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Dendryphiellin J ID: ALA4171739
Chembl Id: CHEMBL4171739
PubChem CID: 145950063
Max Phase: Preclinical
Molecular Formula: C26H35NO5
Molecular Weight: 441.57
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: C=C(/C=N/O)[C@]1(OC)C[C@@]2(C)C(=CC1=O)C=C[C@H](OC(=O)/C=C/C(C)=C/[C@@H](C)CC)[C@@H]2C
Standard InChI: InChI=1S/C26H35NO5/c1-8-17(2)13-18(3)9-12-24(29)32-22-11-10-21-14-23(28)26(31-7,19(4)15-27-30)16-25(21,6)20(22)5/h9-15,17,20,22,30H,4,8,16H2,1-3,5-7H3/b12-9+,18-13+,27-15+/t17-,20-,22-,25+,26+/m0/s1
Standard InChI Key: HGOCAVZPSXRMSN-XRWLQZSQSA-N
Associated Targets(Human) Associated Targets(non-human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 441.57Molecular Weight (Monoisotopic): 441.2515AlogP: 4.96#Rotatable Bonds: 8Polar Surface Area: 85.19Molecular Species: NEUTRALHBA: 6HBD: 1#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 0CX Acidic pKa: 10.53CX Basic pKa: 2.60CX LogP: 5.14CX LogD: 5.14Aromatic Rings: 0Heavy Atoms: 32QED Weighted: 0.14Np Likeness Score: 2.38
References 1. Fang W, Wang J, Wang J, Shi L, Li K, Lin X, Min Y, Yang B, Tang L, Liu Y, Zhou X.. (2018) Cytotoxic and Antibacterial Eremophilane Sesquiterpenes from the Marine-Derived Fungus Cochliobolus lunatus SCSIO41401., 81 (6): [PMID:29786436 ] [10.1021/acs.jnatprod.8b00015 ]