ID: ALA5199784

Max Phase: Preclinical

Molecular Formula: C35H32N10O6

Molecular Weight: 688.70

Associated Items:

Representations

Canonical SMILES:  Cc1cc(-c2cnccn2)ccc1NC(=O)[C@H](CCC(N)=O)n1cc(CNC(=O)c2ccc3ncn(CC(=O)c4ccc(O)c(O)c4)c3c2)nn1

Standard InChI:  InChI=1S/C35H32N10O6/c1-20-12-21(27-16-37-10-11-38-27)2-5-25(20)41-35(51)28(7-9-33(36)49)45-17-24(42-43-45)15-39-34(50)23-3-6-26-29(13-23)44(19-40-26)18-32(48)22-4-8-30(46)31(47)14-22/h2-6,8,10-14,16-17,19,28,46-47H,7,9,15,18H2,1H3,(H2,36,49)(H,39,50)(H,41,51)/t28-/m0/s1

Standard InChI Key:  LNYBACNHYCEJOT-NDEPHWFRSA-N

Associated Targets(Human)

Alkaline phosphatase placental type 103 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 688.70Molecular Weight (Monoisotopic): 688.2506AlogP: 3.06#Rotatable Bonds: 13
Polar Surface Area: 233.13Molecular Species: NEUTRALHBA: 13HBD: 5
#RO5 Violations: 2HBA (Lipinski): 16HBD (Lipinski): 6#RO5 Violations (Lipinski): 3
CX Acidic pKa: 7.84CX Basic pKa: 5.23CX LogP: 1.47CX LogD: 1.33
Aromatic Rings: 6Heavy Atoms: 51QED Weighted: 0.09Np Likeness Score: -1.38

References

1. Bassi G, Favalli N, Pellegrino C, Onda Y, Scheuermann J, Cazzamalli S, Manz MG, Neri D..  (2021)  Specific Inhibitor of Placental Alkaline Phosphatase Isolated from a DNA-Encoded Chemical Library Targets Tumor of the Female Reproductive Tract.,  64  (21.0): [PMID:34709820] [10.1021/acs.jmedchem.1c01103]

Source