ID: ALA2087344

Max Phase: Preclinical

Molecular Formula: C30H28N2O7

Molecular Weight: 528.56

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(N[C@@H]1CO[C@H]2[C@@H]1OC[C@H]2OCc1ccccc1)/C(=C/c1ccc2c(c1)OCO2)NC(=O)c1ccccc1

Standard InChI:  InChI=1S/C30H28N2O7/c33-29(21-9-5-2-6-10-21)31-22(13-20-11-12-24-25(14-20)39-18-38-24)30(34)32-23-16-36-28-26(17-37-27(23)28)35-15-19-7-3-1-4-8-19/h1-14,23,26-28H,15-18H2,(H,31,33)(H,32,34)/b22-13-/t23-,26-,27-,28-/m1/s1

Standard InChI Key:  MNCOOLKRGJFUMT-LRPZBYNHSA-N

Associated Targets(Human)

Kallikrein 7 657 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Kallikrein 5 307 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

Properties

Molecular Weight: 528.56Molecular Weight (Monoisotopic): 528.1897AlogP: 3.05#Rotatable Bonds: 8
Polar Surface Area: 104.35Molecular Species: NEUTRALHBA: 7HBD: 2
#RO5 Violations: 1HBA (Lipinski): 9HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 12.90CX Basic pKa: CX LogP: 3.17CX LogD: 3.17
Aromatic Rings: 3Heavy Atoms: 39QED Weighted: 0.43Np Likeness Score: -0.47

References

1. Freitas RF, Teixeira TS, Barros TG, Santos JA, Kondo MY, Juliano MA, Juliano L, Blaber M, Antunes OA, Abrahão O, Pinheiro S, Muri EM, Puzer L..  (2012)  Isomannide derivatives as new class of inhibitors for human kallikrein 7.,  22  (19): [PMID:22959247] [10.1016/j.bmcl.2012.08.047]

Source