Forodesine
Forodesine Basic information
- Product Name:
- Forodesine
- Synonyms:
-
- Isopamphos
- 4H-Pyrrolo3,2-dpyrimidin-4-one, 7-(2S,3S,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)-2-pyrrolidinyl-1,5-dihydro-
- Forodesine
- 7-[(2S,3S,4R,5R)-3,4-Dihydroxy-5-(hydroxymethyl)-2-pyrrolidinyl]-3,5-dihydro-4H-pyrrolo[3,2-d]pyrimidin-4-one
- Fodosine
- Immucillin-H
- (1S)-1-(9-deazahypoxanthin-9-yl)-1,4-dideoxy-1,4-iMino-D-ribitol, iMMucillin H
- FORODESINE FODOSINE
- CAS:
- 209799-67-7
- MF:
- C11H14N4O4
- MW:
- 266.25
- Mol File:
- 209799-67-7.mol
Forodesine Chemical Properties
- Boiling point:
- 613.5±65.0 °C(Predicted)
- Density
- 2.01
- storage temp.
- Hygroscopic, Refrigerator, under inert atmosphere
- solubility
- PBS (pH 7.2): 5 mg/ml
- form
- A crystalline solid
- pka
- 13.88±0.70(Predicted)
- color
- Light brown to gray
Forodesine Usage And Synthesis
Description
Forodesine is a purine nucleoside analog and purine nucleoside phosphorylase (PNP) inhibitor (IC50s = 1.19, 0.48, 1.24, 0.66, and 1.57 nM for human, mouse, rat, monkey, and dog PNP, respectively). It inhibits phytohemagglutinin A-, mixed lymphocyte reaction-, or IL-2-induced proliferation of isolated human peripheral blood lymphocytes (PBLs; IC50s = <0.1-0.38 μM) in the presence, but not absence, of 2’-deoxyguanosine (dGuo). Forodesine inhibits proliferation of CEM-SS T cell acute lymphoblastic leukemia (T-ALL) cells. In vivo, forodesine (10 mg/kg) prolongs survival in the hu-PBL-SCID mouse model of xenogeneic graft versus host disease (GVHD).
Uses
Treatment of T-Cell malignancies such as acute lymphoblastic leukemia (ALL) and cutaneous T-cell lymphoma (CTCL) Fodosine.
Uses
Fodosine is a 23-pM inhibitor of bovine purine nucleoside phosphorylase (PNP) specifically designed as a transition state mimic.
Definition
ChEBI: Immucillin H is a pyrrolopyrimidine and a dihydroxypyrrolidine.
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