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GW405833 hydrochloride

SIGMA/G1421 - ≥98% (HPLC), solid

Synonym: 1-(2,3-Dichlorobenzoyl)-5-methoxy-2-methyl-(3-(morpholin-4-yl)ethyl)-1H-indole hydrochloride; 242 hydrochloride; L-768; L-768242 hydrochloride; L768242 hydrochloride; ML-SI1 hydrochloride

CAS Number: 180002-83-9
Empirical Formula (Hill Notation): C23H24Cl2N2O3 · HCl
Molecular Weight: 483.82
MDL Number: MFCD09832650
Linear Formula: C23H24Cl2N2O3 · HCl
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-G1421-5MG 5 mg
$143.00
1/EA
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45-G1421-25MG 25 mg
$611.00
1/EA
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assay ≥98% (HPLC)
color white to pink
drug control regulated under CDSA - not available from Sigma-Aldrich Canada
form solid
InChI 1S/C23H24Cl2N2O3.ClH/c1-15-17(8-9-26-10-12-30-13-11-26)19-14-16(29-2)6-7-21(19)27(15)23(28)18-4-3-5-20(24)22(18)25;/h3-7,14H,8-13H2,1-2H3;1H
InChI key JIQYDHDVNNFPMU-UHFFFAOYSA-N
Quality Level 100 
SMILES string Cl.COc1ccc2n(c(C)c(CCN3CCOCC3)c2c1)C(=O)c4cccc(Cl)c4Cl
solubility DMSO: soluble >10 mg/mL
  H2O: insoluble <2 mg/mL
storage condition desiccated
storage temp. 2-8°C
Application: GW405833 hydrochloride has been used as a lysosomal transient receptor potential mucolipin 1 (TRPML1) specific inhibitor to validate if TRPML1 mediates tau release in neurons and also to verify if it mediates the release of lysosomal tau. It has also been used as a TRPML channel blocker to study the effect of mucolipin transient receptor potential cation channel 3 (MCOLN3/TRPML3) function and trafficking on autophagy in HeLa cells.
Biochem/physiol Actions: GW405833 hydrochloride, also known as ML-SI1, is a cell-permeable lysosomal transient receptor potential cation channel, mucolipin subfamily (TRPML) blocker.
Biochem/physiol Actions: GW405833 is a selective cannabanoid CB2 receptor agonist; analgesic. GW405833 binds with high affinity at both human and rat CB2 receptors (Ki′s 3.9 and 3.6 nM); acts as a partial agonist (50% inhibition of forskolin-stimulated cAMP formation compared to full agonist CP55,940). GW405833 has potent analgesic activity in rat models of inflammatory, neuropathic and incisional pain; devoid of CNS effects common with CB1 agonists.
Biochem/physiol Actions: Selective cannabinoid CB2 receptor agonist; analgesic.
Features and Benefits: This compound is featured on the Cannabinoid Receptors  page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here .
Packaging: 5, 25 mg in glass bottle
Symbol GHS06  GHS06
Signal word Danger
Hazard statements H301 - H413
Precautionary statements P273 - P301 + P310 + P330
Hazard Codes T
Risk Statements 25
Safety Statements 45
RIDADR UN 2811 6.1 / PGIII
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥98% (HPLC)
Storage Temp. 2-8°C
UNSPSC 12352200

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