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LGD-6972

Chemical Structure : LGD-6972

CAS No.: 1207989-09-0

LGD-6972 (LGD6972;RVT 1502)

Catalog No.: PC-43093Not For Human Use, Lab Use Only.

LGD-6972 (RVT 1502) is a novel potent, selective, orally bioavailable glucagon receptor (GCGR) antagonist.

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Purity & Documentation Purity: >98% (HPLC)

Biological Activity

LGD-6972 (RVT 1502) is a novel potent, selective, orally bioavailable glucagon receptor (GCGR) antagonist; binds competitively to GCGR with high affinity and selectivity, suppressing both cAMP and glucose production in vitro; reduces acute glucagon-stimulated hyperglycaemia as well as the hyperglycaemia observed in diabetic mouse models in vivo.

Diabetes

Phase 2 Clinical

Physicochemical Properties

M.Wt 702.9008
Formula C43H46N2O5S
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
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Solubility

DMSO: ≥ 31 mg/mL

Chemical Name/SMILES

Ethanesulfonic acid, 2-[[4-[(2R)-2-[4'-(1,1-dimethylethyl)[1,1'-biphenyl]-4-yl]-3-oxo-3-[(2',4',6'-trimethyl[1,1'-biphenyl]-4-yl)amino]propyl]benzoyl]amino]-

References

1. Vajda EG, et al. Diabetes Obes Metab. 2017 Jan;19(1):24-32.

2. Vajda EG, et al. Diabetes. 2012;61(suppl 1):A252. Abstract.

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