Phosphoric Acid

Phosphoric Acid

SCHEMBL9549658

CN(CC[P+](c1ccccc1)(c1ccccc1)c1ccccc1)Cc1ccccc1.CN(CC[P+](c1ccccc1)(c1ccccc1)c1ccccc1)Cc1ccccc1.CN(CC[P+](c1ccccc1)(c1ccccc1)c1ccccc1)Cc1ccccc1.O=P([O-])([O-])[O-]

nearest known ligand 0.48

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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 10)

geneUniProtsupporting neighboursconfidence
▸ SIGMAR1 Q99720 6/20 0.47
▸ CARM1 Q86X55 1/20 0.47
▸ PRMT6 Q96LA8 1/20 0.47
▸ PRMT8 Q9NR22 1/20 0.47
▸ MAOB P27338 4/20 0.43
▸ TMEM97 Q5BJF2 4/20 0.42
▸ APP P05067 2/20 0.42
▸ ACHE P22303 1/20 0.42
▸ ACKR3 P25106 1/20 0.41
▸ HIF1A Q16665 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
Hydrochloric Acid SCHEMBL9549758 0.89 CARM1 (0.55) SIGMAR1CARM1PRMT6PRMT8MAOB
Bromide SCHEMBL9549584 0.89 CARM1 (0.55) SIGMAR1CARM1PRMT6PRMT8MAOB
Acetic Acid SCHEMBL9549681 0.87 CARM1 (0.46) SIGMAR1CARM1PRMT6PRMT8TMEM97
Phosphoric Acid SCHEMBL8972371 0.82 HTR2A (0.50) HIF1A
Phosphoric Acid SCHEMBL9549648 0.78 HIF1A (0.44) SIGMAR1HIF1A
Phosphoric Acid SCHEMBL9549605 0.76 HIF1A (0.45) SIGMAR1TMEM97HIF1A
Phosphoric Acid SCHEMBL9549586 0.76 HTR2A (0.47) SIGMAR1HIF1A
Phosphoric Acid SCHEMBL9067723 0.73 HIF1A (0.54) HIF1A
SCHEMBL1088446 0.72 SIGMAR1 (0.74) SIGMAR1CARM1PRMT6PRMT8MAOB
SCHEMBL7055109 0.72 CARM1 (0.75) SIGMAR1CARM1PRMT6PRMT8MAOB

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 4 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5208317-A Molding materials of cured epoxy resins THE DOW CHEMICAL COMPANY (US) 1993-05-04 — — US disclosed
US-5109099-A ADVANCING EPOXY RESINS IN PRESENCE OF AMINO GROUP-CONTAINING PHOSPHONIUM CATALYST THE DOW CHEMICAL COMPANY (US) 1992-04-28 — — US disclosed
EP-0441243-A2 Precatalyzed catalyst compositions, process for preparing epoxy resins, curable compositions, articles resulting from curing the resultant compositions THE DOW CHEMICAL COMPANY (US) 1991-08-14 — — EP disclosed
US-4981926-A Rapid and selective curing using phosphonium catalyst containing an amine group; polyepoxides THE DOW CHEMICAL COMPANY (US) 1991-01-01 — — US disclosed
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