General Information of Drug (ID: DMX302C)

Drug Name
BMS-690514 Drug Info
Synonyms BMS 690514; BMS690514
Indication
Disease Entry ICD 11 Status REF
Chronic pain MG30 Phase 2 [1]
Cross-matching ID
PubChem CID
11349170
CAS Number
CAS 859853-30-8
TTD Drug ID
DMX302C

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
Sorafenib DMS8IFC Hepatocellular carcinoma 2C12.02 Approved [3]
Lapatinib DM3BH1Y Breast cancer 2C60-2C65 Approved [4]
Gefitinib DM15F0X Solid tumour/cancer 2A00-2F9Z Approved [5]
Erlotinib DMCMBHA Non-small-cell lung cancer 2C25.Y Approved [6]
Vandetanib DMRICNP Solid tumour/cancer 2A00-2F9Z Approved [7]
Dacomitinib DMOH8VY Non-small-cell lung cancer 2C25.Y Approved [8]
BIBW 2992 DMTKD7Q Non-small-cell lung cancer 2C25.Y Approved [9]
SKI-758 DMQ8E9R Ischemia 8B10-8B11 Approved [10]
Epidermal growth factor DMVONE6 Vulnerary ND56.Z Approved [8]
Merimepodib DM0HS92 Breast cancer 2C60-2C65 Approved [11]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
Zidovudine DM4KI7O Human immunodeficiency virus infection 1C62 Approved [12]
Ponatinib DMYGJQO Acute lymphoblastic leukaemia 2A85 Approved [13]
Intedanib DMSTA36 Colorectal cancer 2B91.Z Approved [14]
Midostaurin DMI6E0R Acute myeloid leukaemia 2A60 Approved [7]
Gilteritinib DMWQ4MZ Acute myeloid leukaemia 2A60 Approved [15]
Pexidartinib DMS2J0Z Tenosynovial giant cell tumour 2F7B Approved [16]
Lestaurtinib DMQ2AIJ Acute myeloid leukaemia 2A60 Approved (orphan drug) [17]
Pacritinib DM1T6ZN Myelofibrosis 2A20.2 Phase 3 [12]
AC220 DM8Y4JS Acute myeloid leukaemia 2A60 Phase 3 [18]
Famitinib DMSFWT7 Solid tumour/cancer 2A00-2F9Z Phase 2 [19]
⏷ 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 [20]
Romiplostim DM3U7SZ Thrombocytopenia 3B64 Approved [21]
Regorafenib DMHSY1I Metastatic colorectal cancer 2B91 Approved [13]
Sunitinib DMCBJSR Gastrointestinal cancer 2C11 Approved [22]
Axitinib DMGVH6N Renal cell carcinoma 2C90 Approved [23]
Vandetanib DMRICNP Solid tumour/cancer 2A00-2F9Z Approved [7]
Pazopanib HCl DM6U9CQ Renal cell carcinoma 2C90 Approved [24]
Cabozantinib DMIYDT4 Thyroid cancer 2D10 Approved [25]
Tivozanib DMUKC5L Renal cell carcinoma 2C90 Approved [26]
Lenvatinib DMB1IU4 Thyroid cancer 2D10 Approved [27]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
HKI-272 DM6QOVN Breast cancer 2C60-2C65 Phase 3 [28]
3,4-di-(4-methoxyphenyl)-1H-pyrrole-2,5-dione DMDO175 Discovery agent N.A. Investigative [29]
3,4-diphenyl-1H-pyrrole-2,5-dione DMPK6YT Discovery agent N.A. Investigative [29]
3-(4-methoxyphenyl)-4-phenyl-1H-pyrrole-2,5-dione DMGC7RY Discovery agent N.A. Investigative [29]
BMS-536924 DMXJB4N Discovery agent N.A. Investigative [30]
3-(indole-3-yl)-4-phenyl-1H-pyrrole-2,5-dione DM3EV9N Discovery agent N.A. Investigative [29]
PMID24915291C38 DMBXT9J Discovery agent N.A. Investigative [31]
Geldanamycin-estradiol hybrid DMUSJ96 Discovery agent N.A. Investigative [32]
CL-387785 DMLKFZC Discovery agent N.A. Investigative [33]
HDS-029 DMLRUVA Discovery agent N.A. Investigative [33]
⏷ 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 [2]
ERBB2 messenger RNA (HER2 mRNA) TTR5TV4 ERBB2_HUMAN Inhibitor [2]
Fms-like tyrosine kinase 3 (FLT-3) TTGJCWZ FLT3_HUMAN Inhibitor [2]
Vascular endothelial growth factor receptor 2 (KDR) TTUTJGQ VGFR2_HUMAN Inhibitor [2]

References

1 A novel epidermal growth factor receptor inhibitor promotes apoptosis in non-small cell lung cancer cells resistant to erlotinib. Cancer Res. 2007 Jul 1;67(13):6253-62.
2 Preclinical pharmacokinetics and in vitro metabolism of BMS-690514, a potent inhibitor of EGFR and VEGFR2. J Pharm Sci. 2010 Aug;99(8):3579-93.
3 Nasopharyngeal carcinoma: Current treatment options and future directions. J Nasopharyng Carcinoma, 2014, 1(16): e16.
4 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.
5 Gefitinib ('Iressa', ZD1839) and new epidermal growth factor receptor inhibitors. Br J Cancer. 2004 Feb 9;90(3):566-72.
6 Quantitative prediction of fold resistance for inhibitors of EGFR. Biochemistry. 2009 Sep 8;48(35):8435-48.
7 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.
8 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).
9 Boehringer Ingelheim. Product Development Pipeline. June 2 2009.
10 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.
11 Clinical pipeline report, company report or official report of GlaxoSmithKline (2009).
12 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).
13 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health & Human Services. 2015
14 2014 FDA drug approvals. Nat Rev Drug Discov. 2015 Feb;14(2):77-81.
15 2018 FDA drug approvals.Nat Rev Drug Discov. 2019 Feb;18(2):85-89.
16 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services. 2019
17 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.
18 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
19 Metabolism and bioactivation of famitinib, a novel inhibitor of receptor tyrosine kinase, in cancer patients. Br J Pharmacol. 2013 Apr;168(7):1687-706.
20 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.
21 Anthranilic acid amides: a novel class of antiangiogenic VEGF receptor kinase inhibitors. J Med Chem. 2002 Dec 19;45(26):5687-93.
22 2006 drug approvals: finding the niche. Nat Rev Drug Discov. 2007 Feb;6(2):99-101.
23 Nat Rev Drug Discov. 2013 Feb;12(2):87-90.
24 Hughes B: 2009 FDA drug approvals. Nat Rev Drug Discov. 2010 Feb;9(2):89-92.
25 Clinical pipeline report, company report or official report of Exelixis (2011).
26 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health Human Services
27 Emerging drugs for ovarian cancer. Expert Opin Emerg Drugs. 2008 Sep;13(3):523-36.
28 Identification of genotype-correlated sensitivity to selective kinase inhibitors by using high-throughput tumor cell line profiling. Proc Natl Acad Sci U S A. 2007 Dec 11;104(50):19936-41.
29 Design, synthesis, and biological evaluation of 3,4-diarylmaleimides as angiogenesis inhibitors. J Med Chem. 2006 Feb 23;49(4):1271-81.
30 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.
31 Discovery of a series of 2,5-diaminopyrimidine covalent irreversible inhibitors of Bruton's tyrosine kinase with in vivo antitumor activity. J Med Chem. 2014 Jun 26;57(12):5112-28.
32 Synthesis and evaluation of geldanamycin-estradiol hybrids. Bioorg Med Chem Lett. 1999 May 3;9(9):1233-8.
33 Tyrosine kinase inhibitors. 19. 6-Alkynamides of 4-anilinoquinazolines and 4-anilinopyrido[3,4-d]pyrimidines as irreversible inhibitors of the erbB... J Med Chem. 2006 Feb 23;49(4):1475-85.