ID: ALA4635848

Max Phase: Preclinical

Molecular Formula: C33H43N7O6S

Molecular Weight: 665.82

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CN(C)c1cccc2c(S(=O)(=O)N3CCC[C@H]3C(=O)N[C@@H](CCc3ccccc3)C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)cccc12

Standard InChI:  InChI=1S/C33H43N7O6S/c1-39(2)27-15-6-13-24-23(27)12-7-17-29(24)47(45,46)40-21-9-16-28(40)31(42)37-25(19-18-22-10-4-3-5-11-22)30(41)38-26(32(43)44)14-8-20-36-33(34)35/h3-7,10-13,15,17,25-26,28H,8-9,14,16,18-21H2,1-2H3,(H,37,42)(H,38,41)(H,43,44)(H4,34,35,36)/t25-,26-,28-/m0/s1

Standard InChI Key:  KSPUMTJNNKKZAY-NSVAZKTRSA-N

Associated Targets(Human)

FK506 binding protein 4 257 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: 665.82Molecular Weight (Monoisotopic): 665.2996AlogP: 2.01#Rotatable Bonds: 15
Polar Surface Area: 198.02Molecular Species: ZWITTERIONHBA: 7HBD: 6
#RO5 Violations: 2HBA (Lipinski): 13HBD (Lipinski): 7#RO5 Violations (Lipinski): 3
CX Acidic pKa: 3.64CX Basic pKa: 11.80CX LogP: 0.69CX LogD: 0.69
Aromatic Rings: 3Heavy Atoms: 47QED Weighted: 0.08Np Likeness Score: -0.59

References

1. de la Sierra-Gallay IL, Belnou M, Chambraud B, Genet M, van Tilbeurgh H, Aumont-Nicaise M, Desmadril M, Baulieu EE, Jacquot Y, Byrne C..  (2020)  Bioinspired Hybrid Fluorescent Ligands for the FK1 Domain of FKBP52.,  63  (18): [PMID:32866001] [10.1021/acs.jmedchem.0c00825]

Source