General Information of the Compound
Compound ID
CP0007893
Compound Name
4-[2-(1H-indazol-4-yl)-6-[(4-methanesulfonylpiperazin-1-yl)methyl]thieno[3,2-d]pyrimidin-4-yl]morpholine
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Synonyms
GD9
2-(1H-Indazol-4-yl)-6-(4-methanesulfonylpiperazin-1-ylmethyl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidine
2-(1H-indazol-4-yl)-6-(4-methanesulfonylpiperazin-1-ylmethyl)-4-morpholin-4-ylthieno(3,2-d)pyrimidine
4-(2-(1H-Indazol-4-yl)-6-((4-(methylsulfonyl)piperazin-1-yl)methyl)thieno[3,2-d]pyrimidin-4-yl)morpholine
957054-30-7
AK-40872
CHEBI:65326
GDC 0941
GDC-0941
GDC-0941, GDC0941
GDC0941
ICY00EMP8P
PICTILISIB
Pictilisib
Pictilisib (GDC-0941)
Pictrelisib
Thieno[3,2-d]pyrimidine, 2-(1H-indazol-4-yl)-6-[[4-(methylsulfonyl)-1-piperazinyl]methyl]-4-(4-morpholinyl)-
UNII-ICY00EMP8P
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Structure
Formula
C23H27N7O3S2
Molecular Weight
513.649
Canonical SMILES
CS(=O)(=O)N1CCN(Cc2cc3nc(nc(N4CCOCC4)c3s2)-c2cccc3[nH]ncc23)CC1
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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)
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InChIKey
LHNIIDJUOCFXAP-UHFFFAOYSA-N
CAS
957054-30-7
Physicochemical Property
logP
2.1484
Rotatable Bonds
5
Heavy Atom Count
35
Polar Areas
107.55
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
9
Complexity
35

"RO5" indicates the cutoff set by lipinski's rule of five:

(1) Molecular weight less than 500 Dalton;

(2) xlogp less than 5;

(3) No more than 5 hbonddonor (Hydrogen Bond Donor Count);

(4) No more than 10 hbondacc (Hydrogen Bond Acceptor Count);

(5) No more than 10 rotbonds (Rotatable Bond Count).

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PubChem ID
CID: 17755052
SID: 29212926
ChEMBL ID
CHEMBL521851
DrugBank ID
DB11663
Map of Molecular Bioactivity Related to the Compound
Map of Molecular Bioactivity Related to the Compound

Compound
Cell Line
Protein

Bioactivity Value:

<= 0.1 μM
> 0.1 μM and <= 10 μM
> 10 μM
Imprecise Activity
Table of Molecular Bioactivities Related to the Compound
Protein ID: PT01213, Histone deacetylase 6
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000083 MCF-7 Homo sapiens (Human)  1
1
EC50 > 30000 nM
   TI
   LI
   LO
   TS
Protein ID: PT01045, Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000013 Sf9 Spodoptera frugiperda (Fall armyworm)  3
1
IC50 = 3 nM
   TI
   LI
   LO
   TS
2
Ki = 2.6 nM
   TI
   LI
   LO
   TS
3
Ki = 10.2 nM
   TI
   LI
   LO
   TS
CL000918 MCF7-neo/Her2 Homo sapiens (Human)  1
1
IC50 = 7 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 IC50 = 0.1 nM
2 IC50 = 3 nM
3 IC50 = 4.7 nM
4 IC50 = 6.5 nM
5 IC50 = 7 nM
6 IC50 = 33 nM
7 IC50 = 50.12 nM
8 IC50 = 251.19 nM
9 Kd = 0.76 nM
10 Kd = 0.86 nM
11 Kd = 1.1 nM
12 Kd = 1.2 nM
13 Kd = 1.5 nM
14 Kd = 1.7 nM
15 Kd = 3.7 nM
16 Kd = 4.1 nM
17 Kd = 4.5 nM
18 Kd = 7.1 nM
Protein ID: PT07498, Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000019 Rat1 Rattus norvegicus (Rat)  1
1
IC50 = 52 nM
   TI
   LI
   LO
   TS
Protein ID: PT01033, Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000013 Sf9 Spodoptera frugiperda (Fall armyworm)  2
1
IC50 = 17 nM
   TI
   LI
   LO
   TS
2
IC50 = 33 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 IC50 = 3 nM
2 IC50 = 31 nM
3 IC50 = 32 nM
4 IC50 = 33 nM
5 IC50 = 181 nM
6 IC50 = 251.19 nM
7 IC50 = 324 nM
8 Kd = 2.1 nM
9 Kd = 16 nM
Protein ID: PT06232, Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000019 Rat1 Rattus norvegicus (Rat)  1
1
IC50 = 146 nM
   TI
   LI
   LO
   TS
Protein ID: PT00999, Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000013 Sf9 Spodoptera frugiperda (Fall armyworm)  2
1
IC50 = 3 nM
   TI
   LI
   LO
   TS
2
Ki = 31 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 IC50 = 3 nM
2 IC50 = 4 nM
3 IC50 = 7 nM
4 IC50 = 9 nM
5 IC50 = 12.59 nM
6 IC50 = 15.7 nM
7 IC50 = 50.12 nM
8 IC50 = 75 nM
9 Kd = 3.3 nM
10 Kd = 5 nM
Protein ID: PT01029, Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000013 Sf9 Spodoptera frugiperda (Fall armyworm)  2
1
IC50 = 42 nM
   TI
   LI
   LO
   TS
2
Ki = 1.4 nM
   TI
   LI
   LO
   TS
CL000014 RAW 264.7 Mus musculus (Mouse)  1
1
IC50 = 298 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 IC50 = 12.59 nM
2 IC50 = 66 nM
3 IC50 = 75 nM
4 IC50 = 110.5 nM
5 IC50 = 251.19 nM
6 IC50 = 580 nM
7 IC50 = 746 nM
8 Kd = 7.7 nM
9 Kd = 48 nM
Protein ID: PT00845, RAC-alpha serine/threonine-protein kinase
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000225 MDA-MB-361 Homo sapiens (Human)  1
1
IC50 = 28 nM
   TI
   LI
   LO
   TS
CL000048 PC-3 Homo sapiens (Human)  1
1
IC50 = 37 nM
   TI
   LI
   LO
   TS
CL000102 U-87MG ATCC Homo sapiens (Human)  1
1
IC50 = 46 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 Kd > 10000 nM
Protein ID: PT01065, Serine/threonine-protein kinase mTOR
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000012 Sf21 Spodoptera frugiperda (Fall armyworm)  1
1
IC50 = 134 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 IC50 = 3 nM
2 IC50 = 310 nM
3 IC50 = 410 nM
4 IC50 = 580 nM
5 IC50 = 712 nM
6 IC50 = 959 nM
7 IC50 = 3351 nM
8 Kd = 48 nM
9 Kd = 200 nM
10 Ki = 570 nM
11 Ki = 580 nM
Cell Viability or Cytotoxicity Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000072 A2780 Homo sapiens (Human)  1
1
IC50 = 140 nM
   TI
   LI
   LO
   TS
CL000148 Huh-7 Homo sapiens (Human)  1
1
IC50 = 1720 nM
   TI
   LI
   LO
   TS
CL000225 MDA-MB-361 Homo sapiens (Human)  1
1
IC50 = 720 nM
   TI
   LI
   LO
   TS
Clinical Information about the Compound
Drug 1 ( GDC0941 )
Drug Name GDC0941
Company Genentech
Indication
Non-hodgkin lymphoma
Phase 2
Solid tumour/cancer
Phase 2
Breast cancer
Phase 2
Target(s)
PI3-kinase gamma (PIK3CG)
Inhibitor