Δ2,3'(2'H,3H)-ビ[1H-インドール]-2',3-ジオン

Δ2,3'(2'H,3H)-ビ[1H-インドール]-2',3-ジオン 化学構造式
479-41-4
CAS番号.
479-41-4
化学名:
Δ2,3'(2'H,3H)-ビ[1H-インドール]-2',3-ジオン
别名:
Δ2(3H),3'(2'H)-ビ[1H-インドール]-2',3-ジオン;インジゴレッド;イソインジルビン;クロウピチンB;インジゴプルプリン;Δ2,3'-ビ[インドリン]-2',3-ジオン;Δ2,3'(2'H,3H)-ビ[1H-インドール]-2',3-ジオン;3-(1,3-ジヒドロ-3-オキソ-2H-インドール-2-イリデン)-1,3-ジヒドロ-2H-インドール-2-オン;インジルビン;インデイルビン;Δ2,3′-ビ[インドリン]-2′,3-ジオン;Δ2(3H),3′(2′H)-ビ[1H-インドール]-2′,3-ジオン;1',2'-ジヒドロ-1H,3H-[2,3'-ビインドリリデン]-2',3-ジオン;Δ2,3′(2′H,3H)-ビ[1H-インドール]-2′,3-ジオン
英語名:
Indirubin
英語别名:
INDIGO RED;COUROUPITINE B;2H-Indol-2-one, 3-(1,3-dihydro-3-oxo-2H-indol-2-ylidene)-1,3-dihydro-;c.i.73200;Nsc105327;INDIRUBIN;C.I.75790;Indirabin;Isoindogotin;Indirubin>
CBNumber:
CB9296505
化学式:
C16H10N2O2
分子量:
262.26
MOL File:
479-41-4.mol

Δ2,3'(2'H,3H)-ビ[1H-インドール]-2',3-ジオン 物理性質

融点 :
350°C(lit.)
沸点 :
496.6±45.0 °C(Predicted)
比重(密度) :
1.417±0.06 g/cm3(Predicted)
貯蔵温度 :
-20°C
溶解性:
DMSO(微量)、メタノール(微量、加温)
酸解離定数(Pka):
9.13±0.20(Predicted)
外見 :
紫色の粉末。
色:
非常に濃い赤
極大吸収波長 (λmax):
540nm(DMSO)(lit.)
InChI:
InChI=1S/C16H10N2O2/c19-15-10-6-2-4-8-12(10)17-14(15)13-9-5-1-3-7-11(9)18-16(13)20/h1-8,17H,(H,18,20)
InChIKey:
CRDNMYFJWFXOCH-UHFFFAOYSA-N
SMILES:
N1C2=C(C=CC=C2)C(=C2C(=O)C3=C(N2)C=CC=C3)C1=O
CAS データベース:
479-41-4(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)
RTECS 番号 DU2995000
HSコード  29339900
絵表示(GHS) GHS hazard pictograms
注意喚起語
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
H335 呼吸器への刺激のおそれ 特定標的臓器毒性、単回暴露; 気道刺激性 3 警告 GHS hazard pictograms
注意書き
P264 取扱い後は皮膚をよく洗うこと。
P264 取扱い後は手や顔をよく洗うこと。
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。
P321 特別な処置が必要である(このラベルの... を見よ)。
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。
P362 汚染された衣類を脱ぎ、再使用す場合には洗濯をすること。

Δ2,3'(2'H,3H)-ビ[1H-インドール]-2',3-ジオン 価格 もっと(8)

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) W01TRCI521350 インジゴプルプリン
Indigopurpurin
479-41-4 25mg ¥72600 2024-03-01 購入
富士フイルム和光純薬株式会社(wako) W01CHDASB-00009077 インジルビン
Indirubin
479-41-4 5mg ¥57200 2024-03-01 購入
東京化成工業 I0868 インジルビン >97.0%(HPLC)
Indirubin >97.0%(HPLC)
479-41-4 25mg ¥27800 2024-03-01 購入
関東化学株式会社(KANTO) 49064-57 インジルビン
Indirubin
479-41-4 10mg ¥65000 2024-03-01 購入
Sigma-Aldrich Japan PHL89716 phyproof? Reference Substance
Indirubin phyproof? Reference Substance
479-41-4 10mg ¥68000 2024-03-01 購入

Δ2,3'(2'H,3H)-ビ[1H-インドール]-2',3-ジオン 化学特性,用途語,生産方法

外観

赤色~暗い赤色~濃い紫色粉末~結晶

説明

A further alkaloid isolated from the matured fruit of Couroupita guianensis, this base forms red crystals from EtOH and melts above 340°C. It forms the Nacetyl derivative, m.p. 186°C. The full structure has not yet been established.

物理的性質

Appearance: dark red acicular crystal with sublimate, odorless, and tasteless. Solubility: slightly soluble in dimethyl sulfoxide (DMSO) or tetrahydrofuran, very slightly soluble in chloroform or acetone, and insoluble in ethanol, ethyl ether, or water. Melting point: 348–353 °C. The stability of indirubin is poor that it needs to be stored away from light and thermal environment.

来歴

The report in 1951 showed that indirubin can inhibit eosinophils in the blood of guinea pigs. But this report did not attract attention. Indirubin is the effective component of the traditional Chinese medicine Angelica aloe pill. Since 1966, the scientists in the Institute of Hematonosis, Chinese Academy of Medical Sciences Research, started the research of therapying chronic myelocytic leukemia with the TCM rules using Angelica aloe pills, which had certain effect. Angelica aloe pill consisted of 11 herbs, such as Angelica, Aloe, Rhizoma Coptidis, and natural indigo. It was identified that natural indigo was the effective component of Angelica aloe pill. However, the active ingredient of natural indigo was indirubin.
Indirubin is a novel antileukemia drug, which was found by the medical scientists in China in the middle of the 1970s. It has the effects of antibacterial, antiinflammatory, antitumor, and enhancing immune functions. The compound has been applied to the clinical treatment of chronic myeloid leukemia. Indirubin has the characteristics of reliable clinical curative effect, small side effects, and no obvious inhibitory effect on the bone marrow.

適応症

Indirubin is contained in the fourth volume of the book, “National standards for chemical drugs.”
Indirubin tablets are used for the therapy of chronic myelocytic leukemia in clinical.

一般的な説明

This substance is a primary reference substance with assigned absolute purity (considering chromatographic purity, water, residual solvents, inorganic impurities). The exact value can be found on the certificate. Produced by PhytoLab GmbH & Co. KG

薬理学

The effect of indirubin has anti-inflammatory, antibacterial, detoxification, enhancing immune function anticancer. Indirubin has moderate inhibitory effect for animal-transplanted tumor. 200? mg/kg indirubin subcutaneous or intraperitoneal injection, once daily for 6 consecutive days, had the inhibition effect to rat W256 tumor cancer sarcoma; the inhibition rates were 47–52% and 50–58%, respectively. The chemotherapy index of intraperitoneal injection was 2.23. However, the inhibition rate of 500?mg/kg indirubin by gavage was only 23–33%. Indirubin by perfusion can prolong the survival time of W526 rat. The inhibition rate of Lewis mice’s lung cancer was 43% for 500?mg/kg indirubin orally, once a day for 9–10?days. Indirubin has some inhibition effects on mice breast cancer, but no obvious effect for L1212, P388, and L1210 of lymphocytic leukemia in mice.
The effect of indirubin on chronic myelogenous leukemia is very obvious, which is similar to first clinical choice of Maryland. Indirubin has the advantages of fast curative effect, no obvious inhibition effect of the bone, small bone marrow toxicity, and low side effects. Indirubin may have the effect of improving adrenocorticotropic hormone. In pathological conditions, such as inflammatory diarrhea, protein metabolism disorder, kidney disease, leukemia, and other tumors, urinary excretion of indirubin increased. Indirubin can inhibit synthesis of DNA and destroy the leukemia cells. It was found by electron microscopy that juvenile cells reduced, even disappear completely, with indirubin administration. Indirubin can significantly reduce the size of spleen, increase the concentration of hemoglobin to normal level, and reduce the swelling liver. In addition, indirubin can also enhance the phagocytic ability of animal mononuclear macrophages, which play a role in body immune reaction. So the anticancer effect of this product may be related to improving the body’s immunity.

臨床応用

Indirubin is mainly used for chronic myeloid leukemia; its total effective rate was 87.3%. The effect of indirubin to decrease white blood cells is similar to Maryland. The effect of indirubin to reduce liver is better than that of Maryland. But the remission role of the blood and bone marrow is worse than Maryland, and no cross resistance with Maryland. Indirubin could be used for abnormal bone marrow hyperplasia and eosinophilia.

参考文献

Sen, Mahato, Dutta, Tetrahedron Lett., 609 (1974)

Δ2,3'(2'H,3H)-ビ[1H-インドール]-2',3-ジオン 上流と下流の製品情報

原材料

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Δ2,3'(2'H,3H)-ビ[1H-インドール]-2',3-ジオン 生産企業

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Δ2,3'(2'H,3H)-ビ[1H-インドール]-2',3-ジオン  スペクトルデータ(1HNMR)


479-41-4(Δ2,3'(2'H,3H)-ビ[1H-インドール]-2',3-ジオン)キーワード:


  • 479-41-4
  • [2,3'-Biindolinylidene]-2',3-dione
  • Indirubin (Synthetic), >=98%
  • Indirubin/Folium Isatidis Extract
  • Nsc105327
  • INDIRUBIN (RG)
  • (E)-3-(3-oxoindolin-2-ylidene)indolin-2-one
  • Isoindogotin
  • (delta(sup2,3’)-biindoline)-2’,3-dione
  • 3-(1,3-dihydro-3-oxo-2h-indol-2-ylidene)-1,3-dihydro-2h-indol-2-on
  • c.i.73200
  • 2-(2-oxo-1h-indol-3-ylidene)-1h-indol-3-one
  • INDIGOPURPURIN
  • INDIRUBIN
  • CouroupitineB,IndigoRed,Indigopurpurin
  • 2H-Indol-2-one,3-(1,3-dihydro-3-oxo-2H-indol-
  • 2-ylidene)-1,3-dihydro-
  • Indirubin,Couroupitine B
  • C.I.75790
  • Δ2,3'(2'H,3H)-Bi[1H-indole]-2',3-dione
  • [.delta.2,3'-Biindoline]-2',3-dione
  • 3-(1,3-dihydro-3-oxo-2h-indol-2-ylidene)-1,3-dihydro-
  • Indirubin (Synthetic)
  • Indirubin, 98%, from Isatis tinctoria
  • Indirubin 479-41-4
  • Indirubin>
  • Indirabin
  • Indirubin USP/EP/BP
  • Indirubin (NSC 105327
  • (+)-Hosenkoside K
  • 2H-Indol-2-one, 3-(1,3-dihydro-3-oxo-2H-indol-2-ylidene)-1,3-dihydro-
  • Δ2(3H),3'(2'H)-ビ[1H-インドール]-2',3-ジオン
  • インジゴレッド
  • イソインジルビン
  • クロウピチンB
  • インジゴプルプリン
  • Δ2,3'-ビ[インドリン]-2',3-ジオン
  • Δ2,3'(2'H,3H)-ビ[1H-インドール]-2',3-ジオン
  • 3-(1,3-ジヒドロ-3-オキソ-2H-インドール-2-イリデン)-1,3-ジヒドロ-2H-インドール-2-オン
  • インジルビン
  • インデイルビン
  • Δ2,3′-ビ[インドリン]-2′,3-ジオン
  • Δ2(3H),3′(2′H)-ビ[1H-インドール]-2′,3-ジオン
  • 1',2'-ジヒドロ-1H,3H-[2,3'-ビインドリリデン]-2',3-ジオン
  • Δ2,3′(2′H,3H)-ビ[1H-インドール]-2′,3-ジオン
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