SCHEMBL3113144

SCHEMBL3113144

CCCCCCCCCCCCCCCCCC(=O)OP(=O)([O-])[O-].[Ca+2].[MgH2]

nearest known ligand 0.50

Known targets — ChEMBL curated mechanism

GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHMGCRMMP1MMP13MMP7MMP8PTGS1PTGS2ileSpolrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
DGKA P23743 1/20 0.50
CES2 O00748 4/20 0.48
CES1 P23141 4/20 0.48
LMNA P02545 2/20 0.47
LPAR1 Q92633 3/20 0.47
LPAR4 Q99677 3/20 0.47
LPAR2 Q9HBW0 3/20 0.47
LPAR3 Q9UBY5 3/20 0.47
PAM P19021 2/20 0.46
MAPT P10636 2/20 0.44
MAPK1 P28482 1/20 0.44
LPAR6 P43657 2/20 0.43
LPAR5 Q9H1C0 2/20 0.43
TSHR P16473 1/20 0.43
ENPP2 Q13822 1/20 0.43
DNM1 Q05193 1/20 0.42

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
SCHEMBL28616840 0.98 DGKA (0.52) DGKACES2CES1LMNALPAR1
SCHEMBL29089011 0.98 DGKA (0.52) DGKACES2CES1LMNALPAR1
SCHEMBL8975164 0.98 DGKA (0.52) DGKACES2CES1LMNALPAR1
SCHEMBL28261297 0.96 DGKA (0.53) DGKACES2CES1LMNALPAR1
SCHEMBL28896537 0.96 DGKA (0.53) DGKACES2CES1LMNALPAR1
SCHEMBL3917799 0.96 DGKA (0.53) DGKACES2CES1LMNALPAR1
SCHEMBL28518374 0.94 DGKA (0.52) DGKACES2CES1LMNALPAR1
SCHEMBL28353538 0.94 DGKA (0.52) DGKACES2CES1LMNALPAR1
Zinc Ion SCHEMBL29089010 0.94 DGKA (0.52) DGKACES2CES1LMNALPAR1
Potassium Ion SCHEMBL28377997 0.94 DGKA (0.52) DGKACES2CES1LMNALPAR1

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 8 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20100256199-A1 Crystalline form of an Antimalarial Compound GLAXO GROUP LIMITED 2010-10-07 US disclosed
EP-2220043-A1 CRYSTALLINE FORM OF AN ANTIMALARIAL COMPOUND Glaxo Group Limited (GB) 2010-08-25 EP disclosed
EP-1682126-B1 SUBSTITUTED BENZAZOLES AND USE THEREOF AS INHIBITORS OF RAF KINASE NOVARTIS VACCINES & DIAGNOSTIC (US) 2009-07-01 EP disclosed
WO-2009068623-A1 CRYSTALLINE FORM OF AN ANTIMALARIAL COMPOUND GLAXO GROUP LIMITED (GB) 2009-06-04 WO disclosed
CN-1981747-A Rapidly disintegrating methylcellulose tablets SMITHKLINE BEECHAM CORP (US) 2007-06-20 CN disclosed
CN-1215833-C Rapidly disintegrating methylcellulose tablets SMITHKLINE BEECHAM CORP (US) 2005-08-24 CN disclosed
EP-0361629-B1 Heterocyclic compounds WYETH JOHN & BROTHER LTD (GB) 1994-06-15 EP disclosed
EP-0361629-A2 Heterocyclic compounds JOHN WYETH & BROTHER LIMITED (GB) 1990-04-04 EP 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 (1 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-20100256199-A1 Crystalline form of an Antimalarial Compound CYP3A43, G6PD, PYGL DGKA 4587/4885CES2 3717/4885CES1 2213/4885

“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.