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ZT 52656A hydrochloride
CAS No. 115730-24-0
ZT 52656A hydrochloride( —— )
Catalog No. M22459 CAS No. 115730-24-0
ZT 52656A is a selective agonist of kappa opioid, and used for the prevention or alleviation of pain in the eye.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 1026 | In Stock |
|
| 5MG | 1197 | In Stock |
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| 10MG | 1786 | In Stock |
|
| 25MG | 3031 | In Stock |
|
| 50MG | 3841 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameZT 52656A hydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionZT 52656A is a selective agonist of kappa opioid, and used for the prevention or alleviation of pain in the eye.
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DescriptionZT 52656A is a selective agonist of kappa opioid, and used for the prevention or alleviation of pain in the eye.
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In VitroZT 52656A is a selective kappa opioid agonist, used for the prevention or alleviation of pain in the eye.
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In Vivo——
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Synonyms——
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PathwayEndocrinology/Hormones
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TargetOpioid Receptor
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Recptorkappa opioid receptor
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Research Area——
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Indication——
Chemical Information
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CAS Number115730-24-0
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Formula Weight390.87
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Molecular FormulaC19H26ClF3N2O
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Purity>98% (HPLC)
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SolubilityDMSO:34 mg/mL (86.98 mM; Need ultrasonic)
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SMILESCl.FC(F)(F)c1ccc(CC(=O)N2CCCCC2CN2CCCC2)cc1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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UFP-101
Potent, selective and competitive silent antagonist for the NOP opioid receptor. Binds to NOP with high affinity (pKi = 10.24) and displays > 3000-fold selectivity over δ, μ and κ opioid receptors. Antinociceptive and opposes the action of nociceptin in vivo.
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Endomorphin 2?
Endomorphins-2 (EM-2) could decrease both the frequency and amplitude of the sEPSC of the motoneurons in lamina IX which was reversed by the MOR antagonist CTOP.??
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[(pF)Phe4]Nociceptin...
Highly potent and selective nociceptin/orphanin FQ receptor (OP4) agonist peptide (pKi = 10.68; pEC50 = 9.80). Displays > 8000-fold selectivity over δ, κ, and μ opioid receptors and has relatively long lasting pronociceptive, hypotensive, negative inotropic and feeding stimulation effects in vivo.
