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ID: ALA4866232
Max Phase: Preclinical
Molecular Formula: C27H31F5N4O
Molecular Weight: 522.56
Molecule Type: Unknown
Associated Items:
ID: ALA4866232
Max Phase: Preclinical
Molecular Formula: C27H31F5N4O
Molecular Weight: 522.56
Molecule Type: Unknown
Associated Items:
Canonical SMILES: C[C@@H]1Cc2c([nH]c3ccccc23)[C@@H](c2c(F)cc(NCCN3CC(CF)C3)cc2F)N1CC(F)(F)CO
Standard InChI: InChI=1S/C27H31F5N4O/c1-16-8-20-19-4-2-3-5-23(19)34-25(20)26(36(16)14-27(31,32)15-37)24-21(29)9-18(10-22(24)30)33-6-7-35-12-17(11-28)13-35/h2-5,9-10,16-17,26,33-34,37H,6-8,11-15H2,1H3/t16-,26-/m1/s1
Standard InChI Key: LZLBFPYANSHCCS-AKJBCIBTSA-N
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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 |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Molecular Weight: 522.56 | Molecular Weight (Monoisotopic): 522.2418 | AlogP: 4.72 | #Rotatable Bonds: 9 |
Polar Surface Area: 54.53 | Molecular Species: NEUTRAL | HBA: 4 | HBD: 3 |
#RO5 Violations: 1 | HBA (Lipinski): 5 | HBD (Lipinski): 3 | #RO5 Violations (Lipinski): 1 |
CX Acidic pKa: 12.81 | CX Basic pKa: 7.63 | CX LogP: 4.04 | CX LogD: 3.61 |
Aromatic Rings: 3 | Heavy Atoms: 37 | QED Weighted: 0.36 | Np Likeness Score: -0.54 |
1. Liang J, Zbieg JR, Blake RA, Chang JH, Daly S, DiPasquale AG, Friedman LS, Gelzleichter T, Gill M, Giltnane JM, Goodacre S, Guan J, Hartman SJ, Ingalla ER, Kategaya L, Kiefer JR, Kleinheinz T, Labadie SS, Lai T, Li J, Liao J, Liu Z, Mody V, McLean N, Metcalfe C, Nannini MA, Oeh J, O'Rourke MG, Ortwine DF, Ran Y, Ray NC, Roussel F, Sambrone A, Sampath D, Schutt LK, Vinogradova M, Wai J, Wang T, Wertz IE, White JR, Yeap SK, Young A, Zhang B, Zheng X, Zhou W, Zhong Y, Wang X.. (2021) GDC-9545 (Giredestrant): A Potent and Orally Bioavailable Selective Estrogen Receptor Antagonist and Degrader with an Exceptional Preclinical Profile for ER+ Breast Cancer., 64 (16.0): [PMID:34251202] [10.1021/acs.jmedchem.1c00847] |
Source(1):