growth after 4 days by HCS assay
Cytotoxicity against human MDA-MB-231 cells assessed as reduction in growth after 4 days by HCS assay
[PMID: 31130264]
NCI-H69 GI50
17.5 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against human H69 cells assessed as reduction in growth after 7 days by MTT assay
Cytotoxicity against human H69 cells assessed as reduction in growth after 7 days by MTT assay
[PMID: 31130264]
P388 GI50
100 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against mouse P388 cells assessed as reduction in growth after 24 hrs by MTT assay
Cytotoxicity against mouse P388 cells assessed as reduction in growth after 24 hrs by MTT assay
[PMID: 31130264]
T98G GI50
7.5 1
Compound: 1; (-)-PA-48153C
Cytotoxicity against human T98G cells assessed as reduction in growth after 4 days by MTS assay
Cytotoxicity against human T98G cells assessed as reduction in growth after 4 days by MTS assay
[PMID: 31130264]
体外実験

Pironetin (20-100 ng/mL; 24 hours; 3Y1 cells) treatment arrests the cell cycle progression at G2/M in 3Y1 cells[1].
Pironetin (1-10000 ng/mL; 3 days; HeLa, A2780 and K-NRK cells) treatment inhibits the cell proliferation. IC50 values against these cell lines are almost 10 ng/mL[1].

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

Cell Cycle Analysis[1]

Cell Line: 3Y1 cells
Concentration: 20 ng/mL, 50 ng/mL, 100 ng/mL
Incubation Time: 24 hours
Result: Arrested the cell cycle progression at G2/M in3Y1 cells.

Cell Proliferation Assay[1]

Cell Line: HeLa, A2780 and K-NRK cells
Concentration: 1 ng/mL, 10 ng/mL, 100 ng/mL, 1000 ng/mL and 10000 ng/mL
Incubation Time: 3 days
Result: Inhibited the cell proliferation.
体内実験

Pironetin (0.78-6.25 mg/kg; intraperitoneal injection; daily; for 5 days; female CDF1-SLC mice) treatment shows a moderate antitumor effect, however, a severe weight loss is observed as a side effect[1].

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

Animal Model: Female CDF1-SLC mice (10 weeks) injected with P388 murine leukemia cells[1]
Dosage: 0.78 mg/kg, 1.56 mg/kg, 3.13 mg/kg, 6.25 mg/kg
Administration: Intraperitoneal injection; daily; for 5 days
Result: Showed a moderate antitumor effect.
分子量

324.45

分子式

C19H32O4

CAS 番号
Appearance

Oil

Color

Colorless to off-white

SMILES

O=C1C=C[C@H]([C@H](O1)C[C@H]([C@@H]([C@@H]([C@H](C/C=C/C)C)OC)C)O)CC

輸送条件

Room temperature in continental US; may vary elsewhere.

保管条件
Pure form -20°C 3 years
In solvent -80°C 6 months
  -20°C 1 month
溶剤 & 溶解度
体外: 

DMSO : < 1 mg/mL (insoluble or slightly soluble)

  • Molarity Calculator

  • Dilution Calculator

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

Mass
=
Concentration
×
Volume
×
Molecular Weight *

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)

C1

×
体積 (開始)

V1

=
濃度 (終了)

C2

×
体積 (終了)

V2

In Vivo Dissolution Calculator
Please enter the basic information of animal experiments:

Dosage

mg/kg

Animal weight
(per animal)

g

Dosing volume
(per animal)

μL

Number of animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Calculation results:
Working solution concentration: mg/mL
純度とドキュメンテーション
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:
Pironetin
製品番号:
HY-116446
数量:
MCE 日本正規代理店: