General Information of Drug (ID: DMRIMLJ)

Drug Name
BX-795 Drug Info
Synonyms BX795; BX 795
Indication
Disease Entry ICD 11 Status REF
Discovery agent N.A. Investigative [1]
Cross-matching ID
PubChem CID
10077147
ChEBI ID
CHEMBL91439
CAS Number
CAS 702675-74-9
TTD Drug ID
DMRIMLJ

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
DOT
Drug Status:
Clinical Trial Drug(s)
Investigative Drug(s)
Patented Agent(s)
Approved Drug(s)
Discontinued Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
AR-12 DM4RK6P Lymphoma 2A80-2A86 Phase 1 [4]
L-serine-O-phosphate DMTJ1NH Discovery agent N.A. Investigative [5]
PMID20005102C1 DMMESBW Discovery agent N.A. Investigative [6]
BX-912 DMZA45C Discovery agent N.A. Investigative [2]
PHT-427 DMI96Y3 Discovery agent N.A. Investigative [7]
PF-5177624 DMUOFT0 Solid tumour/cancer 2A00-2F9Z Investigative [8]
GSK-2334470 DM3BI7R Solid tumour/cancer 2A00-2F9Z Investigative [9]
⏷ Show the Full List of 7 Drug(s)
Drug(s) Targeting Checkpoint kinase-1 (CHK1)
Drug Name Drug ID Indication ICD 11 Highest Status REF
LY2603618 DMCXRZF Pancreatic cancer 2C10 Phase 2 [10]
UCN-01 DMUNJZB Non-small-cell lung cancer 2C25.Y Phase 2 [11]
SCH-900776 DM67EMK Solid tumour/cancer 2A00-2F9Z Phase 2 [12]
LY2606368 DM4XMF7 Ovarian cancer 2C73 Phase 2 [13]
LY2880070 DMADEHZ Solid tumour/cancer 2A00-2F9Z Phase 1/2 [14]
RG7741 DMK6P9J Lymphoma 2A80-2A86 Phase 1 [15]
GDC-0425 DMDZ26X Lymphoma 2A80-2A86 Phase 1 [16]
AZD7762 DM1FW0C Solid tumour/cancer 2A00-2F9Z Phase 1 [17]
MK-8776 DMAS1RB Hodgkin lymphoma 2B30 Phase 1 [18]
Diamidothiazole derivative 1 DM02V5Q N. A. N. A. Patented [19]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
R-roscovitine DMSH108 Non-small-cell lung cancer 2C25.Y Phase 2 [20]
Ro 31-7453 DM83QCL Solid tumour/cancer 2A00-2F9Z Phase 2 [21]
PHA848125 DMS2Q9G Thymic cancer 2C27 Phase 2 [22]
TG02 DMZFIGQ Anaplastic astrocytoma 2A00.0 Phase 1/2 [23]
NUV-422 DMQJQNT Malignant glioma 2A00.0 Phase 1/2 [24]
RGB-286638 DMEGOQP Haematological malignancy 2B33.Y Phase 1 [25]
FN-1501 DM7BMD6 Solid tumour/cancer 2A00-2F9Z Phase 1 [26]
AG-024322 DMY4WVK Solid tumour/cancer 2A00-2F9Z Phase 1 [20]
PHA-793887 DM2Y4FG Solid tumour/cancer 2A00-2F9Z Phase 1 [27]
SNS-032 DMEITAS Solid tumour/cancer 2A00-2F9Z Phase 1 [28]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
AMO-02 DMJRU3A Myotonic dystrophy 8C71.0 Phase 2/3 [29]
LY2090314 DMTBFE4 Acute myeloid leukaemia 2A60 Phase 2 [30]
Lithium DMZ3OU6 Bipolar disorder 6A60 Phase 2 [31]
Tideglusib DME4LA1 Alzheimer disease 8A20 Phase 2 [32]
9-ING-41 DM57TY3 Myelofibrosis 2A20.2 Phase 2 [33]
Neu-120 DMXKOUC Parkinson disease 8A00.0 Phase 1/2 [34]
KENPAULLONE DMAGVXW Discovery agent N.A. Patented [35]
CHIR-99021 DMB8MNU Allergic inflammation 4A80-4A85 Patented [36]
TDZD-8 DMG6Q45 Malignant glioma 2A00.0 Patented [37]
AR-A014418 DMUPN01 Ovarian cancer 2C73 Patented [38]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Sorafenib DMS8IFC Adenocarcinoma 2D40 Approved [39]
Romiplostim DM3U7SZ Thrombocytopenia 3B64 Approved [40]
Regorafenib DMHSY1I Gastrointestinal stromal tumour 2B5B Approved [41]
Sunitinib DMCBJSR Acute undifferentiated leukemia Approved [42]
Axitinib DMGVH6N Renal cell carcinoma 2C90 Approved [43]
Vandetanib DMRICNP Solid tumour/cancer 2A00-2F9Z Approved [21]
Pazopanib HCl DM6U9CQ Renal cell carcinoma 2C90 Approved [44]
Fruquintinib DMHOSCQ Colorectal cancer 2B91.Z Approved [45]
Cabozantinib DMIYDT4 Medullary thyroid gland carcinoma Approved [46]
Tivozanib DMUKC5L Renal cell carcinoma 2C90 Approved [47]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
BALANOL DMDLN9E N. A. N. A. Terminated [48]
4-[(3,5-diamino-1H-pyrazol-4-yl)diazenyl]phenol DMSKJ1X Discovery agent N.A. Investigative [49]
Ro-4396686 DM5DMCH Discovery agent N.A. Investigative [50]
PMID20005102C1 DMMESBW Discovery agent N.A. Investigative [6]
[3H]cAMP DMZRQU7 Discovery agent N.A. Investigative [51]
PMID19364658C33 DMSE1C3 Discovery agent N.A. Investigative [52]
BX-912 DMZA45C Discovery agent N.A. Investigative [2]
chelerythrine DMCP1G9 Discovery agent N.A. Investigative [53]
PMID21742770C1 DME3JMH Discovery agent N.A. Investigative [54]
Rp-adenosine 3',5'-cyclic monophosphothioate triethylamine (Rp-cAMPS) DM1JWGH Discovery agent N.A. Investigative [55]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Daunorubicin DMQUSBT Acute monocytic leukemia Approved [56]
Amlexanox DM0DQM5 Respiratory tract inflammation CA07 Approved [3]
Hydrogen peroxide DM1NG5W Infectious disease 1A00-CA43.1 Approved [57]
Acetic Acid, Glacial DM4SJ5Y infection in the ear canal AA0Y Approved [58]
Marinol DM70IK5 Anorexia nervosa cachexia 6B80 Approved [59]
Testosterone DM7HUNW Hot flushes GA30 Approved [60]
Calcitriol DM8ZVJ7 Congenital alopecia LC30 Approved [60]
Motexafin gadolinium DMEJKRF Brain cancer 2A00 Approved [58]
Zoledronate DMIXC7G Adenocarcinoma 2D40 Approved [61]
Melphalan DMOLNHF Hematologic disease 3C0Z Approved [62]
⏷ Show the Full List of 10 Drug(s)

Molecular Interaction Atlas of This Drug

Molecular Interaction Atlas

Drug Therapeutic Target (DTT)
DTT Name DTT ID UniProt ID MOA REF
Checkpoint kinase-1 (CHK1) TTTU902 CHK1_HUMAN Inhibitor [2]
Cyclin-dependent kinase 2 (CDK2) TT7HF4W CDK2_HUMAN Inhibitor [2]
Fungal Protein kinase A (Fung ypkA) TTYVI76 Q56921_YEREN Inhibitor [2]
Glycogen synthase kinase-3 beta (GSK-3B) TTRSMW9 GSK3B_HUMAN Inhibitor [2]
Phosphoinositide dependent protein kinase-1 (PDPK1) TT9QBI6 PDPK1_HUMAN Inhibitor [2]
Vascular endothelial growth factor receptor 2 (KDR) TTUTJGQ VGFR2_HUMAN Inhibitor [2]

Drug Off-Target (DOT)
DOT Name DOT ID UniProt ID Interaction REF
Inhibitor of nuclear factor kappa-B kinase subunit epsilon (IKBKE) OT5VYOSM IKKE_HUMAN Gene/Protein Processing [3]

References

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25 Small-molecule multi-targeted kinase inhibitor RGB-286638 triggers P53-dependent and -independent anti-multiple myeloma activity through inhibition of transcriptional CDKs. Leukemia. 2013 Dec;27(12):2366-75.
26 Discovery of 4-((7H-Pyrrolo[2,3-d]pyrimidin-4-yl)amino)-N-(4-((4-methylpiperazin-1-yl)methyl)phenyl)-1H-pyrazole-3-carboxamide (FN-1501), an FLT3- and CDK-Kinase Inhibitor with Potentially High Efficiency against Acute Myelocytic Leukemia. J Med Chem. 2018 Feb 22;61(4):1499-1518.
27 A first in man, phase I dose-escalation study of PHA-793887, an inhibitor of multiple cyclin-dependent kinases (CDK2, 1 and 4) reveals unexpected h... Cell Cycle. 2011 Mar 15;10(6):963-70.
28 Mechanism of action of SNS-032, a novel cyclin-dependent kinase inhibitor, in chronic lymphocytic leukemia. Blood. 2009 May 7;113(19):4637-45.
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31 The GSK3 kinase inhibitor lithium produces unexpected hyperphosphorylation of -catenin, a GSK3 substrate, in human glioblastoma cells. Biol Open. 2018 Jan 26;7(1):bio030874.
32 Evidence for irreversible inhibition of glycogen synthase kinase-3beta by tideglusib. J Biol Chem. 2012 Jan 6;287(2):893-904.
33 9-ING-41, a small molecule inhibitor of GSK-3beta, potentiates the effects of anticancer therapeutics in bladder cancer. Sci Rep. 2019 Dec 27;9(1):19977.
34 Company report (Neurim Pharmaceuticals)
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36 Selective glycogen synthase kinase 3 inhibitors potentiate insulin activation of glucose transport and utilization in vitro and in vivo. Diabetes. 2003 Mar;52(3):588-95.
37 Identification of novel scaffold of benzothiazepinones as non-ATP competitive glycogen synthase kinase-3beta inhibitors through virtual screening. Bioorg Med Chem Lett. 2012 Dec 1;22(23):7232-6.
38 Fragment and knowledge-based design of selective GSK-3beta inhibitors using virtual screening models. Eur J Med Chem. 2009 Jun;44(6):2361-71.
39 Preclinical overview of sorafenib, a multikinase inhibitor that targets both Raf and VEGF and PDGF receptor tyrosine kinase signaling.Mol Cancer Ther.2008 Oct;7(10):3129-40.
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50 Biological evaluation of a multi-targeted small molecule inhibitor of tumor-induced angiogenesis. Bioorg Med Chem Lett. 2006 Apr 1;16(7):1950-3.
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52 Identification and SAR of squarate inhibitors of mitogen activated protein kinase-activated protein kinase 2 (MK-2). Bioorg Med Chem. 2009 May 1;17(9):3342-51.
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54 A Potent and Selective Quinoxalinone-Based STK33 Inhibitor Does Not Show Synthetic Lethality in KRAS-Dependent Cells. ACS Med Chem Lett. 2012 Dec 13;3(12):1034-1038.
55 Inhibition of protein kinase A activity interferes with long-term, but not short-term, memory of conditioned taste aversions. Behav Neurosci. 2002 Dec;116(6):1070-4.
56 Genetic variants contributing to daunorubicin-induced cytotoxicity. Cancer Res. 2008 May 1;68(9):3161-8. doi: 10.1158/0008-5472.CAN-07-6381.
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58 Motexafin gadolinium and zinc induce oxidative stress responses and apoptosis in B-cell lymphoma lines. Cancer Res. 2005 Dec 15;65(24):11676-88.
59 THC exposure of human iPSC neurons impacts genes associated with neuropsychiatric disorders. Transl Psychiatry. 2018 Apr 25;8(1):89. doi: 10.1038/s41398-018-0137-3.
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62 Bone marrow osteoblast damage by chemotherapeutic agents. PLoS One. 2012;7(2):e30758. doi: 10.1371/journal.pone.0030758. Epub 2012 Feb 17.