Phosphoric Acid

Phosphoric Acid

SCHEMBL9067723

CCC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.CCC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.CCC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.O=P([O-])([O-])[O-]

nearest known ligand 0.54

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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
HIF1A Q16665 1/20 0.54
ALDH1A1 P00352 2/20 0.47
CYP1A2 P05177 1/20 0.47
CYP2D6 P10635 1/20 0.47
TSHR P16473 1/20 0.47
CYP2C19 P33261 1/20 0.47
TRAP1 Q12931 1/20 0.38
CETP P11597 4/20 0.38
FDFT1 P37268 3/20 0.38
MEN1 O00255 1/20 0.36
KMT2A Q03164 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
Butyltriphenylphosphonium SCHEMBL8972698 0.90 HIF1A (0.52) HIF1AALDH1A1CYP1A2CYP2D6TSHR
SCHEMBL7865520 0.87 HIF1A (0.64) HIF1AALDH1A1CYP1A2CYP2D6TSHR
SCHEMBL29421497 0.87 HIF1A (0.70) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Phosphoric Acid SCHEMBL8972445 0.87 HIF1A (0.48) HIF1AALDH1A1CYP1A2CYP2D6TSHR
SCHEMBL7865544 0.85 HIF1A (0.61) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Bromide SCHEMBL164032 0.85 HIF1A (0.67) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Hydrochloric Acid SCHEMBL2039214 0.85 HIF1A (0.67) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Water SCHEMBL3418016 0.85 HIF1A (0.67) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Iodide SCHEMBL297568 0.85 HIF1A (0.67) HIF1AALDH1A1CYP1A2CYP2D6TSHR
Fluoride Ion SCHEMBL31171038 0.85 HIF1A (0.67) HIF1AALDH1A1CYP1A2CYP2D6TSHR

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-5534565-A DICYANDIAMIDE DERIVATIVES FOR LAMINATES ALLIEDSIGNAL INC. (US) 1996-07-09 US disclosed