ChemicalBook >> CAS DataBase List >>Fludarabine phosphate

Fludarabine phosphate

CAS No.
75607-67-9
Chemical Name:
Fludarabine phosphate
Synonyms
FAMP;Fludura;F-ara-AMP;-F-ara-AMP;2-fluoro-araamp;5-Monophosphate;fludarabine hcl;fludara Phosphate;Fludarabin Phosphate;Fludarbine Phopshate
CBNumber:
CB7347825
Molecular Formula:
C10H13FN5O7P
Molecular Weight:
365.21
MDL Number:
MFCD00866418
MOL File:
75607-67-9.mol
MSDS File:
SDS
Last updated:2024-03-18 17:21:11

Fludarabine phosphate Properties

Melting point 203°C(dec.)(lit.)
alpha [α]D20 +10~+14゜(c=0.5,H2O)
Boiling point 864.2±75.0 °C(Predicted)
Density 2.39±0.1 g/cm3(Predicted)
RTECS UO7440900
storage temp. 2-8°C
solubility DMSO: soluble1mg/mL
pka 1.86±0.10(Predicted)
form Powder
color white
Water Solubility Soluble in DMSO or water at 5mg/ml
Merck 14,4126
Stability Hygroscopic
InChIKey GIUYCYHIANZCFB-GFRUICAKSA-N
CAS DataBase Reference 75607-67-9(CAS DataBase Reference)
NCI Dictionary of Cancer Terms fludarabine phosphate
FDA UNII 1X9VK9O1SC
NCI Drug Dictionary fludarabine phosphate

Pharmacokinetic data

Protein binding 19-29%
Excreted unchanged in urine 40-60%
Volume of distribution 0.8-4
Biological half-life 20 / 24

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS08
Signal word  Warning
Hazard statements  H341-H361d
Precautionary statements  P201-P202-P280-P308+P313-P405-P501
WGK Germany  3
HS Code  2934990002
NFPA 704
0
2 0

Fludarabine phosphate price More Price(57)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich Y0002256 Fludarabine for peak identification European Pharmacopoeia (EP) Reference Standard 75607-67-9 Y0002256 $161 2024-03-01 Buy
Sigma-Aldrich F9813 Fludarabine phosphate 75607-67-9 5mg $78.2 2024-03-01 Buy
Sigma-Aldrich 1272204 Fludarabine phosphate 75607-67-9 300mg $436 2024-03-01 Buy
TCI Chemical F0913 Fludarabine Monophosphate >98.0%(HPLC)(T) 75607-67-9 25mg $30 2024-03-01 Buy
TCI Chemical F0913 Fludarabine Monophosphate >98.0%(HPLC)(T) 75607-67-9 100mg $84 2024-03-01 Buy
Product number Packaging Price Buy
Y0002256 Y0002256 $161 Buy
F9813 5mg $78.2 Buy
1272204 300mg $436 Buy
F0913 25mg $30 Buy
F0913 100mg $84 Buy

Fludarabine phosphate Chemical Properties,Uses,Production

Description

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.

Chemical Properties

White or almost white, crystalline powder, hygroscopic.

Originator

Southern Research Institute (U.S.A.)

Uses

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.

Uses

anticonvulsant

Definition

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.

brand name

Fludara (Berlex), Benefluor (Schering AG).

Mechanism of action

Fludarabine phosphate is a cytotoxic purine antimetabolite that acts by inhibiting DNA synthesis. Fludarabine and its soluble derivatives interfere with phosphorylation, e.g., in L 1210 cells. Fludarabine behaves more like an analog of deoxycytidine than adenine or deoxyadenine as indicated by reports demonstrating that the presence of fluorine in the 2-position of the adenine ring alters its function as a substrate for deaminase and nucleoside kinases. This results in differences in biological activity and metabolism. Halogenation does not simply block deamination, but also influences the enzyme that carries out the phosphorylation, as a result cytotoxicity is increased. Fludarabine phosphate may selectively inhibit the incorporation of thymidine and uridine into the DNA molecule by inhibiting both ribonucleotide reductase and DNA polymerase. The maximum tolerated dose (MTD) in heavily pretreated patients with advanced malignancy/solid tumors on the daily regimen was about 15 mg/m2. Granulocytopenia and thrombocytopenia were dose-limiting.

Pharmacology

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%.

Clinical Use

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).

target

DNA synthesis

Drug interactions

Potentially hazardous interactions with other drugs
Antipsychotics: avoid concomitant use with clozapine, increased risk of agranulocytosis.
Cytotoxics: increased pulmonary toxicity with pentostatin (unacceptably high incidence of fatalities); increases intracellular concentration of cytarabine.

Metabolism

Intravenous fludarabine phosphate is rapidly dephosphorylated to fludarabine which is taken up by lymphocytes and rephosphorylated via the enzyme deoxycytidine kinase to the active triphosphate nucleotide. Clearance of fludarabine from the plasma is triphasic; elimination is mostly via renal excretion: 40-60% of an intravenous dose is excreted in the urine. The pharmacokinetics of fludarabine show considerable inter-individual variation

Fludarabine phosphate Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 500)Suppliers
Supplier Tel Email Country ProdList Advantage
Capot Chemical Co.,Ltd.
571-85586718 +8613336195806 sales@capotchem.com China 29797 60
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21691 55
Hangzhou FandaChem Co.,Ltd.
008657128800458; +8615858145714 fandachem@gmail.com China 9348 55
Hubei XinRunde Chemical Co., Ltd.
+8615102730682 bruce@xrdchem.cn CHINA 566 55
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32480 60
career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29914 58
Biochempartner
0086-13720134139 candy@biochempartner.com CHINA 967 58
Shenzhen Nexconn Pharmatechs Ltd
+86-755-89396905 +86-15013857715 admin@nexconn.com China 10248 58
Cangzhou Wanyou New Material Technology Co.,Ltd
18631714998 sales@czwytech.com CHINA 906 58
Xiamen AmoyChem Co., Ltd
+86-592-6051114 +8618959220845 sales@amoychem.com China 6387 58

View Lastest Price from Fludarabine phosphate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Fludarabine Phosphate pictures 2023-03-06 Fludarabine Phosphate
75607-67-9
US $2.70 / g/Bag 10g 99.7% 10000kg Hebei Guanlang Biotechnology Co,.LTD
Fludarabine phosphate pictures 2022-11-05 Fludarabine phosphate
75607-67-9
US $0.00-0.00 / KG 1KG ≥98% HPLC 1-10000KG Changzhou Rokechem Technology Co., Ltd.
Fludarabine phosphate pictures 2022-09-30 Fludarabine phosphate
75607-67-9
US $0.00-0.00 / kg 1kg 98% 1Ton Henan Aochuang Chemical Co.,Ltd.
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) Fludarbine Phopshate Fludarabine Phosphate USP F-ara-A (NSC 312887) Phosphate Fludarabine phosphate 9-bata-D-Arabinofuranosyl-2-fluoroadenine phosphate Fludarabine for system suitability Fluclarabine phosphate ludarabine phosphate 2-fluoro-9-(5-o-phosphono-beta-d-arabinofuranosyl)-9h-purin-6-amin 2-Fluoro-9-β-D-arabinofuranosyladenine5'-monophosphate 2-fluoro-9-β-adenosineabinofuranosyladenine- 5'-monophosphate Fludarabine for system suitability CRS FludarabineMonophosphate> Fludarabine phosphate CRS fludara Phosphate NSC 312887 Phosphate 9H-Purin-6-amine, 2-fluoro-9-(5-O-phosphono-β-D-arabinofuranosyl)- 9H-Purin-6-amine, 2-fluoro-9-(5-O-phosphono-b-D-arabinofuranosyl)- 2-Fluoroadenine 9-beta-D-Arabinofuranoside 5'-Monophosphate Fludarabine phosphate USP/EP/BP Fludarabine Phosphate (NSC 118218) Fludarabine Phosphate (1272204) Fludarabine (NSC-118218) phosphate Fludarabine phosphate 75607-67-9 Fludarabine Phosphate CAS75607-67-9 Fludarabine phosphate salt 9H-Purin-6-amine, 2-fluoro-9-(5-O-phosphono-β-D-arabinofuranosyl)- -F-ara-AMP 75607-67-9