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Forodesine hydrochloride

Catalog No. T11313 CAS 284490-13-7

Synonyms: BCX-1777 hydrochloride, Immucillin-H hydrochloride

Forodesine hydrochloride (BCX-1777 hydrochloride), a potent inhibitor of human lymphocyte proliferation, effectively induces apoptosis in leukemic cells by elevating dGTP levels. This compound is an orally active, highly potent purine nucleoside phosphorylase (PNP) inhibitor, demonstrating IC50 values between 0.48 to 1.57 nM across human, mouse, rat, monkey, and dog PNP.

All products from TargetMol are for Research Use Only. Not for Human or Veterinary or Therapeutic Use.

Forodesine hydrochloride Chemical Structure

Forodesine hydrochloride, CAS 284490-13-7

Pack Size	Availability	Price/USD	Quantity
5 mg	5 days	$ 1,670.00

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Biological Description

Chemical Properties

Storage & Solubility Information

Description	Forodesine hydrochloride (BCX-1777 hydrochloride), a potent inhibitor of human lymphocyte proliferation, effectively induces apoptosis in leukemic cells by elevating dGTP levels. This compound is an orally active, highly potent purine nucleoside phosphorylase (PNP) inhibitor, demonstrating IC50 values between 0.48 to 1.57 nM across human, mouse, rat, monkey, and dog PNP.
Targets&IC50	PNP (human):1.19 nM , PNP (monkey):0.66 nM , PNP (mouse):0.48 nM , PNP (rat):1.24 nM , PNP (dog):1.57 nM
In vitro	Forodesine (BCX-1777), in the presence of 2'-deoxyguanosine (dGuo, 3-10 μM), inhibits human lymphocyte proliferation activated by various agents such as interleukin-2 (IL-2), mixed lymphocyte reaction (MLR) and phytohemagglutinin (PHA) (IC50 values
In vivo	In the hu-PBL-SCID mouse model, Forodesine (BCX-1777) demonstrates efficacy in extending lifespan by two-fold or greater. This compound exhibits outstanding oral bioavailability (63%) in mice. When administered at a single dose of 10 mg/kg, it significantly increases dGuo levels to around 5 μM.

Synonyms	BCX-1777 hydrochloride, Immucillin-H hydrochloride
Molecular Weight	302.71
Formula	C11H15ClN4O4
CAS No.	284490-13-7

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 16.67 mg/mL (55.07 mM), Sonication is recommended.

H2O: 16.67 mg/mL (55.07 mM), Sonication is recommended.

References and Literature

1. Bieghs L, et al. The effects of forodesine in murine and human multiple myeloma cells. Adv Hematol. 2010;2010:131895. 2. Bantia S, et al. Purine nucleoside phosphorylase inhibitor BCX-1777 (Immucillin-H)--a novel potent and orally active immunosuppressive agent. Int Immunopharmacol. 2001 Jun;1(6):1199-210.

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Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO (Master liquid concentration mg/mL)，Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.

Method for preparing in vivo formulation：Take μL DMSO master liquid, next add μL PEG300， mix and clarify, next add μL Tween 80，mix and clarify, next add μL ddH₂O, mix and clarify.

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Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc.

Keywords

Forodesine hydrochloride 284490-13-7 Others BCX-1777 hydrochloride Forodesine Hydrochloride Immucillin-H hydrochloride BCX 1777 Hydrochloride Immucillin-H Hydrochloride BCX-1777 Hydrochloride BCX1777 Hydrochloride inhibitor inhibit

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