Phosphoric Acid

Phosphoric Acid

SCHEMBL9549586

CN(C)CCCC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.CN(C)CCCC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.CN(C)CCCC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.O=P([O-])([O-])[O-]

nearest known ligand 0.47

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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
▸ HRH1 known ✓ P35367 2/20 0.47
▸ HTR2A P28223 2/20 0.47
▸ HIF1A Q16665 1/20 0.45
▸ SIGMAR1 Q99720 1/20 0.43
▸ MAPT P10636 1/20 0.42
▸ ALDH1A1 P00352 1/20 0.41
▸ CYP1A2 P05177 1/20 0.41
▸ CYP2D6 P10635 1/20 0.41
▸ TSHR P16473 1/20 0.41
▸ CYP2C19 P33261 1/20 0.41
▸ TRAP1 Q12931 2/20 0.40
▸ UTS2R Q9UKP6 1/20 0.37
▸ CHRNA7 P36544 2/20 0.37
▸ USP2 O75604 1/20 0.36

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 SCHEMBL8972371 0.90 HTR2A (0.50) HTR2AHRH1HIF1AMAPTALDH1A1
Bromide SCHEMBL8909571 0.90 HTR2A (0.53) HTR2AHRH1HIF1ASIGMAR1ALDH1A1
Hydrochloric Acid SCHEMBL9549516 0.90 HTR2A (0.53) HTR2AHRH1HIF1ASIGMAR1ALDH1A1
Bromide SCHEMBL8782143 0.88 HTR2A (0.52) HTR2AHRH1HIF1ASIGMAR1ALDH1A1
Acetic Acid SCHEMBL9549692 0.87 ALDH1A1 (0.46) HTR2AHRH1HIF1ASIGMAR1MAPT
Bromide SCHEMBL9147651 0.86 HTR2A (0.50) HTR2AHRH1HIF1ASIGMAR1ALDH1A1
Acetic Acid SCHEMBL9848369 0.86 ALDH1A1 (0.45) HTR2AHRH1HIF1ASIGMAR1MAPT
Bromide SCHEMBL190865 0.84 HTR2A (0.60) HTR2AHRH1HIF1ASIGMAR1ALDH1A1
Iodide SCHEMBL4110593 0.84 HTR2A (0.60) HTR2AHRH1HIF1ASIGMAR1ALDH1A1
Hydrochloric Acid SCHEMBL8861752 0.84 HTR2A (0.60) HTR2AHRH1HIF1ASIGMAR1ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5208317-A Molding materials of cured epoxy resins THE DOW CHEMICAL COMPANY (US) 1993-05-04 — — US disclosed
US-5109099-A ADVANCING EPOXY RESINS IN PRESENCE OF AMINO GROUP-CONTAINING PHOSPHONIUM CATALYST THE DOW CHEMICAL COMPANY (US) 1992-04-28 — — US disclosed
EP-0441243-A2 Precatalyzed catalyst compositions, process for preparing epoxy resins, curable compositions, articles resulting from curing the resultant compositions THE DOW CHEMICAL COMPANY (US) 1991-08-14 — — EP disclosed
US-4981926-A Rapid and selective curing using phosphonium catalyst containing an amine group; polyepoxides THE DOW CHEMICAL COMPANY (US) 1991-01-01 — — US disclosed
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