Phosphoric Acid

Phosphoric Acid

SCHEMBL537669

CC(C)(C)c1cc(Cc2cc(C(C)(C)C)cc(C(C)(C)C)c2O)c(O)c(C(C)(C)C)c1.O=P([O-])([O-])[O-].[Na+].[Na+].[Na+]

nearest known ligand 0.53

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 20)

geneUniProtsupporting neighboursconfidence
HSPA5 P11021 2/20 0.53
CYP2C19 P33261 5/20 0.51
CYP2C9 P11712 4/20 0.51
HIF1A Q16665 3/20 0.51
SMN1; SMN2 Q16637 3/20 0.51
CYP2D6 P10635 2/20 0.46
HSD17B10 Q99714 1/20 0.46
NR5A2 O00482 1/20 0.46
NR5A1 Q13285 1/20 0.46
HTT P42858 2/20 0.43
GAA P10253 2/20 0.43
ALDH1A1 P00352 2/20 0.43
XBP1 P17861 1/20 0.43
MAPK1 P28482 1/20 0.43
NPSR1 Q6W5P4 1/20 0.43
CYP1A2 P05177 2/20 0.39
CYP3A4 P08684 1/20 0.39
TSHR P16473 1/20 0.39
NR1I2 O75469 1/20 0.38
HMGCR P04035 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 SCHEMBL30397166 1.00 HSPA5 (0.53) HSPA5CYP2C19CYP2C9HIF1ASMN1; SMN2
Phosphoric Acid SCHEMBL537648 0.97 HSPA5 (0.53) HSPA5CYP2C19CYP2C9HIF1ASMN1; SMN2
Phosphoric Acid SCHEMBL7731612 0.97 HSPA5 (0.53) HSPA5CYP2C19CYP2C9HIF1ASMN1; SMN2
Phosphoric Acid SCHEMBL7731846 0.97 HSPA5 (0.53) HSPA5CYP2C19CYP2C9HIF1ASMN1; SMN2
Phosphoric Acid SCHEMBL7732345 0.97 HSPA5 (0.53) HSPA5CYP2C19CYP2C9HIF1ASMN1; SMN2
Phosphoric Acid SCHEMBL537656 0.90 HSPA5 (0.56) HSPA5CYP2C19CYP2C9HIF1ASMN1; SMN2
SCHEMBL29500375 0.88 HSPA5 (0.66) HSPA5CYP2C19CYP2C9HIF1ASMN1; SMN2
SCHEMBL30903568 0.88 HSPA5 (0.66) HSPA5CYP2C19CYP2C9HIF1ASMN1; SMN2
SCHEMBL39554 0.88 HSPA5 (0.66) HSPA5CYP2C19CYP2C9HIF1ASMN1; SMN2
SCHEMBL538260 0.87 HSPA5 (0.44) HSPA5CYP2C19CYP2C9HIF1ASMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9309408-B2 Additive concentrate and use thereof HOLLAND COLOURS N.V. (NL) 2016-04-12 US claimed
US-20140353550-A1 ADDITIVE CONCENTRATE AND USE THEREOF HOLLAND COLOURS N.V. (NL) 2014-12-04 US claimed
EP-2559726-B1 Additive concentrate and use thereof HOLLAND COLOURS NV (NL) 2014-02-19 EP claimed
WO-2013025098-A1 ADDITIVE CONCENTRATE AND USE THEREOF HOLLAND COLOURS N.V. (NL) 2013-02-21 WO claimed
EP-2559726-A1 Additive concentrate and use thereof Holland Colours N. V. (NL) 2013-02-20 EP claimed
EP-1694368-B1 TERMINAL STERILIZATION OF PREFILLED CONTAINERS BECTON DICKINSON CO (US) 2012-02-08 EP claimed
WO-2024068415-A1 CO-STABILIZERS FOR HYDROXYPHENYL TRIAZINE STABILIZED POLYMERS BASF SE (DE) 2024-04-04 WO disclosed
WO-2024052176-A1 RHEOLOGY MODIFYING OF POLYMERS WITH A RADICAL INITIATOR AND THIOURETHANE BASF SE (DE) 2024-03-14 WO disclosed
US-20230272171-A1 ADDITIVE MIXTURES FOR RHEOLOGY MODIFICATION OF POLYMERS BASF SE (DE) 2023-08-31 US disclosed
US-9309408-B2 Additive concentrate and use thereof HOLLAND COLOURS N.V. (NL) 2016-04-12 US disclosed
US-9085689-B2 Polylactic acid stereocomplex resin composition having improved crystallization rate and method for molding the same LOTTE CHEMICAL CORPORATION (KR) 2015-07-21 US disclosed
US-20140378595-A1 POLYLACTIC ACID STEREOCOMPLEX RESIN COMPOSITION HAVING IMPROVED CRYSTALLIZATION RATE AND METHOD FOR MOLDING THE SAME LOTTE CHEMICAL CORPORATION (KR) 2014-12-25 US disclosed
EP-2816086-A1 Polylactic Acid Stereocomplex Resin Composition having Improved Crystallization Rate and Method for Molding the same Lotte Chemical Corporation (KR) 2014-12-24 EP disclosed
EP-2305317-A1 Terminal sterilization of prefilled containers Becton Dickinson and Company (US) 2011-04-06 EP disclosed
US-20100099808-A1 ENVIRONMENTALLY FRIENDLY MATERIAL USED FOR MAKING PENS BEIFA GROUP CO., LTD. (CN) 2010-04-22 US disclosed
US-20090012466-A1 Terminal Sterilization of Prefilled Containers BECTON, DICKINSON AND COMPANY (US) 2009-01-08 US disclosed
EP-1694368-A4 TERMINAL STERILIZATION OF PREFILLED CONTAINERS BECTON DICKINSON CO (US) 2007-11-07 EP disclosed
EP-1694368-A2 TERMINAL STERILIZATION OF PREFILLED CONTAINERS Becton, Dickinson and Company (US) 2006-08-30 EP disclosed
WO-2005058377-A2 TERMINAL STERILIZATION OF PREFILLED CONTAINERS BECTON, DICKINSON AND COMPANY (US) 2005-06-30 WO disclosed
US-20050129569-A1 Terminal sterilization of prefilled containers BECTON, DICKINSON AND COMPANY 2005-06-16 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 (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-20230272171-A1 ADDITIVE MIXTURES FOR RHEOLOGY MODIFICATION OF POLYMERS TST, INMT, CD44 HSPA5 3353/4885CYP2C19 1505/4885CYP2C9 1656/4885

“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.