aclarubicin
chemical compound
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aclarubicin
Summary
aclarubicin is a type of chemical entity[1]. aclarubicin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (3 views/month).[2]
Key Facts
- aclarubicin's instance of is recorded as type of chemical entity[3].
- aclarubicin's canonical SMILES is recorded as CCC1(CC(C2=C(C1C(=O)OC)C=C3C(=C2O)C(=O)C4=C(C3=O)C=CC=C4O)OC5CC(C(C(O5)C)OC6CC(C(C(O6)C)OC7CCC(=O)C(O7)C)O)N(C)C)O[4].
- aclarubicin's chemical formula is recorded as C₄₂H₅₃NO₁₅[5].
- aclarubicin is a type of methyl (1R,2R,4S)-4-[(2R,5S,6S)-4-(dimethylamino)-5-[(2S,4S,5S,6S)-4-hydroxy-6-methyl-5-[(2R,6S)-6-methyl-5-oxooxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxan-2-yl]oxy-2-ethyl-2,5,7-trihydroxy-6,11-dioxo-3,4-dihydro-1H-tetracene-1-carboxylate[6].
- aclarubicin is used for medication[7].
- aclarubicin's found in taxon is recorded as Streptomyces galilaeus[8].
- aclarubicin's found in taxon is recorded as Micromonospora[9].
- aclarubicin's NCI Thesaurus ID is recorded as C202[10].
- aclarubicin's isomeric SMILES is recorded as CC[C@@]1(O)CC@HC5=C(C=C6C(=O)C7=C(C(O)=CC=C7)C(=O)C6=C5O)[C@H]1C(=O)OCC@HC5=C(C=C6C(=O)C7=C(C(O)=CC=C7)C(=O)C6=C5O)[C@H]">[11].
- aclarubicin's mass is recorded as {'unit': 'Q483261', 'amount': '+811.341519996'}[12].
- aclarubicin's subject has role is recorded as antineoplastic antibiotics[13].
- aclarubicin's subject has role is recorded as topoisomerase II inhibitor[14].
- aclarubicin's stereoisomer of is recorded as Methyl 2-ethyl-2,5,7-trihydroxy-6,11-dioxo-4-({2,3,6-trideoxy-4-O-[2,6-dideoxy-4-O-(6-methyl-5-oxooxan-2-yl)hexopyranosyl]-3-(dimethylamino)hexopyranosyl}oxy)-1,2,3,4,6,11-hexahydrotetracene-1-carboxy late[15].
Why It Matters
aclarubicin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (3 views/month).[2] aclarubicin has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[16]