DC Chemicals · Product datasheet

Giredestrant — Datasheet

CAT. NO. DC40118

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ParameterValue
Chemical NameGiredestrant
CAS No.1953133-47-5
SynonymsGiredestrant;28P3DU6DB3;Giredestrant [INN];GQCXHIKRWBIQMD-AKJBCIBTSA-N;3-((1R,3R)-1-(2,6-Difluoro-4-((1-(3-fluoropropyl)azetidin-3-yl)amino)phenyl)-3-methyl-1,3,4,9-tetrahydro-2H-pyrido(3,4-b)indol-2-yl)-2,2-difluoropropan-1-ol;3-[(1R,3R)-1-[2,6-difluoro-4-[[1-(3-fluoropropyl)azetidin-3-yl]amino]phenyl]-3-methyl-1,3,4,9-tetrahydropyrido[3,4-b]indol-2-yl]-2,2-difluoro-propan-1-ol;2H-Pyrido(3,4-b)indole-2-propanol, 1-(2,6-difluoro-4;GDC-9545
FormulaC27H31F5N4O
M.Wt522.553263902664
SMILESFC(CO)(CN1[C@H](C)CC2C3=CC=CC=C3NC=2[C@H]1C1C(=CC(=CC=1F)NC1CN(CCCF)C1)F)F
Purity98%
StoragePowder-20°C3 years 4°C2 yearsIn solvent-80°C6 months-20°C1 month

Biological Activity

Giredestrant (GDC-9545), a non-steroidal ER ligand, is an orally active and selective estrogen receptor (ER) antagonist. Giredestrant potently competes with estradiol for binding and induces a conformational change within the ER ligand binding domain. Giredestrant has anti-tumor activity[1].

In Vitro

Giredestrant (GDC-9545) is a novel ER antagonist and clinical candidate that combines desirable mechanistic and pre-clinical DMPK attributes. The highly potent in vivo efficacy of Giredestrant likely arises due to the particular combination of high binding potency, full suppression of ER signaling, and an improved DMPK profile[1].

In Vivo

No in vivo data are provided in the current product source. Contact us for further information.

References & source

DC Chemicals original product information

Published experimental findings depend on the model and assay conditions. They do not guarantee equivalent performance in every application. For laboratory research use only.

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