ID: ALA4278915

Max Phase: Preclinical

Molecular Formula: C26H25F3N4O4

Molecular Weight: 514.50

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cn1cc(-c2ccc(C(F)(F)F)cc2CN2CCC3(CC2)CN(c2ccc(C(=O)O)cc2)C(=O)O3)cn1

Standard InChI:  InChI=1S/C26H25F3N4O4/c1-31-14-19(13-30-31)22-7-4-20(26(27,28)29)12-18(22)15-32-10-8-25(9-11-32)16-33(24(36)37-25)21-5-2-17(3-6-21)23(34)35/h2-7,12-14H,8-11,15-16H2,1H3,(H,34,35)

Standard InChI Key:  RJKNDLPQGKNRPC-UHFFFAOYSA-N

Associated Targets(Human)

SSTR5 Tclin Somatostatin receptor 5 (1477 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Sstr5 Somatostatin receptor 5 (112 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: 514.50Molecular Weight (Monoisotopic): 514.1828AlogP: 4.80#Rotatable Bonds: 5
Polar Surface Area: 87.90Molecular Species: ACIDHBA: 6HBD: 1
#RO5 Violations: 1HBA (Lipinski): 8HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 4.07CX Basic pKa: 8.17CX LogP: 1.09CX LogD: 1.04
Aromatic Rings: 3Heavy Atoms: 37QED Weighted: 0.53Np Likeness Score: -1.17

References

1. Liu W, Hussain Z, Zang Y, Sweis RF, Romero FA, Finke PE, Moningka R, Bao J, Plotkin MA, Shang J, Dingley KH, Salituro G, Murphy BA, Howard AD, Ujjainwalla F, Wood HB, Duffy JL..  (2018)  Optimization of Preclinical Metabolism for Somatostatin Receptor Subtype 5-Selective Antagonists.,  (11): [PMID:30429950] [10.1021/acsmedchemlett.8b00306]

Source