capivasertib   Click here for help

GtoPdb Ligand ID: 7709

Synonyms: AZD 5363 | AZD-5363 | AZD5363 | cc-638 | Truqap®
Approved drug PDB Ligand
capivasertib is an approved drug (FDA (2023))
Compound class: Synthetic organic
Comment: Capivasertib (AZD5363) was developed as an inhibitor of the AKT serine/threonine protein kinases [1], and was investigated as a potential therapeutic for solid and haematological malignancies. This compound is now included in AstaZeneca's Open Innovation Pharmacology Toolbox.
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2D Structure
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Physico-chemical Properties
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Hydrogen bond acceptors 7
Hydrogen bond donors 4
Rotatable bonds 7
Topological polar surface area 120.16
Molecular weight 428.17
XLogP 2.44
No. Lipinski's rules broken 0
SMILES / InChI / InChIKey
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Canonical SMILES OCCC(c1ccc(cc1)Cl)NC(=O)C1(N)CCN(CC1)c1ncnc2c1cc[nH]2
Isomeric SMILES OCC[C@@H](c1ccc(cc1)Cl)NC(=O)C1(N)CCN(CC1)c1ncnc2c1cc[nH]2
InChI InChI=1S/C21H25ClN6O2/c22-15-3-1-14(2-4-15)17(6-12-29)27-20(30)21(23)7-10-28(11-8-21)19-16-5-9-24-18(16)25-13-26-19/h1-5,9,13,17,29H,6-8,10-12,23H2,(H,27,30)(H,24,25,26)/t17-/m0/s1
InChI Key JDUBGYFRJFOXQC-KRWDZBQOSA-N
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Summary of Clinical Use Click here for help
Capivasertib was evaluated in clinical trials in patients with various types of advanced solid malignancies. Click here to link to ClinicalTrials.gov's full list of capivasertib trials. First approval was granted by the FDA in November 2023, under which capivasertib (with fulvestrant) was authorised to treat hormone receptor +ve, HER2 -ve locally advanced/metastatic breast cancer with ≥ PIK3CA/AKT1/PTEN genetic alterations (that promote AKT pathway activation). The FoundationOne®CDx assay must be used to confirm the presence of the specified genetic alterations.
Clinical Trials
Clinical Trial ID Title Type Source Comment References
NCT04305496 Capivasertib+Fulvestrant vs Placebo+Fulvestrant as Treatment for Locally Advanced (Inoperable) or Metastatic HR+/HER2- Breast Cancer Phase 3 Interventional AstraZeneca 3