General Information of This Drug (ID: DMJ0936)

Drug Name
PF-03772304   DMJ0936
Synonyms
MTOR inhibitors, Biotica; MTOR inhibitors, Wyeth; PF-04979064; PF-05017255; PF-05168899; WYE-125132; WYE-132; WYE-178; WYE-354; WYE-600; WYE-687; Imidazolo and pyrazolopyrimidine derivatives (cancer), Pfizer; Imidazolopyrimidine derivatives (cancer), Pfizer; Imidazolopyrimidine derivatives (cancer), Wyeth; Non-rapamycin mTOR/PI3K inhibitors (cancer); PI3K/mTOR signalling inhibitors (cancer), Wyeth; Non-rapamycin mTOR/PI3K inhibitors (cancer), Pfizer; 5H-pyrrolo[3,2-d]pyridimine analogs (cancer), Wyeth
Indication
Disease Entry ICD 11 Status REF
Solid tumour/cancer 2A00-2F9Z Investigative [1]
Structure 3D Structure is Not Available
3D MOL 2D MOL

List of Combinatorial Drugs (CBD) Containing This Drug

7 Investigative Drug Combination(s) Consisting of This drug
Normalized Drug Combination Synergy Score
Synergy scores were normalized using Min-Max Scaling to facilitate visual comparisons.
DrugCom Name DrugCom ID Component Drug Indication REF
PF-03772304 + Ruxolitinib DCCZVUG Ruxolitinib T-cell leukemia/lymphoma (Cell Line: ED-40515) [2]
PF-03772304 + Panobinostat DC4KEK3 Panobinostat Diffuse intrinsic pontine glioma (Cell Line: DIPG25) [2]
PF-03772304 + Marizomib DCPL9YV Marizomib Diffuse intrinsic pontine glioma (Cell Line: DIPG25) [2]
PF-03772304 + Idarubicin DCII6T2 Idarubicin Glioblastoma? (Cell Line: T98G) [2]
PF-03772304 + PF-562271 DCZ9V5Z PF-562271 Diffuse large B cell lymphoma (Cell Line: TMD8) [2]
PF-03772304 + Ibrutinib DCSYR2F Ibrutinib Diffuse large B cell lymphoma (Cell Line: TMD8) [2]
PF-03772304 + Ruxolitinib DCCRSR2 Ruxolitinib Hodgkin lymphoma (Cell Line: L-1236) [3]
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⏷ Show the Full List of 7 DrugCom(s)

References

1 Discovery of the Highly Potent PI3K/mTOR Dual Inhibitor PF-04979064 through Structure-Based Drug Design. ACS Med Chem Lett. 2012 Nov 7;4(1):91-7.
2 Recurrent recessive mutation in deoxyguanosine kinase causes idiopathic noncirrhotic portal hypertension.Hepatology. 2016 Jun;63(6):1977-86. doi: 10.1002/hep.28499. Epub 2016 Mar 31.
3 Loss of function mutations in VARS encoding cytoplasmic valyl-tRNA synthetase cause microcephaly, seizures, and progressive cerebral atrophy.Hum Genet. 2018 Apr;137(4):293-303. doi: 10.1007/s00439-018-1882-3. Epub 2018 Apr 24.