General Information of Drug (ID: DMY0UEQ)

Drug Name
VATALANIB Drug Info
Synonyms
Vatalanib; 212141-54-3; Vatalanib base; N-(4-chlorophenyl)-4-(pyridin-4-ylmethyl)phthalazin-1-amine; PTK787; Pynasunate; CGP 79787; Vatalanib free base; PTK-787; Vatalanib (free base); Vatalinib; ZK-232934; CGP-79787; ZK222584; PTK/ZK; CHEMBL101253; N-(4-Chlorophenyl)-4-(4-pyridinylmethyl)-1-phthalazinamine; UNII-5DX9U76296; CHEBI:90620; YCOYDOIWSSHVCK-UHFFFAOYSA-N; 1-(4-chloroanilino)-4-(4-pyridylmethyl)phthalazine; 5DX9U76296; NCGC00181350-01; 1-Phthalazinamine,N-(4-chlorophenyl)-4-(4-pyridinylmethyl)-; DSSTox_CID_26919
Indication
Disease Entry ICD 11 Status REF
Solid tumour/cancer 2A00-2F9Z Phase 2 [1] , [2]
Cross-matching ID
PubChem CID
151194
ChEBI ID
CHEBI:90620
CAS Number
CAS 212141-54-3
TTD Drug ID
DMY0UEQ

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
Drug Status:
Approved Drug(s)
Clinical Trial Drug(s)
Investigative Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Tivozanib DMUKC5L Renal cell carcinoma 2C90 Approved [6]
E-3810 DM42PFT Solid tumour/cancer 2A00-2F9Z Phase 3 [7]
Sulfatinib DMPOTM4 Neuroendocrine cancer 2B72.1 Phase 3 [8]
Fruquintinib DMHOSCQ Solid tumour/cancer 2A00-2F9Z Phase 3 [9]
PI-88 DMGZPX6 Hepatocellular carcinoma 2C12.02 Phase 3 [10]
Taberminogene vadenovec DMW5PHL Vascular restinosis BE2Z Phase 3 [11]
ABT-869 DMREDYP Solid tumour/cancer 2A00-2F9Z Phase 3 [12]
MGCD516 DM752PU Solid tumour/cancer 2A00-2F9Z Phase 2/3 [13]
Famitinib DMSFWT7 Solid tumour/cancer 2A00-2F9Z Phase 2 [14]
MK-2461 DM21WBH Alzheimer disease 8A20 Phase 1/2 [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 [16]
Lapatinib DM3BH1Y Breast cancer 2C60-2C65 Approved [17]
Gefitinib DM15F0X Solid tumour/cancer 2A00-2F9Z Approved [18]
Erlotinib DMCMBHA Non-small-cell lung cancer 2C25.Y Approved [19]
Vandetanib DMRICNP Solid tumour/cancer 2A00-2F9Z Approved [20]
Dacomitinib DMOH8VY Non-small-cell lung cancer 2C25.Y Approved [21]
BIBW 2992 DMTKD7Q Non-small-cell lung cancer 2C25.Y Approved [22]
SKI-758 DMQ8E9R Ischemia 8B10-8B11 Approved [23]
Epidermal growth factor DMVONE6 Vulnerary ND56.Z Approved [21]
Merimepodib DM0HS92 Breast cancer 2C60-2C65 Approved [24]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Romiplostim DM3U7SZ Thrombocytopenia 3B64 Approved [25]
MK-2461 DM21WBH Alzheimer disease 8A20 Phase 1/2 [15]
Sirna-027 DMZTQD8 Exudative age-related macular degeneration 9B78.3Z Phase 1/2 [26]
PMID22765894C8h DMH5RFU Discovery agent N.A. Investigative [27]
2-(1H-indazol-3-yl)-1H-benzo[d]imidazole DM0CSH8 Discovery agent N.A. Investigative [28]
AAL-993 DM35RFH Discovery agent N.A. Investigative [5]
PMID17935989C25 DML8ZBR Discovery agent N.A. Investigative [29]
2-(5-Phenyl-oxazol-2-ylamino)-benzonitrile DMX6QMT Discovery agent N.A. Investigative [4]
4-Chloro-N-(3-chloro-benzoyl)-benzenesulfonamide DMI3OR9 Discovery agent N.A. Investigative [30]
(2-Methoxy-phenyl)-(5-phenyl-oxazol-2-yl)-amine DMQWD75 Discovery agent N.A. Investigative [4]
⏷ 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 [31]
Romiplostim DM3U7SZ Thrombocytopenia 3B64 Approved [32]
Regorafenib DMHSY1I Metastatic colorectal cancer 2B91 Approved [33]
Sunitinib DMCBJSR Gastrointestinal cancer 2C11 Approved [34]
Axitinib DMGVH6N Renal cell carcinoma 2C90 Approved [35]
Vandetanib DMRICNP Solid tumour/cancer 2A00-2F9Z Approved [20]
Pazopanib HCl DM6U9CQ Renal cell carcinoma 2C90 Approved [36]
Cabozantinib DMIYDT4 Thyroid cancer 2D10 Approved [37]
Tivozanib DMUKC5L Renal cell carcinoma 2C90 Approved [6]
Lenvatinib DMB1IU4 Thyroid cancer 2D10 Approved [38]
⏷ 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
Epidermal growth factor receptor (EGFR) TTGKNB4 EGFR_HUMAN Inhibitor [3]
Vascular endothelial growth factor receptor 2 (KDR) TTUTJGQ VGFR2_HUMAN Inhibitor [3]
Vascular endothelial growth factor receptor 3 (FLT-4) TTDCBX5 VGFR3_HUMAN Inhibitor [4]
VEGFR1 messenger RNA (VEGFR1 mRNA) TT1VAUK VGFR1_HUMAN Inhibitor [5]

References

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2 ClinicalTrials.gov (NCT00348790) Vatalanib in Treating Patients With Recurrent or Progressive Meningioma. U.S. National Institutes of Health.
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6 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services
7 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.
8 Clinical pipeline report, company report or official report of Hutchison Medi Pharma.
9 Discovery of fruquintinib, a potent and highly selective small molecule inhibitor of VEGFR 1, 2, 3 tyrosine kinases for cancer therapy. Cancer Biol Ther. 2014;15(12):1635-45.
10 Company report (Medigen)
11 Advances in kinase targeting: current clinical use and clinical trials. Trends Pharmacol Sci. 2014 Nov;35(11):604-20.
12 Preclinical activity of ABT-869, a multitargeted receptor tyrosine kinase inhibitor. Mol Cancer Ther. 2006 Apr;5(4):995-1006.
13 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: 1814).
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 MK-2461, a novel multitargeted kinase inhibitor, preferentially inhibits the activated c-Met receptor. Cancer Res. 2010 Feb 15;70(4):1524-33.
16 Nasopharyngeal carcinoma: Current treatment options and future directions. J Nasopharyng Carcinoma, 2014, 1(16): e16.
17 Triple negative breast cancer--current status and prospective targeted treatment based on HER1 (EGFR), TOP2A and C-MYC gene assessment. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2009 Mar;153(1):13-7.
18 Gefitinib ('Iressa', ZD1839) and new epidermal growth factor receptor inhibitors. Br J Cancer. 2004 Feb 9;90(3):566-72.
19 Quantitative prediction of fold resistance for inhibitors of EGFR. Biochemistry. 2009 Sep 8;48(35):8435-48.
20 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.
21 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: 1797).
22 Boehringer Ingelheim. Product Development Pipeline. June 2 2009.
23 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.
24 Clinical pipeline report, company report or official report of GlaxoSmithKline (2009).
25 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.
26 2011 Pipeline of Sirna Therapeutics.
27 The design, synthesis, and biological evaluation of potent receptor tyrosine kinase inhibitors. Bioorg Med Chem Lett. 2012 Aug 1;22(15):4979-85.
28 Design and structure-activity relationship of 3-benzimidazol-2-yl-1H-indazoles as inhibitors of receptor tyrosine kinases. Bioorg Med Chem Lett. 2006 Jul 1;16(13):3595-9.
29 Macrocyclic ureas as potent and selective Chk1 inhibitors: an improved synthesis, kinome profiling, structure-activity relationships, and prelimina... Bioorg Med Chem Lett. 2007 Dec 1;17(23):6593-601.
30 Acyl sulfonamide anti-proliferatives: benzene substituent structure-activity relationships for a novel class of antitumor agents. J Med Chem. 2004 Oct 21;47(22):5367-80.
31 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.
32 Anthranilic acid amides: a novel class of antiangiogenic VEGF receptor kinase inhibitors. J Med Chem. 2002 Dec 19;45(26):5687-93.
33 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health & Human Services. 2015
34 2006 drug approvals: finding the niche. Nat Rev Drug Discov. 2007 Feb;6(2):99-101.
35 Nat Rev Drug Discov. 2013 Feb;12(2):87-90.
36 Hughes B: 2009 FDA drug approvals. Nat Rev Drug Discov. 2010 Feb;9(2):89-92.
37 Clinical pipeline report, company report or official report of Exelixis (2011).
38 Emerging drugs for ovarian cancer. Expert Opin Emerg Drugs. 2008 Sep;13(3):523-36.