Phosphoric Acid

Phosphoric Acid

SCHEMBL230224

O=P(O)(O)O.O=S(=O)(O)c1ccccc1

nearest known ligand 0.80

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

BTKCACNA1CCACNA1DCACNA1FCACNA1SCACNA2D1CACNA2D2DRD2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQHRH1HTR2AP2RY12

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
TSHR P16473 3/20 0.80
SMN1; SMN2 Q16637 1/20 0.80
POLB P06746 1/20 0.54
CYP2D6 P10635 1/20 0.54
ALDH1A1 P00352 4/20 0.50
TDP1 Q9NUW8 3/20 0.50
HSD17B10 Q99714 2/20 0.50
MMP2 P08253 2/20 0.48
CA12 O43570 2/20 0.48
CA9 Q16790 2/20 0.48
CA14 Q9ULX7 2/20 0.48
LMNA P02545 1/20 0.48
HTR6 P50406 1/20 0.48
NT5E P21589 1/20 0.46
NAPRT Q6XQN6 1/20 0.45
CA2 P00918 3/20 0.44
CA1 P00915 2/20 0.44
MMP1 P03956 1/20 0.44
MMP9 P14780 1/20 0.44
MMP8 P22894 1/20 0.44

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
SCHEMBL125188 0.89 TSHR (1.00) TSHRSMN1; SMN2POLBCYP2D6ALDH1A1
SCHEMBL1079321 0.89 TSHR (1.00) TSHRSMN1; SMN2POLBCYP2D6ALDH1A1
SCHEMBL30812783 0.89 TSHR (1.00) TSHRSMN1; SMN2POLBCYP2D6ALDH1A1
SCHEMBL597672 0.89 TSHR (1.00) TSHRSMN1; SMN2POLBCYP2D6ALDH1A1
SCHEMBL2509 0.89 TSHR (1.00) TSHRSMN1; SMN2POLBCYP2D6ALDH1A1
SCHEMBL30307036 0.89 TSHR (1.00) TSHRSMN1; SMN2POLBCYP2D6ALDH1A1
SCHEMBL30671620 0.89 TSHR (1.00) TSHRSMN1; SMN2POLBCYP2D6ALDH1A1
Benzene SCHEMBL9751882 0.89 TSHR (1.00) TSHRSMN1; SMN2POLBCYP2D6ALDH1A1
SCHEMBL3409457 0.89 TSHR (1.00) TSHRSMN1; SMN2POLBCYP2D6ALDH1A1
SCHEMBL9871011 0.87 TSHR (0.94) TSHRSMN1; SMN2POLBCYP2D6ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-101987891-B Polyolefin resin and nucleating agent-containing composition CHINA PETROLEUM & CHEMICAL 2013-04-10 CN claimed
CN-101987891-A Polyolefin resin and nucleating agent-containing composition CHINA PETROLEUM & CHEMICAL 2011-03-23 CN claimed
US-9643971-B2 Breathing control modulating compounds, and methods of using same GALLEON PHARMACEUTICALS, INC. (US) 2017-05-09 US disclosed
CN-106536523-A Expedient synthesis of sitagliptin 斯特里奥肯公司 2017-03-22 CN disclosed
US-20160046635-A1 NOVEL BREATHING CONTROL MODULATING COMPOUNDS, AND METHODS OF USING SAME GALLEON PHARMACEUTICALS, INC. 2016-02-18 US disclosed
EP-2968329-A1 NOVEL BREATHING CONTROL MODULATING COMPOUNDS, AND METHODS OF USING SAME Galleon Pharmaceuticals, Inc. (US) 2016-01-20 EP disclosed
WO-2014151462-A1 NOVEL BREATHING CONTROL MODULATING COMPOUNDS, AND METHODS OF USING SAME GALLEON PHARMACEUTICALS, INC. (US) 2014-09-25 WO disclosed
US-8710071-B2 Compounds, compositions and methods for reducing lipid levels CVI PHARMACEUTICALS LIMITED (KY) 2014-04-29 US disclosed
CN-101830803-B Method for synthesizing citric acid ester type compound UNIV NORTHWEST NORMAL 2013-04-03 CN disclosed
US-20120004223-A1 COMPOUNDS, COMPOSITIONS AND METHODS FOR REDUCING LIPID LEVELS CVI PHARMACEUTICALS LIMITED (KY) 2012-01-05 US disclosed
CN-101830803-A Method for synthesizing citric acid ester type compound UNIV NORTHWEST NORMAL 2010-09-15 CN disclosed
US-5262446-A Resin acid, esters or abietyl phthalate foaming agent BASF AKTIENGESELLSCHAFT (DE) 1993-11-16 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-20120004223-A1 COMPOUNDS, COMPOSITIONS AND METHODS FOR REDUCING LIPID LEVELS LIPC, LDLR, PCSK9 TSHR 1637/4885SMN1; SMN2 4854/4885POLB 3099/4885
US-20160046635-A1 NOVEL BREATHING CONTROL MODULATING COMPOUNDS, AND METHODS OF USING SAME PRDX5, QDPR, P2RX5 TSHR 3814/4885SMN1; SMN2 378/4885POLB 533/4885

“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.