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Cat. No.: HY-183773

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KOR agonist-9

KOR agonist-9 is a selective kappa opioid receptor (KOR) agonist with an EC₅₀of 1.41 nM. KOR agonist-9 exhibits >125-fold selectivity over μ/δ-opioid receptors. KOR agonist-9 antinociceptive and antipruritic effects in mice. KOR agonist-9 can be used for the research of pain, pruritus.

연구목적의 판매만을 진행합니다. 환자를 대상으로 한 판매는 하지 않습니다.

화학식: C₃₆H₄₅N₃O₄
분자량:583.76

보관:

Please store the product under the recommended conditions in the Certificate of Analysis.

KOR agonist-9 Chemical Structure

Amount: USD 0.00

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Use of MCE Products

Strong Fluorescence Signal / Multi-Disciplinary Applications / High Fluorescence Specificity

Biological Activity
- 제품 설명
- IC₅₀ & Target
- In Vitro
- In Vivo
Chemical Information
순도&문서
References
Calculators
Help & FAQs
Classifications
Bioz

Biological Activity

제품 설명

IC₅₀ & Target

^[1]

κ Opioid Receptor/KOR

0.0016 nM (Ki)

κ Opioid Receptor/KOR

1.41 nM (EC₅₀)

μ Opioid Receptor/MOR

0.20 nM (Ki)

δ Opioid Receptor/DOR

15.15 nM (Ki)

All Opioid Receptor Isoforms :

In Vitro

KOR agonist-9 (compound 10e) (17 h) shows significantly lower potency for β-arrestin recruitment in HTLA-KOR Tango cells (EC₅₀ = 4912 nM) compared to cAMP inhibition, indicating G-protein biased signaling^[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

KOR agonist-9 (compound 10e) (2-20 mg/kg; i.p.; single dose; 4 hours pretreatment) induces dose-dependent antinociception in the mouse acetic acid-induced writhing visceral nociception model^[1].
KOR agonist-9 (5-10 mg/kg; i.p.; single dose; 4 hours pretreatment) induces dose-dependent antipruritic effects in the mouse histamine-induced pruritus model^[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model:

ICR mice (male, 18~22 g)^[1]
Dosage:

2; 5; 10; 15; 20 mg/kg
Administration:

i.p.; single dose; 4 hours pretreatment
Result:

Produced dose-dependent antinociceptive effects.
Showed significant antinociception observed at the 15 mg/kg dose.

Animal Model:

ICR mice (male, 18~22 g)^[1]
Dosage:

5; 10 mg/kg
Administration:

i.p.; single dose; 4 hours pretreatment
Result:

Elicited dose-dependent antipruritic activity.
Showed a significant reduction in scratching bouts observed at the 10 mg/kg dose.

Chemical Information

분자량 583.76
화학식 C₃₆H₄₅N₃O₄
SMILES

COC1=C(O2)C([C@]([C@@H]2[C@]3(OC)[C@@H](N4CCN(C(CC5=CC=CC=C5)=O)CC4)C6)(CC7)[C@@]6(CC3)C(N7CC8CC8)C9)=C9C=C1
선적

Room temperature in continental US; may vary elsewhere.
보관

Please store the product under the recommended conditions in the Certificate of Analysis.

순도&문서

Handling Instructions (2659 KB)

References

[1]. Duan S, et al. Discovery of a highly selective and potent kappa opioid receptor agonist from N-cyclopropylmethyl-7α-piperazinyl -6,14-endoethano-tetrahydronorthebaines. Eur J Med Chem. 2026 May 16;315:118964. [Content Brief]

Calculators

몰농도 계산기

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

Concentration Concentration

Volume Volume

Molecular Weight Molecular Weight

농도 희석 계산기

Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final)

Concentration _(start) Concentration _(start)

Volume _(start) Volume _(start)

Concentration _(final) Concentration _(final)

Volume _(final) Volume _(final)

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

Bioz

Keywords

MOQ

Minimum order quantity

100 mg

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