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Referencia número: HY-178720

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SHR0687

SHR0687 is a selective tetrapeptide kappa opioid receptor (KOR) agonist with an EC₅₀ of 0.53 pM. SHR0687 displays high potency and selectivity over MOR and DOR, with negligible blood-brain barrier penetration. SHR0687 activates KOR specifically, leading to potential modulation of neurological pathways without significant central nervous system effects. SHR0687 can be used for the research of pain.

Para uso exclusivo en investigación. No vendemos a pacientes.

No. CAS: 2168573-03-1
Fòrmula: C₃₉H₆₀N₈O₅
Peso molecular:720.94

Almacenamiento:

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

Data Sheet (270 KB)

SHR0687 Chemical Structure

No. CAS: 2168573-03-1

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Fluorescent Dye

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

Actividad biológica
- Descripciòn
- IC₅₀ & Target
- In Vitro
- Parmacokinetics
- In Vivo
Chemical Information
Pureza y Documentación
Referencias
Calculators
Help & FAQs
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Bioz

Actividad biológica

Descripciòn

IC₅₀ & Target^[1]

κ Opioid Receptor/KOR

0.53 pM (EC₅₀)

μ Opioid Receptor/MOR

>50000 nM (EC₅₀)

δ Opioid Receptor/DOR

>50000 nM (EC₅₀)

Ver todos los productos específicos de isoformas Opioid Receptor :

In Vitro

SHR0687 (Human embryonic kidney cells (HEK293)) does not inhibit hERG channels^[1].
SHR0687 (Human liver microsomes) does not significantly inhibit major CYP isoforms, including CYP1A2, CYP2C9, CYP2C19, CYP2D6, and CYP3A4^[1].

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

Parmacokinetics

Species	Dose	Route	T_1/2	Clearance (CL)	V_z	AUC_0-t
Rat^[1]	1 mg/kg	i.v.	4.78 h	10.5 mL/min/kg	4515 mL/kg	1553 ng·h/mL
Mice^[1]	1 mg/kg	i.v.	0.34 h	10.1 mL/min/kg	297 mL/kg	1656 ng·h/mL
Dog^[1]	0.5 mg/kg	i.v.	4.45 h	3.1 mL/min/kg	1236 mL/kg	2619 ng·h/mL

In Vivo

SHR0687 (0.03-0.3 mg/kg; Intravenous (IV); once) demonstrates analgesic effects in carrageenan-induced pain model in Sprague Dawley rats (SD)^[1].
SHR0687 (1 mg/kg; Intravenous (IV); administration) shows minimal BBB penetration in Sprague Dawley rats (SD)^[1].

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

Animal Model:

Sprague Dawley rats (SD) (150-180 g) were subcutaneously injected with 1% carrageenan (100 μL)^[1]
Dosage:

0.03 mg/kg, 0.1 mg/kg, 0.3 mg/kg
Administration:

i.v.;30 minutes before detection
Result:

A dose-dependent reduction in pain was observed.

Chemical Information

No. CAS 2168573-03-1
Peso molecular 720.94
Fòrmula C₃₉H₆₀N₈O₅
SMILES

C[C@H](C1=CC=CC=C1)CNCC(N[C@H](CC2=CC=CC=C2)C(N[C@H](CC(C)C)C(N[C@H](CCCCN)C(N3CCC(CC3)NC(NC)=O)=O)=O)=O)=O
Envío

Room temperature in continental US; may vary elsewhere.
Almacenamiento

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

Pureza y Documentación

Select Batch:

Pureza: 99.98%

Assay: 99.98%

ee.: 99.98%

Ficha de datos (270 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Instrucciones de manejo (2659 KB)

Referencias

[1]. Li X, et al. Discovery of SHR0687, a Highly Potent and Peripheral Nervous System-Restricted KOR Agonist. ACS Med Chem Lett. 2020;11(11):2151-2155. Published 2020 Sep 14. [Content Brief]

Calculators

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

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Calculadora de dilución

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

Concentration _(start) Concentration _(start)

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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.

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100 mg

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Actividad biológica
- Descripciòn
- IC₅₀ & Target
- In Vitro
- In Vivo
Chemical Information
Pureza y Documentación
Referencias

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SHR0687

Ver todos los productos específicos de isoformas Opioid Receptor

Actividad biológica

Chemical Information

Pureza y Documentación

Referencias

Calculators

Help & FAQs

SHR0687 Related Classifications

HY-178720 Related Classifications