Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
ID: ALA4795846
Max Phase: Preclinical
Molecular Formula: C31H35ClFNO
Molecular Weight: 455.62
Molecule Type: Unknown
Associated Items:
ID: ALA4795846
Max Phase: Preclinical
Molecular Formula: C31H35ClFNO
Molecular Weight: 455.62
Molecule Type: Unknown
Associated Items:
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
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
---|
Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
Molecule Type: Unknown | Topical: No | First In Class: No | Black Box: No |
Chirality: No | Availability: No | Prodrug: No |
MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
---|
Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
---|
Molecular Weight: 455.62 | Molecular Weight (Monoisotopic): 455.2624 | AlogP: 7.44 | #Rotatable Bonds: 8 |
Polar Surface Area: 23.47 | Molecular Species: BASE | HBA: 2 | HBD: 1 |
#RO5 Violations: 1 | HBA (Lipinski): 2 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 1 |
CX Acidic pKa: 9.57 | CX Basic pKa: 8.95 | CX LogP: 6.50 | CX LogD: 5.28 |
Aromatic Rings: 3 | Heavy Atoms: 34 | QED Weighted: 0.36 | Np Likeness Score: -0.20 |
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(1):