Phosphoric Acid

Phosphoric Acid

SCHEMBL5328897

O=C1NC(=O)C2CCCCC12.O=P(O)(O)O

nearest known ligand 0.35

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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
PARP1 P09874 1/20 0.35
MAPT P10636 1/20 0.33
ENO1 P06733 1/20 0.31
MMP2 P08253 4/20 0.31
CA12 O43570 3/20 0.31
CA1 P00915 3/20 0.31
CA2 P00918 3/20 0.31
CA9 Q16790 3/20 0.31
MMP1 P03956 2/20 0.31
PDE4A P27815 4/20 0.31
PDE4B Q07343 4/20 0.31
PDE4C Q08493 4/20 0.31
PDE4D Q08499 4/20 0.31
FDPS P14324 1/20 0.30
MMP8 P22894 1/20 0.30
KDM4E B2RXH2 1/20 0.30
POLB P06746 1/20 0.30
L3MBTL1 Q9Y468 1/20 0.30
MMP3 P08254 1/20 0.30

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
SCHEMBL13557473 0.87 PARP1 (0.40) PARP1MAPTCA1CA2PDE4A
SCHEMBL797221 0.87 PARP1 (0.40) PARP1MAPTCA1CA2PDE4A
SCHEMBL2539347 0.87 PARP1 (0.40) PARP1MAPTCA1CA2PDE4A
SCHEMBL2543825 0.87 PARP1 (0.40) PARP1MAPTCA1CA2PDE4A
SCHEMBL9063186 0.85 MAPT (0.43) PARP1MAPTPDE4APDE4BPDE4C
SCHEMBL11835522 0.85 PARP1 (0.39) PARP1MAPTPDE4APDE4BPDE4C
Hydrochloric Acid SCHEMBL5238010 0.85 PARP1 (0.39) PARP1MAPTPDE4APDE4BPDE4C
SCHEMBL11091560 0.85 PARP1 (0.39) PARP1MAPTPDE4APDE4BPDE4C
SCHEMBL6219549 0.82 PARP1 (0.36) PARP1MAPTPDE4APDE4BPDE4C
SCHEMBL12428067 0.82 PARP1 (0.36) PARP1MAPTPDE4APDE4BPDE4C

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 claimed