Structure via PubChem · Public domain (PubChem)
Chemical data
- Formula
- C62H87N13O16
- Molecular weight
- 1270.4 g/mol
- IUPAC name
- 2,7-diamino-4,6-dimethyl-3-oxo-1-N,9-N-bis[(3R,6S,7R,10S,16S)-7,11,14-trimethyl-2,5,9,12,15-pentaoxo-3,10-di(propan-2-yl)-8-oxa-1,4,11,14-tetrazabicyclo[14.3.0]nonadecan-6-yl]phenoxazine-1,9-dicarboxamide
- SMILES
- C[C@@H]1[C@@H](C(=O)N[C@@H](C(=O)N2CCC[C@H]2C(=O)N(CC(=O)N([C@H](C(=O)O1)C(C)C)C)C)C(C)C)NC(=O)C3=CC(=C(C4=C3N=C5C(=C(C(=O)C(=C5O4)C)N)C(=O)N[C@H]6[C@H](OC(=O)[C@@H](N(C(=O)CN(C(=O)[C@@H]7CCCN7C(=O)[C@H](NC6=O)C(C)C)C)C)C(C)C)C)C)N
- InChIKey
- YXHLJMWYDTXDHS-IRFLANFNSA-N
- XLogP
- 3.1
- Polar surface area
- 382 Ų
- H-bond donors
- 6
- H-bond acceptors
- 19
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
506 papers- Miltirone induces cell death in hepatocellular carcinoma cell through GSDME-dependent pyroptosis.Acta pharmaceutica Sinica. B · 2020
- 7-Aminoactinomycin D for apoptosis staining in flow cytometry.Analytical biochemistry · 2012
- Multiparametric flow cytometric analysis of biochemical and functional events associated with apoptosis and oncosis using the 7-aminoactinomycin D assay.Journal of immunological methods · 2002
- Location of 7-Aminoactinomycin D in Micellar Medium Depends on Ionic Nature of the Surfactant Head Group.Luminescence : the journal of biological and chemical luminescence · 2025
- Actinomycin D and 7-aminoactinomycin D binding to single-stranded DNA.Biochemistry · 1991
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 1269.639
Show 4 more facts
- chemical formula
- C₆₂H₈₇N₁₃O₁₆
- canonical SMILES
- CC1C(C(=O)NC(C(=O)N2CCCC2C(=O)N(CC(=O)N(C(C(=O)O1)C(C)C)C)C)C(C)C)NC(=O)C3=CC(=C(C4=C3N=C5C(=C(C(=O)C(=C5O4)C)N)C(=O)NC6C(OC(=O)C(N(C(=O)CN(C(=O)C7CCCN7C(=O)C(NC6=O)C(C)C)C)C)C(C)C)C)C)N
- isomeric SMILES
- C[C@@H]1[C@@H](C(=O)N[C@@H](C(=O)N2CCC[C@H]2C(=O)N(CC(=O)N([C@H](C(=O)O1)C(C)C)C)C)C(C)C)NC(=O)C3=CC(=C(C4=C3N=C5C(=C(C(=O)C(=C5O4)C)N)C(=O)N[C@H]6[C@H](OC(=O)[C@@H](N(C(=O)CN(C(=O)[C@@H]7CCCN7C(=O)[C@H](NC6=O)C(C)C)C)C)C(C)C)C)C)N
- subject has role
- fluorophore
Sources (1)
via Wikidata · CC0