メチル(4-イソチオシアナトブチル)スルホキシド

メチル(4-イソチオシアナトブチル)スルホキシド 化学構造式
4478-93-7
CAS番号.
4478-93-7
化学名:
メチル(4-イソチオシアナトブチル)スルホキシド
别名:
スルホラファン;スルフォラファン;1-イソチオシアナト-4-(メチルスルフィニル)ブタン;4-(メチルスルフィニル)ブチルイソチオシアナート;メチル(4-イソチオシアナトブチル)スルホキシド;D,L-スルホラファン;R,S-スルホラファン;スルホラファン, D-;R,S-スルホラファン, RESEARCH GRADE;スルホラファン, DL-;DL-スルホラファン;R-スルホラファン;4-メチルスルフィニルブチルイソチオシアナート;1-イソチオシアナト-4-メタンスルフィニルブタン
英語名:
DL-Sulforaphane
英語别名:
sulforaphane;SULPHORAPHANE;sulforaphan;-SuL;foraphane;sulforafan;Sulforaphen;Detoxophane;sulforphane;S-SULFORAPHANE
CBNumber:
CB9765544
化学式:
C6H11NOS2
分子量:
177.29
MOL File:
4478-93-7.mol
MSDS File:
SDS

メチル(4-イソチオシアナトブチル)スルホキシド 物理性質

沸点 :
125-135°C
比重(密度) :
1.17±0.1 g/cm3(Predicted)
貯蔵温度 :
-20°C
溶解性:
DMSO: 40 mg/mL、可溶
外見 :
液体
色:
わずかに黄色
安定性::
光に敏感
LogP:
0.407 (est)
CAS データベース:
4478-93-7(CAS DataBase Reference)
安全性情報
  • リスクと安全性に関する声明
  • 危険有害性情報のコード(GHS)
Sフレーズ  23-24/25
WGK Germany  3
HSコード  29309090
絵表示(GHS) GHS hazard pictograms
注意喚起語 警告
危険有害性情報
コード 危険有害性情報 危険有害性クラス 区分 注意喚起語 シンボル P コード
H315 皮膚刺激 皮膚腐食性/刺激性 2 警告 GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 強い眼刺激 眼に対する重篤な損傷性/眼刺激 性 2A 警告 GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
注意書き
P280 保護手袋/保護衣/保護眼鏡/保護面を着用するこ と。
P302+P352 皮膚に付着した場合:多量の水と石鹸で洗うこと。
P305+P351+P338 眼に入った場合:水で数分間注意深く洗うこと。次にコ ンタクトレンズを着用していて容易に外せる場合は外す こと。その後も洗浄を続けること。
P332+P313 皮膚刺激が生じた場合:医師の診断/手当てを受けるこ と。
P337+P313 眼の刺激が続く場合:医師の診断/手当てを受けること。

メチル(4-イソチオシアナトブチル)スルホキシド 価格 もっと(24)

メーカー 製品番号 製品説明 CAS番号 包装 価格 更新時間 購入
富士フイルム和光純薬株式会社(wako) W01CHDASB-00019385 スルホラファン, DL-
Sulforaphane, DL-
4478-93-7 5mg ¥45000 2024-03-01 購入
富士フイルム和光純薬株式会社(wako) W01CHDASB-00019385 スルホラファン, DL-
Sulforaphane, DL-
4478-93-7 10mg ¥66600 2024-03-01 購入
Sigma-Aldrich Japan S4441 DL-スルホラファン ≥90% (HPLC), synthetic, liquid
DL-Sulforaphane ≥90% (HPLC), synthetic, liquid
4478-93-7 5mg ¥33700 2024-03-01 購入
富士フイルム和光純薬株式会社(wako) W01TRCS699115 D,L-スルホラファン
D,L-Sulforaphane
4478-93-7 25mg ¥54300 2024-03-01 購入
富士フイルム和光純薬株式会社(wako) W01TRCS699115 D,L-スルホラファン
D,L-Sulforaphane
4478-93-7 250mg ¥108000 2024-03-01 購入

メチル(4-イソチオシアナトブチル)スルホキシド 化学特性,用途語,生産方法

用途

スルフォラファン (sulforaphane) とは、ブロッコリーに微量含まれるフィトケミカルの一種。体内の解毒酵素や抗酸化酵素の生成を促進し、体の抗酸化力や解毒力を高める。 通常、植物細胞内では前駆物質であるスルフォラファングルコシノレート (SGS) の状態で存在する。

説明

Sulforaphane is a compound within the isothiocyanate group of organosulfur compounds and mainly found in cruciferous vegetables. It is produced when the enzyme myrosinase transforms glucoraphanin,a prodrug or storage form of SFN, into SFN upon damage to the plant (such as from chewing),which allows the two compounds to mix and react. Glucoraphanin is one of a few molecules known as isothiocyanates, existing alongside Sinigrin (metabolized into allylisothiocyanate).

化学的特性

DL-Sulforaphane (SFN) is a slightly yellow liquid. soluble in DMSO, methanol, or water-like solvents. SFN exists in food in its food-bound form known as Glucoraphanin. It is present in a wide range of vegetables such as cabbage, cauliflower, bok choy, kale, chinese broccoli, mustard, turnip, radish, and watercress.

使用

Potent, selective inducer of phase II detoxification enzymes with anticarcinogenic properties. Occurs naturally in broccoli. It was found to inhibit chemically induced mammary tumor formation in rats. Antitumor agent
LNCaP prostate cancer cells were treated with DL-Sulforaphane to study the effect on androgen receptor. Effects on malathion toxicity was studied in rats by treating them with DL-Sulforaphane.
Nrf2 activation of the antioxidant response element (ARE) is central to cytoprotective gene expression against oxidative and/or electrophilic stress.
Unless activated by inflammatory, environmental, or oxidative stressors, Nrf2 is sequestered in the cytoplasm by its repressor, Keap1.
Because of its protective capabilities, small molecules that activate Nrf2 signaling are being examined as potential anti-cancer or anti-inflammatory agents.
Sulforaphane is an isothiocyanate derived from cruciferous vegetables, including broccoli, that potently induces chemopreventative enzymes via Keap1-Nrf2 signaling and ARE-driven gene expression.
At 15 μM, sulforaphane inhibits class I and II HDAC activity and suppresses tumor growth by inducing cell cycle arrest and apoptosis selectively in various cancerous prostate epithelial cells without affecting normal cells.
Differential effects of sulforaphane on histone deacetylases, cell cycle arrest and apoptosis in normal prostate cells versus hyperplastic and cancerous prostate cells

定義

ChEBI: Sulforaphane is an isothiocyanate having a 4-(methylsulfinyl)butyl group attached to the nitrogen. It has a role as an antineoplastic agent, a plant metabolite, an antioxidant and an EC 3.5.1.98 (histone deacetylase) inhibitor. It is a sulfoxide and an isothiocyanate.

一般的な説明

An isothiocyanate isolated from broccoli that acts as a potent inducer of phase II detoxifying enzymes in mouse tissues and murine hepatoma cells in culture. It has been shown to be an effective agent in prevention of chemically-induced mammary tumors in rats. It also inhibits the phase I cytochrome P450 isoenzymes 2E1 and IA2 which have been associated with the activation of carcinogens. The induction of phase II enzymes is mediated by mitogen-activated protein kinase (MAPK) pathway.

生物活性

Selective inducer of phase II detoxification enzymes with anticarcinogenic properties. Organosulfur compound found in cruciferous vegetables, including broccoli.
Sulforaphane is an anti-cancer, anti-microbial and anti-diabetic compound found in cruciferous vegetables. It induces the production of detoxifying enzymes such as quinone reductase and glutathione S-transferase that cause xenobiotic transformation. Sulforaphane also increases the transcription of tumor suppressor proteins and inhibits histone deacetylases. It modulates inflammatory responses by suppressing the LPS-mediated expression of iNOS, COX-2, IL-1β and TNF-α.

メチル(4-イソチオシアナトブチル)スルホキシド 上流と下流の製品情報

原材料

準備製品


メチル(4-イソチオシアナトブチル)スルホキシド 生産企業

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メチル(4-イソチオシアナトブチル)スルホキシド  スペクトルデータ(MS)


4478-93-7(メチル(4-イソチオシアナトブチル)スルホキシド)キーワード:


  • 4478-93-7
  • sulforafan
  • R-SULFORAPHANE
  • R,S-SULFORAPHANE
  • SULFORAPHANE, L-
  • SULFORAPHANE, DL-
  • SULFORAPHANE, D-
  • S-SULFORAPHANE
  • Methyl(4-isothiocyanatobutyl) sulfoxide
  • Sulforaphen
  • (-)-ISOTHIOCYANATO-(4R)-(METHYLSULFINYL)BUTANE
  • DL-SULPHORAPHANE
  • DL-SULFORAPHANE
  • D-SULFORAPHANE
  • (-)-(4R)-SULFORAPHANE
  • 4-METHYLSULFINYLBUTYL ISOTHIOCYANATE
  • 1-ISOTHISCYANATO-4-(METHYLSULFINYL)-BUTANE
  • 1-ISOTHIOCYANATO-4-(METHYLSULFINYL)-BUTANE
  • (-)1-ISOTHIOCYANATO-4S-(METHYLSULFINYL)-BUTANE
  • (+)1-ISOTHIOCYANATO-4S-(METHYLSULFINYL)-BUTANE
  • ((-)1-ISOTHIOCYANATO-4R-METHYLSULFINYL)BUTANE
  • 1-ISOTHIOCYANATO-4-(METHYLSULFIYL)-BUTANE
  • (+)-1-ISOTHIOCYANATE-4R(METHYLSULFINYL)-BUTANE
  • 4-methylsulfinylbutylimino(thioxo)methane
  • DL-Sulforaphane,1-Isothiocyanato-4-(methylsulfinyl)-butane
  • Detoxophane
  • DL-Sulforaphan
  • Butane,1-isothiocyanato-4-(Methylsulfinyl)-
  • Broccoli Seed Extract/Sulforaphane/Brassica oleracea extract
  • DL-Sulforaphane 4478-93-7
  • Sulforaphane Racemate
  • スルホラファン
  • スルフォラファン
  • 1-イソチオシアナト-4-(メチルスルフィニル)ブタン
  • 4-(メチルスルフィニル)ブチルイソチオシアナート
  • メチル(4-イソチオシアナトブチル)スルホキシド
  • D,L-スルホラファン
  • R,S-スルホラファン
  • スルホラファン, D-
  • R,S-スルホラファン, RESEARCH GRADE
  • スルホラファン, DL-
  • DL-スルホラファン
  • R-スルホラファン
  • 4-メチルスルフィニルブチルイソチオシアナート
  • 1-イソチオシアナト-4-メタンスルフィニルブタン
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