Amsacrine

For research use only. Not for therapeutic Use.

  • CAT Number: I003839
  • CAS Number: 51264-14-3
  • Molecular Formula: C21H19N3O3S
  • Molecular Weight: 393.46
  • Purity: ≥95%
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Amsacrine(Cat No.:I003839), also known as mAMSA, is an antineoplastic agent utilized in cancer treatment. It exerts its therapeutic effects by intercalating into the DNA of tumor cells, disrupting DNA replication and transcription processes. Additionally, amsacrine functions as a topoisomerase II inhibitor, preventing the enzyme from properly managing DNA supercoiling and leading to DNA damage and cell death. The combined actions of DNA intercalation and topoisomerase II inhibition contribute to the cytotoxic effects of amsacrine, making it effective in the treatment of certain types of cancer.


Catalog Number I003839
CAS Number 51264-14-3
Synonyms

N-[4-(acridin-9-ylamino)-3-methoxyphenyl]methanesulfonamide

Molecular Formula C21H19N3O3S
Purity ≥95%
Target Topoisomerase
Solubility DMSO: ≤ 9.3 mg/mL
Storage 2-8°C(protect from light)
IUPAC Name N-[4-(acridin-9-ylamino)-3-methoxyphenyl]methanesulfonamide
InChI InChI=1S/C21H19N3O3S/c1-27-20-13-14(24-28(2,25)26)11-12-19(20)23-21-15-7-3-5-9-17(15)22-18-10-6-4-8-16(18)21/h3-13,24H,1-2H3,(H,22,23)
InChIKey XCPGHVQEEXUHNC-UHFFFAOYSA-N
SMILES COC1=C(C=CC(=C1)NS(=O)(=O)C)NC2=C3C=CC=CC3=NC4=CC=CC=C42
Reference

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<br>[1]. Kanellis J, et al. JNK signalling in human and experimental renal ischaemia/reperfusion injury. Nephrol Dial Transplant. 2010 Sep;25(9):2898-908.
<br>[2]. Thomas D, et al. Inhibition of cardiac HERG currents by the DNA topoisomerase II inhibitor amsacrine: mode of action. Br J Pharmacol. 2004 Jun;142(3):485-94.
<br>[3]. Attia SM. Molecular cytogenetic evaluation of the mechanism of genotoxic potential of amsacrine and nocodazole in mouse bone marrow cells. J Appl Toxicol. 2013 Jun;33(6):426-33.
<br>[4]. Kao-Shan CS, et al. Cytogenetic effects of amsacrine on human lymphocytes in vivo and in vitro. Cancer Treat Rep. 1984 Jul-Aug;68(7-8):989-97.
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