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(2S)-N-[(2S)-1-[[(3S)-2-hydroxyoxolan-3-yl]amino]-4-methyl-1-oxopentan-2-yl]-4-methyl-2-[[2-(10H-phenothiazin-2-yl)acetyl]amino]pentanamide ID: ALA206235
Max Phase: Preclinical
Molecular Formula: C30H40N4O5S
Molecular Weight: 568.74
Molecule Type: Small molecule
Associated Items:
Representations Canonical SMILES: CC(C)C[C@H](NC(=O)Cc1ccc2c(c1)Nc1ccccc1S2)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H]1CCOC1O
Standard InChI: InChI=1S/C30H40N4O5S/c1-17(2)13-23(28(36)34-24(14-18(3)4)29(37)33-21-11-12-39-30(21)38)32-27(35)16-19-9-10-26-22(15-19)31-20-7-5-6-8-25(20)40-26/h5-10,15,17-18,21,23-24,30-31,38H,11-14,16H2,1-4H3,(H,32,35)(H,33,37)(H,34,36)/t21-,23-,24-,30?/m0/s1
Standard InChI Key: HHNHYEDODWWQEY-XIIWGJLCSA-N
Associated Targets(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
Properties Molecular Weight: 568.74Molecular Weight (Monoisotopic): 568.2719AlogP: 3.72#Rotatable Bonds: 11Polar Surface Area: 128.79Molecular Species: NEUTRALHBA: 7HBD: 5#RO5 Violations: 1HBA (Lipinski): 9HBD (Lipinski): 5#RO5 Violations (Lipinski): 1CX Acidic pKa: 11.65CX Basic pKa: CX LogP: 3.66CX LogD: 3.66Aromatic Rings: 2Heavy Atoms: 40QED Weighted: 0.24Np Likeness Score: -0.19
References 1. Auvin S, Pignol B, Navet E, Troadec M, Carré D, Camara J, Bigg D, Chabrier PE.. (2006) Novel dual inhibitors of calpain and lipid peroxidation with enhanced cellular activity., 16 (6): [PMID:16380258 ] [10.1016/j.bmcl.2005.12.036 ]