3-[[1-(4-ピペリジニル)-1H-ピラゾール-4-イル]アミノ]-2,5,13-トリメチル-2,4,5,13-テトラアザ-1H-ベンゾ[4,5]シクロヘプタ[1,2-b]ナフタレン-12(13H)-オン

3-[[1-(4-ピペリジニル)-1H-ピラゾール-4-イル]アミノ]-2,5,13-トリメチル-2,4,5,13-テトラアザ-1H-ベンゾ[4,5]シクロヘプタ[1,2-b]ナフタレン-12(13H)-オン 化学構造式
1613724-42-7
CAS番号.
1613724-42-7
化学名:
3-[[1-(4-ピペリジニル)-1H-ピラゾール-4-イル]アミノ]-2,5,13-トリメチル-2,4,5,13-テトラアザ-1H-ベンゾ[4,5]シクロヘプタ[1,2-b]ナフタレン-12(13H)-オン
别名:
2,6,9-トリメチル-5-{[1-(ピペリジン-4-イル)-1H-ピラゾール-4-イル]アミノ}-2,4,6,9-テトラアザテトラシクロ[9.8.0.03,8.013,18]ノナデカ-1(11),3(8),4,12,14,16,18-ヘプタエン-10-オン;3-[[1-(4-ピペリジニル)-1H-ピラゾール-4-イル]アミノ]-2,5,13-トリメチル-2,4,5,13-テトラアザ-1H-ベンゾ[4,5]シクロヘプタ[1,2-b]ナフタレン-12(13H)-オン
英語名:
HTH-01-015
英語别名:
CS-2296;HTH-01-015;HTH-01-015 >=98% (HPLC);CHSDJDLAKKAWCI-UHFFFAOYSA-N;inhibit,AMPK,AMP-activated protein kinase,HTH 01 015,HTH01015,Inhibitor;5,13-Dihydro-4,5,13-trimethyl-2-[[1-(4-piperidinyl)-1H-pyrazol-4-yl]amino]-6H-naphtho[2,3-e]pyrimido[5,4-b][1,4]diazepin-6-one;4,5,13-Trimethyl-2-((1-(piperidin-4-yl)-1H-pyrazol-4-yl)amino)-5,13-dihydro-6H-naphtho[2,3-e]pyrimido[5,4-b][1,4]diazepin-6-one;6H-Naphtho[2,3-e]pyrimido[5,4-b][1,4]diazepin-6-one, 5,13-dihydro-4,5,13-trimethyl-2-[[1-(4-piperidinyl)-1H-pyrazol-4-yl]amino]-
CBNumber:
CB22715641
化学式:
C26H28N8O
分子量:
468.55
MOL File:
1613724-42-7.mol

3-[[1-(4-ピペリジニル)-1H-ピラゾール-4-イル]アミノ]-2,5,13-トリメチル-2,4,5,13-テトラアザ-1H-ベンゾ[4,5]シクロヘプタ[1,2-b]ナフタレン-12(13H)-オン 物理性質

沸点 :
759.6±70.0 °C(Predicted)
比重(密度) :
1.41±0.1 g/cm3(Predicted)
貯蔵温度 :
-20°C
溶解性:
≥23.45 mg/mL in DMSO; insoluble in H2O; ≥14.67 mg/mL in EtOH with ultrasonic
酸解離定数(Pka):
9.84±0.10(Predicted)
外見 :
色:
白から薄茶色
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)
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
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
P261 粉じん/煙/ガス/ミスト/蒸気/スプレーの吸入を避ける 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。

3-[[1-(4-ピペリジニル)-1H-ピラゾール-4-イル]アミノ]-2,5,13-トリメチル-2,4,5,13-テトラアザ-1H-ベンゾ[4,5]シクロヘプタ[1,2-b]ナフタレン-12(13H)-オン 価格 もっと(4)

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) W01TOC5622
HTH 01-015
1613724-42-7 10mg ¥71000 2024-03-01 購入
富士フイルム和光純薬株式会社(wako) W01TOC5622
HTH 01-015
1613724-42-7 50mg ¥294000 2024-03-01 購入
Sigma-Aldrich Japan SML1446 ≥98% (HPLC)
HTH-01-015 ≥98% (HPLC)
1613724-42-7 5mg ¥25500 2024-03-01 購入
Sigma-Aldrich Japan SML1446 ≥98% (HPLC)
HTH-01-015 ≥98% (HPLC)
1613724-42-7 25mg ¥101000 2024-03-01 購入

3-[[1-(4-ピペリジニル)-1H-ピラゾール-4-イル]アミノ]-2,5,13-トリメチル-2,4,5,13-テトラアザ-1H-ベンゾ[4,5]シクロヘプタ[1,2-b]ナフタレン-12(13H)-オン 化学特性,用途語,生産方法

説明

NUAK1 (also known as AMPK-related kinase 5) and NUAK2 (also known as SNF1/AMPK-related kinase) are members of the AMP-activated protein kinase (AMPK) family of protein kinases that are activated by the liver kinase B1 tumor suppressor kinase. NUAK kinases are thought to have roles in regulating cell adhesion, cancer cell invasion, embryonic development, senescence, proliferation, neuronal polarity, and axon branching. HTH-01-015 is a selective inhibitor of NUAK1 (IC50 = 100 nM) and does not affect the activity of a panel of 139 other kinases, including additional AMPK family members. At 10 μM, HTH-01-015 has been shown to partially inhibit the phosphorylation of the NUAK1 substrate, myosin phosphate-targeting subunit 1 at Ser445. When administered to mouse embryonic fibroblasts in vitro, 10 μM HTH-01-015 inhibits proliferation and migration in a wound-healing assay. It has also been shown to impair the invasive potential of U2OS cells at similar concentrations in a 3D cell invasion assay.

使用

HTH 01-015 is a highly specific protein kinase inhibitor of NUAK1. It inhibits the NUAK1 phosphorylation of myosin phosphate-targeting subunit 1 (MYPT1) substrate.

Biochem/physiol Actions

HTH-01-015 is a potent and selective inhibitor of NUAK1 kinase, a member of the AMPK family that are that are activated by the LKB1 (liver kinaseB1) tumour suppressor kinase and involved in development and proliferation. HTH-01-015 has an IC50 of 100 nM for NUAK1, >100-fold higher than NUAK2, and has no significant inhibition of 139 other kinases tested, including ten AMPK-related kinase family members. Treatment with HTH-01-015 was found to suppress proliferation, restricting cells from entering into mitosis.

3-[[1-(4-ピペリジニル)-1H-ピラゾール-4-イル]アミノ]-2,5,13-トリメチル-2,4,5,13-テトラアザ-1H-ベンゾ[4,5]シクロヘプタ[1,2-b]ナフタレン-12(13H)-オン 上流と下流の製品情報

原材料

準備製品


3-[[1-(4-ピペリジニル)-1H-ピラゾール-4-イル]アミノ]-2,5,13-トリメチル-2,4,5,13-テトラアザ-1H-ベンゾ[4,5]シクロヘプタ[1,2-b]ナフタレン-12(13H)-オン 生産企業

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3-[[1-(4-ピペリジニル)-1H-ピラゾール-4-イル]アミノ]-2,5,13-トリメチル-2,4,5,13-テトラアザ-1H-ベンゾ[4,5]シクロヘプタ[1,2-b]ナフタレン-12(13H)-オン  スペクトルデータ(1HNMR)


1613724-42-7(3-[[1-(4-ピペリジニル)-1H-ピラゾール-4-イル]アミノ]-2,5,13-トリメチル-2,4,5,13-テトラアザ-1H-ベンゾ[4,5]シクロヘプタ[1,2-b]ナフタレン-12(13H)-オン)キーワード:


  • 1613724-42-7
  • HTH-01-015
  • 5,13-Dihydro-4,5,13-trimethyl-2-[[1-(4-piperidinyl)-1H-pyrazol-4-yl]amino]-6H-naphtho[2,3-e]pyrimido[5,4-b][1,4]diazepin-6-one
  • HTH-01-015 >=98% (HPLC)
  • 6H-Naphtho[2,3-e]pyrimido[5,4-b][1,4]diazepin-6-one, 5,13-dihydro-4,5,13-trimethyl-2-[[1-(4-piperidinyl)-1H-pyrazol-4-yl]amino]-
  • CHSDJDLAKKAWCI-UHFFFAOYSA-N
  • CS-2296
  • inhibit,AMPK,AMP-activated protein kinase,HTH 01 015,HTH01015,Inhibitor
  • 4,5,13-Trimethyl-2-((1-(piperidin-4-yl)-1H-pyrazol-4-yl)amino)-5,13-dihydro-6H-naphtho[2,3-e]pyrimido[5,4-b][1,4]diazepin-6-one
  • 2,6,9-トリメチル-5-{[1-(ピペリジン-4-イル)-1H-ピラゾール-4-イル]アミノ}-2,4,6,9-テトラアザテトラシクロ[9.8.0.03,8.013,18]ノナデカ-1(11),3(8),4,12,14,16,18-ヘプタエン-10-オン
  • 3-[[1-(4-ピペリジニル)-1H-ピラゾール-4-イル]アミノ]-2,5,13-トリメチル-2,4,5,13-テトラアザ-1H-ベンゾ[4,5]シクロヘプタ[1,2-b]ナフタレン-12(13H)-オン
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