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Antimycin A8a ID: ALA4290816
Chembl Id: CHEMBL4290816
PubChem CID: 9984612
Max Phase: Preclinical
Molecular Formula: C27H38N2O9
Molecular Weight: 534.61
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: CCC(C)C(=O)O[C@H]1[C@H](C)OC(=O)[C@@H](NC(=O)c2cccc(NC=O)c2O)[C@@H](C)OC(=O)[C@@H]1CCC(C)C
Standard InChI: InChI=1S/C27H38N2O9/c1-7-15(4)25(33)38-23-17(6)37-27(35)21(16(5)36-26(34)19(23)12-11-14(2)3)29-24(32)18-9-8-10-20(22(18)31)28-13-30/h8-10,13-17,19,21,23,31H,7,11-12H2,1-6H3,(H,28,30)(H,29,32)/t15?,16-,17+,19-,21+,23+/m1/s1
Standard InChI Key: QPFFQZIETBZFRR-QSFRASQOSA-N
Associated Targets(non-human) Molecule Features Natural Product: YesOral: 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: 534.61Molecular Weight (Monoisotopic): 534.2577AlogP: 2.95#Rotatable Bonds: 10Polar Surface Area: 157.33Molecular Species: NEUTRALHBA: 9HBD: 3#RO5 Violations: 1HBA (Lipinski): 11HBD (Lipinski): 3#RO5 Violations (Lipinski): 2CX Acidic pKa: 7.51CX Basic pKa: ┄CX LogP: 4.60CX LogD: 4.36Aromatic Rings: 1Heavy Atoms: 38QED Weighted: 0.18Np Likeness Score: 1.06
References 1. Granchi C.. (2018) ATP citrate lyase (ACLY) inhibitors: An anti-cancer strategy at the crossroads of glucose and lipid metabolism., 157 [PMID:30195238 ] [10.1016/j.ejmech.2018.09.001 ]