LMD-009 - 10mM in DMSO , CAS No.950195-51-4

CAS: 950195-51-4 Cat. No.: L656840 Molecular Weight: 471.59 PubChem CID: 91032188
AVAILABLE TO ORDER
GRADE & PURITY 10mM in DMSO
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Size
Status
Price
Qty
1ml
L656840-1ml
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$788.90
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

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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

LMD-009 is a selective CCR8 nonpeptide agonist. LMD-009 mediates chemotaxis, inositol phosphate accumulation, and calcium release in high potencies with EC 50 s from 11 to 87 nM

In Vitro

LMD-009 (0-20 nM; 90 min) stimulates inositol phosphate accumulation in COS-7 cells expressing the human CCR8 receptor. LMD-009 (0-100 nM; 1 h) mediates calcium release in Chinese hamster ovary cells. LMD-009 (0.1 nM-100 μM; 40 min) induces L1.2 cells migration. LMD-009 (0-10 μM; 90 min) exhibits different molecular interaction with CCR8 mutations in COS-7 cells. LMD-009 (0-10 nM; 90 min) exhibits no antagonist activity to other human chemokine receptors. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Cell Viability AssayCell Line: COS-7 cells Concentration: 0-20 nM Incubation Time: 90 min Result: Stimulated inositol phosphate accumulation in COS-7 cells expressing the human CCR8 receptor with an EC 50 value of 11 nM. Inhibited none of the receptors of other human chemokine receptors. Cell Viability AssayCell Line: Chinese hamster ovary cells Concentration: 0-100 nM Incubation Time: 1 hour Result: Regulated calcium release in Chinese hamster ovary cells with an EC 50 value 87 nM. Cell Migration AssayCell Line: Lymphocyte L1.2 cells. Concentration: 0.1 nM- 100 μM Incubation Time: 40 min Result: Exhibited an K i value of 66 nM with L1.2 cells and specifically bound 125 I-CCL1.

IC50& Target:CCR8 11-87 nM (EC 50 )

Specifications

Specifications & Purity
10mM in DMSO
Biochemical and Physiological Mechanisms
LMD-009 is a selective CCR8 nonpeptide agonist. LMD-009 mediates chemotaxis, inositol phosphate accumulation, and calcium release in high potencies with EC 50 s from 11 to 87 nM.
Storage
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
Names and Identifiers
Isomeric SMILES COC1=CC=CC=C1OC2=CC=CC(=C2)CN3CCC4(CC3)C(=O)NCN4CCC5=CC=CC=C5
PubChem CID 91032188
Molecular Weight 471.59

Documentation

📋 Safety Data Sheet (SDS)

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

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✅ Certificate of Analysis (COA)

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

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📊 Datasheet

Quick-reference summary of product specifications and applications.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Solution Calculators
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