A multimodal receptor antagonist
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AVN-101 (hydrochloride)

Item No. 38791

Technical Information
Formal Name
2,3,4,5-tetrahydro-2,8-dimethyl-5-(2-phenylethyl)-1H-pyrido[4,3-b]indole, monohydrochloride
CAS Number
1061354-48-0
Molecular Formula
C21H24N2 • HCl
Formula Weight
Purity
≥98%
Formulation
A crystalline solid
DMF: 10 mg/mlDMSO: 5 mg/mlEthanol: 1 mg/ml
λmax
227 nm
SMILES
CN(C1)CCC2=C1C3=C(C=CC(C)=C3)N2CCC4=CC=CC=C4.Cl
InChi Code
InChI=1S/C21H24N2.ClH/c1-16-8-9-20-18(14-16)19-15-22(2)12-11-21(19)23(20)13-10-17-6-4-3-5-7-17;/h3-9,14H,10-13,15H2,1-2H3;1H
InChi Key
RKLJJDFIWWRTEJ-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    AVN-101 is a multimodal receptor antagonist.1 It is an antagonist of the serotonin (5-HT) receptor subtypes 5-HT7, 5-HT2C, 5-HT2A, and 5-HT6 (Kis = 0.153, 1.17, 1.56, and 2.04 nM, respectively). It is selective for these receptors over 5-HT2B, 5-HT5A, 5-HT1A, and 5-HT1B receptors (Kis = 10.6, 20.8, 61, and 720 nM, respectively). It is also an antagonist of α2A-, α2B-, α2C-, α1B-, α1A-, and α1D-adrenergic receptors (Kis = 0.41, 1.77, 3.55, 9.4, 18.9, and 30.2 nM, respectively), as well as histamine H1 and H2 (Kis = 0.58 and 89 nM, respectively), but not H3, receptors. AVN-101 (0.2, 1, and 5 mg/kg) increases the time spent in the open arms of the elevated plus maze in mice. It also reduces immobility in the forced swim test and prevents scopolamine-induced amnesia in a passive avoidance test in mice when administered at a dose of 0.05 mg/kg.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Ivachtchenko, A.V., Lavrovsky, Y., and Okun, I. AVN-101: A multi-target drug candidate for the treatment of CNS disorders. J. Alzheimers Dis. 53(2), (2016).