General Information of Drug (ID: DMBZMYT)

Drug Name
Pyridine derivative 18 Drug Info
Synonyms PMID27646564-Compound-5
Cross-matching ID
TTD Drug ID
DMBZMYT

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
Drug Status:
Approved Drug(s)
Clinical Trial Drug(s)
Patented Agent(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Pexidartinib DMS2J0Z Tenosynovial giant cell tumour 2F7B Approved [2]
Sulfatinib DMPOTM4 Neuroendocrine cancer 2B72.1 Phase 3 [3]
ARRY-382 DM0VGDC Solid tumour/cancer 2A00-2F9Z Phase 2 [3]
BLZ-945 DMG1LVA Amyotrophic lateral sclerosis 8B60.0 Phase 2 [3]
Cabiralizumab DMGE058 Pancreatic cancer 2C10 Phase 2 [4]
FPA-008 DM3ZN6Y Autoimmune diabetes 5A10 Phase 1/2 [5]
DCC-3014 DMHW289 Solid tumour/cancer 2A00-2F9Z Phase 1/2 [6]
PLX7486 DM0IVGU Pancreatic cancer 2C10 Phase 1 [3]
TPX-0022 DMC2IJN Solid tumour/cancer 2A00-2F9Z Phase 1 [7]
SNDX-6352 DM8ZROW Solid tumour/cancer 2A00-2F9Z Phase 1 [3]
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Drug Name Drug ID Indication ICD 11 Highest Status REF
Romiplostim DM3U7SZ Thrombocytopenia 3B64 Approved [8]
Ripretinib DM958QB Gastrointestinal stromal tumour 2B5B Approved [9]
Olaratumab DMNYOIX Soft tissue sarcoma 2B57 Approved [10]
Avapritinib DMK2GZX Gastrointestinal stromal tumour 2B5B Approved [11]
E-3810 DM42PFT Solid tumour/cancer 2A00-2F9Z Phase 3 [12]
CP-868596 DMZIM37 Gastrointestinal cancer 2C11 Phase 3 [13]
Famitinib DMSFWT7 Solid tumour/cancer 2A00-2F9Z Phase 2 [14]
XL-820 DMMHX9K Solid tumour/cancer 2A00-2F9Z Phase 2 [15]
MP470 DMELUAK Solid tumour/cancer 2A00-2F9Z Phase 2 [16]
MEDI-575 DMI9WVM Glioblastoma multiforme 2A00.0 Phase 2 [17]
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Drug Name Drug ID Indication ICD 11 Highest Status REF
Imatinib DM7RJXL Acute lymphoblastic leukaemia 2A85 Approved [18]
Sorafenib DMS8IFC Hepatocellular carcinoma 2C12.02 Approved [19]
Romiplostim DM3U7SZ Thrombocytopenia 3B64 Approved [20]
Regorafenib DMHSY1I Metastatic colorectal cancer 2B91 Approved [21]
Ponatinib DMYGJQO Acute lymphoblastic leukaemia 2A85 Approved [21]
Pazopanib HCl DM6U9CQ Renal cell carcinoma 2C90 Approved [22]
Pexidartinib DMS2J0Z Tenosynovial giant cell tumour 2F7B Approved [2]
Ripretinib DM958QB Gastrointestinal stromal tumour 2B5B Approved [9]
Famitinib DMSFWT7 Solid tumour/cancer 2A00-2F9Z Phase 2 [14]
XL-820 DMMHX9K Solid tumour/cancer 2A00-2F9Z Phase 2 [15]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Sorafenib DMS8IFC Hepatocellular carcinoma 2C12.02 Approved [19]
Romiplostim DM3U7SZ Thrombocytopenia 3B64 Approved [8]
Becaplermin DM1R5X4 Diabetic complication 5A2Y Approved [23]
E-3810 DM42PFT Solid tumour/cancer 2A00-2F9Z Phase 3 [12]
Famitinib DMSFWT7 Solid tumour/cancer 2A00-2F9Z Phase 2 [14]
XL-820 DMMHX9K Solid tumour/cancer 2A00-2F9Z Phase 2 [15]
MK-2461 DM21WBH Alzheimer disease 8A20 Phase 1/2 [24]
SNN-0031 DM2X3BR Brain injury NA07.Z Phase 1/2 [25]
TAK-593 DMNFZOT Solid tumour/cancer 2A00-2F9Z Phase 1 [26]
PMID25656651-Compound-21a DMCKAON N. A. N. A. Patented [27]
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Drug(s) Targeting Proto-oncogene c-Ret (RET)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Romiplostim DM3U7SZ Thrombocytopenia 3B64 Approved [28]
Regorafenib DMHSY1I Metastatic colorectal cancer 2B91 Approved [21]
Ponatinib DMYGJQO Acute lymphoblastic leukaemia 2A85 Approved [21]
Vandetanib DMRICNP Solid tumour/cancer 2A00-2F9Z Approved [18]
Selpercatinib DMZR15V Non-small-cell lung cancer 2C25.Y Approved [29]
Pralsetinib DMWU0I2 Non-small-cell lung cancer 2C25.Y Approved [30]
MGCD516 DM752PU Solid tumour/cancer 2A00-2F9Z Phase 2/3 [31]
CEP-32496 DMAO04B Solid tumour/cancer 2A00-2F9Z Phase 1/2 [3]
TPX-0046 DMIVE67 Solid tumour/cancer 2A00-2F9Z Phase 1/2 [32]
GSK3179106 DM2KCIP Inflammatory bowel disease DD72 Phase 1 [33]
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Drug Name Drug ID Indication ICD 11 Highest Status REF
Zidovudine DM4KI7O Human immunodeficiency virus infection 1C62 Approved [34]
Ponatinib DMYGJQO Acute lymphoblastic leukaemia 2A85 Approved [21]
Intedanib DMSTA36 Colorectal cancer 2B91.Z Approved [35]
Midostaurin DMI6E0R Acute myeloid leukaemia 2A60 Approved [18]
Gilteritinib DMWQ4MZ Acute myeloid leukaemia 2A60 Approved [36]
Pexidartinib DMS2J0Z Tenosynovial giant cell tumour 2F7B Approved [2]
Lestaurtinib DMQ2AIJ Acute myeloid leukaemia 2A60 Approved (orphan drug) [37]
Pacritinib DM1T6ZN Myelofibrosis 2A20.2 Phase 3 [34]
AC220 DM8Y4JS Acute myeloid leukaemia 2A60 Phase 3 [3]
Famitinib DMSFWT7 Solid tumour/cancer 2A00-2F9Z Phase 2 [14]
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Drug Name Drug ID Indication ICD 11 Highest Status REF
Sorafenib DMS8IFC Hepatocellular carcinoma 2C12.02 Approved [19]
Romiplostim DM3U7SZ Thrombocytopenia 3B64 Approved [38]
Regorafenib DMHSY1I Metastatic colorectal cancer 2B91 Approved [21]
Sunitinib DMCBJSR Gastrointestinal cancer 2C11 Approved [39]
Axitinib DMGVH6N Renal cell carcinoma 2C90 Approved [40]
Vandetanib DMRICNP Solid tumour/cancer 2A00-2F9Z Approved [18]
Pazopanib HCl DM6U9CQ Renal cell carcinoma 2C90 Approved [22]
Cabozantinib DMIYDT4 Thyroid cancer 2D10 Approved [41]
Tivozanib DMUKC5L Renal cell carcinoma 2C90 Approved [42]
Lenvatinib DMB1IU4 Thyroid cancer 2D10 Approved [43]
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Drug(s) Targeting Proto-oncogene c-Src (SRC)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Dasatinib DMJV2EK Chronic myelogenous leukaemia 2A20.0 Approved [18]
Bosutinib DMTI8YE Breast cancer 2C60-2C65 Approved [18]
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 [3]
CP-868596 DMZIM37 Gastrointestinal cancer 2C11 Phase 3 [3]
Masitinib DMRSNEU Amyotrophic lateral sclerosis 8B60.0 Phase 3 [33]
KX-01 DMF0NA9 Actinic keratosis EK90.0 Phase 3 [46]
Saracatinib DMBLHGP Hematologic tumour 2B33.Y Phase 2 [47]
TPX-0046 DMIVE67 Solid tumour/cancer 2A00-2F9Z Phase 1/2 [32]
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Molecular Interaction Atlas of This Drug

Molecular Interaction Atlas

Drug Therapeutic Target (DTT)
DTT Name DTT ID UniProt ID MOA REF
Fms-like tyrosine kinase 3 (FLT-3) TTGJCWZ FLT3_HUMAN Inhibitor [1]
Macrophage colony-stimulating factor 1 receptor (CSF1R) TT7MRDV CSF1R_HUMAN Inhibitor [1]
Platelet-derived growth factor receptor alpha (PDGFRA) TT8FYO9 PGFRA_HUMAN Inhibitor [1]
Platelet-derived growth factor receptor beta (PDGFRB) TTI7421 PGFRB_HUMAN Inhibitor [1]
Proto-oncogene c-Ret (RET) TT4DXQT RET_HUMAN Inhibitor [1]
Proto-oncogene c-Src (SRC) TT6PKBN SRC_HUMAN Inhibitor [1]
Tyrosine-protein kinase Kit (KIT) TTX41N9 KIT_HUMAN Inhibitor [1]
Vascular endothelial growth factor receptor 2 (KDR) TTUTJGQ VGFR2_HUMAN Inhibitor [1]

References

1 RET kinase inhibitors: a review of recent patents (2012-2015).Expert Opin Ther Pat. 2017 Jan;27(1):91-99.
2 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services. 2019
3 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
4 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
5 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
6 Clinical pipeline report, company report or official report of Deciphera Pharmaceuticals.
7 Clinical pipeline report, company report or official report of Turning Point Therapeutics.
8 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.
9 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services. 2020
10 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.
11 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services. 2020
12 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.
13 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.
14 Metabolism and bioactivation of famitinib, a novel inhibitor of receptor tyrosine kinase, in cancer patients. Br J Pharmacol. 2013 Apr;168(7):1687-706.
15 National Cancer Institute Drug Dictionary (drug id 452042).
16 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.
17 Clinical pipeline report, company report or official report of MedImmune (2011).
18 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.
19 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.
20 New anilinophthalazines as potent and orally well absorbed inhibitors of the VEGF receptor tyrosine kinases useful as antagonists of tumor-driven a... J Med Chem. 2000 Jun 15;43(12):2310-23.
21 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health & Human Services. 2015
22 Hughes B: 2009 FDA drug approvals. Nat Rev Drug Discov. 2010 Feb;9(2):89-92.
23 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health & Human Services.
24 MK-2461, a novel multitargeted kinase inhibitor, preferentially inhibits the activated c-Met receptor. Cancer Res. 2010 Feb 15;70(4):1524-33.
25 Company report (Neuronova)
26 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.
27 Bcr-Abl tyrosine kinase inhibitors: a patent review.Expert Opin Ther Pat. 2015 Apr;25(4):397-412.
28 Synthesis, structure-activity relationship and crystallographic studies of 3-substituted indolin-2-one RET inhibitors. Bioorg Med Chem. 2010 Feb 15;18(4):1482-96.
29 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services. 2020
30 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services. 2020
31 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: 2185).
32 Clinical pipeline report, company report or official report of Turning Point Therapeutics.
33 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
34 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: 1807).
35 2014 FDA drug approvals. Nat Rev Drug Discov. 2015 Feb;14(2):77-81.
36 2018 FDA drug approvals.Nat Rev Drug Discov. 2019 Feb;18(2):85-89.
37 Lestaurtinib (CEP701) is a JAK2 inhibitor that suppresses JAK2/STAT5 signaling and the proliferation of primary erythroid cells from patients with ... Blood. 2008 Jun 15;111(12):5663-71.
38 Anthranilic acid amides: a novel class of antiangiogenic VEGF receptor kinase inhibitors. J Med Chem. 2002 Dec 19;45(26):5687-93.
39 2006 drug approvals: finding the niche. Nat Rev Drug Discov. 2007 Feb;6(2):99-101.
40 Nat Rev Drug Discov. 2013 Feb;12(2):87-90.
41 Clinical pipeline report, company report or official report of Exelixis (2011).
42 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services
43 Emerging drugs for ovarian cancer. Expert Opin Emerg Drugs. 2008 Sep;13(3):523-36.
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 Novel dual Src/Abl inhibitors for hematologic and solid malignancies.Expert Opin Investig Drugs.2010 Aug;19(8):931-45.