Phosphoric Acid

Phosphoric Acid

SCHEMBL9318099

COc1cccc(C[P+](c2ccc(C)cc2)(c2ccc(C)cc2)c2ccc(C)cc2)c1.COc1cccc(C[P+](c2cccc(C)c2)(c2cccc(C)c2)c2cccc(C)c2)c1.O=P([O-])(O)O.[Cl-]

nearest known ligand 0.43

Full drug profile on Sugi Atlas →

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 19)

geneUniProtsupporting neighboursconfidence
MMP13 P45452 2/20 0.43
L3MBTL1 Q9Y468 1/20 0.41
MAOB P27338 2/20 0.41
ACHE P22303 1/20 0.41
TAAR1 Q96RJ0 2/20 0.41
MEN1 O00255 1/20 0.41
KMT2A Q03164 1/20 0.41
TP53 P04637 3/20 0.39
LMNA P02545 1/20 0.39
HSD17B2 P37059 1/20 0.39
SMN1; SMN2 Q16637 2/20 0.38
MAPT P10636 1/20 0.38
KDM4E B2RXH2 1/20 0.38
NPC1 O15118 1/20 0.38
TSHR P16473 1/20 0.38
NFKB1 P19838 1/20 0.38
RAB9A P51151 1/20 0.38
NFKB2 Q00653 1/20 0.38
RELA Q04206 1/20 0.38

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
Phosphoric Acid SCHEMBL9318089 0.96 MAOB (0.42) MMP13L3MBTL1MAOBACHETAAR1
Phosphoric Acid SCHEMBL7197782 0.90 ACHE (0.47) MMP13MAOBACHETAAR1HSD17B2
Phosphoric Acid SCHEMBL7197903 0.90 TAAR1 (0.47) MMP13L3MBTL1MAOBACHETAAR1
Phosphoric Acid SCHEMBL9318706 0.87 MAOB (0.38) MMP13MAOBACHETAAR1MEN1
Hydrochloric Acid SCHEMBL7195803 0.86 ACHE (0.55) MAOBACHETAAR1HSD17B2
Hydrochloric Acid SCHEMBL7198118 0.86 TAAR1 (0.53) MMP13L3MBTL1MAOBACHETAAR1
Acetic Acid SCHEMBL8750057 0.84 ACHE (0.46) MMP13MAOBACHETAAR1MEN1
Acetic Acid SCHEMBL8750051 0.84 L3MBTL1 (0.47) MMP13L3MBTL1MAOBTAAR1MEN1
Bromide SCHEMBL7201341 0.84 TAAR1 (0.53) MMP13L3MBTL1MAOBACHETAAR1
Iodide SCHEMBL7197885 0.84 TAAR1 (0.53) MMP13L3MBTL1MAOBACHETAAR1

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-5310853-A Epoxy resins THE DOW CHEMICAL COMPANY (US) 1994-05-10 US disclosed