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Postion:Product Catalog >Farudodstat
Farudodstat
  • Farudodstat

Farudodstat NEW

Price $40 $64 $129
Package 5mg 10mg 25mg
Min. Order:
Supply Ability: 10g
Update Time: 2026-01-20

Product Details

Product Name: Farudodstat CAS No.: 1035688-66-4
Purity: 98.36% Supply Ability: 10g
Release date: 2026/01/20

Product Introduction

Bioactivity

NameFarudodstat
DescriptionFarudodstat (ASLAN003) is an orally active and potent inhibitor of DHODH (Human Dihydroorotate Dehydrogenase) with antitumor activity, showing potential as a first-in-class candidate in AML [Acute Myeloid Leukemia].
In vitroASLAN003 is a highly potent dihydroorotate dehydrogenase inhibitor that induces differentiation, as well as reduces cell proliferation and viability, of acute myeloid leukemia cell lines and primary acute myeloid leukemia blasts including in chemo-resistant cells. Apoptotic pathways are triggered by ASLAN003, and it also significantly inhibits protein synthesis and activates AP-1 transcription, contributing to its differentiation promoting capacity[2].
In vivoASLAN003 substantially reduces leukemic burden and prolongs survival in acute myeloid leukemia xenograft mice and acute myeloid leukemia patient-derived xenograft models. Notably, the drug has no evident effect on normal hematopoietic cells and exhibits excellent safety profiles in mice, even after a prolonged period of administration. ASLAN003 is an agent targeting dihydroorotate dehydrogenase with potential in the treatment of acute myeloid leukemia. ASLAN003 is currently being evaluated in phase 2a clinical trial in acute myeloid leukemia patients[2].
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information10% DMSO+40% PEG300+5% Tween 80+45% Saline : 4 mg/mL (11.23 mM), Sonication is recommended.
DMSO : 250 mg/mL (701.62 mM), Sonication is recommended.
KeywordsTHP-1 | synthesis | RPL6 | RNASynthesis | RNA Synthesis | protein | orally | OPP | myeloid | MOLM-14 | leukemia | KG-1 | Inhibitor | inhibit | Farudodstat | EIF4B | DNASynthesis | DNA/RNA Synthesis | DNA Synthesis | Dihydroorotate Dehydrogenase | DHODH | caspase-8 | caspase-7 | caspase-3 | ASLAN-003 | ASLAN 003 | Apoptosis | AP-1 | AML | acute
Inhibitors RelatedStavudine | Aceglutamide | Tamoxifen | Urea | Cysteamine hydrochloride | Metronidazole | Guanidine hydrochloride | Citric Acid Triammonium | Thymidine | Dimethyl phthalate | Alginic acid | Dextran sulfate sodium salt (MW 5000)
Related Compound LibrariesBioactive Compound Library | Anti-Cancer Clinical Compound Library | Drug Repurposing Compound Library | Anti-Viral Compound Library | Inhibitor Library | Mitochondria-Targeted Compound Library | Anti-Aging Compound Library | Bioactive Compounds Library Max | Anti-Infection Compound Library | Anti-Cancer Active Compound Library | Anti-Cancer Drug Library | Transcription Factor-Targeted Compound Library

Company Profile Introduction

Target Molecule Corp. (TargetMol) is a global high-tech enterprise, headquartered in Boston, MA, specializing in chemical and biological research product and service to meet the research needs of global customers. TargetMol has evolved into one of the biggest global compound library and small molecule suppliers and a customer based on 40+ countries. TargetMol offers over 80 types of compound libraries and a wide range of high-quality research chemicals including inhibitors, activator, natural compounds, peptides, inhibitory antibodies, and novel life-science kits, for laboratory and scientific use. Besides, virtual screening service is also available for customers who would like to conduct the computer-aided drug discovery.

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Product name Price   Suppliers Update time
$40.00/5mg
VIP6Y
TargetMol Chemicals Inc.
2026-01-20

TargetMol Chemicals Inc.

4YR United StatesUnited States
  • Since: 2011-01-07
  • Address: 36 Washington Street, Wellesley Hill, USA
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