Phosphoric Acid

Phosphoric Acid

SCHEMBL1019439

CCN(CC)CC.CCN(CC)CC.O=P(O)(O)O

nearest known ligand 0.46

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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
FDPS P14324 4/20 0.46
MMP2 P08253 3/20 0.46
MMP1 P03956 2/20 0.46
MMP3 P08254 2/20 0.46
MMP8 P22894 2/20 0.46
CA2 P00918 1/20 0.38
LAP3 P28838 1/20 0.35
LMNA P02545 1/20 0.35
PPIP5K2 O43314 1/20 0.34
LPAR3 Q9UBY5 3/20 0.33
KDM4E B2RXH2 1/20 0.33
THRB P10828 1/20 0.33
MAPK1 P28482 1/20 0.33
HSD17B10 Q99714 1/20 0.33
LPAR2 Q9HBW0 1/20 0.33
CHRM2 P08172 1/20 0.33
CHRM4 P08173 1/20 0.33
CHRM5 P08912 1/20 0.33
CHRM1 P11229 1/20 0.33
CHRM3 P20309 1/20 0.33

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 SCHEMBL28801115 1.00 FDPS (0.46) FDPSMMP2MMP1MMP3MMP8
Phosphoric Acid SCHEMBL16093844 1.00 FDPS (0.46) FDPSMMP2MMP1MMP3MMP8
Phosphoric Acid SCHEMBL192006 1.00 FDPS (0.46) FDPSMMP2MMP1MMP3MMP8
Phosphoric Acid SCHEMBL192007 1.00 FDPS (0.46) FDPSMMP2MMP1MMP3MMP8
Phosphoric Acid SCHEMBL9359318 1.00 FDPS (0.46) FDPSMMP2MMP1MMP3MMP8
Phosphoric Acid SCHEMBL21359160 1.00 FDPS (0.46) FDPSMMP2MMP1MMP3MMP8
Phosphoric Acid SCHEMBL23751823 0.97 FDPS (0.43) FDPSMMP2MMP1MMP3MMP8
Phosphoric Acid SCHEMBL8575235 0.97 FDPS (0.43) FDPSMMP2MMP1MMP3MMP8
Phosphoric Acid SCHEMBL28610245 0.97 FDPS (0.43) FDPSMMP2MMP1MMP3MMP8
Phosphoric Acid SCHEMBL28500444 0.97 FDPS (0.43) FDPSMMP2MMP1MMP3MMP8

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 63 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118414344-A Chemical synthesis of cytidine-5' -monophosphate-N-glycyl-sialic acid 89生物公司 2024-07-30 CN claimed
JP-60067424-A None JP disclosed
CN-120020261-A Method for total synthesis of N-glycan 中国科学院上海药物研究所 2025-05-20 CN disclosed
CN-112513263-B Method for producing a compound of a foliol 弗门尼舍有限公司 2025-01-10 CN disclosed
CN-118414344-A Chemical synthesis of cytidine-5' -monophosphate-N-glycyl-sialic acid 89生物公司 2024-07-30 CN disclosed
CN-108886175-B Silicon-based solid electrolyte for rechargeable batteries 巴斯夫公司 2022-08-02 CN disclosed
CN-107710462-B Electrochemical hydrogen storage electrode and battery 巴斯夫公司 2022-08-02 CN disclosed
US-11345907-B2 Method for producing albicanol compounds FIRMENICH SA (CH) 2022-05-31 US disclosed
US-20220162188-A1 ISOPRENOIDS AND METHODS OF MAKING THEREOF NORTH CAROLINA STATE UNIVERSITY 2022-05-26 US disclosed
EP-3911740-A1 ISOPRENOIDS AND METHODS OF MAKING THEREOF North Carolina State University (US) 2021-11-24 EP disclosed
US-5668171-A Halogenated mevalonate compositions and uses thereof in ras-dependent cell growth BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 1997-09-16 US disclosed
US-5643958-A ANTITUMOR BANYU PHARMACEUTICAL CO., LTD. (JP) 1997-07-01 US disclosed
EP-0776884-A1 SUBSTITUTED AMIDE DERIVATIVE BANYU PHARMACEUTICAL CO., LTD. (JP) 1997-06-04 EP disclosed
WO-1995013058-A1 HALOGENATED MEVALONATE COMPOSITIONS AND USES THEREOF IN RAS-DEPENDENT CELL GROWTH BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 1995-05-18 WO disclosed
EP-0216855-A4 RUBBER POLYMERASES AND METHODS FOR THEIR PRODUCTION AND USE. GOODYEAR TIRE & RUBBER (US) 1989-04-12 EP disclosed
US-4792615-A HYDROLYSIS OF A-DIHYDROPOLYPRENYL DICHLOROPHOSPHATE WITH ALKALI OR ALKALINE EARTH METAL HYDROXIDE; POLYISOPRENE NAKAGAWA NAOSHI (JP) 1988-12-20 US disclosed
EP-0216855-A1 RUBBER POLYMERASES AND METHODS FOR THEIR PRODUCTION AND USE THE GOODYEAR TIRE & RUBBER COMPANY (US) 1987-04-08 EP disclosed
US-4638028-A Rubber polymerases and methods for their production and use GOODYEAR TIRE & RUBBER COMPANY (US) 1987-01-20 US disclosed
WO-1986006095-A1 RUBBER POLYMERASES AND METHODS FOR THEIR PRODUCTION AND USE THE GOODYEAR TIRE & RUBBER COMPANY (US) 1986-10-23 WO disclosed
JP-S6067424-A CARCINOSTATIC AGENT NISSHIN FLOUR MILLING CO LTD 1985-04-17 JP 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-20220162188-A1 ISOPRENOIDS AND METHODS OF MAKING THEREOF GGPS1, SQLE, FDPS FDPS 3/4885MMP2 4083/4885MMP1 4385/4885

“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.