GBT-440
CAS No. 1446321-46-5
GBT-440( GBT 440 | GBT440 | Voxelotor )
Catalog No. M11895 CAS No. 1446321-46-5
A new potent allosteric effector of sickle cell hemoglobin; increases the affinity of hemoglobin for oxygen and consequently inhibits its polymerization when subjected to hypoxic conditions.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
Size | Price / USD | Stock | Quantity |
5MG | 46 | In Stock |
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10MG | 67 | In Stock |
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25MG | 110 | In Stock |
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50MG | 178 | In Stock |
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100MG | 332 | In Stock |
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200MG | 494 | In Stock |
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500MG | Get Quote | In Stock |
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1G | Get Quote | In Stock |
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Biological Information
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Product NameGBT-440
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NoteResearch use only, not for human use.
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Brief DescriptionA new potent allosteric effector of sickle cell hemoglobin; increases the affinity of hemoglobin for oxygen and consequently inhibits its polymerization when subjected to hypoxic conditions.
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DescriptionA new potent allosteric effector of sickle cell hemoglobin; increases the affinity of hemoglobin for oxygen and consequently inhibits its polymerization when subjected to hypoxic conditions; orally bioavailable and partitions highly and favorably into the red blood cell with a RBC/plasma ratio of ~150.Anemia Phase 3 Clinical(In Vitro):Voxelotor (GBT440) binds to the N-terminal a chain of haemoglobin (Hb), increases haemoglobin S (HbS) affinity for oxygen, delays in vitro HbS polymerization and prevents sickling of red blood cells (RBCs).(In Vivo):Voxelotor (GBT440; 100-150 mg/kg; administered twice a day by oral gavage for 9-12 days) reduces ex vivo sickling and prolongs red blood cells (RBCs) half-life in a murine model of sickle cell disease (SCD).Voxelotor shows T1/2s of 11.7, 19.1±1.5, 66.0±11, 28.8±4.0 hours for mouse (70 mg/kg; i.v.), rat (1.6 mg/kg; i.v.), dog (1 mg/kg; i.v.), and momkey (1 mg/kg; i.v.), respectively.Voxelotor shows Cmaxs of 81.9, 71.2±6.0, 5.56±1.6, and 25.2±5.5 μg/mL for mouse (30 mg/kg; p.o.), rat (7.2 mg/kg; p.o.), dog (2.5 mg/kg; p.o.), and momkey (4.25 mg/kg; p.o.), respectively.
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In Vitro——
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In VivoAnimal Model:HbSS Townes knock-in sickle mice (SS mice)Dosage:100 and 150 mg/kg Administration:Oral administration; twice a day; for 9-12 days Result:Reduced haemolysis.Animal Model:C57BL/6J mice, Sprague-Dawley rats, Beagle dogs and Cynomolgus monkeys Dosage:70, 1.6, 1 and 1 mg/kg for mice, rats, dogs and monkeys, respectively.Oral (PO: 30, 7 2, 2 5 and 4 3 mg/kg, respectively) Result:T1/2s of 11.7, 19.1±1.5, 66.0±11, 28.8±4.0 hours for mouse (70 mg/kg; i.v.), rat (1.6 mg/kg; i.v.), dog (1 mg/kg; i.v.), and momkey (1 mg/kg; i.v.), respectively.Cmaxs of 81.9, 71.2±6.0,5.56±1.6, and 25.2±5.5 μg/mL for mouse (30 mg/kg; p.o.), rat (7.2 mg/kg; p.o.), dog (2.5 mg/kg; p.o.), and momkey (4.25 mg/kg; p.o.), respectively.
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SynonymsGBT 440 | GBT440 | Voxelotor
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PathwayOthers
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TargetOther Targets
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RecptorOther Targets
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Research AreaOther Indications
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IndicationAnemia
Chemical Information
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CAS Number1446321-46-5
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Formula Weight337.3725
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Molecular FormulaC19H19N3O3
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Purity>98% (HPLC)
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Solubility10 mM in DMSO
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SMILESO=CC1=C(OCC2=CC=CN=C2C3=CC=NN3C(C)C)C=CC=C1O
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Chemical NameBenzaldehyde, 2-hydroxy-6-[[2-[1-(1-methylethyl)-1H-pyrazol-5-yl]-3-pyridinyl]methoxy]-
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Metcalf B, et al. ACS Med Chem Lett. 2017 Jan 23;8(3):321-326.
2. Oksenberg D, et al. Br J Haematol. 2016 Oct;175(1):141-53.
3. Dufu K, et al. Hematol Rep. 2016 Sep 28;8(3):6637.
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