Products for Research Use Only

Pictilisib

CAT: 0804-HY-50094-01Size: 10 mgDry Ice: NoHazardous: No
Product image 1
1 / 1
CAT#:0804-HY-50094-01Size:10 mg
Selected
24/48H Stock Items & 2 to 6 Weeks non Stock Items.
Quick Request Actions
Description
Pictilisib (GDC-0941) is a potent inhibitor of PI3Kα/δ with an IC50 of 3 nM, with modest selectivity against p110β (11-fold) and p110γ (25-fold) .
CAS Number
957054-30-7
Product Name Alternative
GDC-0941
UNSPSC
12352005
Hazard Statement
H302, H315, H319, H335
Target
Apoptosis; Autophagy; PI3K
Type
Reference compound
Related Pathways
Apoptosis; Autophagy; PI3K/Akt/mTOR
Applications
Cancer-Kinase/protease
Field of Research
Cancer
Assay Protocol
https://www.medchemexpress.com/GDC-0941.html
Purity
99.80
Solubility
DMSO : 100 mg/mL (ultrasonic; warming; heat to 60°C)
Smiles
CS(N1CCN(CC2=CC3=C(C(N4CCOCC4)=NC(C5=CC=CC6=C5C=NN6)=N3)S2)CC1)(=O)=O
Molecular Formula
C23H27N7O3S2
Molecular Weight
513.64
Precautions
H302, H315, H319, H335
References & Citations
[1]Wallin JJ, et al. GDC-0941, a novel class I selective PI3K inhibitor, enhances the efficacy of RP-56976 in human breast cancer models by increasing cell death in vitro and in vivo.Clin Cancer Res. 2012 Jul 15;18 (14) :3901-11. Epub 2012 May 14.|[2]Wullschleger S, et al. Quantitative MRI establishes the efficacy of PI3K inhibitor (GDC-0941) multi-treatments in PTEN-deficient mice lymphoma.Anticancer Res. 2012 Feb;32 (2) :415-20.|[3]Zou ZQ, et al. The novel dual PI3K/mTOR inhibitor GDC-0941 synergizes with the MEK inhibitor U0126 in non-small cell lung cancer cells.Mol Med Report. 2012 Feb;5 (2) :503-8.|[4]Burrows N, et al. GDC-0941 inhibits metastatic characteristics of thyroid carcinomas by targeting both the phosphoinositide-3 kinase (PI3K) and hypoxia-inducible factor-1α (HIF-1α) pathways.J Clin Endocrinol Metab. 2011 Dec;96 (12) :E1934-43. Epub 2011 Oct|[5]Folkes AJ, et al. The identification of 2- (1H-indazol-4-yl) -6- (4-methanesulfonyl-piperazin-1-ylmethyl) -4-morpholin-4-yl-thieno[3,2-d]pyrimidine (GDC-0941) as a potent, selective, orally bioavailable inhibitor of class I PI3 kinase for the treatment of cancer . J Med Chem. 2008 Sep 25;51 (18) :5522-32.|[6]Ni J, et al. Functional characterization of an isoform-selective inhibitor of PI3K-p110β as a potential anticancer agent. Cancer Discov. 2012 May;2 (5) :425-33.|[7]Cheng H, et al. A genetic mouse model of invasive endometrial cancer driven by concurrent loss of Pten and Lkb1 Is highly responsive to mTOR inhibition. Cancer Res. 2014 Jan 1;74 (1) :15-23.
Shipping Conditions
Room Temperature
Storage Conditions
-20°C, 3 years; 4°C, 2 years (Powder)
Scientific Category
Reference compound1
Clinical Information
Phase 2
Isoform
PI3Kα; PI3Kβ; PI3Kγ; PI3Kδ
Citation 01
Anticancer Res. 2025 Apr;45 (4) :1355-1366.|Arab J Gastroenterol. 2025 Feb;26 (1) :104-111.|Biochem Biophys Res Commun. 2025 Jun 12:776:152203.|Biochem J. 2022 Oct 14;479 (19) :2131-2151.|Bioorg Med Chem Lett. 2012 Mar 1;22 (5) :1874-8. |bioRxiv. 2020 Mar.|bioRxiv. 2025 Jul 23:2025.07.18.665614.|bioRxiv. 2025 May 16.|bioRxiv. 2025 Sep 20:2025.09.17.676669.|Br J Cancer. 2021 Apr;124 (9) :1581-1591.|Cancer Discov. 2012 May;2 (5) :425-33.|Cancer Med. 2025 Sep;14 (18) :e71227.|Cancer Res. 2014 Jan 1;74 (1) :15-23.|Cancer Res. 2024 Sep 16;84 (18) :2985-3003.|Cancers. 2020 Jul 16;12 (7) :1918.|Cell Biosci. 2022 Aug 21;12 (1) :135.|Cell Cycle. 2019 Jul;18 (13) :1513-1522.|Cell Metab. 2012 Mar 7;15 (3) :382-94.|Cell Metab. 2021 Nov 2;33 (11) :2247-2259.e6.|Cell Rep. 2023 May 29;42 (6) :112570.|Cell Syst. 2020 Jan 22;10 (1) :66-81.e11.|Cell. 2023 Jun 22;186 (13) :2929-2949.e20.|Cell. 2025 May 29;188 (11) :3065-3080.e21. |Chem Biodivers. 2025 Apr;22 (4) :e202403291.|Debreceni egyettemmolekularis orvostudomany. 2024 Dec.|Free Radic Biol Med. 2025 Oct 30:242:275-287.|Gastroenterology. 2025 Oct 27:S0016-5085 (25) 05903-7.|Harvard Medical School LINCS LIBRARY|Int J Clin Exp Pathol. 2017;10 (3) :3033-3042.|Int J Oncol. 2017 Sep;51 (3) :823-831.|J Cell Biol. 2020 Dec 7;219 (12) :e202001031.|J Clin Endocrinol Metab. 2021 Jan 1;106 (1) :e232-e246.|J Clin Invest. 2023 Jan 17;133 (2) :e153470.|J Pharm Anal. 2025 May;15 (5) :101092.|J Surg Res. 2023 Feb:282:137-146.|J Virol. 2025 Aug 25:e0022125.|Lipids Health Dis. 2024 Sep 4;23 (1) :282.|MedComm (2020) . 2024 Aug 12;5 (8) :e684.|Mol Cell. 2025 Aug 7;85 (15) :2973-2987.e6.|Molecules. 2019 Apr 1;24 (7) :1260.|Molecules. 2020 Apr 23;25 (8) :1980.|Nat Biomed Eng. 2018 Aug;2 (8) :578-588.|Nat Cancer. 2024 Mar;5 (3) :433-447.|Nat Chem Biol. 2017 Jan;13 (1) :38-45.|Nat Chem Biol. 2025 Mar;21 (3) :432-442.|Nat Commun. 2015 Oct 7;6:8501. |Nat Commun. 2016 Feb 2;7:10438.|Nature. 2018 Aug;560 (7719) :499-503.|Oncogene. 2016 Jun 9;35 (23) :2961-70. |Oncol Lett. 2023 Nov 15;27 (1) :18.|Oncol Rep. 2023 Jul;50 (1) :131.|Oncotarget. 2016 Aug 16;7 (33) :53515-53525.|Oncotarget. 2016 May 31;7 (22) :32641-51. |Patent. US20210236501A1.|Patent. US20220313694A1.|Research Square Preprint. 2024 Nov 26.|Sci Rep. 2021 Jan 11;11 (1) :291.|Sci Signal. 2021 Dec 21;14 (714) :eabj0057.|Sci Signal. 2025 Sep 2;18 (902) :eadw3231.|Sci Transl Med. 2013 Jul 31;5 (196) :196ra99.|Sci Transl Med. 2018 Jul 18;10 (450) :eaaq1093.|Tierärztliche Hochschule Hannover. 2021 Jul.|Transl Oncol. 2022 Jan;15 (1) :101260.|Cell Rep. 2020 Sep 29;32 (13) :108196.

Chemical Information

Pictilisib

Pictrelisib is a sulfonamide composed of indazole, morpholine, and methylsulfonyl-substituted piperazine rings bound to a thienopyrimidine ring. It has a role as an EC 2.7.1.137 (phosphatidylinositol 3-kinase) inhibitor. It is a thienopyrimidine, a member of piperazines, a sulfonamide, a member of indazoles and a member of morpholines.

CAS Number957054-30-7
PubChem CID17755052
IUPAC Name4-[2-(1H-indazol-4-yl)-6-[(4-methylsulfonylpiperazin-1-yl)methyl]thieno[3,2-d]pyrimidin-4-yl]morpholine
Molecular FormulaC23H27N7O3S2
Molecular Weight513.6
XLogP1.6
Topological Polar Surface Area144
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count10
Rotatable Bond Count5
Heavy Atom Count35
Formal Charge0
Complexity831
SMILES
CS(=O)(=O)N1CCN(CC1)CC2=CC3=C(S2)C(=NC(=N3)C4=C5C=NNC5=CC=C4)N6CCOCC6
InChI
InChI=1S/C23H27N7O3S2/c1-35(31,32)30-7-5-28(6-8-30)15-16-13-20-21(34-16)23(29-9-11-33-12-10-29)26-22(25-20)17-3-2-4-19-18(17)14-24-27-19/h2-4,13-14H,5-12,15H2,1H3,(H,24,27)
InChIKey
LHNIIDJUOCFXAP-UHFFFAOYSA-N
Chemical Structure
2D Structure
2D structure of Pictilisib
CAS: 957054-30-7
CID: 17755052
Formula: C23H27N7O3S2
MW: 513.6
Interactive 3D Structure
Loading 3D structure...
Computed Properties
PropertyValue
Molecular Weight513.6
XLogP31.6
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count10
Rotatable Bond Count5
Exact Mass513.16168010
Monoisotopic Mass513.16168010
Topological Polar Surface Area144 Ų
Heavy Atom Count35
Formal Charge0
Complexity831
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count1
Compound Is CanonicalizedYes