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

General Information of Drug (ID: DMABITD)

• Drug Name: Tetradecyl-phosphonic acid Drug Info
• Synonyms: Tetradecylphosphonic acid; 4671-75-4; Phosphonic acid, tetradecyl-; 1-Tetradecanephosphonic acid; Tetradecanephosphonic acid; Tetradecyl phosphonic acid; n-Tetradecylphosphonic acid; 1-Tetradecylphosphonic Acid; Phosphonic acid, P-tetradecyl-; EINECS 225-118-1; BRN 1784271; CHEMBL190999; P-tetradecyl-Phosphonic acid; C14H31O3P; tetradecylphosphonate; AC1L2V5G; 14; SCHEMBL19906; 4-04-00-03566 (Beilstein Handbook Reference); Tetradecylphosphonic acid, 97%; DTXSID7063550; CTK3J7960

Indication

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

• Cross-matching ID:
  PubChem CID: 78401
  CAS Number: CAS 4671-75-4
  TTD Drug ID: DMABITD

Molecule-Related Drug Atlas

Drug(s) Targeting Lysophosphatidic acid receptor 1 (LPAR1)

Drug Name	Drug ID	Indication	ICD 11	Highest Status	REF
SAR-100842	DMDMQW0	Fibrosis	GA14-GC01	Phase 2	[2]
BMS-986020	DMHMV6E	Scleroderma	4A42	Phase 2	[3]
BMS-986278	DMD27RW	Pulmonary fibrosis	CB03.4	Phase 2	[4]
BMS-986337	DM9GC6L	Pulmonary fibrosis	CB03.4	Phase 1	[5]
BMS-986202	DM8TAI9	Idiopathic pulmonary fibrosis	CB03.4	Preclinical	[6]
LPA	DMI5XR1	Discovery agent	N.A.	Investigative	[7]
Ki16425	DMJTDK9	Discovery agent	N.A.	Investigative	[8]
dioctanoylglycerol pyrophosphate	DM0QY1V	Discovery agent	N.A.	Investigative	[9]
2-oleoyl-LPA	DMN9OS1	Discovery agent	N.A.	Investigative	[10]
dodecyl-thiophosphate	DMAJVPI	Discovery agent	N.A.	Investigative	[1]

Molecular Interaction Atlas of This Drug

Drug Therapeutic Target (DTT)

DTT Name	DTT ID	UniProt ID	MOA	REF
Lysophosphatidic acid receptor 1 (LPAR1)	TTQ6S1K	LPAR1_HUMAN	Inhibitor	[1]

References

• [1] 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.
• [2] Promising Pharmacological Directions in the World of Lysophosphatidic Acid Signaling. Biomol Ther (Seoul) 2015 January; 23(1): 1-11.
• [3] Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
• [4] Phase 2 trial design of BMS-986278, a lysophosphatidic acid receptor 1 (LPA(1)) antagonist, in patients with idiopathic pulmonary fibrosis (IPF) or progressive fibrotic interstitial lung disease (PF-ILD). BMJ Open Respir Res. 2021 Dec;8(1):e001026.
• [5] ClinicalTrials.gov (NCT04550195) A Double-Blind, Placebo-Controlled, Randomized, Single and Multiple Ascending Dose Study of the Safety and Tolerability, and Pharmacokinetics (Including Food Effect, pH Effect and Japanese Bridging Study) of BMS-986337 Following Oral Administration in Healthy Participants. U.S.National Institutes of Health.
• [6] Pharmacokinetic and pharmacodynamic characterization of an oral lysophosphatidic acid type 1 receptor-selective antagonist. J Pharmacol Exp Ther. 2011 Mar;336(3):693-700.
• [7] Diversity of lysophosphatidic acid receptor-mediated intracellular calcium signaling in early cortical neurogenesis. J Neurosci. 2010 May 26;30(21):7300-9.
• [8] Targeting lysophosphatidic acid receptor type 1 with Debio 0719 inhibits spontaneous metastasis dissemination of breast cancer cells independently of cell proliferation and angiogenesis. Int J Oncol. 2012 Apr;40(4):1133-41.
• [9] Short-chain phosphatidates are subtype-selective antagonists of lysophosphatidic acid receptors. Mol Pharmacol. 2001 Oct;60(4):776-84.
• [10] 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.