Phosphoric Acid

Phosphoric Acid

SCHEMBL9105394

CCC(CC)c1ccccc1.O=P(O)(O)O

nearest known ligand 0.50

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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 11)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.50
SRC P12931 1/20 0.50
HDAC8 Q9BY41 1/20 0.48
HDAC6 Q9UBN7 1/20 0.48
POLB P06746 2/20 0.47
CCR5 P51681 1/20 0.46
ACP3 P15309 6/20 0.46
AOC3 Q16853 1/20 0.43
GABBR2 O75899 1/20 0.42
GABBR1 Q9UBS5 1/20 0.42
ANPEP P15144 1/20 0.42

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
SCHEMBL169508 0.86 LMNA (0.56) LMNAHDAC8HDAC6CCR5AOC3
Hypochlorous Acid SCHEMBL11415854 0.84 LMNA (0.56) LMNAHDAC8HDAC6POLBCCR5
Ammonia Solution, Strong SCHEMBL1640901 0.84 LMNA (0.54) LMNAHDAC8HDAC6CCR5AOC3
Selenic Acid SCHEMBL29153976 0.83 LMNA (0.50) LMNAHDAC8HDAC6POLBCCR5
Methylamine SCHEMBL27931105 0.81 LMNA (0.52) LMNACCR5AOC3GABBR2GABBR1
Phenylpropanol SCHEMBL27669001 0.81 LMNA (0.79) LMNASRCPOLBACP3AOC3
SCHEMBL28726898 0.78 CCR5 (0.46) LMNAHDAC8HDAC6POLBCCR5
SCHEMBL9192188 0.78 CCR5 (0.46) LMNAHDAC8HDAC6POLBCCR5
SCHEMBL15569831 0.78 LMNA (0.50) LMNAHDAC8HDAC6CCR5AOC3
Formamide SCHEMBL28078765 0.78 CCR5 (0.46) LMNAHDAC8HDAC6CCR5AOC3

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
US-20120142690-A1 Substituted piperidines BAYER PHARMA AKTIENGESELLSCHAFT (DE) 2012-06-07 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20120142690-A1 Substituted piperidines VHL, PIR, PIGO LMNA 385/4885SRC 3814/4885HDAC8 2563/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.