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Merck

Q3251

Quinacrine dihydrochloride

≥90% (TLC), powder, MAO-A/B inhibitor

Synonyme(s) :

6-Chloro-9-(4-diethylamino-1-methylbutylamino)-2-methoxyacridine dihydrochloride, Atebrin dihydrochloride, Mepacrine dihydrochloride

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A propos de cet article

Formule empirique (notation de Hill) :
C23H30ClN3O · 2HCl
Numéro CAS:
Poids moléculaire :
472.88
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352101
EC Number:
200-700-8
MDL number:
Beilstein/REAXYS Number:
4834013
Assay:
≥90%
Form:
powder
Quality level:
Service technique
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Nom du produit

Quinacrine dihydrochloride, ≥90%

biological source

synthetic

Quality Level

assay

≥90%

form

powder

mp

257 °C

solubility

H2O: soluble, clear to hazy

originator

Bayer

SMILES string

Cl[H].Cl[H].CCN(CC)CCCC(C)Nc1c2ccc(Cl)cc2nc3ccc(OC)cc13

InChI

1S/C23H30ClN3O.2ClH/c1-5-27(6-2)13-7-8-16(3)25-23-19-11-9-17(24)14-22(19)26-21-12-10-18(28-4)15-20(21)23;;/h9-12,14-16H,5-8,13H2,1-4H3,(H,25,26);2*1H

InChI key

UDKVBVICMUEIKS-UHFFFAOYSA-N

Gene Information

General description

Quinacrine is an acridine derivative and a potent antimalarial agent.

Application

Quinacrine dihydrochloride has been used:
  • in its uptake and accumulation studies in mouse lung slices using fluorescence microscope
  • in the staining of ATP vesicles in mesenchymal stem cells (MSCs)
  • in uptake-release assay for characterization of dense granule functionality of platelets

Biochem/physiol Actions

Non-selective MAO-A/B inhibitor.
Quinacrine has anthelmintic functionality and used in the female sterilization. It is used to treat systemic lupus erythematosus and rheumatic diseases. Apart from malaria, Quinacrine is effective for treating giardia and tapeworm infections. It inhibits nicotinamide adenine dinucleotide phosphate (NADPH) oxidase activity in addition to monoamine oxidase inhibition.

Features and Benefits

This compound was developed by Bayer. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

Preparation Note

Stock solutions are stable for up to 60 h at 20°C.

Other Notes

This product is not assigned an expiration date or recommended retest date.


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Hazard Classifications

Acute Tox. 4 Oral

Classe de stockage

11 - Combustible Solids

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WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves



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Contenu apparenté

Product Information Sheet


Denise De Zanet et al.
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A new biosensor for the real-time analysis of thrombus formation is reported. The fast and accurate monitoring of the individual thrombotic risk represents a challenge in cardiovascular diagnostics and in treatment of hemostatic diseases. Thrombus volume, as representative index of
Abnormal differentiation of B cells and megakaryocytes in patients with Roifman syndrome
Heremans J, et al.
The Journal of Allergy and Clinical Immunology, 142(2), 630-646 (2018)
Mayur Nimbadas Devare et al.
Aging cell, 19(6), e13151-e13151 (2020-05-26)
Glucose controls the phosphorylation of silent information regulator 2 (Sir2), a NAD+ -dependent protein deacetylase, which regulates the expression of the ATP-dependent proton pump Pma1 and replicative lifespan (RLS) in yeast. TORC1 signaling, which is a central regulator of cell