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Clinical data | |
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AHFS/ Drugs.com | International Drug Names |
Routes of administration | IV |
ATC code | |
Legal status | |
Legal status |
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Identifiers | |
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CAS Number | |
PubChem CID | |
ChemSpider | |
UNII | |
KEGG | |
ChEBI | |
ChEMBL | |
CompTox Dashboard ( EPA) | |
ECHA InfoCard | 100.055.277 |
Chemical and physical data | |
Formula | C42H53NO15 |
Molar mass | 811.878 g·mol−1 |
3D model ( JSmol) | |
Melting point | 151 to 153 °C (304 to 307 °F) (decomposes) |
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Aclarubicin ( INN) or aclacinomycin A [1] is an anthracycline drug [2] that is used in the treatment of cancer. Soil bacteria Streptomyces galilaeus can produce aclarubicin. It can induce histone eviction from chromatin upon intercalation. [3] [4]
![]() | |
Clinical data | |
---|---|
AHFS/ Drugs.com | International Drug Names |
Routes of administration | IV |
ATC code | |
Legal status | |
Legal status |
|
Identifiers | |
| |
CAS Number | |
PubChem CID | |
ChemSpider | |
UNII | |
KEGG | |
ChEBI | |
ChEMBL | |
CompTox Dashboard ( EPA) | |
ECHA InfoCard | 100.055.277 |
Chemical and physical data | |
Formula | C42H53NO15 |
Molar mass | 811.878 g·mol−1 |
3D model ( JSmol) | |
Melting point | 151 to 153 °C (304 to 307 °F) (decomposes) |
| |
| |
![]() ![]() |
Aclarubicin ( INN) or aclacinomycin A [1] is an anthracycline drug [2] that is used in the treatment of cancer. Soil bacteria Streptomyces galilaeus can produce aclarubicin. It can induce histone eviction from chromatin upon intercalation. [3] [4]