Send us a Message

Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   


The Chemical Entities of Biological Interest (ChEBI) ontology is downloaded weekly from EMBL-EBI at The data is made available under the Creative Commons License (CC BY 3.0, For more information see: Degtyarenko et al. (2008) ChEBI: a database and ontology for chemical entities of biological interest. Nucleic Acids Res. 36, D344–D350.

go back to main search page
Accession:CHEBI:173077 term browser browse the term
Definition: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.
Synonyms:exact_synonym: 2-amino-N-{7-methoxy-8-[3-(morpholin-4-yl)propoxy]-2,3-dihydroimidazo[1,2-c]quinazolin-5-yl}pyrimidine-5-carboxamide
 related_synonym: BAY 80-6946;   BAY80-6946;   Formula=C23H28N8O4;   InChI=1S/C23H28N8O4/c1-33-19-17(35-10-2-6-30-8-11-34-12-9-30)4-3-16-18(19)28-23(31-7-5-25-20(16)31)29-21(32)15-13-26-22(24)27-14-15/h3-4,13-14H,2,5-12H2,1H3,(H2,24,26,27)(H,28,29,32);   InChIKey=PZBCKZWLPGJMAO-UHFFFAOYSA-N;   SMILES=COC1=C(OCCCN2CCOCC2)C=CC2=C1N=C(NC(=O)C1=CN=C(N)N=C1)N1CCN=C21;   copanlisibum
 xref: CAS:1032568-63-0;   Chemspider:25069683;   DrugBank:DB12483;   Drug_Central:5256;   KEGG:D10867
 xref_mesh: MESH:C000589253
 xref: PDBeChem:6E2;   PMID:24170767;   PMID:24852792;   PMID:24942196;   PMID:25528022;   PMID:27310202;   PMID:27672108;   PMID:28714036;   PMID:30147333;   PMID:30174412;   PMID:30430191;   PMID:30813760;   PMID:30962952;   PMID:31934607;   PMID:32126142;   PMID:32183683;   PMID:32371592;   PMID:32483262;   PMID:32576028;   PMID:32658557;   PMID:33108585;   PMID:33110476;   PMID:33125719;   PMID:33139695;   PMID:33289918;   PMID:33352201;   PMID:33531838;   PMID:33560394;   PMID:33687623;   PMID:33771771;   PMID:33799597;   PMID:33839692;   PMID:33848462;   PMID:33879868;   PMID:33889376;   PMID:33942546;   Wikipedia:Copanlisib

show annotations for term's descendants           Sort by:
copanlisib term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Akt1 AKT serine/threonine kinase 1 decreases phosphorylation ISO copanlisib results in decreased phosphorylation of AKT1 protein CTD PMID:31445927 NCBI chr 6:131,713,716...131,735,319
Ensembl chr 6:131,713,720...131,733,921
JBrowse link
G Fas Fas cell surface death receptor affects response to substance ISO copanlisib affects the susceptibility to FAS protein CTD PMID:31445927 NCBI chr 1:231,798,963...231,832,591
Ensembl chr 1:231,798,960...231,832,591
JBrowse link
G Tnf tumor necrosis factor increases response to substance ISO copanlisib results in increased susceptibility to TNF protein CTD PMID:31445927 NCBI chr20:3,622,011...3,624,629
Ensembl chr20:3,622,011...3,624,629
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  CHEBI ontology 19812
    role 19761
      biological role 19761
        biochemical role 19381
          apoptosis inducer 13237
            copanlisib 3
              copanlisib dihydrochloride 0
Path 2
Term Annotations click to browse term
  CHEBI ontology 19812
    subatomic particle 19811
      composite particle 19811
        hadron 19811
          baryon 19811
            nucleon 19811
              atomic nucleus 19811
                atom 19811
                  main group element atom 19708
                    p-block element atom 19708
                      carbon group element atom 19630
                        carbon atom 19620
                          organic molecular entity 19620
                            organic group 18728
                              organic divalent group 18719
                                organodiyl group 18719
                                  carbonyl group 18667
                                    carbonyl compound 18667
                                      carboxylic acid 18364
                                        carboacyl group 17482
                                          univalent carboacyl group 17482
                                            carbamoyl group 17298
                                              carboxamide 17298
                                                monocarboxylic acid amide 15014
                                                  pyrimidinecarboxamide 3
                                                    copanlisib 3
                                                      copanlisib dihydrochloride 0
paths to the root