Endomorphin 1 acetate - ≥99% , CAS No.1276123-71-7

CAS: 1276123-71-7 Cat. No.: E650817 Molecular Weight: 670.75
AVAILABLE TO ORDER
GRADE & PURITY ≥99%
Storage
Protected from light,Argon charged,Desiccated,Store at -80°C
Shipped In
Dry ice packs + Cold packs
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
5mg
E650817-5mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$110.90
10mg
E650817-10mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$154.90
25mg
E650817-25mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$264.90
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Why this grade

≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Protected from light,Argon charged,Desiccated,Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

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Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Endomorphin 1 acetate, a high affinity, highly selective agonist of the μ-opioid receptor ( K i : 1.11 nM), displays reasonable affinities for kappa 3 binding sites, with K i value between 20 and 30 nM. Endomorphin 1 acetate has antinociceptive properties.

In Vitro

Endomorphin 1 acetate inhibits Forskolin (1 μM) stimulated cyclic AMP formation with a pIC 50 value of 8.03 in In CHOμ cells . Endomorphin 1 (1-10 μM) acetate increases interleukin-8 secretion in Caco-2 cells. Endomorphin 1 (1 μM) acetate inhibits excitatory transmission in adult rat substantia gelatinosa neurons. MCE has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Endomorphin 1 (i.c.v.) acetate shows antinociceptive properties in mice, with an ED 50 value of 6.16 nM. Endomorphin 1 (50 μg/kg, i.v., rats) acetate alleviates myocardial ischemia/reperfusion injury (MIRI) by inhibiting the inflammatory response. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: ICR mice. Dosage: 6.16 nM (ED 50 ) Administration: Intracerebroventricularly (i.c.v.) injection Result: Inhibited dose-dependently the tail-flick response. Animal Model: Rats. Dosage: 50 μg/kg Administration: Intravenously following LAD ligation for 25 min, subsequently the LAD was reperfused for 120 min. Result: Alleviated MIRI by reducing the production of free radicals. Dncreased LDH and CK-MB activities. Increased SOD activity and decreased MDA content. Decreased IL-6 and TNF-α plasma content.

Form:Solid

IC50& Target:μ Opioid Receptor/MOR 1.11 nM (Ki)

Specifications

Specifications & Purity
≥99%
Biochemical and Physiological Mechanisms
Endomorphin 1 acetate, a high affinity, highly selective agonist of the μ-opioid receptor ( K i : 1.11 nM), displays reasonable affinities for kappa 3 binding sites, with K i value between 20 and 30 nM. Endomorphin 1 acetate has antinociceptive properties
Storage
Protected from light, Argon charged, Desiccated, Store at -80°C
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Action Type
AGONIST
Purity
≥99%
Names and Identifiers
Molecular Weight 670.75

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
SolubilityDMSO : 125 mg/mL (186.36 mM; Need ultrasonic)
Solution Calculators
Reviews

Customer Reviews

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