ID: ALA4743069

Max Phase: Preclinical

Molecular Formula: C28H35N5O7

Molecular Weight: 553.62

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  N[C@@H]1CCC(=O)NCC[C@@H](C(=O)NCc2ccccc2CC(=O)O)NC(=O)C[C@H](Cc2ccc(O)cc2)NC1=O

Standard InChI:  InChI=1S/C28H35N5O7/c29-22-9-10-24(35)30-12-11-23(28(40)31-16-19-4-2-1-3-18(19)14-26(37)38)33-25(36)15-20(32-27(22)39)13-17-5-7-21(34)8-6-17/h1-8,20,22-23,34H,9-16,29H2,(H,30,35)(H,31,40)(H,32,39)(H,33,36)(H,37,38)/t20-,22+,23-/m0/s1

Standard InChI Key:  YPOQRJZHCULELI-WWNPGLIZSA-N

Associated Targets(Human)

Interleukin-1 receptor antagonist protein 102 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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

Properties

Molecular Weight: 553.62Molecular Weight (Monoisotopic): 553.2536AlogP: -0.13#Rotatable Bonds: 7
Polar Surface Area: 199.95Molecular Species: ACIDHBA: 7HBD: 7
#RO5 Violations: 2HBA (Lipinski): 12HBD (Lipinski): 8#RO5 Violations (Lipinski): 3
CX Acidic pKa: 4.22CX Basic pKa: 8.20CX LogP: -3.10CX LogD: -3.16
Aromatic Rings: 2Heavy Atoms: 40QED Weighted: 0.25Np Likeness Score: 0.34

References

1. Barlow, Nicholas, Vanga, Sudarsana Reddy, Savmarker, Jonas, Sandstrom, Anja, Burns, Peta, Hallberg, Anders, Aqvist, Johan, Gutierrez-de-Teran, Hugo, Hallberg, Mathias, Larhed, Mats, Chai, Siew Yeen, Thompson, Philip E..  (2020)  Macrocyclic peptidomimetics as inhibitors of insulin-regulated aminopeptidase (IRAP),  11  (2): [PMID:33479630] [10.1039/c9md00485h]

Source