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| BAY 80-6946 (Copanlisib) Basic information |
Product Name: | BAY 80-6946 (Copanlisib) | Synonyms: | BAY 80-6946 (Copanlisib);7-methoxy-8-(3-morpholinopropoxy)-2,3-dihydroimidazo[1,2-c]quinazolin-5-amine;BAY80-6946;2-Amino-N-[2,3-dihydro-7-methoxy-8-[3-(4-morpholinyl)propoxy]imidazo[1,2-c]quinazolin-5-yl]-5-pyrimidinecarboxamide;Copanlisib;5-Pyrimidinecarboxamide, 2-amino-N-[2,3-dihydro-7-methoxy-8-[3-(4-morpholinyl)propoxy]imidazo[1,2-c]quinazolin-5-yl]-;Copanlisib(BAY80-6946);Copanlisib, 98%, an ATP-competitive selective class-I PI3 kinases inhibitor | CAS: | 1032568-63-0 | MF: | C23H28N8O4 | MW: | 480.52 | EINECS: | | Product Categories: | Inhibitors;Akt;PI3K/Akt/mTOR;mTOR;PI3K | Mol File: | 1032568-63-0.mol | |
| BAY 80-6946 (Copanlisib) Chemical Properties |
density | 1.51 | storage temp. | Store at -20°C | solubility | insoluble in DMSO; insoluble in H2O; insoluble in EtOH | form | solid | pka | 8.42±0.20(Predicted) |
| BAY 80-6946 (Copanlisib) Usage And Synthesis |
Uses | BAY 80-6946 is a highly selective intravenous PI3K inhibitor with potent p110α and p110δ activities in tumor cell lines and xenograft models. | Definition | ChEBI: Copanlisib is an imidazoquinazoline that is 2,3-dihydroimidazo[1,2-c]quinazoline substituted by (2-aminopyrimidine-5-carbonyl)amino, methoxy, and 3-(morpholin-4-yl)propoxy groups at positions 5, 7 and 8, respectively. It is a intravenous pan-class I PI3K inhibitor used for the treatment of relapsed follicular lymphoma in patients who have received at least 2 prior systemic therapies. It has a role as an EC 2.7.1.137 (phosphatidylinositol 3-kinase) inhibitor, an antineoplastic agent and an apoptosis inducer. It is a member of morpholines, an aromatic ether, a diether, a tertiary amino compound, a secondary carboxamide, a pyrimidinecarboxamide, an aminopyrimidine and an imidazoquinazoline. |
| BAY 80-6946 (Copanlisib) Preparation Products And Raw materials |
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