1. GPCR/G Protein
    Neuronal Signaling
  2. mAChR
  3. Levetimide

Levetimide 

Cat. No.: HY-105545A Purity: 99.18% ee.: 100.00%
Handling Instructions

Levetimide is a potent and stereoselective inhibitor of [3H](+)pentazocine binding, with a Ki of 2.2 nM.

For research use only. We do not sell to patients.

Levetimide Chemical Structure

Levetimide Chemical Structure

CAS No. : 21888-99-3

Size Price Stock Quantity
10 mM * 1 mL in DMSO USD 165 In-stock
Estimated Time of Arrival: December 31
10 mg USD 150 In-stock
Estimated Time of Arrival: December 31
50 mg USD 450 In-stock
Estimated Time of Arrival: December 31
100 mg   Get quote  
200 mg   Get quote  

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Based on 1 publication(s) in Google Scholar

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Description

Levetimide is a potent and stereoselective inhibitor of [3H](+)pentazocine binding, with a Ki of 2.2 nM[1].

In Vitro

Levetimide potently inhibits [3H]DTG binding although without stereoselectivity (Ki value of 103 nM) [1].

Molecular Weight

362.46

Formula

C₂₃H₂₆N₂O₂

CAS No.

21888-99-3

SMILES

O=C(N1)[[email protected]](C2=CC=CC=C2)(CCC1=O)C3CCN(CC3)CC4=CC=CC=C4

Shipping

Room temperature in continental US; may vary elsewhere

Storage
Powder -20°C 3 years
  4°C 2 years
In solvent -80°C 6 months
  -20°C 1 month
Solvent & Solubility
In Vitro: 

DMSO : ≥ 100 mg/mL (275.89 mM)

*"≥" means soluble, but saturation unknown.

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.7589 mL 13.7946 mL 27.5893 mL
5 mM 0.5518 mL 2.7589 mL 5.5179 mL
10 mM 0.2759 mL 1.3795 mL 2.7589 mL
*Please refer to the solubility information to select the appropriate solvent.
References
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Levetimide
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HY-105545A
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