Structure via PubChem · Public domain (PubChem)
Chemical data
- Formula
- C29H37NO5
- Molecular weight
- 479.6 g/mol
- IUPAC name
- (1S,4E,6R,10R,12E,14S,15S,17S,18S,19S)-19-benzyl-6,15-dihydroxy-10,17-dimethyl-16-methylidene-2-oxa-20-azatricyclo[12.7.0.01,18]henicosa-4,12-diene-3,21-dione
- SMILES
- C[C@@H]1CCC[C@H](/C=C/C(=O)O[C@]23[C@@H](/C=C/C1)[C@@H](C(=C)[C@H]([C@H]2[C@@H](NC3=O)CC4=CC=CC=C4)C)O)O
- InChIKey
- GBOGMAARMMDZGR-TYHYBEHESA-N
- XLogP
- 3.4
- Polar surface area
- 95.9 Ų
- H-bond donors
- 3
- H-bond acceptors
- 5
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
7,894 papers- Cytochalasin B, cytokinesis, and the contractile ring.Frontiers of biology · 1978
- Effects of cytochalasin B on endocytosis and exocytosis.Frontiers of biology · 1978
- Mitochondrial aggregation caused by cytochalasin B compromises the efficiency and safety of three-parent embryo.Molecular human reproduction · 2022
- Cytochalasin B induces cellular DNA fragmentation.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 1990
- Cytochalasin B reacts with thiols.FEBS letters · 1976
via PubMed
Wikidata facts
- Subclass of
- cytochalasin
- Mass
- 479.267173
Show 4 more facts
- found in taxon
- Phoma
- canonical SMILES
- CC1CCCC(C=CC(=O)OC23C(C=CC1)C(C(=C)C(C2C(NC3=O)CC4=CC=CC=C4)C)O)O
- isomeric SMILES
- C[C@@H]1CCC[C@H](/C=C/C(=O)O[C@]23[C@@H](/C=C/C1)[C@@H](C(=C)[C@H]([C@H]2[C@@H](NC3=O)CC4=CC=CC=C4)C)O)O
- chemical formula
- C₂₉H₃₇NO₅
via Wikidata · CC0