General Information of Drug Combination (ID: DCJL92N)

Drug Combination Name
MK-4827 SNX-2112
Indication
Disease Entry Status REF
Non small cell carcinoma Investigative [1]
Component Drugs MK-4827   DMLYGH4 SNX-2112   DMB5A80
Small molecular drug Small molecular drug
2D MOL 2D MOL
3D MOL 3D MOL
High-throughput Screening Result Testing Cell Line: SKMES1
Zero Interaction Potency (ZIP) Score: 7.25
Bliss Independence Score: 6.69
Loewe Additivity Score: 8.66
LHighest Single Agent (HSA) Score: 9.46

Molecular Interaction Atlas of This Drug Combination

Molecular Interaction Atlas (MIA)
Indication(s) of MK-4827
Disease Entry ICD 11 Status REF
Ovarian cancer 2C73 Phase 3 [2]
Breast cancer 2C60-2C65 Phase 2 [3]
Ewing sarcoma 2B52 Phase 1 [3]
MK-4827 Interacts with 1 DTT Molecule(s)
DTT Name DTT ID UniProt ID Mode of Action REF
Poly [ADP-ribose] polymerase (PARP) TTEBCY8 NOUNIPROTAC Modulator [5]
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MK-4827 Interacts with 3 DME Molecule(s)
DME Name DME ID UniProt ID Mode of Action REF
Cytochrome P450 1A1 (CYP1A1) DE6OQ3W CP1A1_HUMAN Metabolism [6]
Carboxylesterase 1 (CES1) DEB30C5 EST1_HUMAN Metabolism [7]
Beta-glucuronidase (GUSB) DEP54UE BGLR_HUMAN Metabolism [7]
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MK-4827 Interacts with 1 DOT Molecule(s)
DOT Name DOT ID UniProt ID Mode of Action REF
Histone H2AX (H2AX) OT18UX57 H2AX_HUMAN Increases Expression [8]
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Indication(s) of SNX-2112
Disease Entry ICD 11 Status REF
Discovery agent N.A. Investigative [4]
SNX-2112 Interacts with 1 DTT Molecule(s)
DTT Name DTT ID UniProt ID Mode of Action REF
Heat shock protein 90 alpha (HSP90A) TT78R5H HS90A_HUMAN Inhibitor [4]
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SNX-2112 Interacts with 14 DOT Molecule(s)
DOT Name DOT ID UniProt ID Mode of Action REF
Inhibitor of nuclear factor kappa-B kinase subunit alpha (CHUK) OTLF4ZB1 IKKA_HUMAN Decreases Expression [9]
Poly polymerase 1 (PARP1) OT310QSG PARP1_HUMAN Increases Cleavage [9]
Apoptosis regulator Bcl-2 (BCL2) OT9DVHC0 BCL2_HUMAN Decreases Expression [9]
Endoplasmic reticulum chaperone BiP (HSPA5) OTFUIRAO BIP_HUMAN Decreases Expression [9]
Endoplasmin (HSP90B1) OT02XLBR ENPL_HUMAN Decreases Expression [9]
RAC-alpha serine/threonine-protein kinase (AKT1) OT8H2YY7 AKT1_HUMAN Decreases Expression [9]
Caspase-3 (CASP3) OTIJRBE7 CASP3_HUMAN Increases Expression [9]
Caspase-9 (CASP9) OTD4RFFG CASP9_HUMAN Increases Expression [9]
Cytochrome c (CYCS) OTBFALJD CYC_HUMAN Affects Localization [9]
Transcription factor p65 (RELA) OTUJP9CN TF65_HUMAN Decreases Expression [9]
Apoptosis regulator BAX (BAX) OTAW0V4V BAX_HUMAN Increases Expression [9]
Bcl-2-like protein 1 (BCL2L1) OTRC5K9O B2CL1_HUMAN Decreases Expression [9]
Heat shock protein 75 kDa, mitochondrial (TRAP1) OTNG0L8J TRAP1_HUMAN Decreases Expression [9]
Caspase-8 (CASP8) OTA8TVI8 CASP8_HUMAN Increases Activity [9]
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⏷ Show the Full List of 14 DOT(s)

Test Results of This Drug Combination in Other Disease Systems

Indication DrugCom ID Cell Line Status REF
Ewing sarcoma-peripheral primitive neuroectodermal tumour DCQOSV7 ES2 Investigative [10]
Breast carcinoma DC863YI ZR751 Investigative [11]
Breast carcinoma DC7HYCK KPL1 Investigative [11]
Breast carcinoma DCA9DX4 OCUBM Investigative [11]
Carcinoma DCJ44T6 OV90 Investigative [11]
Carcinoma DC6Z2I9 EFM192B Investigative [11]
Carcinoma DCYZGOT MDAMB436 Investigative [11]
Colon adenocarcinoma DC2ROHE LOVO Investigative [11]
Colon carcinoma DCQIQ79 RKO Investigative [11]
Invasive ductal carcinoma DC0XGVK T-47D Investigative [11]
Rectal adenocarcinoma DCN643W SW837 Investigative [11]
Adenocarcinoma DCIKDDC CAOV3 Investigative [1]
Adenocarcinoma DC0L2WK OVCAR3 Investigative [1]
Adenocarcinoma DCHW25O A427 Investigative [1]
Adenocarcinoma DCZZOHN NCIH1650 Investigative [1]
Adenocarcinoma DCVNSN7 NCIH2122 Investigative [1]
Adenocarcinoma DCNL3AP NCIH23 Investigative [1]
Adenocarcinoma DCFNTKC NCIH520 Investigative [1]
Adenocarcinoma DCYAYYW COLO320DM Investigative [1]
Adenocarcinoma DCVFKNW DLD1 Investigative [1]
Adenocarcinoma DCI0IQB HCT116 Investigative [1]
Adenocarcinoma DC8VEIK HT29 Investigative [1]
Adenocarcinoma DCEKHIK SW-620 Investigative [1]
Amelanotic melanoma DC8ESVA A2058 Investigative [1]
Germ cell tumour DCJT3AG PA1 Investigative [1]
Large cell lung carcinoma DCFXI48 NCI-H460 Investigative [1]
Malignant melanoma DCBPB7L HT144 Investigative [1]
Malignant melanoma DCCYUYS SKMEL30 Investigative [1]
Malignant melanoma DC96WY2 UACC62 Investigative [1]
Malignant melanoma DC8Q5PN A375 Investigative [1]
Mesothelioma DCX2XY6 MSTO Investigative [1]
Ovarian endometrioid adenocarcinoma DCHMI4S A2780 Investigative [1]
Ovarian serous cystadenocarcinoma DCPDGB7 SK-OV-3 Investigative [1]
Prostate carcinoma DCPGJ6F LNCAP Investigative [1]
Prostate carcinoma DCWDV0K VCAP Investigative [1]
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⏷ Show the Full List of 35 DrugCom(s)

References

1 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.
2 ClinicalTrials.gov (NCT03602859) A Phase 3 Comparison of Platinum-based Therapy With TSR-042 and Niraparib Versus Standard of Care (SOC) Platinum-based Therapy as First-line Treatment of Stage III or IV Nonmucinous Epithelial Ovarian Cancer (FIRST). U.S. National Institutes of Health.
3 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
4 Heat shock protein 90: inhibitors in clinical trials. J Med Chem. 2010 Jan 14;53(1):3-17.
5 Interpreting expression profiles of cancers by genome-wide survey of breadth of expression in normal tissues. Genomics 2005 Aug;86(2):127-41.
6 Discovery of 2-{4-[(3S)-piperidin-3-yl]phenyl}-2H-indazole-7-carboxamide (MK-4827): a novel oral poly(ADP-ribose)polymerase (PARP) inhibitor efficacious in BRCA-1 and -2 mutant tumors. J Med Chem. 2009 Nov 26;52(22):7170-85.
7 Summary of FDA-approved anticancer cytotoxic drugs at May 2019.
8 Autophagy up-regulated by MEK/ERK promotes the repair of DNA damage caused by aflatoxin B1. Toxicol Mech Methods. 2022 Feb;32(2):87-96. doi: 10.1080/15376516.2021.1968985. Epub 2021 Aug 26.
9 The Hsp90 inhibitor SNX-2112, induces apoptosis in multidrug resistant K562/ADR cells through suppression of Akt/NF-B and disruption of mitochondria-dependent pathways. Chem Biol Interact. 2013 Sep 5;205(1):1-10. doi: 10.1016/j.cbi.2013.06.007. Epub 2013 Jun 15.
10 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.
11 Biologically active neutrophil chemokine pattern in tonsillitis.Clin Exp Immunol. 2004 Mar;135(3):511-8. doi: 10.1111/j.1365-2249.2003.02390.x.