The store will not work correctly when cookies are disabled.
JavaScript seems to be disabled in your browser. For the best experience on our site, be sure to turn on Javascript in your browser.
Meroantarctine C ID: ALA5219164
Chembl Id: CHEMBL5219164
PubChem CID: 168298110
Max Phase: Preclinical
Molecular Formula: C25H32O9
Molecular Weight: 476.52
Associated Items:
Names and Identifiers Canonical SMILES: COC(=O)[C@H]1C(=O)O[C@]2(/C=C(\C)C(C)=O)[C@]34CC[C@H](OC(C)=O)C(C)(C)[C@H]3[C@H](C[C@]12C)OC4=O
Standard InChI: InChI=1S/C25H32O9/c1-12(13(2)26)10-25-23(6,17(19(28)31-7)20(29)34-25)11-15-18-22(4,5)16(32-14(3)27)8-9-24(18,25)21(30)33-15/h10,15-18H,8-9,11H2,1-7H3/b12-10+/t15-,16-,17-,18+,23+,24+,25-/m0/s1
Standard InChI Key: LUOQRFJKUAAOQC-FDHYQUGASA-N
Associated Targets(Human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Topical: 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: 476.52Molecular Weight (Monoisotopic): 476.2046AlogP: 2.30#Rotatable Bonds: 4Polar Surface Area: 122.27Molecular Species: NEUTRALHBA: 9HBD: 0#RO5 Violations: 0HBA (Lipinski): 9HBD (Lipinski): 0#RO5 Violations (Lipinski): 0CX Acidic pKa: CX Basic pKa: CX LogP: 2.30CX LogD: 2.30Aromatic Rings: 0Heavy Atoms: 34QED Weighted: 0.26Np Likeness Score: 2.18
References 1. Leshchenko EV, Antonov AS, Dyshlovoy SA, Berdyshev DV, Hauschild J, Zhuravleva OI, Borkunov GV, Menshov AS, Kirichuk NN, Popov RS, Gerasimenko AV, Udovenko AA, Graefen M, Bokemeyer C, von Amsberg G, Yurchenko AN.. (2022) Meroantarctines A-C, Meroterpenoids with Rearranged Skeletons from the Alga-Derived Fungus Penicillium antarcticum KMM 4685 with Potent p-Glycoprotein Inhibitory Activity., 85 (12.0): [PMID:36413729 ] [10.1021/acs.jnatprod.2c00677 ]