Phosphoric Acid

Phosphoric Acid

SCHEMBL5312301

CCCCCCCCCC(=O)C(N)(C(=O)CCCCCCCCC)C(=O)CCCCCCCCC.O=P(O)(O)O

nearest known ligand 0.53

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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 9)

geneUniProtsupporting neighboursconfidence
FAAH O00519 8/20 0.53
CES1 P23141 8/20 0.53
CES2 O00748 5/20 0.53
MEN1 O00255 1/20 0.53
CYP1A2 P05177 1/20 0.53
KMT2A Q03164 1/20 0.53
HSD17B10 Q99714 1/20 0.53
SMPD1 P17405 4/20 0.50
FDPS P14324 2/20 0.50

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
SCHEMBL638951 0.92 FAAH (0.61) FAAHCES1CES2MEN1CYP1A2
SCHEMBL2573096 0.92 FAAH (0.61) FAAHCES1CES2MEN1CYP1A2
Fluoride SCHEMBL10493503 0.90 FAAH (0.59) FAAHCES1CES2MEN1CYP1A2
Hydrochloric Acid SCHEMBL219232 0.90 FAAH (0.59) FAAHCES1CES2MEN1CYP1A2
Hydrochloric Acid SCHEMBL196410 0.90 FAAH (0.59) FAAHCES1CES2MEN1CYP1A2
Water SCHEMBL3120172 0.90 FAAH (0.59) FAAHCES1CES2MEN1CYP1A2
Iodide SCHEMBL8433341 0.90 FAAH (0.59) FAAHCES1CES2MEN1CYP1A2
Bromide SCHEMBL1244460 0.90 FAAH (0.59) FAAHCES1CES2MEN1CYP1A2
Bromide SCHEMBL6552300 0.90 FAAH (0.59) FAAHCES1CES2MEN1CYP1A2
Water SCHEMBL11595702 0.90 FAAH (0.59) FAAHCES1CES2MEN1CYP1A2

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
CN-107074794-B Method for producing polyvalent glycidyl compound 昭和电工株式会社 2019-09-24 CN disclosed
CN-107074794-A Method for producing polyvalent glycidyl compound 昭和电工株式会社 2017-08-18 CN disclosed
US-20070215351-A1 Use of phosphorus and nitrogen containing formulations in secondary oil recovery operations ENVIROFUELS, LLC (US) 2007-09-20 US disclosed
WO-2007089474-A2 THE USE OF PHOSPHORUS AND NITROGEN CONTAINING FORMULATIONS IN SECONDARY OIL RECOVERY OPERATIONS ENVIROFUELS, LLC (US) 2007-08-09 WO disclosed