Details of the Drug Combination

General Information of Drug Combination (ID: DC9Z8IP)

Drug Combination Name

SCH 727965 SCH-900776

Indication

Disease Entry	Status	REF
Carcinoma	Investigative	[1]

Component Drugs

SCH 727965 DMCJLD1

SCH-900776 DM67EMK

Small molecular drug

2D MOL

3D MOL

High-throughput Screening Result

Testing Cell Line: OV90

Zero Interaction Potency (ZIP) Score: 1.38

Bliss Independence Score: 4.37

Loewe Additivity Score: 2.15

LHighest Single Agent (HSA) Score: 5.61

Molecular Interaction Atlas of This Drug Combination

Molecular Interaction Atlas (MIA)

Indication(s) of SCH 727965

Disease Entry	ICD 11	Status	REF
Acute lymphoblastic leukaemia	2A85	Discontinued in Phase 3	[2]

SCH 727965 Interacts with 3 DTT Molecule(s)

DTT Name	DTT ID	UniProt ID	Mode of Action	REF
Cyclin-dependent kinase 9 (CDK9)	TT1LVF2	CDK9_HUMAN	Inhibitor	[4]
Cyclin-dependent kinase 1 (CDK1)	TTH6V3D	CDK1_HUMAN	Inhibitor	[4]
Cyclin-dependent kinase 2 (CDK2)	TT7HF4W	CDK2_HUMAN	Inhibitor	[4]
------------------------------------------------------------------------------------

SCH 727965 Interacts with 7 DOT Molecule(s)

DOT Name	DOT ID	UniProt ID	Mode of Action	REF
Retinoblastoma-associated protein (RB1)	OTQJUJMZ	RB_HUMAN	Decreases Phosphorylation	[5]
Poly polymerase 1 (PARP1)	OT310QSG	PARP1_HUMAN	Increases Cleavage	[5]
Breast cancer type 1 susceptibility protein (BRCA1)	OT5BN6VH	BRCA1_HUMAN	Decreases Expression	[6]
Breast cancer type 2 susceptibility protein (BRCA2)	OTF1XSV1	BRCA2_HUMAN	Decreases Expression	[6]
DNA repair protein RAD51 homolog 1 (RAD51)	OTNVWGC1	RAD51_HUMAN	Decreases Expression	[6]
Fanconi anemia group D2 protein (FANCD2)	OTVEB5LF	FACD2_HUMAN	Decreases Expression	[6]
Cyclin-dependent kinase 12 (CDK12)	OTZUDGNU	CDK12_HUMAN	Decreases Activity	[6]
------------------------------------------------------------------------------------


⏷ Show the Full List of 7 DOT(s)

Indication(s) of SCH-900776

Disease Entry	ICD 11	Status	REF
Solid tumour/cancer	2A00-2F9Z	Phase 2	[3]

SCH-900776 Interacts with 1 DTT Molecule(s)

DTT Name	DTT ID	UniProt ID	Mode of Action	REF
Checkpoint kinase-1 (CHK1)	TTTU902	CHK1_HUMAN	Inhibitor	[7]
------------------------------------------------------------------------------------

Test Results of This Drug Combination in Other Disease Systems

Indication	DrugCom ID	Cell Line	Status	REF
Ewing sarcoma-peripheral primitive neuroectodermal tumour	DCTFAHC	ES2	Investigative	[8]
Carcinoma	DCYGQRW	MDAMB436	Investigative	[1]
Colon carcinoma	DC7U843	RKO	Investigative	[1]
Invasive ductal carcinoma	DCLL6ON	T-47D	Investigative	[1]
Adenocarcinoma	DCA6RV1	CAOV3	Investigative	[9]
Adenocarcinoma	DCO77CY	A427	Investigative	[9]
Adenocarcinoma	DC4V54L	NCIH520	Investigative	[9]
Adenocarcinoma	DC7K0MG	COLO320DM	Investigative	[9]
Adenocarcinoma	DC29FJP	DLD1	Investigative	[9]
Adenocarcinoma	DCFSSX6	HT29	Investigative	[9]
Adenocarcinoma	DC4XTCM	HCT116	Investigative	[9]
Amelanotic melanoma	DCJL27L	A2058	Investigative	[9]
Germ cell tumour	DCVDCC9	PA1	Investigative	[9]
Large cell lung carcinoma	DCMJTED	NCI-H460	Investigative	[9]
Malignant melanoma	DCV9UV4	A375	Investigative	[9]
Malignant melanoma	DCPBTAA	HT144	Investigative	[9]
Malignant melanoma	DCDGA0L	RPMI7951	Investigative	[9]
Malignant melanoma	DC7HJMU	SKMEL30	Investigative	[9]
Malignant melanoma	DCOXZUA	UACC62	Investigative	[9]
Mesothelioma	DCMC99S	MSTO	Investigative	[9]
Ovarian endometrioid adenocarcinoma	DC5VA04	A2780	Investigative	[9]
Prostate carcinoma	DCMTY2S	VCAP	Investigative	[9]
------------------------------------------------------------------------------------


⏷ Show the Full List of 22 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	URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 7379).
3	URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 7943).
4	Cell cycle kinases as therapeutic targets for cancer. Nat Rev Drug Discov. 2009 Jul;8(7):547-66.
5	Dinaciclib (SCH 727965), a novel and potent cyclin-dependent kinase inhibitor. Mol Cancer Ther. 2010 Aug;9(8):2344-53. doi: 10.1158/1535-7163.MCT-10-0324. Epub 2010 Jul 27.
6	CDK12 Inhibition Reverses De Novo and Acquired PARP Inhibitor Resistance in BRCA Wild-Type and Mutated Models of Triple-Negative Breast Cancer. Cell Rep. 2016 Nov 22;17(9):2367-2381. doi: 10.1016/j.celrep.2016.10.077.
7	Targeting the replication checkpoint using SCH 900776, a potent and functionally selective CHK1 inhibitor identified via high content screening. Mol Cancer Ther. 2011 Apr;10(4):591-602.
8	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.
9	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.