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Gageopeptide D ID: ALA5273349
Chembl Id: CHEMBL5273349
Max Phase: Preclinical
Molecular Formula: C38H70N4O9
Molecular Weight: 727.00
Associated Items:
Names and Identifiers Canonical SMILES: CCC(C)CC(C)CCCCC[C@@H](O)CC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)O
Standard InChI: InChI=1S/C38H70N4O9/c1-10-26(8)21-27(9)14-12-11-13-15-28(43)22-33(44)39-30(18-23(2)3)36(48)40-29(16-17-34(45)46)35(47)41-31(19-24(4)5)37(49)42-32(38(50)51)20-25(6)7/h23-32,43H,10-22H2,1-9H3,(H,39,44)(H,40,48)(H,41,47)(H,42,49)(H,45,46)(H,50,51)/t26?,27?,28-,29+,30+,31+,32+/m1/s1
Standard InChI Key: UZGWGZSRLAITPB-SMSJGLPFSA-N
Associated Targets(non-human) Molecule Features Natural Product: YesOral: 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: 727.00Molecular Weight (Monoisotopic): 726.5143AlogP: 4.79#Rotatable Bonds: 28Polar Surface Area: 211.23Molecular Species: ACIDHBA: 7HBD: 7#RO5 Violations: 2HBA (Lipinski): 13HBD (Lipinski): 7#RO5 Violations (Lipinski): 3CX Acidic pKa: 3.67CX Basic pKa: CX LogP: 5.53CX LogD: -0.81Aromatic Rings: 0Heavy Atoms: 51QED Weighted: 0.06Np Likeness Score: 0.60
References 1. El-Hossary EM, Cheng C, Hamed MM, Hamed MM, El-Sayed Hamed AN, Ohlsen K, Hentschel U, Abdelmohsen UR.. (2017) Antifungal potential of marine natural products., 126 [PMID:27936443 ] [10.1016/j.ejmech.2016.11.022 ]