Phosphoric Acid

Phosphoric Acid

SCHEMBL5096408

CCN(CC)C1N(C)CCN1C.O=P(O)(O)O

nearest known ligand 0.32

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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
FDPS P14324 1/20 0.32
MMP1 P03956 1/20 0.32
MMP2 P08253 1/20 0.32
MMP3 P08254 1/20 0.32
MMP8 P22894 1/20 0.32
HTR1A P08908 1/20 0.31
MEN1 O00255 1/20 0.30
GAA P10253 1/20 0.30
HTT P42858 1/20 0.30
KMT2A Q03164 1/20 0.30

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 SCHEMBL17433546 0.64 S1PR1 (0.31)
Phosphoric Acid SCHEMBL27482642 0.64 CYP1A2 (0.43) FDPSMMP1MMP2MMP3HTR1A
Phosphoric Acid SCHEMBL11271597 0.62 S1PR1 (0.43)
Phosphoric Acid SCHEMBL28801115 0.61 FDPS (0.46) FDPSMMP1MMP2MMP3MMP8
Phosphoric Acid SCHEMBL9359318 0.61 FDPS (0.46) FDPSMMP1MMP2MMP3MMP8
Phosphoric Acid SCHEMBL192007 0.61 FDPS (0.46) FDPSMMP1MMP2MMP3MMP8
N,N-Dimethylethanaminium SCHEMBL9049895 0.61 FDPS (0.46) FDPSMMP1MMP2MMP3MMP8
N,N-Dimethylethanaminium SCHEMBL9049890 0.61 FDPS (0.46) FDPSMMP1MMP2MMP3MMP8
Phosphoric Acid SCHEMBL192006 0.61 FDPS (0.46) FDPSMMP1MMP2MMP3MMP8
Phosphoric Acid SCHEMBL21359160 0.61 FDPS (0.46) FDPSMMP1MMP2MMP3MMP8

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-7439395-B2 Process for the preparation of guanidinium salts MERCK PATENT GMBH (DE) 2008-10-21 US disclosed
US-20070135645-A1 Process for the preparation of guanidinium salts MERCK PATENT GMBH (DE) 2007-06-14 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 (1 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-20070135645-A1 Process for the preparation of guanidinium salts GMPS, AGPS, PFAS FDPS 84/4885MMP1 4667/4885MMP2 4826/4885

“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.