GDC-0276

CAT: 0804-HY-114237-01Size: 5 mgDry Ice: NoHazardous: No

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CAT#:0804-HY-114237-01Size:5 mg

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Description

GDC-0276 is a potent, selective, reversible and orally active NaV1.7 inhibitor with an IC50 value of 0.4 nM. GDC-0276 is well tolerated and exhibits a good pharmacokinetic profile. GDC-0276 has the potential for the treatment of pain and to address shortcomings of existing pain medications, such as addiction and off-target side effects[1].

CAS Number

1494581-70-2

Product Name Alternative

Adonitol-1-13C; Adonite-1-13C, Adonitol-2-13C; Adonite-2-13C

UNSPSC

12352005

Target

Sodium Channel

Type

Reference compound

Related Pathways

Membrane Transporter/Ion Channel

Applications

Neuroscience-Neuromodulation

Field of Research

Neurological Disease

Assay Protocol

https://www.medchemexpress.com/gdc-0276.html

Purity

99.69

Solubility

DMSO : 125 mg/mL (ultrasonic)

Smiles

O=C(NS(=O)(N1CCC1)=O)C2=CC(C3CC3)=C(OCC4(C5)CC6CC5CC(C6)C4)C=C2F

Molecular Formula

C24H31FN2O4S

Molecular Weight

462.58

References & Citations

[1]Rothenberg ME, et al. Safety, Tolerability, and Pharmacokinetics of GDC-0276, a Novel NaV1.7 Inhibitor, in a First-in-Human, Single- and Multiple-Dose Study i|[2]Steven J. McKerrall, et al. Nav1.7 inhibitors for the treatment of chronic pain. Bioorganic & Medicinal Chemistry Letters (2018) |[3]Takahashi RH, et al.Unequal Absorption of Radiolabeled and Nonradiolabeled Drug from the Oral Dose Leads to Incorrect Estimates of Drug Absorption and Circulating Metabolites in a Mass Balance Study.Drug Metab Lett. 2019;13 (1) :37-44.

Shipping Conditions

Room Temperature

Storage Conditions

-20°C, 3 years; 4°C, 2 years (Powder)

Scientific Category

Reference compound1

Clinical Information

Phase 1

Isoform

Nav1.7

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T11377-01	GDC-0276
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BA6397-1	GDC-0339
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GDC-0276

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