Phosphoric Acid

Phosphoric Acid

SCHEMBL5329669

O=C(CN1CCN(c2cc(F)ccc2OC2CCCC2)CC1)CN1C(=O)C2CC(O)C(O)CC2C1=O.O=P(O)(O)O

nearest known ligand 0.38

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Known targets — ChEMBL curated mechanism

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

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 19)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 2/20 0.38
KMT2A Q03164 2/20 0.38
RAB9A P51151 1/20 0.37
ALDH1A1 P00352 2/20 0.34
MAPT P10636 1/20 0.34
HTR1A P08908 3/20 0.34
HTR7 P34969 2/20 0.34
PDE4A P27815 2/20 0.33
PDE4B Q07343 2/20 0.33
PDE4C Q08493 2/20 0.33
PDE4D Q08499 2/20 0.33
DRD2 P14416 1/20 0.33
HTR2A P28223 1/20 0.33
GPR6 P46095 4/20 0.33
TSHR P16473 2/20 0.33
GRIN1 Q05586 1/20 0.33
GRIN2B Q13224 1/20 0.33
SMN1; SMN2 Q16637 1/20 0.33
CLK1 P49759 1/20 0.32

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
SCHEMBL4535333 0.97 MEN1 (0.40) MEN1KMT2ARAB9AALDH1A1MAPT
Hydrochloric Acid SCHEMBL4526384 0.96 MEN1 (0.39) MEN1KMT2ARAB9AALDH1A1MAPT
Succinic Acid SCHEMBL5330872 0.92 MEN1 (0.37) MEN1KMT2ARAB9AALDH1A1MAPT
SCHEMBL5329692 0.92 MEN1 (0.35) MEN1KMT2ARAB9AALDH1A1MAPT
Cadaverine Tartrate SCHEMBL5328277 0.92 MEN1 (0.36) MEN1KMT2ARAB9AALDH1A1MAPT
Fumaric Acid SCHEMBL5326133 0.92 MEN1 (0.36) MEN1KMT2ARAB9AALDH1A1MAPT
Maleic Acid SCHEMBL5326128 0.92 MEN1 (0.36) MEN1KMT2ARAB9AALDH1A1MAPT
Phosphoric Acid SCHEMBL5303126 0.91 MEN1 (0.38) MEN1KMT2ARAB9AALDH1A1MAPT
Phosphoric Acid SCHEMBL5328350 0.90 RAB9A (0.47) MEN1KMT2ARAB9AALDH1A1HTR1A
Phosphoric Acid SCHEMBL5329987 0.87 HTR1A (0.45) HTR1AHTR7DRD2HTR2A

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
WO-2007010504-A2 ACID ADDITION SALTS OF ISOINDOLES ACTING AS ADRENERGIC RECEPTOR ANTAGONISTS RANBAXY LABORATORIES LIMITED (IN) 2007-01-25 WO disclosed