Cytochalasin K
AlkaPlorer ID: AK294168
Synonym: Cytochalasin Kasp
IUPAC Name: 18-benzyl-7,14-dihydroxy-7,9,15,16-tetramethyl-2,4-dioxa-19-azatricyclo[11.7.0.01,17]icosa-5,11,15-triene-3,8,20-trione
Structure
SMILES: CC1=C(C)C2C(CC3=CC=CC=C3)N=C(O)C23OC(=O)OC=CC(C)(O)C(=O)C(C)CC=CC3C1O
InChI: InChI=1S/C28H33NO7/c1-16-9-8-12-20-23(30)18(3)17(2)22-21(15-19-10-6-5-7-11-19)29-25(32)28(20,22)36-26(33)35-14-13-27(4,34)24(16)31/h5-8,10-14,16,20-23,30,34H,9,15H2,1-4H3,(H,29,32)
InChIKey: WDDZJZXADGVZLS-UHFFFAOYSA-N
Reference
Characterization of Mycotypha Metabolites Found to be Inhibitors of Cell Adhesion Molecules.
PubChem CID: 75051784
LOTUS: LTS0111045
COCONUT: CNP0216005.6
Source
| Species | Genus | Family | Order | Class | Phylum | Kingdom | Domain |
|---|---|---|---|---|---|---|---|
| Aspergillus clavatus | Aspergillus | Aspergillaceae | Eurotiales | Eurotiomycetes | Ascomycota | Fungi | Eukaryota |
| None | Arthrinium | Apiosporaceae | Xylariales | Sordariomycetes | Ascomycota | Fungi | Eukaryota |
Properties Information
Molecule Weight: 495.5720000000002
TPSA？: 125.65000000000002
MolLogP？: 3.832900000000002
Number of H-Donors: 3
Number of H-Acceptors: 7
RingCount: 4
Activities Information
| Organism | Target Name | Standard Type | Standard Value | Standard Units | doi |
|---|