Phosphoric Acid

Phosphoric Acid

SCHEMBL4552489

Nc1ccc2ccccc2n1.O=P(O)(O)O

nearest known ligand 0.76

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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 20)

geneUniProtsupporting neighboursconfidence
BACE1 P56817 5/20 0.76
NCF1 P14598 1/20 0.76
NOS2 P35228 1/20 0.76
PLAU P00749 4/20 0.50
ALDH1A1 P00352 2/20 0.49
MAPT P10636 2/20 0.49
GAA P10253 1/20 0.49
HDAC8 Q9BY41 1/20 0.46
MGAM O43451 1/20 0.46
RAB9A P51151 3/20 0.43
NPC1 O15118 2/20 0.43
MEN1 O00255 2/20 0.43
KMT2A Q03164 2/20 0.43
SMN1; SMN2 Q16637 2/20 0.42
NFKB1 P19838 1/20 0.42
NFKB2 Q00653 1/20 0.42
RELA Q04206 1/20 0.42
CA12 O43570 1/20 0.42
CA9 Q16790 1/20 0.42
CYP1A2 P05177 1/20 0.42

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
SCHEMBL38775 0.87 BACE1 (1.00) BACE1NCF1NOS2PLAUALDH1A1
SCHEMBL29374605 0.87 BACE1 (1.00) BACE1NCF1NOS2PLAUALDH1A1
Formaldehyde SCHEMBL27626837 0.85 BACE1 (0.86) BACE1NCF1NOS2PLAUALDH1A1
Formaldehyde SCHEMBL27992884 0.85 BACE1 (0.86) BACE1NCF1NOS2PLAUALDH1A1
Hydrochloric Acid SCHEMBL7041585 0.85 BACE1 (0.95) BACE1NCF1NOS2PLAUALDH1A1
SCHEMBL31425238 0.85 BACE1 (0.95) BACE1NCF1NOS2PLAUALDH1A1
SCHEMBL28580629 0.85 BACE1 (0.95) BACE1NCF1NOS2PLAUALDH1A1
Methane SCHEMBL5014377 0.85 BACE1 (0.95) BACE1NCF1NOS2PLAUALDH1A1
Hydrochloric Acid SCHEMBL29933599 0.85 BACE1 (0.95) BACE1NCF1NOS2PLAUALDH1A1
SCHEMBL30834682 0.85 BACE1 (0.95) BACE1NCF1NOS2PLAUALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20160058749-A1 TREATMENTS FOR NEUROPATHY CHILDRENS MEDICAL CENTER (US) 2016-03-03 US disclosed
US-7863295-B2 Treatments for neuropathy CHILDREN'S MEDICAL CENTER CORPORATION (US) 2011-01-04 US disclosed
US-20090203735-A1 TREATMENTS FOR NEUROPATHY NIH-DEITR 2009-08-13 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20160058749-A1 TREATMENTS FOR NEUROPATHY NGF, BDNF, NTRK2 BACE1 1661/4885NCF1 192/4885NOS2 491/4885
US-20090203735-A1 TREATMENTS FOR NEUROPATHY NGF, BDNF, NTRK2 BACE1 1661/4885NCF1 192/4885NOS2 491/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.