Phosphoric Acid

Phosphoric Acid

SCHEMBL9001330

CCCCCCCCCCCCCCCCCC(=O)NC(CC)C(C)[N+](C)(C)O.O=P([O-])([O-])[O-].[H+].[H+]

nearest known ligand 0.51

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Known targets — ChEMBL curated mechanism

ADRA1AADRA1BADRA1DADRB1ADRB2ADRB3CYP11B1DPP4FGFR1FGFR2FGFR3FGFR4HRH1JAK1JAK2JAK3KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITNAOPRD1OPRK1OPRM1PPDGFRBPIK3CDSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASMOTYK2polrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Phosphoric Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 2/20 0.51
KMT2A Q03164 2/20 0.51
FAAH O00519 2/20 0.51
MAPK1 P28482 1/20 0.51
CPT2 P23786 1/20 0.46
CPT1A P50416 1/20 0.46
CPT1B Q92523 1/20 0.46
PLA2G10 O15496 1/20 0.46
PLA2G4A P47712 2/20 0.45
PLA2G1B P04054 1/20 0.45
PLA2G2A P14555 1/20 0.45
DNM1 Q05193 1/20 0.43
LPAR3 Q9UBY5 1/20 0.41
THRB P10828 1/20 0.41

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
Phosphoric Acid SCHEMBL3172731 0.96 MEN1 (0.50) MEN1KMT2AFAAHMAPK1CPT2
SCHEMBL3166335 0.93 FAAH (0.59) MEN1KMT2AFAAHMAPK1CPT2
SCHEMBL11274282 0.89 FAAH (0.51) MEN1KMT2AFAAHMAPK1CPT2
SCHEMBL11363461 0.89 FAAH (0.51) MEN1KMT2AFAAHMAPK1CPT2
Phosphoric Acid SCHEMBL10489010 0.82 FAAH (0.57) MEN1KMT2AFAAHMAPK1CPT2
SCHEMBL12435848 0.77 FAAH (0.67) MEN1KMT2AFAAHMAPK1PLA2G10
SCHEMBL12435872 0.77 FAAH (0.67) MEN1KMT2AFAAHMAPK1PLA2G10
SCHEMBL1310123 0.74 CPT2 (0.51) MEN1KMT2AFAAHMAPK1CPT2
SCHEMBL118838 0.74 CPT2 (0.51) MEN1KMT2AFAAHMAPK1CPT2
SCHEMBL339771 0.74 CPT2 (0.51) MEN1KMT2AFAAHMAPK1CPT2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0653974-B1 METHOD OF MAKING A COATED ABRASIVE ARTICLE CONTAINING A CONDUCTIVE BACKING MINNESOTA MINING & MFG (US) 1996-09-18 EP disclosed