Details of the Drug Combination

General Information of Drug Combination (ID: DC2X2FE)

Drug Combination Name
SY-1425 TEM
Indication
Disease Entry Status REF
Colon adenocarcinoma Investigative [1]
Component Drugs SY-1425   DMH8UF0 TEM   DMLNFWU
N.A. Small molecular drug
High-throughput Screening Result Testing Cell Line: COLO 205
Zero Interaction Potency (ZIP) Score: 1.86
Bliss Independence Score: 3.69
Loewe Additivity Score: 2.68
LHighest Single Agent (HSA) Score: 2.09

Molecular Interaction Atlas of This Drug Combination

Molecular Interaction Atlas (MIA)
Indication(s) of SY-1425
Disease Entry ICD 11 Status REF
Acute myeloid leukaemia 2A60 Phase 1 [2]
Myelodysplastic syndrome 2A37 Phase 1 [2]
SY-1425 Interacts with 1 DTT Molecule(s)
DTT Name DTT ID UniProt ID Mode of Action REF
Retinoic acid receptor alpha (RARA) TTW38KT RARA_HUMAN Agonist [2]
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Indication(s) of TEM
Disease Entry ICD 11 Status REF
Postherpetic neuralgia 1E91.5 Phase 2 [3]

Test Results of This Drug Combination in Other Disease Systems

Indication DrugCom ID Cell Line Status REF
Adult T acute lymphoblastic leukemia DCSSUD1 MOLT-4 Investigative [4]
Glioma DC8FGGC SF-268 Investigative [4]
Invasive ductal carcinoma DCUPKHT T-47D Investigative [1]
Adenocarcinoma DCR954W HCT116 Investigative [5]
Amelanotic melanoma DC80FIE MDA-MB-435 Investigative [5]
Non-small cell lung carcinoma DCYFHO6 HOP-92 Investigative [5]
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⏷ Show the Full List of 6 DrugCom(s)

References

1 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.
2 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
3 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800030055)
4 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.
5 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.