Przejdź do zawartości
Merck

C6628

Chloroquine diphosphate salt

98.5-101.0% (EP), powder or crystals, autophagy inhibitor, meets EP testing specifications

Synonim(y):

N4-(7-chloroquinolin-4-yl)-N1,N1-diethylpentane-1,4-diamine diphosphate, N4-(7-Chloro-4-quinolinyl)-N1,N1-dimethyl-1,4-pentanediamine diphosphate salt

Zaloguj się, aby wyświetlić ceny organizacyjne i kontraktowe.

Wybierz wielkość

25 G

310,00 zł

50 G

579,00 zł

100 G

1050,00 zł

250 G

1880,00 zł

310,00 zł


Skontaktuj się z Obsługą Klienta, aby uzyskać informacje na temat dostępności

Zamów zamówienie zbiorcze

Informacje o tej pozycji

Wzór empiryczny (zapis Hilla):
C18H26ClN3 · 2H3PO4
Numer CAS:
Masa cząsteczkowa:
515.86
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352107
EC Number:
200-055-2
MDL number:
Beilstein/REAXYS Number:
4223142
Assay:
98.5-101.0% (EP)
Form:
powder or crystals
Quality level:

Przejdź do

Pomoc techniczna
Potrzebujesz pomocy? Nasz zespół doświadczonych naukowców chętnie Ci pomoże.
Pozwól nam pomóc

Nazwa produktu

Chloroquine diphosphate salt, powder or crystals, 98.5-101.0% (EP), meets EP testing specifications

Quality Level

agency

meets EP testing specifications

assay

98.5-101.0% (EP)

form

powder or crystals

mp

192-198 °C

antibiotic activity spectrum

parasites

mode of action

enzyme | inhibits

SMILES string

OP(O)(O)=O.OP(O)(O)=O.CCN(CC)CCCC(C)Nc1ccnc2cc(Cl)ccc12

InChI

1S/C18H26ClN3.2H3O4P/c1-4-22(5-2)12-6-7-14(3)21-17-10-11-20-18-13-15(19)8-9-16(17)18;2*1-5(2,3)4/h8-11,13-14H,4-7,12H2,1-3H3,(H,20,21);2*(H3,1,2,3,4)

InChI key

QKICWELGRMTQCR-UHFFFAOYSA-N

Gene Information

human ... ABCC1(4363)

Porównaj podobne pozycje

Wyświetl pełne porównanie

Pokaż różnice

1 of 4

Ta pozycja
1118000C7874BP1101
assay

98.5-101.0% (EP)

assay

-

assay

≥98% (HPLC)

assay

-

form

powder or crystals

form

powder

form

powder

form

solid

Quality Level

200

Quality Level

-

Quality Level

100

Quality Level

-

mp

192-198 °C

mp

200 °C (dec.) (lit.)

mp

-

mp

238-241 °C

antibiotic activity spectrum

parasites

antibiotic activity spectrum

-

antibiotic activity spectrum

-

antibiotic activity spectrum

-

mode of action

enzyme | inhibits

mode of action

-

mode of action

-

mode of action

-

General description

Chloroquine effectively eliminates the erythrocytic forms of malaria parasites at all developmental stages, although it does not impact the sporozoites. It also functions as an antibiotic. In addition, it can be utilized at a concentration of 200 mg/mL (PBS, pH 5.0) to dissociate antigen-antibody complexes without denaturing red blood cell antigens. Recent research indicates chloroquine′s potential as an antitumor medication for cancer treatment along with chemotherapy and radiation. Its antimalarial effects are achieved by inhibiting the polymerization of heme into hemozoin, which serves as a food source for the malarial parasite. Chloroquine forms a complex with the drug-hemozoin, capping the polymerizing chain and preventing further polymerization. As a result, free heme accumulates in the food vacuole, exerting toxic effects on the parasite. Additionally, chloroquine acts as an anti-autoimmune therapy by binding to transcriptional factors on T helper 17 cells and inhibiting their differentiation. Chloroquine diphosphate (CQ) is frequently employed as an inhibitor of the autophagic pathway. The combined use of chloroquine diphosphate and salidroside initiates apoptosis in human liver cells by modulating mitochondrial dysfunction and autophagy.
Chloroquine is a member of quinolone family and is a weak intercalating agent. Chloroquine is used for treating amebiasis, rheumatoid arthritis, discoid and systemic lupus erythematosus.

Application

DNA intercalator. Also used to increase transfection efficiency.
Chloroquine diphosphate salt has been used :
  • in in vitro antiplasmodial assays
  • in transfection and infection assays
  • in autophagy inhibition
  • in differentiation of induced pluripotent stem (iPS) cells into cardiomyocytes
  • in flow treatment of infected blood

Biochem/physiol Actions

Standard anti-malarial drug. Substrate for MRP in multidrug resistant cell line and inhibits photoaffinity labeling of MRP by quinoline-based photoactive drug IAAQ (N-[4-[1-hydroxy-2-(dibutylamino)ethyl]quinolin-8-yl]-4-azidosalicylamide).

Features and Benefits

This compound is a featured product for ADME Tox research. Click here to discover more featured ADME Tox products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.
Ta strona może zawierać tekst przetłumaczony maszynowo.

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Klasa składowania

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


Wybierz jedną z najnowszych wersji:

Certyfikaty analizy (CoA)

Lot/Batch Number

Nie widzisz odpowiedniej wersji?

Jeśli potrzebujesz konkretnej wersji, możesz wyszukać konkretny certyfikat według numeru partii lub serii.

Masz już ten produkt?

Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Screening of medicinal plants from Reunion Island for antimalarial and cytotoxic activity
Jonville MC, et al.
Journal of Ethnopharmacology, 120(3), 382-386 (2008)
E2F1 modulates p38 MAPK phosphorylation via transcriptional regulation of ASK1 and Wip1
Hershko T, et al.
The Journal of Biological Chemistry, 281(42), 31309-31316 (2006)
Ototoxicity of chloroquine
Matz GJ and Naunton RF
Archives of Otolaryngology, 88(4), 370-372 (1968)
Ecotoxicological evaluation of the antimalarial drug chloroquine
Zurita JL, et al.
Aquatic Toxicology (Amsterdam, Netherlands), 75(2), 97-107 (2005)
Mechanism of inhibition of DNA gyrase by analogues of nalidixic acid: the target of the drugs is DNA
Shen LL and Pernet AG
Proceedings of the National Academy of Sciences of the USA, 82(2), 307-311 (1985)

Produkty

Discover Bioactive Small Molecules for ADME/Tox

Protein-based drug transporters are expressed in Sf9 cells. Understanding the specific mechanisms of tumor cell transporters is an essential aspect of chemotherapeutic drug design.

We presents an article on Autophagy in Cancer Promotes Therapeutic Resistance

Powiązane treści

Numer pozycji handlu globalnego

SKUNUMER GTIN
C6628-100G04061833511398
C6628-250G04061833629246
C6628-25G04061833511404
C6628-50G04061833511411

Questions

1–4 of 4 Questions  
  1. How should I store the product in powder? Ambient temperature?

    1 answer
    1. Yes, this product in powdered format should be stored in ambient temperature.

      Helpful?

  2. In primary neuron culture, what concentration is used for chloroquine and what solvent is used to dissolve it?

    1 answer
    1. Per “Preparation Instructions” in the Data Sheet, Chloroquine diphosphate salt is soluble in water (50 mg/mL).
      https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/documents/564/826/c6628dat-ms.pdf

      For more guidance on use in cell culture applications, we kindly ask you to navigate to the link https://www.sigmaaldrich.com/techservice, click on "Product Technical Inquires" under the Products Section with all the required information so that a member of our team can reach out to you to assist further. Thank you.

      Helpful?

  3. salve per la sua preparazione, in che soluzione si deve sciogliere ?

    1 answer
    1. This product is soluble at 50 mg/mL in water. Please see the link below to review the product datasheet:
      https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/documents/564/826/c6628dat-ms.pdf

      Helpful?

  4. How should I store stock solutions of this product? For how long should I store?

    1 answer
    1. Stock solutions should be protected from light and may be stored at 4 °C or in aliquots at -20 °C. The time frame for solution storage has not been determined.

      Please see the link below to review the product datasheet:
      https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/documents/564/826/c6628dat-ms.pdf

      Helpful?

Reviews

No rating value

Active Filters

Nasz zespół naukowców ma doświadczenie we wszystkich obszarach badań, w tym w naukach przyrodniczych, materiałoznawstwie, syntezie chemicznej, chromatografii, analityce i wielu innych dziedzinach.

Skontaktuj się z zespołem ds. pomocy technicznej