A racemic mixture of (S)-(+)-LY426965 and (R)-(–)-LY426965
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Product Type

Biochemicals

(±)-LY426965 (hydrochloride)

Item No. 32568

Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
1-cyclohexyl-4-[4-(2-methoxyphenyl)-1-piperazinyl]-2-methyl-2-phenyl-1-butanone, dihydrochloride
CAS Number
228418-81-3
Molecular Formula
C28H38N2O2 • 2HCl
Formula Weight
507.5
Purity
≥98%
Formulation (Request formulation change)
A solid
Solubility(Learn about Variance in Solubility)
DMSO: 25 mg/ml
SMILES
O=C(C(C)(CCN1CCN(CC1)C2=C(OC)C=CC=C2)C3=CC=CC=C3)C4CCCCC4.Cl.Cl
InChi Code
InChI=1S/C28H38N2O2.2ClH/c1-28(24-13-7-4-8-14-24,27(31)23-11-5-3-6-12-23)17-18-29-19-21-30(22-20-29)25-15-9-10-16-26(25)32-2;;/h4,7-10,13-16,23H,3,5-6,11-12,17-22H2,1-2H3;2*1H
InChi Key
MWAFGTLMPGKRHD-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    1 mg

    $49

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    5 mg

    $190

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    10 mg

    $329

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    25 mg

    $702

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    Product Description

    (±)-LY426965 is a racemic mixture of the serotonin (5-HT) receptor subtype 5-HT1A antagonist (S)-(+)-LY426965 and (R)-(–)-LY426965.1,2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Kaplin, A.I., Hendrix, C.W., and Rahn, K.A. Methods for reducing anxiety and impulsivity in subjects initiating treatment with serotonin reuptake inhibitors. WO2014209991A1, (2014).

    2. Denmark, S.E., and Fu, J. Asymmetric construction of quaternary centers by enantioselective allylation: Application to the synthesis of the serotonin antagonist LY426965. Org. Lett. 4(11), 1951-1953 (2002).