Phosphoric Acid

Phosphoric Acid

SCHEMBL8972445

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

nearest known ligand 0.49

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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 14)

geneUniProtsupporting neighboursconfidence
HIF1A Q16665 1/20 0.48
CETP P11597 4/20 0.45
TRAP1 Q12931 2/20 0.44
ALDH1A1 P00352 1/20 0.43
CYP1A2 P05177 1/20 0.43
CYP2D6 P10635 1/20 0.43
TSHR P16473 1/20 0.43
CYP2C19 P33261 1/20 0.43
GGPS1 O95749 2/20 0.42
EPHX2 P34913 1/20 0.41
PKM P14618 1/20 0.41
CES2 O00748 1/20 0.41
CES1 P23141 1/20 0.41
ENPP2 Q13822 1/20 0.41

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 0.93 HIF1A (0.52) HIF1ACETPTRAP1ALDH1A1CYP1A2
SCHEMBL7871283 0.91 HIF1A (0.54) HIF1ATRAP1ALDH1A1CYP1A2CYP2D6
SCHEMBL7871293 0.91 HIF1A (0.54) HIF1ATRAP1ALDH1A1CYP1A2CYP2D6
Decyltriphenylphosphonium SCHEMBL29772910 0.91 HIF1A (0.58) HIF1ATRAP1ALDH1A1CYP1A2CYP2D6
SCHEMBL29375680 0.91 HIF1A (0.58) HIF1ATRAP1ALDH1A1CYP1A2CYP2D6
SCHEMBL31168138 0.91 HIF1A (0.58) HIF1ATRAP1ALDH1A1CYP1A2CYP2D6
SCHEMBL31614995 0.91 HIF1A (0.58) HIF1ATRAP1ALDH1A1CYP1A2CYP2D6
SCHEMBL7874678 0.89 HIF1A (0.52) HIF1ATRAP1ALDH1A1CYP1A2CYP2D6
SCHEMBL7872995 0.89 HIF1A (0.52) HIF1ATRAP1ALDH1A1CYP1A2CYP2D6
Bromide SCHEMBL1866839 0.89 HIF1A (0.56) HIF1ATRAP1ALDH1A1CYP1A2CYP2D6

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
US-5578694-A MELT POLYCONDENSATION OF AROMATIC DIOL AND DIARYL CARBONATE; ESTER INTERCHANGE USING PHOSPHONIUM CATALYST MITSUBISHI CHEMICAL CORPORATION (JP) 1996-11-26 US disclosed
EP-0703262-A2 Process for producing aromatic polycarbonate Mitsubishi Chemical Corporation (JP) 1996-03-27 EP disclosed