A GCGR antagonist
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LGD 6972 (ammonium salt)

Item No. 40961

Technical Information
Formal Name
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]-ethanesulfonic acid, monoammonium salt
Molecular Formula
C43H45N2O5S • NH4
Formula Weight
Purity
≥95%
Formulation
A solid
DMSO: Sparingly soluble: 1-10 mg/mlEthanol: Sparingly soluble: 1-10 mg/ml
SMILES
CC1=C(C2=CC=C(C=C2)NC([C@@H](C3=CC=C(C4=CC=C(C=C4)C(C)(C)C)C=C3)CC5=CC=C(C=C5)C(NCCS(=O)([O-])=O)=O)=O)C(C)=CC(C)=C1.[NH4+]
InChi Code
InChI=1S/C43H46N2O5S.H3N/c1-28-25-29(2)40(30(3)26-28)35-17-21-38(22-18-35)45-42(47)39(27-31-7-9-36(10-8-31)41(46)44-23-24-51(48,49)50)34-13-11-32(12-14-34)33-15-19-37(20-16-33)43(4,5)6;/h7-22,25-26,39H,23-24,27H2,1-6H3,(H,44,46)(H,45,47)(H,48,49,50);1H3/t39-;/m1./s1
InChi Key
VZJMFAKZCPXIGY-DRRLCDGFSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    LGD 6972 is a glucagon receptor (GCGR) antagonist.1 In vivo, LGD 6972 reduces glucagon-induced hyperglycemia in wild-type mice and reduces blood glucose levels in mouse models of diabetes.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Vajda, E.G., Logan, D., Lasseter, K., et alPharmacokinetics and pharmacodynamics of single and multiple doses of the glucagon receptor antagonist LGD-6972 in healthy subjects and subjects with type 2 diabetes mellitus. Diabetes Obes. Metab. 19(1), 24-32 (2017).