SDZ NKT 343
Tocris Bioscience, part of Bio-Techne | Catalog # 2394
Highly selective human NK1 antagonist
Key Product Details
Description
Highly selective human NK1 antagonist
Product Description
SDZ NKT 343 is a highly selective human tachykinin NK1 receptor antagonist (IC50 values are 0.62 and 451 nM for human and rat receptors respectively) that displays > 130-fold selectivity over human NK2 and NK3 receptors. Potently antagonizes SP-induced Ca2+ efflux in vitro and inhibits mechanical hyperalgesia in vivo.Product Specifications
Molecular Weight
579.65
Formula
C33H33N5O5
Storage
Store at +4°C
Purity
≥98% (HPLC)
Chemical Name
1-[[(2-Nitrophenyl)amino]carbonyl]-L-prolyl-N-methyl-3-(2-naphthalenyl)-N-(phenylmethyl)-L-alaninamide
CAS Number
180046-99-5
PubChem ID
9851211
InChI Key
PCVSIMQAFWRUEC-JDXGNMNLSA-N
SMILES
O=C(NC3=C([N+]([O-])=O)C=CC=C3)N1[C@H]([C@@](N[C@H]([C@@](N(C)CC4=CC=CC=C4)=O)CC2=CC=C(C=CC=C5)C5=C2)=O)CCC1
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Solubility
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| DMSO | 57.97 | 100 | |
| Ethanol | 57.97 | 100 |
Preparing Stock Solutions
for SDZ NKT 343
The following data is based on the product molecular weight 579.65
Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which all affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 1 mM | 1.73 mL | 8.63 mL | 17.25 mL |
| 5 mM | 0.35 mL | 1.73 mL | 3.45 mL |
| 10 mM | 0.17 mL | 0.86 mL | 1.73 mL |
| 50 mM | 0.03 mL | 0.17 mL | 0.35 mL |
Calculators
Molarity Calculator
Dilution Calculator
Reconstitution Calculator
Background References
References are publications that support the biological activity of the product.
- Walpole 2-Nitrophenylcarbamoyl-(S)-prolyl-(S)-3-(2-naphthyl)alanyl-N-benzyl-N-methylamide (SDZ NKT 343), a potent human NK1 tachykinin receptor antagonist with good oral analgesic activity in chronic pain models. J.Med.Chem. 1998 PMID: 9703462
- Campbell Selective neurokinin-1 receptor antagonists are anti-hyperalgesic in a model of neuropathic pain in the guinea-pig. Neuroscience. 1998 PMID: 9758219
- Walpole Comparative, general pharmacology of SDZ NKT 343, a novel, selective NK1 receptor antagonist. Br.J.Pharmacol. 1998 PMID: 9630347
Product Specific Notices for SDZ NKT 343
For research use only
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