Phosphoric Acid

Phosphoric Acid

SCHEMBL28852148

O=P(O)(O)O.OCc1ccc(C(F)(F)F)cc1

nearest known ligand 0.47

Full drug profile on Sugi Atlas →

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 20)

geneUniProtsupporting neighboursconfidence
PTPN2 P17706 3/20 0.47
PTPN1 P18031 3/20 0.47
PTPN6 P29350 3/20 0.47
PGK1 P00558 2/20 0.47
PGK2 P07205 2/20 0.47
PTPN11 Q06124 2/20 0.47
CA12 O43570 1/20 0.46
CA1 P00915 1/20 0.46
MMP2 P08253 1/20 0.46
TAAR1 Q96RJ0 1/20 0.45
ACP3 P15309 2/20 0.44
BTN3A1 O00481 1/20 0.44
IDO1 P14902 3/20 0.44
PSEN1 P49768 1/20 0.44
PSEN2 P49810 1/20 0.44
APH1B Q8WW43 1/20 0.44
NCSTN Q92542 1/20 0.44
APH1A Q96BI3 1/20 0.44
PSENEN Q9NZ42 1/20 0.44
CES2 O00748 1/20 0.43

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
SCHEMBL96239 0.89 TAAR1 (0.54) TAAR1IDO1PSEN1PSEN2APH1B
Hydrochloric Acid SCHEMBL30282379 0.87 IDO1 (0.54) TAAR1IDO1PSEN1PSEN2APH1B
Hydroxyamine SCHEMBL9048789 0.85 TAAR1 (0.56) TAAR1IDO1PSEN1PSEN2APH1B
SCHEMBL1781036 0.83 KIF11 (0.58) CA1TAAR1IDO1PSEN1PSEN2
SCHEMBL5509990 0.83 SRD5A2 (0.55) TAAR1IDO1PSEN1PSEN2APH1B
SCHEMBL15437156 0.83 TAAR1 (0.59) TAAR1IDO1
SCHEMBL28109891 0.81 TAAR1 (0.47) TAAR1IDO1PSEN1PSEN2APH1B
SCHEMBL2995687 0.79 PGK1 (0.72) PTPN2PTPN1PTPN6PGK1PGK2
SCHEMBL1451054 0.78 LTA4H (0.59) TAAR1IDO1
SCHEMBL6250682 0.78 IDO1 (0.46) TAAR1IDO1PSEN1PSEN2APH1B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115125553-B Electrochemical synthesis method of alcohol 绍兴久孚新材料科技有限公司 2023-12-22 CN disclosed
CN-115125553-A Electrochemical synthesis method of alcohol 绍兴久孚新材料科技有限公司 2022-09-30 CN disclosed