Merck
  • SML2577
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SML2577

Sigma-Aldrich

Pixantrone dimaleate

≥98% (HPLC)

Synonym(s):
2-Azaanthracene-9,10-dione dimaleate, 6,9-Bis[(2-aminoethyl)amino]benzo[g]isoquinoline-5,10-dione dimaleate, BBR 2778, BBR-2778, BBR2778, Pixantrone maleate
Empirical Formula (Hill Notation):
C17H19N5O2 · C8H8O8
CAS Number:
Molecular Weight:
557.51
Numer MDL:

próba

≥98% (HPLC)

forma

powder

warunki przechowywania

desiccated

kolor

purple to dark blue

rozpuszczalność

H2O: 2 mg/mL, clear

temp. przechowywania

2-8°C

InChI

1S/C17H19N5O2.2C4H4O4/c18-4-7-21-12-1-2-13(22-8-5-19)15-14(12)16(23)10-3-6-20-9-11(10)17(15)24;2*5-3(6)1-2-4(7)8/h1-3,6,9,21-22H,4-5,7-8,18-19H2;2*1-2H,(H,5,6)(H,7,8)/b;2*2-1+

InChI key

SVAGFBGXEWPNJC-LVEZLNDCSA-N

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Pixantrone dimaleate ≥98% (HPLC)

Sigma-Aldrich

SML2577

Pixantrone dimaleate

Pilocarpine nitrate meets USP testing specifications

Sigma-Aldrich

P0597

Pilocarpine nitrate

Pilocarpine nitrate meets USP testing specifications

Sigma-Aldrich

P0597

Pilocarpine nitrate

Pilocarpine nitrate British Pharmacopoeia (BP) Reference Standard

BP503

Pilocarpine nitrate

assay

≥98% (HPLC)

assay

-

assay

-

assay

-

form

powder

form

crystals

form

crystals

form

-

storage condition

desiccated

storage condition

-

storage condition

-

storage condition

-

color

purple to dark blue

color

-

color

-

color

-

solubility

H2O: 2 mg/mL, clear

solubility

-

solubility

-

solubility

-

storage temp.

2-8°C

storage temp.

-

storage temp.

-

storage temp.

2-8°C

Działania biochem./fizjol.

Pixantrone (BBR 2778) is an aza-anthracenedione with enhanced antitumor activity due to its DNA-intercalating and topoisomerase II-poisoning activity. Pixantrone shows no signs of acute or delayed cardiotoxicity seen with anthracyclines mitoxantrone and doxorubicin (DOX), while exhibiting comparable in vivo efficacy against solid tumors in mice. Tests conducted on human myocardial strips ex vivo shows that not only pixantrone does not form superoxide anion and hydrogen peroxide (O2•− and H2O2) seen with DOX due to redox activation, pixantrone and its metabolites, especially N-dealkylated, show competitive inhibition against DOX reduction. While mitoxantrone does not form O2•− and H2O2 on its own, it synergizes with DOX to form more O2•− and H2O2, whose formation and subsequent production of the long-lived metabolite doxorubicinol contribute to DOX cardiotoxicity.

piktogramy

Health hazard

Hasło ostrzegawcze

Warning

Zwroty wskazujące rodzaj zagrożenia

Zwroty wskazujące środki ostrożności

Klasyfikacja zagrożeń

Muta. 2 - Repr. 2

Kod klasy składowania

13 - Non Combustible Solids

WGK

WGK 3

Temperatura zapłonu °F

Not applicable

Temperatura zapłonu °C

Not applicable

Certificate of Analysis

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Certificate of Origin

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