SCHEMBL2224897

SCHEMBL2224897

CCCCCCCCOCC(COP(=O)(O)OP(=O)(O)O)OCCCCCCCC

nearest known ligand 0.78

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
LPAR3 Q9UBY5 13/20 0.78
LPAR1 Q92633 12/20 0.78
LPAR2 Q9HBW0 8/20 0.65
LPAR5 Q9H1C0 6/20 0.55
PLA2G2C Q5R387 1/20 0.52
LPAR6 P43657 5/20 0.51
LPAR4 Q99677 5/20 0.51
AKT1 P31749 4/20 0.48
AKT2 P31751 3/20 0.48
AKT3 Q9Y243 3/20 0.48
PIK3R1 P27986 2/20 0.48
PIK3CA P42336 2/20 0.48
PLCG2 P16885 1/20 0.48
GAB1 Q13480 1/20 0.48

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL6854208 0.99 LPAR3 (0.76) LPAR3LPAR1LPAR2LPAR5PLA2G2C
SCHEMBL2813163 0.88 LPAR3 (1.00) LPAR3LPAR1LPAR2LPAR5PLA2G2C
SCHEMBL31198159 0.88 LPAR3 (1.00) LPAR3LPAR1LPAR2LPAR5PLA2G2C
SCHEMBL30443866 0.88 LPAR3 (1.00) LPAR3LPAR1LPAR2LPAR5PLA2G2C
SCHEMBL10896195 0.88 LPAR3 (1.00) LPAR3LPAR1LPAR2LPAR5PLA2G2C
SCHEMBL5055004 0.88 LPAR3 (1.00) LPAR3LPAR1LPAR2LPAR5PLA2G2C
SCHEMBL2814732 0.88 LPAR3 (1.00) LPAR3LPAR1LPAR2LPAR5PLA2G2C
SCHEMBL496845 0.88 LPAR3 (1.00) LPAR3LPAR1LPAR2LPAR5PLA2G2C
SCHEMBL31439420 0.88 LPAR3 (1.00) LPAR3LPAR1LPAR2LPAR5PLA2G2C
SCHEMBL29353224 0.88 LPAR3 (1.00) LPAR3LPAR1LPAR2LPAR5PLA2G2C

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 28 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1918287-A2 LPA receptor agonists and antagonists and methods of use THE UNIVERSITY OF TENNESSEE RESEARCH CORPORATION (US) 2008-05-07 EP claimed
US-20050261252-A1 LPA receptor agonists and antagonists and methods of use MILLER DUANE D 2005-11-24 US claimed
JP-2004506604-A 2004-03-04 JP claimed
EP-1263752-A4 LPA RECEPTOR AGONISTS AND ANTAGONISTS AND METHODS OF USE UNIV TENNESSEE RES CORP (US) 2003-07-30 EP claimed
US-20030027800-A1 LPA receptor agonists and antagonists and methods of use NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2003-02-06 US claimed
EP-1263752-A2 LPA RECEPTOR AGONISTS AND ANTAGONISTS AND METHODS OF USE THE UNIVERSITY OF TENNESSEE RESEARCH CORPORATION (US) 2002-12-11 EP claimed
WO-2001071022-A2 LPA RECEPTOR AGONISTS AND ANTAGONISTS AND METHODS OF USE THE UNIVERSITY OF TENNESSEE RESEARCH CORPORATION (US) 2001-09-27 WO claimed
WO-2011091167-A2 LYSOPHOSPHATIDIC ACID RECEPTOR TARGETING FOR SCLERODERMA AND OTHER FIBROTIC DISEASES THE GENERAL HOSPITAL CORPORATION (US) 2011-07-28 WO disclosed
US-20100239501-A1 GENE SENSITIVE TO BONE/JOINT DISEASE AND USE THEREOF RIKEN (JP) 2010-09-23 US disclosed
US-20100143381-A1 LYSOPHOSPHATIDIC ACID RECEPTOR TARGETING FOR LUNG DISEASE THE GENERAL HOSPITAL CORPORATION 2010-06-10 US disclosed
EP-2153847-A1 GENE SENSITIVE TO BONE/JOINT DISEASE AND USE THEREOF Riken (JP) 2010-02-17 EP disclosed
WO-2008112201-A2 LYSOPHOSPHATIDIC ACID RECEPTOR TARGETING FOR LUNG DISEASE THE GENERAL HOSPITAL CORPORATION (US) 2008-09-18 WO disclosed
EP-1918287-A2 LPA receptor agonists and antagonists and methods of use THE UNIVERSITY OF TENNESSEE RESEARCH CORPORATION (US) 2008-05-07 EP disclosed
EP-1427424-A2 LPA RECEPTOR AGONISTS AND ANTAGONISTS AND METHODS OF USE THE UNIVERSITY OF TENNESSEE RESEARCH CORPORATION (US) 2004-06-16 EP disclosed
EP-1263752-A4 LPA RECEPTOR AGONISTS AND ANTAGONISTS AND METHODS OF USE UNIV TENNESSEE RES CORP (US) 2003-07-30 EP disclosed
US-20030130237-A1 LPA receptor agonists and antagonists and methods of use MILLER DUANE D (US) 2003-07-10 US disclosed
WO-2003024402-A2 LPA RECEPTOR AGONISTS AND ANTAGONISTS AND METHODS OF USE THE UNIVERSITY OF TENNESSEE RESEARCH CORPORATION (US) 2003-03-27 WO disclosed
US-20030027800-A1 LPA receptor agonists and antagonists and methods of use NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2003-02-06 US disclosed
EP-1263752-A2 LPA RECEPTOR AGONISTS AND ANTAGONISTS AND METHODS OF USE THE UNIVERSITY OF TENNESSEE RESEARCH CORPORATION (US) 2002-12-11 EP disclosed
WO-2001071022-A2 LPA RECEPTOR AGONISTS AND ANTAGONISTS AND METHODS OF USE THE UNIVERSITY OF TENNESSEE RESEARCH CORPORATION (US) 2001-09-27 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (3 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20050261252-A1 LPA receptor agonists and antagonists and methods of use LPAR1, LPAR2, LPAR3 LPAR3 3/4885LPAR1 1/4885LPAR2 2/4885
US-20030027800-A1 LPA receptor agonists and antagonists and methods of use LPAR1, LPAR2, LPAR3 LPAR3 3/4885LPAR1 1/4885LPAR2 2/4885
US-20030130237-A1 LPA receptor agonists and antagonists and methods of use LPAR1, LPAR2, LPAR5 LPAR3 4/4885LPAR1 1/4885LPAR2 2/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.