Details of the Drug-Related molecule(s) Interaction Atlas

General Information of Drug (ID: DMLT1N3)

• Drug Name: decavanadate Drug Info
• Synonyms: Decavanidate

Indication

Disease Entry	ICD 11	Status	REF
Discovery agent	N.A.	Investigative	[1]

• Cross-matching ID:
  PubChem CID: 5311062
  TTD Drug ID: DMLT1N3

Molecule-Related Drug Atlas

Drug(s) Targeting IP3 receptor isoform 1 (ITPR1)

Drug Name	Drug ID	Indication	ICD 11	Highest Status	REF
PIP2	DMOZV7N	Discovery agent	N.A.	Investigative	[2]
inositol 2,4,5-trisphosphate	DM43G5Z	Discovery agent	N.A.	Investigative	[2]
xestospongin C	DM4YQR2	Discovery agent	N.A.	Investigative	[2]

Drug(s) Targeting P2X purinoceptor 7 (P2RX7)

Drug Name	Drug ID	Indication	ICD 11	Highest Status	REF
CE-224535	DMFCLT6	Arthralgia	ME82	Phase 2/3	[7]
AZD9056	DMJGYPK	Chronic obstructive pulmonary disease	CA22	Phase 2	[8]
LY3857210	DMZO2V2	Pain	MG30-MG3Z	Phase 2	[9]
BIL010t	DMV1EA9	Alzheimer disease	8A20	Phase 1/2	[10]
EVT 401	DMOG8IE	Rheumatoid arthritis	FA20	Phase 1	[11]
SGM-1019	DMDAHEL	Inflammatory bowel disease	DD72	Phase 1	[12]
GSK1482160	DMWDQOV	Pain	MG30-MG3Z	Phase 1	[13]
JNJ-55308942	DM0QZJX	Anhedonia	MB24.2	Phase 1	[10]
JNJ-54175446	DMQ5ZVK	Major depressive disorder	6A70.3	Phase 1	[14]
JNJ-479655	DMDU6GN	Alzheimer disease	8A20	Clinical trial	[15]

Drug(s) Targeting IP3 receptor isoform 2 (IP3R2)

Drug Name	Drug ID	Indication	ICD 11	Highest Status	REF
inositol 2,4,5-trisphosphate	DM43G5Z	Discovery agent	N.A.	Investigative	[3]

Drug(s) Targeting Long transient receptor potential channel 4 (TRPM4)

Drug Name	Drug ID	Indication	ICD 11	Highest Status	REF
AMP-PNP	DMTOK1D	Discovery agent	N.A.	Investigative	[16]
PIP2	DMOZV7N	Discovery agent	N.A.	Investigative	[17]
adenosine diphosphate	DMFUHKP	N. A.	N. A.	Investigative	[16]
BTP2	DMNM63G	Discovery agent	N.A.	Investigative	[18]
9-phenanthrol	DMJFBQ1	Discovery agent	N.A.	Investigative	[19]

Molecular Interaction Atlas of This Drug

Drug Therapeutic Target (DTT)

DTT Name	DTT ID	UniProt ID	MOA	REF
IP3 receptor isoform 1 (ITPR1)	TT5HWAT	ITPR1_HUMAN	Antagonist	[2]
IP3 receptor isoform 2 (IP3R2)	TTK9OV3	ITPR2_HUMAN	Antagonist	[3]
IP3 receptor isoform 3 (ITPR3)	TTH1769	ITPR3_HUMAN	Antagonist	[4]
Long transient receptor potential channel 4 (TRPM4)	TTJ2HKA	TRPM4_HUMAN	Activator	[5]
P2X purinoceptor 7 (P2RX7)	TT473XN	P2RX7_HUMAN	Antagonist	[6]

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: 2459).
• [2] 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: 743).
• [3] 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: 744).
• [4] 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: 745).
• [5] Decavanadate modulates gating of TRPM4 cation channels. J Physiol. 2004 Nov 1;560(Pt 3):753-65.
• [6] Decavanadate, a P2X receptor antagonist, and its use to study ligand interactions with P2X7 receptors. Eur J Pharmacol. 2006 Mar 18;534(1-3):19-29.
• [7] Efficacy and safety of CE-224,535, an antagonist of P2X7 receptor, in treatment of patients with rheumatoid arthritis inadequately controlled by methotrexate. J Rheumatol. 2012 Apr;39(4):720-7.
• [8] Clinical pipeline report, company report or official report of AstraZeneca (2009).
• [9] Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2023. Adis Insight
• [10] Antibodies and venom peptides: new modalities for ion channels. Nat Rev Drug Discov. 2019 May;18(5):339-357.
• [11] Molecular and functional properties of P2X receptors ecent progress and persisting challenges. Purinergic Signal. 2012 September; 8(3): 375-417.
• [12] Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
• [13] Clinical pipeline report, company report or official report of GlaxoSmithKline (2009).
• [14] Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
• [15] Pharmacological characterization of a novel centrally permeable P2X7 receptor antagonist: JNJ-47965567. Br J Pharmacol. 2013 Oct;170(3):624-40.
• [16] Intracellular nucleotides and polyamines inhibit the Ca2+-activated cation channel TRPM4b. Pflugers Arch. 2004 Apr;448(1):70-5.
• [17] Phosphatidylinositol 4,5-bisphosphate rescues TRPM4 channels from desensitization. J Biol Chem. 2005 Nov 25;280(47):39185-92.
• [18] A pyrazole derivative potently inhibits lymphocyte Ca2+ influx and cytokine production by facilitating transient receptor potential melastatin 4 ch... Mol Pharmacol. 2006 Apr;69(4):1413-20.
• [19] 9-phenanthrol inhibits human TRPM4 but not TRPM5 cationic channels. Br J Pharmacol. 2008 Apr;153(8):1697-705.