Ipatasertib dihydrochloride
Based on 66 publication(s) in Google Scholar
Ipatasertib dihydrochloride (GDC-0068 dihydrochloride) is a highly selective and ATP-competitive pan-Akt inhibitor with IC50s of 5, 18 and 8 nM for Akt1, Akt2 and Akt3, respectively.
For research use only. We do not sell to patients.
- Purity: 99.19%
- CAS No.: 1396257-94-5
- Formula: C24H34Cl3N5O2
- Molecular Weight:530.92
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Storage:
4°C, sealed storage, away from moisture
* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
Publications Citing Use of MedChemExpress (MCE) Ipatasertib dihydrochloride
More- Cell Metab. 2021 Nov 2;33(11):2247-2259.e6. [Abstract]
- Blood. 2023 Sep 14;142(11):973-988. [Abstract]
- Nat Cell Biol. 2025 Jan;27(1):73-86. [Abstract]
- Cancer Res. 2021 May 1;81(9):2470-2480. [Abstract]
- Nat Commun. 2025 Feb 25;16(1):1774. [Abstract]
- Nat Commun. 2024 Dec 12;15(1):10476. [Abstract]
- Mol Cell. 2020 Sep 17;79(6):1008-1023.e4. [Abstract]
- Mol Cell. 2019 Jan 3;73(1):22-35.e6. [Abstract]
- Nat Chem Biol. 2025 Aug;21(8):1194-1204. [Abstract]
- Sci Transl Med. 2018 Jul 18;10(450):eaaq1093. [Abstract]
- Sci Adv. 2025 Apr 25;11(17):eads6385. [Abstract]
- Sci Adv. 2023 Mar 22;9(12):eadd5028. [Abstract]
- Biomaterials. 2024 Mar:305:122462. [Abstract]
- Small. 2026 May;22(30):e73336. [Abstract]
- Int J Biol Sci. 2025 Jan 27;21(4):1545-1565. [Abstract]
- Oncogene. 2025 Sep;44(34):3142-3148. [Abstract]
- Int J Biol Macromol. 2026 May:362:152113. [Abstract]
- Haematologica. 2020 Mar;105(3):661-673. [Abstract]
- EMBO Mol Med. 2025 Feb;17(2):336-364. [Abstract]
- Br J Cancer. 2025 Sep 4. [Abstract]
- Cell Rep. 2021 Feb 16;34(7):108744. [Abstract]
- Mol Cancer Ther. 2024 Oct 1;23(10):1404-1417. [Abstract]
- Biochem Pharmacol. 2020 Oct:180:114145. [Abstract]
- Life Sci. 2021 Jul 15:277:119520. [Abstract]
- Life Sci. 2020 Sep 1:256:117955. [Abstract]
- Oncoimmunology. 2018 Aug 6;7(10):e1488565. [Abstract]
- EMBO Rep. 2020 Mar 4;21(3):e49129. [Abstract]
- Cancer Immunol Immunother. 2020 Nov;69(11):2259-2273. [Abstract]
- Sci Rep. 2025 Aug 17;15(1):30048. [Abstract]
- Int J Cancer. 2021 Sep 1;149(5):1137-1149. [Abstract]
- Cancers (Basel). 2023 Nov 14;15(22):5407. [Abstract]
- Neuropharmacology. 2026 Nov 1:298:111050. [Abstract]
- Oncol Rep. 2018 Aug;40(2):635-646. [Abstract]
- Mol Oncol. 2025 Jul 13. [Abstract]
- Mol Oncol. 2024 Mar;18(3):726-742. [Abstract]
- Skelet Muscle. 2021 Mar 15;11(1):6. [Abstract]
- Ren Fail. 2025 Dec;47(1):2580064. [Abstract]
- Front Oncol. 2021 Nov 24:11:766298. [Abstract]
- J Cell Biochem. 2024 Aug;125(8):e30613. [Abstract]
- Int J Hyperthermia. 2024 Feb 13;41(1):2310017. [Abstract]
- Steroids. 2025 Nov:223:109692. [Abstract]
- Biochem Biophys Res Commun. 2025 Aug 30:776:152203. [Abstract]
- Onco Targets Ther. 2020 Aug 18:13:8197-8208. [Abstract]
- Biomed Chromatogr. 2020 Oct;34(10):e4923. [Abstract]
- Biomed Chromatogr. 2020 Oct;34(10):e4920. [Abstract]
- Res Sq. 2026 Jun 15:rs.3.rs-9941989. [Abstract]
- J Mol Liq. 2026 May 23;457:129686.
- bioRxiv. 2026 Apr 9.
- Res Sq. 2026 Jan 15.
- Technical University of Dresden. 2025.
- Universite du Quebec. 2025.
- Preprints. 2025 Nov 18.
- bioRxiv. 2025 May 4:2025.04.29.651320. [Abstract]
- bioRxiv. 2025 March 20.
- bioRxiv. 2024 August 26.
- Research Square Preprint. 2024 Nov 26.
- bioRxiv. 2024 August 18.
- bioRxiv. 2024 September 07.
- bioRxiv. 2024 Jan 16.
- SSRN. 2023 Jun 20.
- Patent. US20220313694A1.
- Cold Spring Harb Mol Case Stud. 2022 Jan 10;8(1):a006140. [Abstract]
- Oxid Med Cell Longev. 2021 Jan 12:2021:3010548. [Abstract]
- Elife. 2020 Dec 7:9:e61405. [Abstract]
- Radboud University Nijmegen. 2019 Oct.
- Oncotarget. 2016 May 17;7(20):29131-42. [Abstract]
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Cell Proliferation/Viability Assay
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WB
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WB
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WB
Biological Activity
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Akt1 5 nM (IC50) |
Akt3 8 nM (IC50) |
Akt2 18 nM (IC50) |
PKA 3100 nM (IC50) |
Ipatasertib shows more than 600 and more than 100-fold selectivity for Akt1 in IC50 against the closely related kinases PKA and p70S6K, respectively. When tested at 1 μM in a panel of 230 protein kinases, which includes 36 human AGC family members, Ipatasertib inhibits only 3 other kinases by more than 70% at 1 μM concentration (PRKG1α, PRKG1β, and p70S6K). IC50s measured for these 3 kinases are 98, 69, and 860 nM, respectively. Thus, with the exception of PKG1 (relative to which Ipatasertib is >10-fold more selective for Akt1), Ipatasertib displays a more than 100-fold selectivity for Akt1 over the next most potently inhibited non-Akt kinase, p70S6K, in the screening kinase panel. The relationship between pharmacokinetics (PK) and pharmacodynamics (PD) of Ipatasertib is investigated in 3 xenograft models that showed dose-dependent response to drug treatment: MCF7-neo/HER2, TOV-21G.x1, and LNCaP. The mean cell viability IC50 of Ipatasertib in these 3 cell lines is 2.56, 0.44, and 0.11 μM, respectively[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
| NCT Number | Sponsor | Condition | Start Date |
Phase
|
|---|---|---|---|---|
| NCT01329991 | Plexxikon| | 2011-05 | PHASE1 |
Chemical Information
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CAS No. 1396257-94-5
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Appearance Solid
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Molecular Weight 530.92
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Formula C24H34Cl3N5O2
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Color Light yellow to yellow
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SMILES
ClC1=CC=C([C@@H](CNC(C)C)C(N2CCN(C3=C([C@H](C)C[C@H]4O)C4=NC=N3)CC2)=O)C=C1.[H]Cl.[H]Cl
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Synonyms
GDC-0068 dihydrochloride; RG-7440 dihydrochloride
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
4°C, sealed storage, away from moisture
* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
Publications (66)
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Journal Impact Factor
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Most Recent
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Cell Metab
2021 Nov 2;33(11):2247-2259.e6. PMID: 34731655 -
Blood
DLBCL associated NOTCH2 mutations escape ubiquitin-dependent degradation and promote chemo-resistance. [Abstract]2023 Sep 14;142(11):973-988. PMID: 37235754 -
Nat Cell Biol
Chromosome mis-segregation triggers cell cycle arrest through a mechanosensitive nuclear envelope checkpoint. [Abstract]2025 Jan;27(1):73-86. PMID: 39779939 -
Cancer Res
Genomic Alterations in PIK3CA-Mutated Breast Cancer Result in mTORC1 Activation and Limit the Sensitivity to PI3Kα Inhibitors. [Abstract]2021 May 1;81(9):2470-2480. PMID: 33685991 -
Nat Commun
Attenuated growth factor signaling during cell death initiation sensitizes membranes towards peroxidation. [Abstract]2025 Feb 25;16(1):1774. PMID: 40000627
Ipatasertib dihydrochloride purchased from MedChemExpress. Usage Cited in: Nat Commun. 2025 Feb 25;16(1):1774. [Abstract]
Viable cell numbers and PUFA-PC ratio after treatment with LY294002 (iPI3K, 10 µM), picropodophyllin (iRTK, 10 µM), ipatasertib (iAkt, 10 µM), or fatostatin (iSREBP1, 20 µM) for 48 h.
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Nat Commun
An actin bracket-induced elastoplastic transition determines epithelial folding irreversibility. [Abstract]2024 Dec 12;15(1):10476. PMID: 39668169 -
Mol Cell
DNA Damage Promotes TMPRSS2-ERG Oncoprotein Destruction and Prostate Cancer Suppression via Signaling Converged by GSK3β and WEE1. [Abstract]2020 Sep 17;79(6):1008-1023.e4. PMID: 32871104 -
Mol Cell
Phosphorylated RB Promotes Cancer Immunity by Inhibiting NF-κB Activation and PD-L1 Expression. [Abstract]2019 Jan 3;73(1):22-35.e6. PMID: 30527665 -
Nat Chem Biol
2025 Aug;21(8):1194-1204. PMID: 39934397 -
Sci Transl Med
PP2A inhibition is a druggable MEK inhibitor resistance mechanism in KRAS-mutant lung cancer cells. [Abstract]2018 Jul 18;10(450):eaaq1093. PMID: 30021885 -
Sci Adv
2025 Apr 25;11(17):eads6385. PMID: 40279411 -
Sci Adv
Breast tumors interfere with endothelial TRAIL at the premetastatic niche to promote cancer cell seeding. [Abstract]2023 Mar 22;9(12):eadd5028. PMID: 36947620 -
Biomaterials
FAK-p38 signaling serves as a potential target for reverting matrix stiffness-modulated liver sinusoidal endothelial cell defenestration. [Abstract]2024 Mar:305:122462. PMID: 38171118 -
Small
High-Throughput Single-Cell Biochip System for Functional Interrogation of Protein Interactions in Living Cells. [Abstract]2026 May;22(30):e73336. PMID: 41944250 -
Int J Biol Sci
High-dose Ascorbate Exhibits Anti-proliferative and Anti-invasive Effects Dependent on PTEN/AKT/mTOR Pathway in Endometrial Cancer in vitro and in vivo. [Abstract]2025 Jan 27;21(4):1545-1565. PMID: 39990670 -
Oncogene
Identification of RAPGEF3 as the therapeutic vulnerability of basal-subtype lung squamous cell carcinoma. [Abstract]2025 Sep;44(34):3142-3148. PMID: 40781157 -
Int J Biol Macromol
Acetylation of GPRC5A at Lys348 facilitates cisplatin resistance and promotes the recurrence and poor prognosis in ovarian cancer. [Abstract]2026 May:362:152113. PMID: 42009151 -
Haematologica
2020 Mar;105(3):661-673. PMID: 31289202 -
EMBO Mol Med
2025 Feb;17(2):336-364. PMID: 39748059 -
Br J Cancer
Inhibition of YB-1 phosphorylation enhances cisplatin activity and disrupts cell division in pleural mesothelioma. [Abstract]2025 Sep 4. PMID: 40908296 -
Cell Rep
An acetyl-histone vulnerability in PI3K/AKT inhibition-resistant cancers is targetable by both BET and HDAC inhibitors. [Abstract]2021 Feb 16;34(7):108744. PMID: 33596421 -
Mol Cancer Ther
AKT Inhibition Sensitizes to Polo-Like Kinase 1 Inhibitor Onvansertib in Prostate Cancer. [Abstract]2024 Oct 1;23(10):1404-1417. PMID: 38894678 -
Biochem Pharmacol
20(S)-ginsenoside Rg3 promotes myoblast differentiation and protects against myotube atrophy via regulation of the Akt/mTOR/FoxO3 pathway. [Abstract]2020 Oct:180:114145. PMID: 32653593
Ipatasertib dihydrochloride purchased from MedChemExpress. Usage Cited in: Biochem Pharmacol. 2020 Oct:180:114145. [Abstract]
C2C12 myoblasts were pre-incubated with 2.5 μM GDC-0068 for 30 min then treated with 0.2 μM S-Rg3. After incubation with S-Rg3 for 72 h and 24 h, Western blotting is used to detect levels of Myf5 and myogenin in C2C12 myoblasts after incubation of cells with S-Rg3 for 120 h. GDC-0068 inhibits S-Rg3-activated phosphorylation of Akt and mTOR in C2C12 myoblasts.
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Life Sci
Early-senescent bone marrow mesenchymal stem cells promote C2C12 cell myogenic differentiation by preventing the nuclear translocation of FOXO3. [Abstract]2021 Jul 15:277:119520. PMID: 33887345 -
Life Sci
2020 Sep 1:256:117955. PMID: 32534038 -
Oncoimmunology
Ex vivo AKT-inhibition facilitates generation of polyfunctional stem cell memory-like CD8+ T cells for adoptive immunotherapy. [Abstract]2018 Aug 6;7(10):e1488565. PMID: 30288356 -
EMBO Rep
2020 Mar 4;21(3):e49129. PMID: 32030864 -
Cancer Immunol Immunother
Cell composition and expansion strategy can reduce the beneficial effect of AKT-inhibition on functionality of CD8+ T cells. [Abstract]2020 Nov;69(11):2259-2273. PMID: 32504246 -
Sci Rep
Dendrobium officinale Kimura & Migo polysaccharide ameliorates skin photoaging by promoting angiogenesis. [Abstract]2025 Aug 17;15(1):30048. PMID: 40820014 -
Int J Cancer
Effects of Metformin on the virus/host cell crosstalk in human papillomavirus-positive cancer cells. [Abstract]2021 Sep 1;149(5):1137-1149. PMID: 33844847 -
Cancers (Basel)
Oleic Acid Exhibits Anti-Proliferative and Anti-Invasive Activities via the PTEN/AKT/mTOR Pathway in Endometrial Cancer. [Abstract]2023 Nov 14;15(22):5407. PMID: 38001668 -
Neuropharmacology
Hypericin alleviates high glucose-induced ferroptosis in cultured rat satellite glial cells via targeting P2X7R to activate the Akt/GSK3β/Nrf2 axis. [Abstract]2026 Nov 1:298:111050. PMID: 42214457 -
Oncol Rep
Evaluation of anticancer agents using patient-derived tumor organoids characteristically similar to source tissues. [Abstract]2018 Aug;40(2):635-646. PMID: 29917168 -
Mol Oncol
Olaparib synergy screen reveals Exemestane induces replication stress in triple-negative breast cancer. [Abstract]2025 Jul 13. PMID: 40652528 -
Mol Oncol
Dual targeting of the androgen receptor and PI3K/AKT/mTOR pathways in prostate cancer models improves antitumor efficacy and promotes cell apoptosis. [Abstract]2024 Mar;18(3):726-742. PMID: 38225213 -
Skelet Muscle
MiR-1290 promotes myoblast differentiation and protects against myotube atrophy via Akt/p70/FoxO3 pathway regulation. [Abstract]2021 Mar 15;11(1):6. PMID: 33722298
Ipatasertib dihydrochloride purchased from MedChemExpress. Usage Cited in: Skelet Muscle. 2021 Mar 15;11(1):6. [Abstract]
The western blot analysis and quantification of phosphorylated and all forms of AKT and P70, MyoG, and MyoD, after transfecting miR-1290/miR-NC with or without GDC0068. GDC-0068 inhibits miR-1290-activated phosphorylation of AKT and P70 in C2C12 myoblasts.
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Ren Fail
A multi-omics landscape of programmed cell death in acetaminophen-induced acute kidney injury. [Abstract]2025 Dec;47(1):2580064. PMID: 41249093 -
Front Oncol
Zotatifin, an eIF4A-Selective Inhibitor, Blocks Tumor Growth in Receptor Tyrosine Kinase Driven Tumors. [Abstract]2021 Nov 24:11:766298. PMID: 34900714
Ipatasertib dihydrochloride purchased from MedChemExpress. Usage Cited in: Front Oncol. 2021 Nov 24:11:766298. [Abstract]
Ipatasertib (0.625, 1.25, 5 µM; 24 h) increases the phosphorylation of AKT in MFM-223 FGFR2amp cells.
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J Cell Biochem
2024 Aug;125(8):e30613. PMID: 38860522 -
Int J Hyperthermia
Impacts of hyperthermic chemotherapeutic agent on cytotoxicity, chemoresistance-related proteins and PD-L1 expression in human gastric cancer cells. [Abstract]2024 Feb 13;41(1):2310017. PMID: 38350654 -
Steroids
Kobochromone A, a polyphenol in Carex kobomugi, suppresses androgen signaling induced by 11-oxygenated androgens and enhances the efficacy of AKT inhibitors in triple-negative breast cancer cells. [Abstract]2025 Nov:223:109692. PMID: 41015102 -
Biochem Biophys Res Commun
Loss of DNA replication fork protection by TIMELESS degradation supports oncogene-induced senescence. [Abstract]2025 Aug 30:776:152203. PMID: 40517672 -
Onco Targets Ther
Inhibition of PI3K-AKT Signaling Blocks PGE2-Induced COX-2 Expression in Lung Adenocarcinoma. [Abstract]2020 Aug 18:13:8197-8208. PMID: 32904445 -
Biomed Chromatogr
2020 Oct;34(10):e4923. PMID: 32558944 -
Biomed Chromatogr
A validated LC-MS/MS method for the quantification of capivasertib in dog plasma: Application to its pharmacokinetics study. [Abstract]2020 Oct;34(10):e4920. PMID: 32537750 -
Res Sq
ERG function in prostate cells is regulated by distinct positive feedback loops depending on AKT signaling status. [Abstract]2026 Jun 15:rs.3.rs-9941989. PMID: 42370241 -
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bioRxiv
2025 May 4:2025.04.29.651320. PMID: 40654780 -
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Cold Spring Harb Mol Case Stud
Functional impact and targetability of PI3KCA, GNAS, and PTEN mutations in a spindle cell rhabdomyosarcoma with MYOD1 L122R mutation. [Abstract]2022 Jan 10;8(1):a006140. PMID: 35012940 -
Oxid Med Cell Longev
2021 Jan 12:2021:3010548. PMID: 33505580 -
Elife
2020 Dec 7:9:e61405. PMID: 33284104 -
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Oncotarget
Dual inhibition of AKT/FLT3-ITD by A674563 overcomes FLT3 ligand-induced drug resistance in FLT3-ITD positive AML. [Abstract]2016 May 17;7(20):29131-42. PMID: 27074558
Solvent & Solubility
DMSO : 100 mg/mL (188.35 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
H2O : ≥ 41 mg/mL (77.22 mM)
* "≥" means soluble, but saturation unknown.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Select the appropriate dissolution method based on your experimental animal and administration route.
- For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
- To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for In Vivo experiments, it is recommended to prepare freshly and use it on the same day.
- The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.
Add each solvent one by one: 10% DMSO 40% PEG300 5% Tween-80 45% Saline
Solubility: ≥ 2.08 mg/mL (3.92 mM); Clear solution
This protocol yields a clear solution of ≥ 2.08 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (20.8 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.
Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
Add each solvent one by one: 10% DMSO 90% (20% SBE-β-CD in Saline)
Solubility: ≥ 2.08 mg/mL (3.92 mM); Clear solution
This protocol yields a clear solution of ≥ 2.08 mg/mL (saturation unknown).
Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (20.8 mg/mL) to 900 μL 20% SBE-β-CD in Saline, and mix evenly.
Preparation of 20% SBE-β-CD in Saline (4°C, storage for one week): 2 g SBE-β-CD powder is dissolved in 10 mL Saline, completely dissolve until clear.
For the following dissolution methods, please prepare the working solution directly:
It is recommended to prepare fresh solutions and use them promptly within a short period of time.
The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.
Add each solvent one by one: PBS
Solubility: 16.67 mg/mL (31.40 mM); Clear solution; Need ultrasonic
Please enter the basic information of animal experiments:
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Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
Working solution concentration: 0.22 mg/mL
This product has good water solubility, please refer to the measured solubility data in water/PBS/Saline for details.
Protocol
The 384-well plates are seeded with 2,000 cells per well in a volume of 54 μL per well followed by incubation at 37°C under 5% CO2 overnight (~16 hours). Compounds (e.g., Ipatasertib) are diluted in DMSO to generate the desired stock concentrations then added in a volume of 6 μL per well. All treatments are tested in quadruplicates. After 4 days incubation, relative numbers of viable cells are estimated using CellTiter-Glo and total luminescence is measured on a Wallac Multilabel Reader. The concentration of drug resulting in IC50 is calculated from a 4-parameter curve analysis (XLfit) and is determined from a minimum of 3 experiments. For cell lines that failed to achieve an IC50, the highest concentration tested (10 μM) is listed[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Mice[2]
In vivo efficacy is evaluated in multiple tumor cell line- and patient-derived xenograft models. Cells or tumor fragments are implanted subcutaneously into the flank of immunocompromised mice. Female or male nude (nu/nu) or severe combined immunodeficient mice (SCID)/beige mice are used. The LuCaP35V patient-derived primary tumors are obtained; male mice are castrated before implantation of tumor fragments. After implantation of tumor cells or fragments into mice, tumors are monitored until they reached mean tumor volumes of 180 to 350 mm3 and distributed into groups of 8 to 10 animals/group. Ipatasertib is formulated in 0.5% methylcellulose/0.2% Tween-80 (MCT) and administered daily (QD), via oral (per os; PO) gavage. RP-56976 is formulated in 3% EtOH/97% saline and dosed intravenously (IV) every week (QW) at 2.5 or 7.5 mg/kg. NSC 241240 is formulated in saline and dosed intraperitoneally (IP) weekly at 50 mg/kg.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Purity & Documentation
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Data Sheet (283 KB)
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SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
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Handling Instructions (2659 KB)
References
[1]. Blake JF, et al. Discovery and preclinical pharmacology of a selective ATP-competitive Akt inhibitor (GDC-0068) for the treatment of human tumors. J Med Chem. 2012 Sep 27;55(18):8110-27. [Content Brief]
[2]. Lin J, et al. Targeting activated Akt with GDC-0068, a novel selective Akt inhibitor that is efficacious in multiple tumor models. Clin Cancer Res. 2013 Apr 1;19(7):1760-72. [Content Brief]
Complete Stock Solution Preparation Table
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| H2O / DMSO | 1 mM | 1.8835 mL | 9.4176 mL | 18.8352 mL | 47.0881 mL |
| 5 mM | 0.3767 mL | 1.8835 mL | 3.7670 mL | 9.4176 mL | |
| 10 mM | 0.1884 mL | 0.9418 mL | 1.8835 mL | 4.7088 mL | |
| 15 mM | 0.1256 mL | 0.6278 mL | 1.2557 mL | 3.1392 mL | |
| 20 mM | 0.0942 mL | 0.4709 mL | 0.9418 mL | 2.3544 mL | |
| 25 mM | 0.0753 mL | 0.3767 mL | 0.7534 mL | 1.8835 mL | |
| 30 mM | 0.0628 mL | 0.3139 mL | 0.6278 mL | 1.5696 mL | |
| 40 mM | 0.0471 mL | 0.2354 mL | 0.4709 mL | 1.1772 mL | |
| 50 mM | 0.0377 mL | 0.1884 mL | 0.3767 mL | 0.9418 mL | |
| 60 mM | 0.0314 mL | 0.1570 mL | 0.3139 mL | 0.7848 mL | |
| DMSO | 80 mM | 0.0235 mL | 0.1177 mL | 0.2354 mL | 0.5886 mL |
| 100 mM | 0.0188 mL | 0.0942 mL | 0.1884 mL | 0.4709 mL |
* Note: If you choose water as the stock solution, please dilute it to the working solution, then filter and sterilize it with a 0.22 μm filter before use.