General Information of Drug (ID: DMOZEW9)

Drug Name
PD-0173955 Drug Info
Synonyms PD-17395
Indication
Disease Entry ICD 11 Status REF
Discovery agent N.A. Investigative [1]
Cross-matching ID
PubChem CID
447077
ChEBI ID
CHEBI:49791
CAS Number
CAS 260415-63-2
TTD Drug ID
DMOZEW9

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
Drug Status:
Approved Drug(s)
Clinical Trial Drug(s)
Investigative Drug(s)
Patented Agent(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Dasatinib DMJV2EK Blast phase chronic myelogenous leukemia, BCR-ABL1 positive Approved [4]
VX-680 DM93YKJ Solid tumour/cancer 2A00-2F9Z Phase 2 [4]
JNJ-26483327 DMSQ3AZ Solid tumour/cancer 2A00-2F9Z Phase 1 [5]
ISIS-CRP DMQDUG4 Cardiovascular disease BA00-BE2Z Phase 1 [6]
RO-316233 DMAGLPW Discovery agent N.A. Investigative [7]
Bisindolylmaleimide-I DMOQJZC Discovery agent N.A. Investigative [7]
4,5,6,7-tetrabromo-1H-benzo[d][1,2,3]triazole DMN9YOB Discovery agent N.A. Investigative [8]
CI-1040 DMF3DZX Discovery agent N.A. Investigative [7]
AMP-PNP DMTOK1D Discovery agent N.A. Investigative [9]
BMS-536924 DMXJB4N Discovery agent N.A. Investigative [10]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Imatinib DM7RJXL Acute lymphoblastic leukaemia 2A85 Approved [4]
Dasatinib DMJV2EK Blast phase chronic myelogenous leukemia, BCR-ABL1 positive Approved [4]
Nilotinib DM7HXWT Chronic myelogenous leukaemia 2A20.0 Approved [11]
Asciminib DM7EVUF Chronic myeloid leukaemia 2A20 Approved [12]
Radotinib DMWA74Y leukaemia 2A60-2B33 Phase 3 [13]
ABL 001 DMMF5K4 Chronic myeloid leukaemia 2A20 Phase 3 [14]
ICLUSIG DM1SQSE Acute lymphoblastic leukaemia 2A85 Phase 3 [15]
Bafetinib DM7586F Bone disease FC0Z Phase 2 [16]
AN-019 DMJ7QP8 Chronic myelogenous leukaemia 2A20.0 Phase 2 [17]
HQP1351 DMQ30X2 Chronic myeloid leukaemia 2A20 Phase 2 [18]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Romiplostim DM3U7SZ Thrombocytopenia 3B64 Approved [19]
Intedanib DMSTA36 Colorectal cancer 2B91.Z Approved [20]
Pemigatinib DM819JF Cholangiocarcinoma 2C12.10 Approved [21]
Infigratinib DMNKBEC Cholangiocarcinoma 2C12.10 Approved [22]
E-3810 DM42PFT Solid tumour/cancer 2A00-2F9Z Phase 3 [23]
Sulfatinib DMPOTM4 Neuroendocrine cancer 2B72.1 Phase 3 [24]
ARQ-087 DM02BVQ Intrahepatic cholangiocarcinoma 2C12.10 Phase 3 [25]
AZD4547 DM3827C Solid tumour/cancer 2A00-2F9Z Phase 2/3 [26]
Debio 1347 DMZW50O Solid tumour/cancer 2A00-2F9Z Phase 2 [27]
AM-001 DMGVQI8 Actinic keratosis EK90.0 Phase 2 [28]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Romiplostim DM3U7SZ Thrombocytopenia 3B64 Approved [29]
Ripretinib DM958QB Gastrointestinal stromal tumour 2B5B Approved [30]
Olaratumab DMNYOIX Soft tissue sarcoma 2B57 Approved [31]
Avapritinib DMK2GZX Gastrointestinal stromal tumour 2B5B Approved [32]
E-3810 DM42PFT Solid tumour/cancer 2A00-2F9Z Phase 3 [23]
CP-868596 DMZIM37 Gastrointestinal cancer 2C11 Phase 3 [33]
Famitinib DMSFWT7 Solid tumour/cancer 2A00-2F9Z Phase 2 [34]
XL-820 DMMHX9K Solid tumour/cancer 2A00-2F9Z Phase 2 [35]
MP470 DMELUAK Solid tumour/cancer 2A00-2F9Z Phase 2 [36]
MEDI-575 DMI9WVM Glioblastoma multiforme 2A00.0 Phase 2 [37]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Sorafenib DMS8IFC Adenocarcinoma 2D40 Approved [38]
Romiplostim DM3U7SZ Thrombocytopenia 3B64 Approved [29]
Becaplermin DM1R5X4 Diabetic complication 5A2Y Approved [39]
E-3810 DM42PFT Solid tumour/cancer 2A00-2F9Z Phase 3 [23]
Famitinib DMSFWT7 Solid tumour/cancer 2A00-2F9Z Phase 2 [34]
XL-820 DMMHX9K Solid tumour/cancer 2A00-2F9Z Phase 2 [35]
MK-2461 DM21WBH Alzheimer disease 8A20 Phase 1/2 [40]
SNN-0031 DM2X3BR Brain injury NA07.Z Phase 1/2 [41]
TAK-593 DMNFZOT Solid tumour/cancer 2A00-2F9Z Phase 1 [42]
Pyridine derivative 18 DMBZMYT N. A. N. A. Patented [43]
⏷ Show the Full List of 10 Drug(s)
Drug(s) Targeting Proto-oncogene c-Src (SRC)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Dasatinib DMJV2EK Blast phase chronic myelogenous leukemia, BCR-ABL1 positive Approved [4]
Bosutinib DMTI8YE Blast phase chronic myelogenous leukemia, BCR-ABL1 positive Approved [4]
SKI-758 DMQ8E9R Ischemia 8B10-8B11 Approved [44]
Herbimycin A DM6YWBF Solid tumour/cancer 2A00-2F9Z Approved [45]
AL3818 DM3WP0N Alveolar soft part sarcoma 2A60-2C35 Phase 3 [27]
CP-868596 DMZIM37 Gastrointestinal cancer 2C11 Phase 3 [27]
Masitinib DMRSNEU Amyotrophic lateral sclerosis 8B60.0 Phase 3 [46]
KX-01 DMF0NA9 Actinic keratosis EK90.0 Phase 3 [47]
Saracatinib DMBLHGP Hematologic tumour 2B33.Y Phase 2 [48]
TPX-0046 DMIVE67 Solid tumour/cancer 2A00-2F9Z Phase 1/2 [49]
⏷ 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
Fibroblast growth factor receptor 1 (FGFR1) TTRLW2X FGFR1_HUMAN Inhibitor [2]
Fusion protein Bcr-Abl (Bcr-Abl) TTS7G69 BCR_HUMAN-ABL1_HUMAN Inhibitor [3]
LCK tyrosine protein kinase (LCK) TT860QF LCK_HUMAN Inhibitor [2]
Platelet-derived growth factor receptor alpha (PDGFRA) TT8FYO9 PGFRA_HUMAN Inhibitor [2]
Platelet-derived growth factor receptor beta (PDGFRB) TTI7421 PGFRB_HUMAN Inhibitor [2]
Proto-oncogene c-Src (SRC) TT6PKBN SRC_HUMAN Inhibitor [2]

References

1 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: 5699).
2 Biochemical and cellular effects of c-Src kinase-selective pyrido[2, 3-d]pyrimidine tyrosine kinase inhibitors. Biochem Pharmacol. 2000 Oct 1;60(7):885-98.
3 Structural insights into the ATP binding pocket of the anaplastic lymphoma kinase by site-directed mutagenesis, inhibitor binding analysis, and hom... J Med Chem. 2006 Sep 21;49(19):5759-68.
4 A comparison of physicochemical property profiles of marketed oral drugs and orally bioavailable anti-cancer protein kinase inhibitors in clinical development. Curr Top Med Chem. 2007;7(14):1408-22.
5 National Cancer Institute Drug Dictionary (drug id 596693).
6 The selectivity of protein kinase inhibitors: a further update. Biochem J. 2007 Dec 15;408(3):297-315.
7 Specificity and mechanism of action of some commonly used protein kinase inhibitors. Biochem J. 2000 Oct 1;351(Pt 1):95-105.
8 Optimization of protein kinase CK2 inhibitors derived from 4,5,6,7-tetrabromobenzimidazole. J Med Chem. 2004 Dec 2;47(25):6239-47.
9 The Protein Data Bank. Nucleic Acids Res. 2000 Jan 1;28(1):235-42.
10 Discovery of a (1H-benzoimidazol-2-yl)-1H-pyridin-2-one (BMS-536924) inhibitor of insulin-like growth factor I receptor kinase with in vivo antitum... J Med Chem. 2005 Sep 8;48(18):5639-43.
11 2007 FDA drug approvals: a year of flux. Nat Rev Drug Discov. 2008 Feb;7(2):107-9.
12 Asciminib in Chronic Myeloid Leukemia after ABL Kinase Inhibitor Failure. N Engl J Med. 2019 Dec 12;381(24):2315-2326.
13 Danusertib, an aurora kinase inhibitor.Expert Opin Investig Drugs.2012 Mar;21(3):383-93.
14 ABL001, a Potent Allosteric Inhibitor of BCR-ABL, Prevents Emergence of Resistant Disease When Administered in Combination with Nilotinib in an in Vivo Murine Model of Chronic Myeloid Leukemia, NorthBuilding, 2014, 120-125.
15 Ponatinib efficacy and safety in Philadelphia chromosome-positive leukemia: final 5-year results of the phase 2 PACE trial. Blood. 2018 Jul 26;132(4):393-404.
16 Interpreting expression profiles of cancers by genome-wide survey of breadth of expression in normal tissues. Genomics 2005 Aug;86(2):127-41.
17 Design, synthesis and preclinical evaluation of NRC-AN-019. Int J Oncol. 2013 Jan;42(1):168-78.
18 Preclinical development of HQP1351, a multikinase inhibitor targeting a broad spectrum of mutant KIT kinases, for the treatment of imatinib-resistant gastrointestinal stromal tumors. Cell Biosci. 2019 Oct 26;9:88.
19 Anthranilic acid amides: a novel class of antiangiogenic VEGF receptor kinase inhibitors. J Med Chem. 2002 Dec 19;45(26):5687-93.
20 2014 FDA drug approvals. Nat Rev Drug Discov. 2015 Feb;14(2):77-81.
21 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services. 2020
22 Pharmacological inhibition of fibroblast growth factor (FGF) receptor signaling ameliorates FGF23-mediated hypophosphatemic rickets. J Bone Miner Res. 2013 Apr;28(4):899-911.
23 E-3810 is a potent dual inhibitor of VEGFR and FGFR that exerts antitumor activity in multiple preclinical models. Cancer Res. 2011 Feb 15;71(4):1396-405.
24 Clinical pipeline report, company report or official report of Hutchison Medi Pharma.
25 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. (Target id: 1808).
26 AZD4547: an orally bioavailable, potent, and selective inhibitor of the fibroblast growth factor receptor tyrosine kinase family. Cancer Res. 2012 Apr 15;72(8):2045-56.
27 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
28 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800029917)
29 Discovery of 5-[5-fluoro-2-oxo-1,2- dihydroindol-(3Z)-ylidenemethyl]-2,4- dimethyl-1H-pyrrole-3-carboxylic acid (2-diethylaminoethyl)amide, a novel... J Med Chem. 2003 Mar 27;46(7):1116-9.
30 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services. 2020
31 A phase I study of olaratumab, an anti-platelet-derived growth factor receptor alpha (PDGFRalpha) monoclonal antibody, in patients with advanced solid tumors. Cancer Chemother Pharmacol. 2014 Mar;73(3):595-604.
32 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services. 2020
33 The FLT3 and PDGFR inhibitor crenolanib is a substrate of the multidrug resistance protein ABCB1 but does not inhibit transport function at pharmacologically relevant concentrations.Invest New Drugs.2015 Apr;33(2):300-9.
34 Metabolism and bioactivation of famitinib, a novel inhibitor of receptor tyrosine kinase, in cancer patients. Br J Pharmacol. 2013 Apr;168(7):1687-706.
35 National Cancer Institute Drug Dictionary (drug id 452042).
36 Phase 1B study of amuvatinib in combination with five standard cancer therapies in adults with advanced solid tumors. Cancer Chemother Pharmacol. 2014 Jul;74(1):195-204.
37 Clinical pipeline report, company report or official report of MedImmune (2011).
38 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.
39 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health & Human Services.
40 MK-2461, a novel multitargeted kinase inhibitor, preferentially inhibits the activated c-Met receptor. Cancer Res. 2010 Feb 15;70(4):1524-33.
41 Company report (Neuronova)
42 Biochemical characterization of TAK-593, a novel VEGFR/PDGFR inhibitor with a two-step slow binding mechanism. Biochemistry. 2011 Feb 8;50(5):738-51.
43 RET kinase inhibitors: a review of recent patents (2012-2015).Expert Opin Ther Pat. 2017 Jan;27(1):91-99.
44 Synthesis and Src kinase inhibitory activity of a series of 4-[(2,4-dichloro-5-methoxyphenyl)amino]-7-furyl-3-quinolinecarbonitriles. J Med Chem. 2006 Dec 28;49(26):7868-76.
45 In vivo antitumor activity of herbimycin A, a tyrosine kinase inhibitor, targeted against BCR/ABL oncoprotein in mice bearing BCR/ABL-transfected cells. Leuk Res. 1994 Nov;18(11):867-73.
46 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
47 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
48 Novel dual Src/Abl inhibitors for hematologic and solid malignancies.Expert Opin Investig Drugs.2010 Aug;19(8):931-45.
49 Clinical pipeline report, company report or official report of Turning Point Therapeutics.