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Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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T413710-5mg | 5mg | In stock | $75.90 | |
T413710-10mg | 10mg | In stock | $118.90 | |
T413710-25mg | 25mg | In stock | $267.90 | |
T413710-100mg | 100mg | In stock | $489.90 |
p110δ Selective Inhibitors
Synonyms | Phenyl chloroformate [UN2746] [Poison] | Taselisib | DB12108 | 1282512-48-4 | Caswell No. 215B | A-dimethyl-1H-pyrazole-1-acetamide | A, | EX-A1581 | HY-13898 | NCGC00387039-02 | SCHEMBL1485247 | Q4272672 | Taselisib (USAN/INN) | UNII-L08J2O299M | BG1662 |
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Specifications & Purity | Moligand™, ≥99% |
Biochemical and Physiological Mechanisms | Taselisib (GDC 0032, RG7604) is a potent, next-generation β isoform-sparing PI3K inhibitor targeting PI3Kα/δ/γ with Ki of 0.29 nM/0.12 nM/0.97nM, >10 fold selective over PI3Kβ. |
Storage Temp | Store at -20°C |
Shipped In | Ice chest + Ice pads |
Grade | Moligand™ |
Action Type | INHIBITOR |
Mechanism of action | PI3-kinase class I inhibitor |
Product Description | Information Taselisib (GDC 0032, RG7604) is a potent, next-generation β isoform-sparing PI3K inhibitor targetingPI3Kα/δ/γwithKiof 0.29 nM/0.12 nM/0.97nM, >10 fold selective over PI3Kβ. Targets PI3Kδ (Cell-free assay); PI3Kα (Cell-free assay); PI3Kγ (Cell-free assay); PI3Kβ (Cell-free assay); C2β (Cell-free assay) 14554,0.12 nM(Ki); 0.29 nM(Ki); 0.97 nM(Ki); 9.1 nM(Ki); 292 nM In vitro GDC-0032 is an orally bioavailable, potent, and selective inhibitor of Class I PI3Kα, δ, and γ isoforms, with 30 fold less inhibition of the PI3K β isoform relative to the PI3Kα isoform. Preclinical data show that GDC-0032 has increased activity against PI3Kα isoform (PIK3CA) mutant and HER2-amplified cancer cell lines. GDC-0032 inhibits MCF7-neo/HER2 cells proliferation with IC50 of 2.5 nM. In vivo GDC-0032 pharmacokinetics is approximately dose proportional and time independent with a mean t1/2 of 40 hours. The combination of GDC-0032 enhances activity of fulvestrant resulting in tumor regressions and tumor growth delay (91% tumor growth inhibition (TGI)). In addition, the combination of GDC-0032 with tamoxifen enhances the efficacy of tamoxifen in vivo (102%TGI for GDC-0032). Cell Research(from reference) Cell lines:MCF7-neo/HER2 Cells Incubation Time:3 and 4 days |
ALogP | 2.47 |
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HBD Count | 1 |
Rotatable Bond | 5 |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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IUPAC Name | 2-methyl-2-[4-[2-(5-methyl-2-propan-2-yl-1,2,4-triazol-3-yl)-5,6-dihydroimidazo[1,2-d][1,4]benzoxazepin-9-yl]pyrazol-1-yl]propanamide |
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INCHI | InChI=1S/C24H28N8O2/c1-14(2)32-22(27-15(3)29-32)19-13-30-8-9-34-20-10-16(6-7-18(20)21(30)28-19)17-11-26-31(12-17)24(4,5)23(25)33/h6-7,10-14H,8-9H2,1-5H3,(H2,25,33) |
InChi Key | BEUQXVWXFDOSAQ-UHFFFAOYSA-N |
Canonical SMILES | CC1=NN(C(=N1)C2=CN3CCOC4=C(C3=N2)C=CC(=C4)C5=CN(N=C5)C(C)(C)C(=O)N)C(C)C |
Isomeric SMILES | CC1=NN(C(=N1)C2=CN3CCOC4=C(C3=N2)C=CC(=C4)C5=CN(N=C5)C(C)(C)C(=O)N)C(C)C |
PubChem CID | 51001932 |
Molecular Weight | 460.53 |
PubChem CID | 51001932 |
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ChEMBL Ligand | CHEMBL2387080 |
CAS Registry No. | 1282512-48-4 |
RCSB PDB Ligand | 799 |
Enter Lot Number to search for COA:
Find and download the COA for your product by matching the lot number on the packaging.
Lot Number | Certificate Type | Date | Item |
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F2310596 | Certificate of Analysis | Nov 28, 2022 | T413710 |
F2310599 | Certificate of Analysis | Nov 28, 2022 | T413710 |
F2310600 | Certificate of Analysis | Nov 28, 2022 | T413710 |
F2310601 | Certificate of Analysis | Nov 28, 2022 | T413710 |
F2310605 | Certificate of Analysis | Nov 28, 2022 | T413710 |
F2310606 | Certificate of Analysis | Nov 28, 2022 | T413710 |
F2230495 | Certificate of Analysis | Jun 07, 2022 | T413710 |
F2230496 | Certificate of Analysis | Jun 07, 2022 | T413710 |
Solubility | Solubility (25°C) In vitro DMSO: 70 mg/mL warmed with 50ºC Water: bath (151.99 mM); Ethanol: 7 mg/mL warmed with 50ºC Water: bath (15.19 mM); Water: Insoluble; |
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DMSO(mg / mL) Max Solubility | 70 |
DMSO(mM) Max Solubility | 151.998784 |
Water(mg / mL) Max Solubility | <1 |
Starting at $241.90
1. Ndubaku CO, Heffron TP, Staben ST, Baumgardner M, Blaquiere N, Bradley E, Bull R, Do S, Dotson J, Dudley D et al.. (2013) Discovery of 2-{3-[2-(1-isopropyl-3-methyl-1H-1,2-4-triazol-5-yl)-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepin-9-yl]-1H-pyrazol-1-yl}-2-methylpropanamide (GDC-0032): a β-sparing phosphoinositide 3-kinase inhibitor with high unbound exposure and robust in vivo antitumor activity.. J Med Chem, 56 (11): (4597-610). [PMID:23662903] |
2. Lopez S, Schwab CL, Cocco E, Bellone S, Bonazzoli E, English DP, Schwartz PE, Rutherford T, Angioli R, Santin AD. (2014) Taselisib, a selective inhibitor of PIK3CA, is highly effective on PIK3CA-mutated and HER2/neu amplified uterine serous carcinoma in vitro and in vivo.. Gynecol Oncol, 135 (2): (312-7). [PMID:25172762] |