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製品番号: HY-121889

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FQ

FQ is a tyrosinase inhibitor that effectively inhibits the diphenolase activity of mushroom tyrosinase (IC₅₀=120 μM). FQ can be used in the study of pigmentation.

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: 190838-76-7
分子式: C₁₄H₉FN₂O
分子量:240.23

保管条件:

Please store the product under the recommended conditions in the Certificate of Analysis.

Data Sheet (267 KB)

FQ 構造式

CAS 番号: 190838-76-7

容量

価格（税別）

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数量

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生物活性
- 製品説明
- IC₅₀ & Target
- Cellular Effect
- 臨床実験
化学情報
純度とドキュメンテーション
参考文献
Calculators
Help & FAQs
関連分類
Bioz

生物活性

製品説明

FQ is a tyrosinase inhibitor that effectively inhibits the diphenolase activity of mushroom tyrosinase (IC₅₀=120 μM). FQ can be used in the study of pigmentation^[1].

IC₅₀ & Target

IC50：120 μM (Tyrosinase Diphenolase) ^[1]

Cellular Effect

Cell Line	Type	Value	Description	References
1A9	ED₅₀	>20 μg/mL Compound: 10	In vitro effective concentration required to reduce the number of human ovarian cancer (1A9) after 3-day incubation In vitro effective concentration required to reduce the number of human ovarian cancer (1A9) after 3-day incubation	[PMID: 11354375]
A549	ED₅₀	7.5 μg/mL Compound: 10	In vitro effective concentration required to reduce the number of human lung carcinoma (A-549) after 3-day incubation In vitro effective concentration required to reduce the number of human lung carcinoma (A-549) after 3-day incubation	[PMID: 11354375]
COLO 205	IC₅₀	10 μM Compound: 9b	Antiproliferative activity against human COLO205 cells by MTT assay Antiproliferative activity against human COLO205 cells by MTT assay	[PMID: 22749421]
H9	EC₅₀	9.18 μM Compound: 10	Concentration required to inhibit viral replication in acutely infected H9 lymphocytes when tested for anti-HIV activity Concentration required to inhibit viral replication in acutely infected H9 lymphocytes when tested for anti-HIV activity	[PMID: 11354375]
H9	IC₅₀	38.8 μM Compound: 10	Concentration required to inhibit uninfected H9 cell growth when tested for anti-HIV activity Concentration required to inhibit uninfected H9 cell growth when tested for anti-HIV activity	[PMID: 11354375]
K562	IC₅₀	17 μM Compound: 9b	Antiproliferative activity against human K562 cells by MTT assay Antiproliferative activity against human K562 cells by MTT assay	[PMID: 22749421]
KB	ED₅₀	>20 μg/mL Compound: 10	In vitro effective concentration required to reduce the number of Human epidermoid carcinoma cells (KB) of nasopharynx after 3-day incubation In vitro effective concentration required to reduce the number of Human epidermoid carcinoma cells (KB) of nasopharynx after 3-day incubation	[PMID: 11354375]
KB	ED₅₀	6.5 μg/mL Compound: 10	In vitro effective concentration required to reduce the number of P-glycoprotein-expressing human epidermoid carcinoma cells (KB-VIN) of nasopharynx after 3-day incubation In vitro effective concentration required to reduce the number of P-glycoprotein-expressing human epidermoid carcinoma cells (KB-VIN) of nasopharynx after 3-day incubation	[PMID: 11354375]
MCF7	ED₅₀	>20 μg/mL Compound: 10	In vitro effective concentration required to reduce the number of human breast cancer (MCF-7) after 3-day incubation In vitro effective concentration required to reduce the number of human breast cancer (MCF-7) after 3-day incubation	[PMID: 11354375]
MDA-MB-231	IC₅₀	20 μM Compound: 9b	Antiproliferative activity against human MDA-MB-231 cells by MTT assay Antiproliferative activity against human MDA-MB-231 cells by MTT assay	[PMID: 22749421]
Sf21	IC₅₀	1102 nM Compound: 13f	Inhibition of N-terminal GST-tagged human TNKS-2 (849 to 1166 residues) expressed in in insect sf21 cells preincubated for 2 hrs followed by substrate addition measured after 30 mins Inhibition of N-terminal GST-tagged human TNKS-2 (849 to 1166 residues) expressed in in insect sf21 cells preincubated for 2 hrs followed by substrate addition measured after 30 mins	[PMID: 27163581]
SK-MEL-2	ED₅₀	>20 μg/mL Compound: 10	In vitro effective concentration required to reduce the number of human melanoma cancer (SKMEL-2) after 3-day incubation In vitro effective concentration required to reduce the number of human melanoma cancer (SKMEL-2) after 3-day incubation	[PMID: 11354375]

臨床実験

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

化学情報

CAS 番号 190838-76-7
分子量 240.23
分子式 C₁₄H₉FN₂O
SMILES

O=C1N=C(NC2=C1C=CC=C2)C3=CC=C(C=C3)F
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

バッチを選択:

純度: 99.98%

Assay: 99.98%

ee.: 99.98%

データシート (267 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]. Wang R, et al. 2-(4-Fluorophenyl)-quinazolin-4(3H)-one as a novel tyrosinase inhibitor: Synthesis, inhibitory activity, and mechanism. Bioorg Med Chem. 2016 Oct 1;24(19):4620-4625. [Content Brief]

Calculators

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)

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.

Bioz

Keywords

MOQ

Minimum order quantity

100 mg

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