General Information of Drug (ID: DMAWLGI)

Drug Name
PMID26924192-Compound-105 Drug Info
Cross-matching ID
PubChem CID
118548311
TTD Drug ID
DMAWLGI

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
Drug Status:
Clinical Trial Drug(s)
Patented Agent(s)
Investigative Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
CPI-0610 DMPXOYJ Myelofibrosis 2A20.2 Phase 3 [2]
OTX-015 DMI8RG1 Acute myeloid leukaemia 2A60 Phase 1/2 [2]
PLX2853 DMX168L Acute myeloid leukaemia 2A60 Phase 1/2 [3]
RVX-208 DM1LO8K Alzheimer disease 8A20 Phase 1/2 [2]
INCB57643 DMBGU7V Advanced malignancy 2A00-2F9Z Phase 1/2 [3]
ABBV-744 DMTEA9C Acute myeloid leukaemia 2A60 Phase 1 [3]
(+)-JQ1 DM1CZSJ Testicular cancer 2C80 Phase 1 [4]
GSK525762 DMPAWBN Haematological malignancy 2B33.Y Phase 1 [2]
TEN010 DM4UOY5 Advanced solid tumour 2A00-2F9Z Phase 1 [2]
AZD5153 DMW4GM2 Solid tumour/cancer 2A00-2F9Z Phase 1 [3]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
ABBV-744 DMTEA9C Acute myeloid leukaemia 2A60 Phase 1 [3]
PMID26924192-Compound-104 DM346EU N. A. N. A. Patented [1]
PMID26924192-Compound-102 DMEJ107 N. A. N. A. Patented [1]
PMID26924192-Compound-103 DMWOCP7 N. A. N. A. Patented [1]
Pyrrolo-pyrrolone derivative 1 DMN4SE5 N. A. N. A. Patented [1]
XD14 DMUMACD Discovery agent N.A. Investigative [5]
GW841819X DMRL9IN Discovery agent N.A. Investigative [6]
PMID24000170C36 DMHUWZS Discovery agent N.A. Investigative [7]
PMID24000170C38 DMOLRIY Discovery agent N.A. Investigative [7]
I-BET151 DMYRUH2 Discovery agent N.A. Investigative [8]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
OTX-015 DMI8RG1 Acute myeloid leukaemia 2A60 Phase 1/2 [2]
ABBV-744 DMTEA9C Acute myeloid leukaemia 2A60 Phase 1 [3]
PMID26924192-Compound-104 DM346EU N. A. N. A. Patented [1]
PMID26924192-Compound-102 DMEJ107 N. A. N. A. Patented [1]
PMID26924192-Compound-103 DMWOCP7 N. A. N. A. Patented [1]
Pyrrolo-pyrrolone derivative 1 DMN4SE5 N. A. N. A. Patented [1]
PMID26924192-Compound-106 DM9HRZJ N. A. N. A. Patented [1]
XD14 DMUMACD Discovery agent N.A. Investigative [5]
GW841819X DMRL9IN Discovery agent N.A. Investigative [6]
PMID24000170C36 DMHUWZS Discovery agent N.A. Investigative [7]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
(+)-JQ1 DM1CZSJ Testicular cancer 2C80 Phase 1 [9]
PMID26924192-Compound-104 DM346EU N. A. N. A. Patented [1]
PMID26924192-Compound-102 DMEJ107 N. A. N. A. Patented [1]
PMID26924192-Compound-103 DMWOCP7 N. A. N. A. Patented [1]
XD14 DMUMACD Discovery agent N.A. Investigative [5]

Molecular Interaction Atlas of This Drug

Molecular Interaction Atlas

Drug Therapeutic Target (DTT)
DTT Name DTT ID UniProt ID MOA REF
Bromodomain testis-specific protein (BRDT) TT7CPI5 BRDT_HUMAN Inhibitor [1]
Bromodomain-containing protein 2 (BRD2) TTDP48B BRD2_HUMAN Inhibitor [1]
Bromodomain-containing protein 3 (BRD3) TTHE657 BRD3_HUMAN Inhibitor [1]
Bromodomain-containing protein 4 (BRD4) TTRA6BO BRD4_HUMAN Inhibitor [1]

References

1 BET inhibitors in cancer therapeutics: a patent review.Expert Opin Ther Pat. 2016;26(4):505-22.
2 Targeting bromodomains: epigenetic readers of lysine acetylation.Nat Rev Drug Discov.2014 May;13(5):337-56.
3 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
4 Selective inhibition of BET bromodomains. Nature. 2010 Dec 23;468(7327):1067-73.
5 4-Acyl pyrroles: mimicking acetylated lysines in histone code reading. Angew Chem Int Ed Engl. 2013 Dec 23;52(52):14055-9.
6 Discovery and characterization of small molecule inhibitors of the BET family bromodomains. J Med Chem. 2011 Jun 9;54(11):3827-38.
7 Naphthyridines as novel BET family bromodomain inhibitors. ChemMedChem. 2014 Mar;9(3):580-9.
8 Inhibition of BET recruitment to chromatin as an effective treatment for MLL-fusion leukaemia. Nature. 2011 Oct 2;478(7370):529-33.
9 Small-molecule inhibition of BRDT for male contraception. Cell. 2012 Aug 17;150(4):673-84.