ID: ALA4795846

Max Phase: Preclinical

Molecular Formula: C31H35ClFNO

Molecular Weight: 455.62

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Cl.Oc1ccc(/C(=C(\CCCF)c2ccccc2)c2ccc(C3CCN(C4CC4)CC3)cc2)cc1

Standard InChI:  InChI=1S/C31H34FNO.ClH/c32-20-4-7-30(25-5-2-1-3-6-25)31(27-12-16-29(34)17-13-27)26-10-8-23(9-11-26)24-18-21-33(22-19-24)28-14-15-28;/h1-3,5-6,8-13,16-17,24,28,34H,4,7,14-15,18-22H2;1H/b31-30+;

Standard InChI Key:  FLNNRZRUOBBJOO-FJISBNMDSA-N

Associated Targets(Human)

Estrogen-related receptor gamma 587 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Estrogen-related receptor alpha 573 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Estrogen-related receptor beta 173 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Estrogen receptor alpha 17718 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: 455.62Molecular Weight (Monoisotopic): 455.2624AlogP: 7.44#Rotatable Bonds: 8
Polar Surface Area: 23.47Molecular Species: BASEHBA: 2HBD: 1
#RO5 Violations: 1HBA (Lipinski): 2HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 9.57CX Basic pKa: 8.95CX LogP: 6.50CX LogD: 5.28
Aromatic Rings: 3Heavy Atoms: 34QED Weighted: 0.36Np Likeness Score: -0.20

References

1. Kim J,Hwang H,Yoon H,Lee JE,Oh JM,An H,Ji HD,Lee S,Cha E,Ma MJ,Kim DS,Lee SJ,Kadayat TM,Song J,Lee SW,Jeon JH,Park KG,Lee IK,Jeon YH,Chin J,Cho SJ.  (2020)  An orally available inverse agonist of estrogen-related receptor gamma showed expanded efficacy for the radioiodine therapy of poorly differentiated thyroid cancer.,  205  [PMID:32758860] [10.1016/j.ejmech.2020.112501]

Source