Nemorubicin Chemical Properties

Boiling point:

852.2±65.0 °C(Predicted)

Density 

1.55±0.1 g/cm3(Predicted)

storage temp. 

Store at -20°C

solubility 

DMSO:60.0(Max Conc. mg/mL);101.0(Max Conc. mM)

pka

7.35±0.60(Predicted)

form 

Powder

color 

Orange to reddish brown

InChIKey

CTMCWCONSULRHO-UZGLGGDGNA-N

SMILES

C12C[C@@](C[C@]([H])(O[C@@H]3O[C@H]([C@@H](O)[C@@H](N4CCO[C@H](OC)C4)C3)C)C=1C(O)=C1C(=O)C3=C(OC)C=CC=C3C(=O)C1=C2O)(O)C(=O)CO |&1:2,4,7,9,10,12,17,r|

Nemorubicin Usage And Synthesis

Uses

Nemorubicin is a doxorubicin derivative that differs significantly from its parent drug in terms of spectrum of antitumor activity, metabolism and toxicity profile. The drug is active on tumors resistant to alkylating agents, topoisomerase II inhibitors and platinum derivatives. It works primarily through topoisomerase I inhibition. Of note, Nemorubicin is active in cells with upregulation of the nucleotide excision repair (NER) pathway, where current therapies fail. Nemorubicin is biotransformed in the liver into cytotoxic metabolites that may further contribute to render this drug highly active against primary liver tumors or liver metastases.

Definition

ChEBI: Nemorubicin is a member of morpholines, an anthracycline antibiotic, a primary alpha-hydroxy ketone and a tertiary alpha-hydroxy ketone. It is functionally related to a doxorubicin.

in vivo

target

cancer

Nemorubicin(108852-90-0)Related Product Information

• 1,8-Dihydroxyanthraquinone
• Adriamycin
• Doxorubicinone
• Nemorubicin
• Idarubicin
• Chrysophanic acid
• 2-Ethyl anthraquinone
• DIETHANOL PROPANOLAMINE
• N,N-BIS(2-HYDROXYETHYL)ISOPROPANOLAMINE
• 1,5-DIHYDROXYANTHRAQUINONE
• 2,4-DIMETHYL-2'-METHOXYBENZOPHENONE
• 2,4-DIMETHYL-3'-METHOXYBENZOPHENONE
• 2,5-DIMETHYL-3'-METHOXYBENZOPHENONE
• N-ETHYL-TETRAHYDRO-2H-PYRAN-4-AMINE
• 14-Hydroxy Carminomycin
• 2-METHOXY-3'-METHYLBENZOPHENONE
• ISLANDICIN
• Feudomycin A