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Meroantarctine A ID: ALA5218977
Chembl Id: CHEMBL5218977
PubChem CID: 168299527
Max Phase: Preclinical
Molecular Formula: C27H34O8
Molecular Weight: 486.56
Associated Items:
Names and Identifiers Canonical SMILES: COC(=O)[C@@]1(C(=O)C(C)=O)C(C)=C(C)C=C2[C@]34CC[C@H](OC(C)=O)C(C)(C)[C@H]3[C@H](C[C@@]21C)OC4=O
Standard InChI: InChI=1S/C27H34O8/c1-13-11-18-25(7,27(14(13)2,23(32)33-8)21(30)15(3)28)12-17-20-24(5,6)19(34-16(4)29)9-10-26(18,20)22(31)35-17/h11,17,19-20H,9-10,12H2,1-8H3/t17-,19-,20+,25-,26+,27-/m0/s1
Standard InChI Key: FWFOPDKYJQYRCZ-MFQZQTJMSA-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: 486.56Molecular Weight (Monoisotopic): 486.2254AlogP: 3.27#Rotatable Bonds: 4Polar Surface Area: 113.04Molecular Species: NEUTRALHBA: 8HBD: 0#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 0#RO5 Violations (Lipinski): 0CX Acidic pKa: CX Basic pKa: CX LogP: 3.07CX LogD: 3.07Aromatic Rings: 0Heavy Atoms: 35QED Weighted: 0.26Np Likeness Score: 2.17
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 ]