りん酸フルダラビン

りん酸フルダラビン 化学構造式
75607-67-9
CAS番号.
75607-67-9
化学名:
りん酸フルダラビン
别名:
フルダラビンホスファート;りん酸フルダラビン;フルダラビンリン酸エステル;9-(5-O-ホスホノ-β-D-アラビノフラノシル)-2-フルオロ-9H-プリン-6-アミン;2-フルオロ-9-(5-O-ホスホノ-β-D-アラビノフラノシル)-9H-プリン-6-アミン;フルダラ;2-フルオロアデニン9-β-D-アラビノフラノシド5'-一りん酸;9-(β-D-アラビノフラノシル)-2-フルオロアデニン5'-一りん酸;フルダラビンリン酸エステル (JAN);{[(2R,3S,4S,5R)-5-(6-アミノ-2-フルオロ-9H-プリン-9-イル)-3,4-ジヒドロキシオキソラン-2-イル]メトキシ}ホスホン酸
英語名:
Fludarabine phosphate
英語别名:
FAMP;Fludura;F-ara-AMP;-F-ara-AMP;2-fluoro-araamp;5-Monophosphate;fludarabine hcl;fludara Phosphate;Fludarabin Phosphate;Fludarbine Phopshate
CBNumber:
CB7347825
化学式:
C10H13FN5O7P
分子量:
365.21
MOL File:
75607-67-9.mol
MSDS File:
SDS

りん酸フルダラビン 物理性質

融点 :
203°C(dec.)(lit.)
比旋光度 :
[α]D20 +10~+14゜(c=0.5,H2O)
沸点 :
864.2±75.0 °C(Predicted)
比重(密度) :
2.39±0.1 g/cm3(Predicted)
RTECS 番号:
UO7440900
貯蔵温度 :
2-8°C
溶解性:
DMSO:可溶1mg/mL
酸解離定数(Pka):
1.86±0.10(Predicted)
外見 :
色:
白い
水溶解度 :
DMSOまたは水に5mg/mlで可溶
Merck :
14,4126
安定性::
吸湿性
InChIKey:
GIUYCYHIANZCFB-GFRUICAKSA-N
CAS データベース:
75607-67-9(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)
WGK Germany  3
HSコード  2934990002
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
H341 遺伝性疾患のおそれの疑い 生殖細胞変異原性 2 警告 P201,P202, P281, P308+P313, P405,P501
注意書き
P201 使用前に取扱説明書を入手すること。
P202 全ての安全注意を読み理解するまで取り扱わないこ と。
P280 保護手袋/保護衣/保護眼鏡/保護面を着用するこ と。
P308+P313 暴露または暴露の懸念がある場合:医師の診断/手当てを 受けること。
P405 施錠して保管すること。
P501 内容物/容器を...に廃棄すること。

りん酸フルダラビン 価格 もっと(23)

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) W01USP1272204 りん酸フルダラビン
Fludarabine Phosphate
75607-67-9 300mg ¥94200 2024-03-01 購入
富士フイルム和光純薬株式会社(wako) W01TRCF425005 りん酸フルダラビン
Fludarabine Phosphate
75607-67-9 1g ¥363600 2024-03-01 購入
東京化成工業 F0913 りん酸フルダラビン >98.0%(HPLC)(T)
Fludarabine Monophosphate >98.0%(HPLC)(T)
75607-67-9 25mg ¥7400 2024-03-01 購入
東京化成工業 F0913 りん酸フルダラビン >98.0%(HPLC)(T)
Fludarabine Monophosphate >98.0%(HPLC)(T)
75607-67-9 100mg ¥21300 2024-03-01 購入
Sigma-Aldrich Japan Y0002256 European Pharmacopoeia (EP) Reference Standard
Fludarabine for peak identification European Pharmacopoeia (EP) Reference Standard
75607-67-9 Y0002256 ¥20400 2024-03-01 購入

りん酸フルダラビン 化学特性,用途語,生産方法

外観

白色~うすい褐色, 結晶性粉末~粉末

溶解性

水に溶ける。

用途

DNA ポリメラーゼ及び RNA ポリメラーゼを阻害し、DNA/RNA 合成阻害 作用を示します。

効能

抗悪性腫瘍薬, 代謝拮抗薬

商品名

フルダラ (サノフィ); フルダラ (サノフィ)

使用上の注意

不活性ガス封入

説明

Fludarabine phosphate is an antimetabolite indicated for the treatment of B cell lymphocytic leukemia. It is reportedly effective in patients refractory to other therapies. Fludarabine phosphate acts by inhibiting primer RNA synthesis. Its side effects include bone marrow suppression, anemia, thrombocytopenia and neutropenia.

化学的特性

White or almost white, crystalline powder, hygroscopic.

使用

Fludarabine phosphate is used for the treatment of chronic lymphatic leukemia and low-grade lymphoma. In the circulation,fludarabine phosphate is immediately dephosphorylated to the nucleoside fludarabine. About 30-40% of nucleoside fludarabine is excreted into the urine. In addition, fludarabine is metabolized into a hypoxanthine metabolite also excreted in the urine.Intracellularly,fludarabine is stepwise rephosphorylated to the active triphosphate. Deoxycytidine kinase is the dominant, if not the exclusive,enzyme for the formation of the monophosphate. Adenylate kinase and nucleoside diphosphate kinase are believed to be involved in the formation of the diphosphate and triphosphate,respectively.

定義

ChEBI: Fludarabine phosphate is a purine arabinonucleoside monophosphate having 2-fluoroadenine as the nucleobase. A prodrug, it is rapidly dephosphorylated to 2-fluoro-ara-A and then phosphorylated intracellularly by deoxycytidine kinase to the active triphosphate, 2-fluoro-ara-ATP. Once incorporated into DNA, 2-fluoro-ara-ATP functions as a DNA chain terminator. It is used for the treatment of adult patients with B-cell chronic lymphocytic leukemia (CLL) who have not responded to, or whose disease has progressed during, treatment with at least one standard alkylating-agent containing regimenas. It has a role as an antimetabolite, an antineoplastic agent, an immunosuppressive agent, an antiviral agent, a prodrug and a DNA synthesis inhibitor. It is an organofluorine compound, a nucleoside analogue and a purine arabinonucleoside monophosphate. It derives from a 2-fluoroadenine.

薬理学

Fludarabine phosphate is rapidly dephosphorylated to 2-fluoro-ara-A and then phosphorylated intracellularly by deoxycytidine kinase to the active triphosphate, 2-fluoro-ara-ATP. This metabolite appears to act by inhibiting DNA polymerase alpha, ribonucleotide reductase and DNA primase, thus inhibiting DNA synthesis. The mechanism of action of this antimetabolite is not completely characterized and may be multi-faceted.
Phase I studies in humans have demonstrated that fludarabine phosphate is rapidly converted to the active metabolite, 2-fluoro-ara-A, within minutes after intravenous infusion.
Consequently, clinical pharmacology studies have focused on 2-fluoro-ara-A pharmacokinetics. After the five daily doses of 25 mg 2-fluoro-ara-AMP/m2 to cancer patients infused over 30 minutes, 2-fluoro-ara-A concentrations show a moderate accumulation. During a 5-day treatment schedule, 2-fluoro-ara-A plasma trough levels increased by a factor of about 2. The terminal half-life of 2-fluoro-ara-A was estimated as approximately 20 hours. In vitro, plasma protein binding of fludarabine ranged between 19% and 29%.

臨床応用

Fludarabine phosphate (Fludara ® ), is a fluorinated nucleotide analog of the antiviral agent vidarabine, 9-β-D-arabinofuranosyladenine(ara-A), which differs only by the presence of a fluorine atom at position 2 of the purine moiety and a phosphate group at position 5 of the arabinose moiety (Plunkett et al., 1993). These structural modifications result in increased aqueous solubility and resistance to enzymatic degradation by adenosine deaminases compared to vidarabine (Brockman et al., 1977; Plunkett et al., 1990). Fludarabine phosphate is indicated for the treatment of patients with B-cell chronic lymphocytic leukemia (CLL) who have not responded to or whose disease has progressed during treatment with at least one standard alkylating agent containing regimen (Boogaerts et al., 2001; Rossi et al., 2004).

りん酸フルダラビン 上流と下流の製品情報

原材料

準備製品


りん酸フルダラビン 生産企業

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りん酸フルダラビン  スペクトルデータ(1HNMR、MS)


75607-67-9(りん酸フルダラビン)キーワード:


  • 75607-67-9
  • 2-fluoro-9-(5-o-phosphono-beta-d-arabinofuranosyl)-9h-purin-6-amine
  • 2-fluoro-araamp
  • 9-beta-arabinofuranosyl-2-fluoroadenine-5’-phosphate
  • 5-Monophosphate
  • 9-BETA-D-ARABINOFURANOSYL-2-FLUOROADENINE-5'-DIHYDROGEN PHOSPHATE
  • FLUDARUBINE PHOSPHATE
  • FLUDARABINE PHOSPHATE
  • 9-bata-d-arabinofuranosyl-2-fluoroadenine phosphate
  • FludarabinePhosphateFdaInspected
  • FludarabinePhosphateUsp28
  • fludarabine hcl
  • 9-BETA-D-ARABINOFURANOSYL-2-FLUOROADENINE PHOSPHATE
  • 9-beta-d-arabinofuranosyl-2-fluoroadenine5’-monophosphate
  • fludarabinemonophosphate
  • Fludarabin Phosphate
  • Fludarabine Phosphate (300 mg)
  • Fludarabine Phosphate(Fludara)
  • ((2R,3S,4S,5R)-5-(6-AMINO-2-FLUORO-9H-PURIN-9-YL)-3,4-DIHYDROXYTETRAHYDROFURAN-2-YL)METHYL DIHYDROGEN PHOSPHATE
  • FLUDARABINE PHOSPHATE (FLUDARABINE 5''-MONOPHOSPHATE)
  • 2-Fluoro-9-(5-O-phosphono-β-D-arabinofuranosyl)-9H-purin-6-amine
  • 9-(5-O-Phosphono-β-D-arabinofuranosyl)-2-fluoro-9H-purine-6-amine
  • F-ara-AMP
  • 9-β-Arabinofuranosyl-2-fluoroadenine-5'-monophosphate
  • Fludarabine 5'-Phosphate
  • Fludarabine Phosphate API
  • FAMP
  • Fludarabine 5'-Monophosphate
  • Fludura
  • Fludrarbine Phosphate
  • Fludarabine Phosphate (Suitable to use for Tablet)
  • フルダラビンホスファート
  • りん酸フルダラビン
  • フルダラビンリン酸エステル
  • 9-(5-O-ホスホノ-β-D-アラビノフラノシル)-2-フルオロ-9H-プリン-6-アミン
  • 2-フルオロ-9-(5-O-ホスホノ-β-D-アラビノフラノシル)-9H-プリン-6-アミン
  • フルダラ
  • 2-フルオロアデニン9-β-D-アラビノフラノシド5'-一りん酸
  • 9-(β-D-アラビノフラノシル)-2-フルオロアデニン5'-一りん酸
  • フルダラビンリン酸エステル (JAN)
  • {[(2R,3S,4S,5R)-5-(6-アミノ-2-フルオロ-9H-プリン-9-イル)-3,4-ジヒドロキシオキソラン-2-イル]メトキシ}ホスホン酸
  • 抗腫瘍代謝拮抗物質
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