ID: ALA4798682

Max Phase: Preclinical

Molecular Formula: C28H29ClN4O4S

Molecular Weight: 553.08

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CC(=O)N1CCC2(CC1)c1cc(C(=O)NCc3ccccc3Cl)ccc1N(S(=O)(=O)c1cccnc1)C2C

Standard InChI:  InChI=1S/C28H29ClN4O4S/c1-19-28(11-14-32(15-12-28)20(2)34)24-16-21(27(35)31-17-22-6-3-4-8-25(22)29)9-10-26(24)33(19)38(36,37)23-7-5-13-30-18-23/h3-10,13,16,18-19H,11-12,14-15,17H2,1-2H3,(H,31,35)

Standard InChI Key:  ADIMLYDNRFSNCC-UHFFFAOYSA-N

Associated Targets(Human)

Gonadotropin-releasing hormone receptor 3398 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: 553.08Molecular Weight (Monoisotopic): 552.1598AlogP: 4.14#Rotatable Bonds: 5
Polar Surface Area: 99.68Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 1HBA (Lipinski): 8HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 1.07CX LogP: 2.54CX LogD: 2.54
Aromatic Rings: 3Heavy Atoms: 38QED Weighted: 0.51Np Likeness Score: -1.36

References

1. Panknin O,Wagenfeld A,Bone W,Bender E,Nowak-Reppel K,Fernández-Montalván AE,Nubbemeyer R,Bäurle S,Ring S,Schmees N,Prien O,Schäfer M,Friedrich C,Zollner TM,Steinmeyer A,Mueller T,Langer G.  (2020)  Discovery and Characterization of BAY 1214784, an Orally Available Spiroindoline Derivative Acting as a Potent and Selective Antagonist of the Human Gonadotropin-Releasing Hormone Receptor as Proven in a First-In-Human Study in Postmenopausal Women.,  63  (20): [PMID:32960053] [10.1021/acs.jmedchem.0c01076]

Source