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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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X124864-5mg | 5mg | In stock | $177.90 | |
X124864-10mg | 10mg | In stock | $248.90 | |
X124864-25mg | 25mg | In stock | $560.90 | |
X124864-50mg | 50mg | In stock | $872.90 | |
X124864-100mg | 100mg | In stock | $1,210.90 |
Potent and selective mTOR inhibitor; antitumor
Synonyms | XL388 | 1251156-08-7 | XL-388 | (7-(6-aminopyridin-3-yl)-2,3-dihydrobenzo[f][1,4]oxazepin-4(5H)-yl)(3-fluoro-2-methyl-4-(methylsulfonyl)phenyl)methanone | XL 388 | B7I5G3Z7XR | [7-(6-aminopyridin-3-yl)-3,5-dihydro-2H-1,4-benzoxazepin-4-yl]-(3-fluoro-2-methyl-4-methyl |
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Specifications & Purity | Moligand™, ≥98% |
Biochemical and Physiological Mechanisms | Potent and selective mTOR inhibitor (IC50= 9.9 nM). Inhibits mTOR activity in an ATP-competitive manner. Exhibits >300-fold selectivity for mTOR over PI 3-K and a range of other kinases. Displays antitumor activity in athymic nude mice implanted with tumo |
Storage Temp | Store at -20°C |
Shipped In | Ice chest + Ice pads |
Grade | Moligand™ |
Action Type | INHIBITOR |
Mechanism of action | Inhibitor of mechanistic target of rapamycin kinase |
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IUPAC Name | [7-(6-aminopyridin-3-yl)-3,5-dihydro-2H-1,4-benzoxazepin-4-yl]-(3-fluoro-2-methyl-4-methylsulfonylphenyl)methanone |
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INCHI | InChI=1S/C23H22FN3O4S/c1-14-18(5-7-20(22(14)24)32(2,29)30)23(28)27-9-10-31-19-6-3-15(11-17(19)13-27)16-4-8-21(25)26-12-16/h3-8,11-12H,9-10,13H2,1-2H3,(H2,25,26) |
InChi Key | LNFBAYSBVQBKFR-UHFFFAOYSA-N |
Canonical SMILES | CC1=C(C=CC(=C1F)S(=O)(=O)C)C(=O)N2CCOC3=C(C2)C=C(C=C3)C4=CN=C(C=C4)N |
Isomeric SMILES | CC1=C(C=CC(=C1F)S(=O)(=O)C)C(=O)N2CCOC3=C(C2)C=C(C=C3)C4=CN=C(C=C4)N |
PubChem CID | 59604787 |
Molecular Weight | 455.5 |
PubChem CID | 59604787 |
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ChEMBL Ligand | CHEMBL2333365 |
CAS Registry No. | 1251156-08-7 |
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Lot Number | Certificate Type | Date | Item |
---|---|---|---|
H23071011 | Certificate of Analysis | Jul 21, 2023 | X124864 |
H23071024 | Certificate of Analysis | Jul 21, 2023 | X124864 |
H23071031 | Certificate of Analysis | Jul 21, 2023 | X124864 |
H23071032 | Certificate of Analysis | Jul 21, 2023 | X124864 |
H23071069 | Certificate of Analysis | Jul 21, 2023 | X124864 |
H23071070 | Certificate of Analysis | Jul 21, 2023 | X124864 |
H23071072 | Certificate of Analysis | Jul 21, 2023 | X124864 |
H23071073 | Certificate of Analysis | Jul 21, 2023 | X124864 |
H23071074 | Certificate of Analysis | Jul 21, 2023 | X124864 |
H23071076 | Certificate of Analysis | Jul 21, 2023 | X124864 |
Solubility | Solvent:DMSO, Max Conc. mg/mL: 24.6, Max Conc. mM: 50 |
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1. Takeuchi CS, Kim BG, Blazey CM, Ma S, Johnson HW, Anand NK, Arcalas A, Baik TG, Buhr CA, Cannoy J et al.. (2013) Discovery of a novel class of highly potent, selective, ATP-competitive, and orally bioavailable inhibitors of the mammalian target of rapamycin (mTOR).. J Med Chem, 56 (6): (2218-34). [PMID:23394126] |