製品番号: HY-13518

ピセアタンノール

(別名: Piceatannol; Astringenin; trans-Piceatannol)

25 Cited Publications

カスタマーレビュー

Based on 25 publication(s) in Google Scholar

Piceatannol is a well-known Syk inhibitor and reduces the expression of iNOS induced by TNF. Piceatannol is an effective agent for research of acute lung injury (ALI). Piceatannol is a naturally occurring polyphenolic stilbene found in various fruits and vegetables and exhibits anticancer and anti-inflammatory properties. Piceatannol induces apoptosis in DLBCL cell lines. Piceatannol induces autophagy and apoptosis in MOLT-4 human leukemia cells.

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。

純度: 98.97%
CAS 番号: 10083-24-6
分子式: C₁₄H₁₂O₄
分子量:244.24

保管条件:

Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 1 year , -20°C, 6 months

Piceatannol 構造式

CAS 番号: 10083-24-6

容量

価格（税別）

在庫状況

数量

Sample (0.1mg)

In-stock

(In Japan)

Apply Now

お問い合わせ Ask For Quote & Lead Time Consult sales personnel for more information Check price and availability お問い合わせ Ask For Quote & Lead Time Consult sales personnel for more information Check price and availability

バルクお問い合わせ

Amount: USD 0.00

* アイテムを追加する前、数量をご選択ください

Top Publications Citing

Use of MCE Products

Fluorescent Dye

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

生物活性
- 製品説明
- Cellular Effect
- 体外実験
- 体内実験
- 臨床実験
化学情報
Publications (25)
溶剤 & 溶解度
- 体外
- 体内
純度とドキュメンテーション
参考文献
Help & FAQs
Bioz

生物活性

製品説明

Piceatannol is a well-known Syk inhibitor and reduces the expression of iNOS induced by TNF. Piceatannol is an effective agent for research of acute lung injury (ALI)^[1]. Piceatannol is a naturally occurring polyphenolic stilbene found in various fruits and vegetables and exhibits anticancer and anti-inflammatory properties^[2]. Piceatannol induces apoptosis in DLBCL cell lines^[3]. Piceatannol induces autophagy and apoptosis in MOLT-4 human leukemia cells^[4].

Endogenous Metabolite アイソフォーム固有の製品をすべて表示 :

Cellular Effect

Cell Line	Type	Value	Description	References
A2780	IC₅₀	41 μM Compound: 4	Antiproliferative activity against human A2780 cells after 2 days by Alamar Blue assay Antiproliferative activity against human A2780 cells after 2 days by Alamar Blue assay	[PMID: 24239390]
BV-2	IC₅₀	80.51 μM Compound: 29	Antineuroinflammatory activity in mouse BV2 cells assessed as inhibition of LPS-induced NO production after 24 hrs in presence of LPS by Griess reaction based assay Antineuroinflammatory activity in mouse BV2 cells assessed as inhibition of LPS-induced NO production after 24 hrs in presence of LPS by Griess reaction based assay	[PMID: 28911817]
HCT-116	IC₅₀	5 μM Compound: Trans-Piceatannol	Anticancer activity against human HCT-116 cells assessed as cell growth inhibition Anticancer activity against human HCT-116 cells assessed as cell growth inhibition	[PMID: 32485531]
J774	IC₅₀	13 μM Compound: 5	Antiinflammatory activity in mouse J774 cells assessed as reduction in LPS-induced IL6 expression after 24 hrs by ELISA Antiinflammatory activity in mouse J774 cells assessed as reduction in LPS-induced IL6 expression after 24 hrs by ELISA	[PMID: 29726680]
J774	IC₅₀	2.6 μM Compound: 5	Antiinflammatory activity in mouse J774 cells assessed as reduction in LPS-induced nitric oxide production after 24 hrs by Griess assay Antiinflammatory activity in mouse J774 cells assessed as reduction in LPS-induced nitric oxide production after 24 hrs by Griess assay	[PMID: 29726680]
J774	IC₅₀	4 μM Compound: 5	Antiinflammatory activity in mouse J774 cells assessed as reduction in LPS-induced MCP1 expression after 24 hrs by ELISA Antiinflammatory activity in mouse J774 cells assessed as reduction in LPS-induced MCP1 expression after 24 hrs by ELISA	[PMID: 29726680]
NCI-H522	EC₅₀	17 μM Compound: Piceatannol	Antiproliferative activity against human NCI-H522 cells after 72 hrs by WST8 assay Antiproliferative activity against human NCI-H522 cells after 72 hrs by WST8 assay	[PMID: 28169168]
NCI-H522	EC₅₀	23 μM Compound: Piceatannol	Antiproliferative activity against human NCI-H522 cells after 48 hrs by WST8 assay Antiproliferative activity against human NCI-H522 cells after 48 hrs by WST8 assay	[PMID: 28169168]
NCI-H522	EC₅₀	53 μM Compound: Piceatannol	Antiproliferative activity against human NCI-H522 cells after 24 hrs by WST8 assay Antiproliferative activity against human NCI-H522 cells after 24 hrs by WST8 assay	[PMID: 28169168]
U373-MAGI	EC₅₀	21.4 μM Compound: 1b	Antiviral activity against HIV1 infected in human U373-MAGI cells expressing CXCR4 assessed as inhibition of viral infection preincubated for 2 hrs prior to infection followed by compound wash out measured after 48 hrs by single round replication assay Antiviral activity against HIV1 infected in human U373-MAGI cells expressing CXCR4 assessed as inhibition of viral infection preincubated for 2 hrs prior to infection followed by compound wash out measured after 48 hrs by single round replication assay	[PMID: 23010273]

体外実験

Piceatannol is a resveratrol metabolite^[2].
SYK inhibitor Piceatannol (3.125, 6.25, 12.5, 25, and 50 μM; 72 hours) inhibits cell growth of six diffuse large B cell lymphomas (DLBCL) cell lines (SUDHL-6, U2392,DOHH2,Karpas 422, VAL, OCI Ly19) with IC₅₀s of 18 μM, 25 μM, 37 μM, 48 μM, >50 μM and >50 μM, respectively^[3].

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

Cell Cytotoxicity Assay^[3]

Cell Line:

Six DLBCL cell lines (Karpas 422, VAL, SUDHL-6, OCI Ly19, U2392 and DOHH2)
Concentration:

3.125, 6.25, 12.5, 25, and 50 μM
Incubation Time:

72 hours
Result:

The IC₅₀s were 18 μM in SUDHL-6, 25 μM in U2392, 37 mM in DOHH2, 48 μM in Karpas 422 and higher than 50 μM in OCI-Ly19 and in VAL.

体内実験

Piceatannol (10, 20, and 40 mg/kg) inhibits the pulmonary edema and reduces the infiltration of inflammatory cells induced by lipopolysaccharide^[1].
Piceatannol (10, 20, and 40 mg/kg) alleviates the myeloperoxidase activity and inhibits the production of iNOS and COX-2 expressions in lung tissuesinduced by lipopolysaccharide^[1].
Piceatannol (10, 20, and 40 mg/kg; intraperitoneally 1 h) treatment alleviates inflammatory response by inhibiting the activation of TLR/NF-κB signaling pathway in lung tissues during acute lung injury (ALI) induced by LPS^[1].

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

Animal Model:

Male C57BL/6 mice (40-50 g)^[1]
Dosage:

10, 20, and 40 mg/kg
Administration:

Intraperitoneally 1 h before LPS challenge
Result:

Significantly reduced the pulmonary edema induced by LPS.

臨床実験

NCT Number	Sponsor	Condition	Start Date	Phase A549
NCT01329991	Plexxikon\|		2011-05	PHASE1

化学情報

CAS 番号 10083-24-6
性状 Solid
分子量 244.24
分子式 C₁₄H₁₂O₄
Color Light yellow to khaki
SMILES

OC1=CC=C(/C=C/C2=CC(O)=CC(O)=C2)C=C1O
別名

Piceatannol; Astringenin; trans-Piceatannol
Structure Classification
- Stilbenes
Initial Source
- Microorganisms
輸送条件

Room temperature in continental US; may vary elsewhere.

保管条件

Powder	-20°C	3 years
	4°C	2 years
In solvent	-80°C	1 year
	-20°C	6 months

Publications (25)

All WBFlow CytometryIFCell Imaging/StainingIP

Sort by:

Journal Impact Factor

Nature

Submicrometre sampling of living cells by macrophages. [Abstract]

2026 Jun;654(8118):495-503. PMID: 42056510
Cell

Immune Checkpoint Inhibition Overcomes ADCP-Induced Immunosuppression by Macrophages. [Abstract]

2018 Oct 4;175(2):442-457.e23. PMID: 30290143

Piceatannol purchased from MedChemExpress. Usage Cited in: Cell. 2018 Oct 4;175(2):442-457.e23. [Abstract]

Syk inhibitors (R406 and Piceatannol) are added during the induction of trastuzumab-dependent BT-474 phagocytosis. The binding of the phagosome marker Rab7 to AIM2 in macrophages are evaluated by co-immunoprecipitation.
Nat Commun

CD36 facilitates fatty acid uptake by dynamic palmitoylation-regulated endocytosis. [Abstract]

2020 Sep 21;11(1):4765. PMID: 32958780

Piceatannol purchased from MedChemExpress. Usage Cited in: Nat Commun. 2020 Sep 21;11(1):4765. [Abstract]

3T3-L1 adipocytes were pretreated with serum-free medium for 4 h and Piceatannol (Pice., 40 μM) for 1 h, followed by treatment with BSA or BSA-conjugated oleate (100 μM) for 30 min. Cells were harvested for immunoblotting with indicated antibodies. The results showed that Piceatannol largely abolished oleic acid-induced phosphorylation of VAV and JNK by inhibiting SYK in 3T3-L1 adipocytes.

Piceatannol purchased from MedChemExpress. Usage Cited in: Nat Commun. 2020 Sep 21;11(1):4765. [Abstract]

3T3-L1 adipocytes were pretreated with serum-free medium for 4 h and Piceatannol (40 μM) for 1 h, followed by treatment with BSA or BSA-conjugated oleate (100 μM) for 1 h. Cells were harvested for immunostaining assays.
Carbohydr Polym

Decoding the pharmacokinetics of intravenous lentinan: A multiscale journey from the blood to hepatic Kupffer cells' lysosomes. [Abstract]

2026 Feb 15:374:124706. PMID: 41371850
Carbohydr Polym

Insights into oral lentinan immunomodulation: Dectin-1-mediated lymphatic transport from Peyer's patch M cells to mononuclear phagocytes. [Abstract]

2024 Dec 15:346:122586. PMID: 39245482
Carbohydr Polym

Metabolic degradation of polysaccharides from Lentinus edodes by Kupffer cells via the Dectin-1/Syk signaling pathway. [Abstract]

2023 Oct 1:317:121108. PMID: 37364942
Carbohydr Polym

Innate immune receptors co-recognition of polysaccharides initiates multi-pathway synergistic immune response. [Abstract]

2023 Apr 1:305:120533. PMID: 36737186
Pharmacol Res

Cardamonin retards progression of autosomal dominant polycystic kidney disease via inhibiting renal cyst growth and interstitial fibrosis. [Abstract]

2020 May;155:104751. PMID: 32151678
Food Front

2023 Jun 10.
Phytother Res

Pterostilbene Exhibits Broad-Spectrum Antiviral Activity by Targeting the Enterovirus Capsid, Inactivating Viral Particles, Blocking Viral Binding, and Protecting Mice From Lethal EV-A71 Challenge. [Abstract]

2025 Apr 16. PMID: 40235439
Fundam Res

2024 Apr 15.

Piceatannol purchased from MedChemExpress. Usage Cited in: Fundam Res. 2024 Apr 15.

pSHP2 expression in Raw264.7 cells stimulated with 20 ng/mL of recombinant IL-10 for 24 h in the presence of the inhibitors PP2 (10 µM), UNC2025 (5 µM) or Piceatannol (40 µM).
Cell Mol Life Sci

Tropomodulin1 exacerbates inflammatory response in macrophages by negatively regulating LPS-induced TLR4 endocytosis. [Abstract]

2024 Sep 14;81(1):402. PMID: 39276234

Piceatannol purchased from MedChemExpress. Usage Cited in: Cell Mol Life Sci. 2024 Sep 14;81(1):402. [Abstract]

The cell surface expression of TLR4 on wild type (WT) or TOT/Tmod1^−/− BMDMs as determined by flow cytometry. The BMDMs were pretreated with Piceatannol (PIC, 75 µM; 30 min), an Syk inhibitor, or solvent (DMSO), and then stimulated with LPS for 0, 30, 60, and 120 min. The data was expressed as percentage of surface TLR4 by dividing the fluorescence intensities at any time points by the fluorescence intensity at 0 min. n = 7 biological replicates. Flow cytometry data revealed that PIC (75 µM; 30 min) treatment impaired the effects of LPS on surface TLR4.

Piceatannol purchased from MedChemExpress. Usage Cited in: Cell Mol Life Sci. 2024 Sep 14;81(1):402. [Abstract]

The colocalization of TLR4 (red) with early endosome marker EEA-1 (green) in Piceatannol (PIC, 75 µM; 30 min)-pretreated WT or TOT/Tmod1^−/− BMDMs at 0 and 10 min after LPS treatment as observed by confocal microscopy (left panels). The nuclei were counterstained with DAPI (blue). Scale bar = 10 μm.
J Agric Food Chem

Resveratrol Reactivates Latent HIV through Increasing Histone Acetylation and Activating Heat Shock Factor 1. [Abstract]

2017 Jun 7;65(22):4384-4394. PMID: 28471170
Inflammation

Oroxylin A-induced Trained Immunity Promotes LC3-associated Phagocytosis in Macrophage in Protecting Mice Against Sepsis. [Abstract]

2024 Dec;47(6):2196-2214. PMID: 38739341
Eur J Pharmacol

Piceatannol alleviates liver ischaemia/reperfusion injury by inhibiting TLR4/NF-κB/NLRP3 in hepatic macrophages. [Abstract]

2023 Dec 5:960:176149. PMID: 37866744
Int Immunopharmacol

Piceatannol-mediated JAK2/STAT3 signaling pathway inhibition contributes to the alleviation of oxidative injury and collagen synthesis during pulmonary fibrosis. [Abstract]

2022 Oct:111:109107. PMID: 35932616
Sci Rep

Enhancement of melanoma aggressiveness via p38-MAPK, HIF-1α pathways, and metabolic reprogramming induced by Candida albicans. [Abstract]

2025 Nov 17;15(1):40227. PMID: 41249785
Chem Biol Drug Des

Piceatannol selectively inhibited the JNK3 enzyme and augmented apoptosis through inhibition of Bcl-2/Cyt-c/caspase-dependent pathways in the oxygen-glucose deprived SHSY-5Y cell lines: In silico and in vitro study. [Abstract]

2024 Feb;103(2):e14458. PMID: 38383061
Naunyn Schmiedebergs Arch Pharmacol

Piceatannol improved cerebral blood flow and attenuated JNK3 and mitochondrial apoptotic pathway in a global ischemic model to produce neuroprotection. [Abstract]

2024 Jan;397(1):479-496. PMID: 37470802
Mol Immunol

IL-4 plays an essential role in DnaJ-ΔA146Ply-mediated immunoprotection against Streptococcus pneumoniae in mice. [Abstract]

2022 Mar;143:105-113. PMID: 35114487
Mycopathologia

MiR-146a Negatively Regulates Aspergillus fumigatus-Induced TNF-α and IL-6 Secretion in THP-1 Macrophages. [Abstract]

2021 Jun;186(3):341-354. PMID: 34089172
Cell Physiol Biochem

Stimulation of Eryptosis, the Suicidal Erythrocyte Death by Piceatannol. [Abstract]

2016;38(6):2300-10. PMID: 27197738
Stony Brook University

2025.
bioRxiv

2025 January 18.
Universidad Del Pais Vasco

2023 Jun 22.

溶剤 & 溶解度

体外:

DMSO : 97.47 mg/mL (399.07 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

H₂O : < 0.1 mg/mL (insoluble)

View the Complete Stock Solution Preparation Table

Preparing Stock Solutions

View the Complete Stock Solution Preparation Table

Concentration Solvent Mass

1 mg

5 mg

10 mg

Concentration

Solvent

Mass

1 mM

4.0943 mL

20.4717 mL

40.9433 mL

5 mM

0.8189 mL

4.0943 mL

8.1887 mL

10 mM

0.4094 mL

2.0472 mL

4.0943 mL

Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.

Storage method and period of stock solution: -80°C, 1 year; -20°C, 6 months. When stored at -80°C, please use it within 1 year. When stored at -20°C, please use it within 6 months.

モル濃度計算機

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

Mass Mass

濃度濃度

体積体積

分子量分子量

希釈計算機

濃度 _(開始) × 体積 _(開始) = 濃度 _(終了) × 体積 _(終了)

濃度 _(開始) 濃度 _(開始)

体積 _(開始) 体積 _(開始)

濃度 _(終了) 濃度 _(終了)

体積 _(終了) 体積 _(終了)

体内:

Select the appropriate dissolution method based on your experimental animal and administration route.

Stock Solution Working Solution

For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for In Vivo experiments, it is recommended to prepare freshly and use it on the same day.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

Protocol 1

Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline

Solubility: ≥ 2.5 mg/mL (10.24 mM); Clear solution

This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.

Protocol 2

Add each solvent one by one: 10% DMSO 90% (20% SBE-β-CD in Saline)

Solubility: ≥ 2.5 mg/mL (10.24 mM); Clear solution

This protocol yields a clear solution of ≥ 2.5 mg/mL (saturation unknown).

Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (25.0 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.

In Vivo Dissolution Calculator

Please enter the basic information of animal experiments:

Dosage Dosage
mg/kg
Animal Weight (Per Animal) Animal Weight (Per Animal)
g
Dosing Volume (Per Animal) Dosing Volume (Per Animal)
μL
Number of Animals Number of Animals

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.

Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.

Please enter your animal formula composition:

%
DMSO +

Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
%
+
+
%
Tween-80 + +
%
Saline +

The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).

Working solution concentration: 0.22 mg/mL

純度とドキュメンテーション

バッチを選択:

純度: 99.98%

Assay: 99.98%

ee.: 99.98%

データシート (278 KB)
SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Portuguese - PT (393 KB)
COA (2659 KB)
元素分析報告書 (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
取扱説明書 (2659 KB)

参考文献

[1]. Lu-Yuan Peng,et al. Protective Effect of Piceatannol Against Acute Lung Injury Through Protecting the Integrity of Air-Blood Barrier and Modulating the TLR4/NF-κB Signaling Pathway Activation. Front Pharmacol. 2020 Jan 22;10:1613. [Content Brief]

[2]. Jonathan Kershaw, et al. The Therapeutic Potential of Piceatannol, a Natural Stilbene, in Metabolic Diseases: A Review. J Med Food. 2017 May;20(5):427-438. [Content Brief]

[3]. Andrea Rinaldi, et al. In vitro efficacy of tyrosine kinase inhibitors: SYK and BCR-ABL inhibitors in lymphomas.Hematol Oncol. 2011 Sep;29(3):164-6. [Content Brief]

[4]. Kamila Siedlecka-Kroplewska, et al. Induction of autophagy, apoptosis and aquisition of resistance in response to piceatannol toxicity in MOLT-4 human leukemia cells. Toxicol In Vitro. 2019 Sep;59:12-25. [Content Brief]

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

Complete Stock Solution Preparation Table

Storage method and period of stock solution: -80°C, 1 year; -20°C, 6 months. When stored at -80°C, please use it within 1 year. When stored at -20°C, please use it within 6 months.

Optional Solvent	Concentration Solvent Mass	1 mg	5 mg	10 mg	25 mg
DMSO	1 mM	4.0943 mL	20.4717 mL	40.9433 mL	102.3583 mL
	5 mM	0.8189 mL	4.0943 mL	8.1887 mL	20.4717 mL
	10 mM	0.4094 mL	2.0472 mL	4.0943 mL	10.2358 mL
	15 mM	0.2730 mL	1.3648 mL	2.7296 mL	6.8239 mL
	20 mM	0.2047 mL	1.0236 mL	2.0472 mL	5.1179 mL
	25 mM	0.1638 mL	0.8189 mL	1.6377 mL	4.0943 mL
	30 mM	0.1365 mL	0.6824 mL	1.3648 mL	3.4119 mL
	40 mM	0.1024 mL	0.5118 mL	1.0236 mL	2.5590 mL
	50 mM	0.0819 mL	0.4094 mL	0.8189 mL	2.0472 mL
	60 mM	0.0682 mL	0.3412 mL	0.6824 mL	1.7060 mL
	80 mM	0.0512 mL	0.2559 mL	0.5118 mL	1.2795 mL
	100 mM	0.0409 mL	0.2047 mL	0.4094 mL	1.0236 mL

Keywords

Piceatannol

25 Cited Publications

100 mg お問い合わせ

Subscribe to the

MedChemExpress

Newsletter

製品名:
製品番号:
数量:
日本の代理先をお選びください:

製品名:
CAS 番号:
生物種:
純度:
数量:

ピセアタンノール

Apoptosis Compound Library

Kinase Inhibitor Library

Metabolism/Protease Compound Library

Protein Tyrosine Kinase Compound Library

Natural Product Library

Anti-Cancer Compound Library

Clinical Compound Library

Autophagy Compound Library

Lipid Compound Library

Traditional Chinese Medicine Active Compound Library

Anti-Blood Cancer Compound Library

Food-Sourced Compound Library

Anti-Cancer Natural Product Library

Plant-Sourced Natural Product Library

Human Metabolite Library

Anti-Pulmonary Fibrosis Compound Library

Mitochondrial Toxicity Compound Library

Cell Death Library

Anti-Hematopathy Compound Library

Bioactive Compound Library Max

Kinase Inhibitor Library Mini

Natural Product Library Plus

Clinical Compound Library Plus

Natural Product and Natural Product-Like Compound Library

Bioactive Compound Library

Miao Ethnicity Medicine Compound Library

PBCRBS Traditional Chinese Medicine Compound Library

Heat-Clearing and Detoxification Traditional Chinese Medicine Compound Library

Protein Kinase Compound Library

Non-Alcoholic Fatty Liver Disease (NAFLD) Compound Library

RO5 Drug-like Natural Product Library

High-Throughput Bioactive Compound Library

High-Throughput Natural Product Library

Ancient Chinese Classical Formulas Traditional Chinese Medicine Active Compound Library

Anti-Rheumatic Arthritis Compound Library

Mass Spectrometry Human Metabolite Library

Diarrhea-Related Traditional Chinese Medicine Active Compound Library

Posttranslational Modification Library

RNA Binding Bioactive Compound Library

Mass Spectrometry Natural Product Library

MedChemExpress（MCE）の使用を引用している文献 Piceatannol

Endogenous Metabolite アイソフォーム固有の製品をすべて表示

生物活性

化学情報

Publications (25)

溶剤 & 溶解度

純度とドキュメンテーション

参考文献

Help & FAQs

Complete Stock Solution Preparation Table

Piceatannol 関連分類

製品番号: HY-13518