exo-N-[5-({3-[5-(Acetyl-hydroxy-amino)-pentylcarbamoyl]-propionyl}-hydroxy-amino)-pentyl]-N'-{5-[(bicyclo[2.2.1]heptane-2-carbonyl)-amino]-pentyl}-N'-hydroxy-succinamide

ID: ALA4203749

Chembl Id: CHEMBL4203749

PubChem CID: 145977788

Max Phase: Preclinical

Molecular Formula: C33H58N6O9

Molecular Weight: 682.86

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CC(=O)N(O)CCCCCNC(=O)CCC(=O)N(O)CCCCCNC(=O)CCC(=O)N(O)CCCCCNC(=O)[C@H]1C[C@H]2CC[C@H]1C2

Standard InChI:  InChI=1S/C33H58N6O9/c1-25(40)37(46)20-8-2-5-17-34-29(41)13-15-31(43)38(47)21-9-3-6-18-35-30(42)14-16-32(44)39(48)22-10-4-7-19-36-33(45)28-24-26-11-12-27(28)23-26/h26-28,46-48H,2-24H2,1H3,(H,34,41)(H,35,42)(H,36,45)/t26-,27-,28-/m0/s1

Standard InChI Key:  IPQAKGCFDRGPCY-KCHLEUMXSA-N

Alternative Forms

  1. Parent:

    ALA4203749

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Associated Targets(Human)

SK-N-BE(2)-M17 (195 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 682.86Molecular Weight (Monoisotopic): 682.4265AlogP: 2.52#Rotatable Bonds: 25
Polar Surface Area: 208.92Molecular Species: NEUTRALHBA: 9HBD: 6
#RO5 Violations: 2HBA (Lipinski): 15HBD (Lipinski): 6#RO5 Violations (Lipinski): 3
CX Acidic pKa: 7.92CX Basic pKa: CX LogP: -0.42CX LogD: -0.55
Aromatic Rings: Heavy Atoms: 48QED Weighted: 0.05Np Likeness Score: -0.06

References

1. Telfer TJ, Liddell JR, Duncan C, White AR, Codd R..  (2017)  Adamantyl- and other polycyclic cage-based conjugates of desferrioxamine B (DFOB) for treating iron-mediated toxicity in cell models of Parkinson's disease.,  27  (8): [PMID:28285915] [10.1016/j.bmcl.2017.03.001]

Source