Phosphoric Acid

Phosphoric Acid

SCHEMBL1223979

CCCCCCCCC=CCCCCCCCC(=O)C[N+](C)(C)C(=O)CCCCCCCC=CCCCCCCCC.CCCCCCCCC=CCCCCCCCC(=O)C[N+](C)(C)C(=O)CCCCCCCC=CCCCCCCCC.CCCCCCCCC=CCCCCCCCC(=O)C[N+](C)(C)C(=O)CCCCCCCC=CCCCCCCCC.O=P([O-])([O-])[O-]

nearest known ligand 0.54

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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
KCNH2 known ✓ Q12809 1/20 0.49
FABP3 P05413 6/20 0.54
FAAH O00519 5/20 0.53
TERT O14746 3/20 0.49
MAPT P10636 2/20 0.49
BLM P54132 2/20 0.49
HSD17B10 Q99714 2/20 0.49
FABP4 P15090 2/20 0.49
PTPN1 P18031 2/20 0.49
PPARG P37231 2/20 0.49
PPARD Q03181 2/20 0.49
PPARA Q07869 2/20 0.49
GMNN O75496 1/20 0.49
USP2 O75604 1/20 0.49
LMNA P02545 1/20 0.49
CYP1A2 P05177 1/20 0.49
POLB P06746 1/20 0.49
CYP2C9 P11712 1/20 0.49
ALOX15 P16050 1/20 0.49
APEX1 P27695 1/20 0.49

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 SCHEMBL28049027 1.00 FABP3 (0.54) FABP3FAAHTERTMAPTBLM
SCHEMBL2905137 0.94 FAAH (0.58) FABP3FAAHTERTMAPTBLM
Propane SCHEMBL741627 0.93 FAAH (0.57) FABP3FAAHTERTMAPTBLM
Propane SCHEMBL28144123 0.93 FAAH (0.57) FABP3FAAHTERTMAPTBLM
Propane SCHEMBL26102539 0.91 FAAH (0.55) FABP3FAAHTERTMAPTBLM
SCHEMBL8432352 0.85 FABP3 (0.70) FABP3FAAHTERTMAPTBLM
SCHEMBL16061965 0.84 KMT2A (0.50) FABP3MAPTHSD17B10FABP4PTPN1
SCHEMBL1720049 0.84 KMT2A (0.50) FABP3MAPTHSD17B10FABP4PTPN1
Phosphoric Acid SCHEMBL28049090 0.83 FABP3 (0.62) FABP3FAAHTERTMAPTBLM
Propane SCHEMBL743689 0.83 KMT2A (0.48) FABP3MAPTHSD17B10FABP4PTPN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240366507-A1 Methods of Treating Neurologic Disorders GEORGETOWN UNIVERSITY 2024-11-07 US claimed
US-10668172-B2 Treatment for exposure to nerve agent GEORGETOWN UNIVERSITY (US) 2020-06-02 US claimed
EP-2968598-B1 TREATMENT FOR EXPOSURE TO NERVE AGENT UNIV GEORGETOWN (US) 2020-05-27 EP claimed
US-20180126004-A1 TREATMENT FOR EXPOSURE TO NERVE AGENT GEORGETOWN UNIVERSITY 2018-05-10 US claimed
US-9878055-B2 Treatment for exposure to nerve agent GEORGETOWN UNIVERSITY (US) 2018-01-30 US claimed
US-9480750-B2 Preparation of antibody or an antibody fragment targeted immunoliposomes for systemic administration of therapeutic or diagnostic agents and uses thereof GEORGETOWN UNIVERSITY (US) 2016-11-01 US claimed
EP-2175835-B1 METHODS FOR GENERATING IMMUNE RESPONSE USING CATIONIC-LIPOSOME-MEDIATED NUCLEIC ACID DELIVERY UNIV GEORGETOWN (US) 2016-04-20 EP claimed
US-20150252372-A1 PREPARATION OF ANTIBODY OR AN ANTIBODY FRAGMENT TARGETED IMMUNOLIPOSOMES FOR SYSTEMIC ADMINISTRATION OF THERAPEUTIC OR DIAGNOSTIC AGENTS AND USES THEREOF GEORGETOWN UNIVERSITY 2015-09-10 US claimed
US-20150224201-A1 PREPARATION OF ANTIBODY OR AN ANTIBODY FRAGMENT TARGETED IMMUNOLIPOSOMES FOR SYSTEMIC ADMINISTRATION OF THERAPEUTIC OR DIAGNOSTIC AGENTS AND USES THEREOF GEORGETOWN UNIVERSITY 2015-08-13 US claimed
US-9034330-B2 Preparation of antibody or an antibody fragment-targeted immunoliposomes for systemic administration of therapeutic or diagnostic agents and uses thereof GEORGETOWN UNIVERSITY (US) 2015-05-19 US claimed
US-20070134154-A1 Tumor-Targeted nanodelivery systems to improve early MRI detection of cancer GEORGETOWN UNVERSITY (US) 2007-06-14 US claimed
WO-2007047981-A2 TUMOR-TARGETED NANODELIVERY SYSTEMS TO IMPROVE EARLY MRI DETECTION OF CANCER GEORGETOWN UNIVERSITY (US) 2007-04-26 WO claimed
US-20070065499-A1 Preparation of antibody or an antibody fragment-targeted immunoliposomes for systemic administration of therapeutic or diagnostic agents and uses thereof GEORGETOWN UNIVERSITY (US) 2007-03-22 US claimed
EP-1595142-A4 METHOD FOR EVALUATING THE EFFICACY OF CERTAIN CANCER TREATMENTS UNIV GEORGETOWN (US) 2006-08-23 EP claimed
EP-1633327-A1 METHOD FOR IMPROVING STABILITY AND SHELF-LIFE OF LIPOSOME COMPLEXES GEORGETOWN UNIVERSITY (US) 2006-03-15 EP claimed
EP-1595142-A2 METHOD FOR EVALUATING THE EFFICACY OF CERTAIN CANCER TREATMENTS GEORGETOWN UNIVERSITY (US) 2005-11-16 EP claimed
US-20050002998-A1 Method for improving stability and shelf-life of liposome complexes GEORGETOWN UNIVERSITY (US) 2005-01-06 US claimed
WO-2005000271-A1 METHOD FOR IMPROVING STABILITY AND SHELF-LIFE OF LIPOSOME COMPLEXES GEORGETOWN UNIVERSITY (US) 2005-01-06 WO claimed
US-20040241088-A1 Method for evaluating the efficacy of certain cancer treatments GEORGETOWN UNIVERSITY 2004-12-02 US claimed
WO-2004066946-A2 METHOD FOR EVALUATING THE EFFICACY OF CERTAIN CANCER TREATMENTS GEORGETOWN UNIVERSITY (US) 2004-08-12 WO claimed

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

For each of this compound's patents that has machine-readable text (3 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-20150224201-A1 PREPARATION OF ANTIBODY OR AN ANTIBODY FRAGMENT TARGETED IMMUNOLIPOSOMES FOR SYSTEMIC ADMINISTRATION OF THERAPEUTIC OR DIAGNOSTIC AGENTS AND USES THEREOF CHMP4B, PLTP, FCGRT KCNH2 2946/4885FABP3 1875/4885FAAH 1658/4885
US-20070065499-A1 Preparation of antibody or an antibody fragment-targeted immunoliposomes for systemic administration of therapeutic or diagnostic agents and uses thereof CHMP4B, FCGRT, EXOSC5 KCNH2 2689/4885FABP3 2159/4885FAAH 2406/4885
US-20150252372-A1 PREPARATION OF ANTIBODY OR AN ANTIBODY FRAGMENT TARGETED IMMUNOLIPOSOMES FOR SYSTEMIC ADMINISTRATION OF THERAPEUTIC OR DIAGNOSTIC AGENTS AND USES THEREOF CHMP4B, FCGRT, EXOSC5 KCNH2 2750/4885FABP3 2087/4885FAAH 2228/4885

“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.