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Dendryphiellin I ID: ALA4160097
Chembl Id: CHEMBL4160097
PubChem CID: 139590020
Max Phase: Preclinical
Molecular Formula: C25H32O5
Molecular Weight: 412.53
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: C=C(C=O)[C@]1(O)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/C25H32O5/c1-7-16(2)12-17(3)8-11-23(28)30-21-10-9-20-13-22(27)25(29,18(4)14-26)15-24(20,6)19(21)5/h8-14,16,19,21,29H,4,7,15H2,1-3,5-6H3/b11-8+,17-12+/t16-,19-,21-,24+,25+/m0/s1
Standard InChI Key: DPMXZAGDKLVQHB-SSTGVLRWSA-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: 412.53Molecular Weight (Monoisotopic): 412.2250AlogP: 4.04#Rotatable Bonds: 7Polar Surface Area: 80.67Molecular Species: NEUTRALHBA: 5HBD: 1#RO5 Violations: 0HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski): 0CX Acidic pKa: 12.28CX Basic pKa: CX LogP: 4.49CX LogD: 4.49Aromatic Rings: 0Heavy Atoms: 30QED Weighted: 0.30Np Likeness Score: 3.08
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 ]