General Information of Drug (ID: DMPCLTW)

Drug Name
dodecylphosphate Drug Info
Synonyms FAP12; dodecanol phosphate; FAP-12; lauryl phosphate
Indication
Disease Entry ICD 11 Status REF
Discovery agent N.A. Investigative [1]
Cross-matching ID
PubChem CID
1550836
TTD Drug ID
DMPCLTW

Molecule-Related Drug Atlas

Molecule-Related Drug Atlas
Molecule Type:
DTT
Drug Status:
Investigative Drug(s)
Clinical Trial Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
LPA DMI5XR1 Discovery agent N.A. Investigative [3]
Ki16425 DMJTDK9 Discovery agent N.A. Investigative [4]
2-oleoyl-LPA DMN9OS1 Discovery agent N.A. Investigative [5]
dodecyl-thiophosphate DMAJVPI Discovery agent N.A. Investigative [6]
oleoyl-thiophosphate DM1TAM9 Discovery agent N.A. Investigative [6]
NAEPA DM38XWZ Discovery agent N.A. Investigative [7]
BrP-LPA DMPGEO1 Discovery agent N.A. Investigative [8]
PMID18178086C15 DMA2OWK Discovery agent N.A. Investigative [9]
decyl dihydrogen phosphate DMNKDT5 Discovery agent N.A. Investigative [2]
GRI977143 DM3A0TE Discovery agent N.A. Investigative [10]
⏷ Show the Full List of 10 Drug(s)
Drug Name Drug ID Indication ICD 11 Highest Status REF
SAR-100842 DMDMQW0 Fibrosis GA14-GC01 Phase 2 [11]
LPA DMI5XR1 Discovery agent N.A. Investigative [12]
Ki16425 DMJTDK9 Discovery agent N.A. Investigative [4]
dioctanoylglycerol pyrophosphate DM0QY1V Discovery agent N.A. Investigative [13]
2-oleoyl-LPA DMN9OS1 Discovery agent N.A. Investigative [5]
dodecyl-thiophosphate DMAJVPI Discovery agent N.A. Investigative [6]
oleoyl-thiophosphate DM1TAM9 Discovery agent N.A. Investigative [6]
VPC12249 DM6F0VR Discovery agent N.A. Investigative [14]
NAEPA DM38XWZ Discovery agent N.A. Investigative [7]
VPC32183 DMLK3I9 Discovery agent N.A. Investigative [15]
⏷ 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
Lysophosphatidate-3 receptor (LPAR3) TTE2YJR LPAR3_HUMAN Antagonist [2]
Lysophosphatidic acid receptor 2 (LPAR2) TTB7Y8I LPAR2_HUMAN Agonist [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: 4031).
2 Fatty alcohol phosphates are subtype-selective agonists and antagonists of lysophosphatidic acid receptors. Mol Pharmacol. 2003 May;63(5):1032-42.
3 Synthesis and biological evaluation of phosphonic and thiophosphoric acid derivatives of lysophosphatidic acid. Bioorg Med Chem Lett. 2004 Jul 5;14(13):3473-6.
4 Ki16425, a subtype-selective antagonist for EDG-family lysophosphatidic acid receptors. Mol Pharmacol. 2003 Oct;64(4):994-1005.
5 Lysophosphatidic acid (LPA) receptors of the EDG family are differentially activated by LPA species. Structure-activity relationship of cloned LPA receptors. FEBS Lett. 2000 Jul 28;478(1-2):159-65.
6 Synthesis, structure-activity relationships, and biological evaluation of fatty alcohol phosphates as lysophosphatidic acid receptor ligands, activ... J Med Chem. 2005 Jul 28;48(15):4919-30.
7 LPA and its analogs-attractive tools for elucidation of LPA biology and drug development. Curr Med Chem. 2008;15(21):2122-31.
8 Dual activity lysophosphatidic acid receptor pan-antagonist/autotaxin inhibitor reduces breast cancer cell migration in vitro and causes tumor regression in vivo. Cancer Res. 2009 Jul 1;69(13):5441-9.
9 Discovery of potent LPA2 (EDG4) antagonists as potential anticancer agents. Bioorg Med Chem Lett. 2008 Feb 1;18(3):1037-41.
10 Virtual screening for LPA2-specific agonists identifies a nonlipid compound with antiapoptotic actions. Mol Pharmacol. 2012 Dec;82(6):1162-73.
11 Promising Pharmacological Directions in the World of Lysophosphatidic Acid Signaling. Biomol Ther (Seoul) 2015 January; 23(1): 1-11.
12 Molecular cloning and characterization of a novel human G-protein-coupled receptor, EDG7, for lysophosphatidic acid. J Biol Chem. 1999 Sep 24;274(39):27776-85.
13 Short-chain phosphatidates are subtype-selective antagonists of lysophosphatidic acid receptors. Mol Pharmacol. 2001 Oct;60(4):776-84.
14 Activity of 2-substituted lysophosphatidic acid (LPA) analogs at LPA receptors: discovery of a LPA1/LPA3 receptor antagonist. Mol Pharmacol. 2001 Dec;60(6):1173-80.
15 Initial structure-activity relationships of lysophosphatidic acid receptor antagonists: discovery of a high-affinity LPA1/LPA3 receptor antagonist. Bioorg Med Chem Lett. 2004 Jun 7;14(11):2735-40.