Phosphoric Acid

Phosphoric Acid

SCHEMBL5718136

N#[N+]c1ccc(Nc2ccccc2)cc1.N#[N+]c1ccc(Nc2ccccc2)cc1.N#[N+]c1ccc(Nc2ccccc2)cc1.O=P([O-])([O-])[O-]

nearest known ligand 0.48

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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
ALDH1A1 P00352 6/20 0.48
HSD17B10 Q99714 5/20 0.48
ALOX12 P18054 4/20 0.48
L3MBTL1 Q9Y468 4/20 0.48
TSHR P16473 3/20 0.48
TDP1 Q9NUW8 3/20 0.48
ALOX15 P16050 2/20 0.48
PTGS1 P23219 1/20 0.48
SLC6A2 P23975 1/20 0.48
MAPK1 P28482 1/20 0.48
PTGS2 P35354 1/20 0.48
HTR2B P41595 1/20 0.48
HPGD P15428 3/20 0.43
CYP3A4 P08684 4/20 0.41
HTT P42858 2/20 0.41
CASP3 P42574 1/20 0.41
SENP7 Q9BQF6 1/20 0.41
MAPT P10636 4/20 0.41
CYP1A2 P05177 1/20 0.41
CYP2C9 P11712 1/20 0.41

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
SCHEMBL9854058 0.93 ALDH1A1 (0.45) ALDH1A1HSD17B10ALOX12L3MBTL1TSHR
Phosphoric Acid SCHEMBL5718141 0.93 ALDH1A1 (0.45) ALDH1A1HSD17B10ALOX12L3MBTL1TSHR
SCHEMBL741543 0.88 ALDH1A1 (0.62) ALDH1A1HSD17B10ALOX12L3MBTL1TSHR
Formaldehyde SCHEMBL8778614 0.86 ALDH1A1 (0.54) ALDH1A1HSD17B10ALOX12L3MBTL1TSHR
Bromide SCHEMBL8910214 0.86 ALDH1A1 (0.59) ALDH1A1HSD17B10ALOX12L3MBTL1TSHR
Hydrochloric Acid SCHEMBL8911949 0.86 ALDH1A1 (0.59) ALDH1A1HSD17B10ALOX12L3MBTL1TSHR
Sulfuric Acid SCHEMBL2959599 0.85 ALDH1A1 (0.48) ALDH1A1HSD17B10ALOX12L3MBTL1TSHR
Hydrochloric Acid SCHEMBL10936047 0.84 ALDH1A1 (0.56) ALDH1A1HSD17B10ALOX12L3MBTL1TSHR
Hydrochloric Acid SCHEMBL11570682 0.84 ALDH1A1 (0.56) ALDH1A1HSD17B10ALOX12L3MBTL1TSHR
Sulfuric Acid SCHEMBL5718123 0.82 SNCA (0.49) ALDH1A1HSD17B10ALOX12L3MBTL1TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0616702-B1 AQUEOUS-PROCESSABLE TONABLE IMAGING ELEMENT DU PONT (US) 2001-05-30 EP claimed
EP-0542858-B1 PROCESS FOR FORMING A COLORED IMAGE USING AN AQUEOUS DEVELOPABLE PRECOLORED DIAZO IMAGING ELEMENT DU PONT (US) 1997-12-29 EP claimed
US-5534380-A PHOTOSENSITIVE COLORED IMAGES ON SUPPORTS WITH TONERS E. I. DU PONT DE NEMOURS AND COMPANY (US) 1996-07-09 US claimed
US-5443937-A Diazo resins E. I. DU PONT DE NEMOURS AND COMPANY (US) 1995-08-22 US claimed
US-5401603-A Aqueous-processable imaging element tonable at room temperature before and after exposure to actinic radiation E. I. DU PONT DE NEMOURS AND COMPANY (US) 1995-03-28 US claimed
EP-0616702-A1 AQUEOUS-PROCESSABLE TONABLE IMAGING ELEMENT E.I. DU PONT DE NEMOURS AND COMPANY (US) 1994-09-28 EP claimed
WO-1993012469-A1 AQUEOUS-PROCESSABLE TONABLE IMAGING ELEMENT E.I. DU PONT DE NEMOURS AND COMPANY (US) 1993-06-24 WO claimed
EP-0542858-A1 PPROCESS FOR FORMING A COLORED IMAGE USING AN AQUEOUS DEVELOPABLE PRECOLORED DIAZO IMAGING ELEMENT E.I. DU PONT DE NEMOURS AND COMPANY (US) 1993-05-26 EP claimed
WO-1992002857-A1 AQUEOUS DEVELOPABLE PRECOLORED DIAZO IMAGING ELEMENT E.I. DU PONT DE NEMOURS AND COMPANY (US) 1992-02-20 WO claimed
CN-113168095-B Lithographic printing plate precursor 易客发有限公司 2024-05-24 CN disclosed
EP-1093019-B1 Process for forming a colored image having a dominant attribute DU PONT (US) 2006-12-27 EP disclosed
EP-1093018-B1 Analog and digital proofing image DU PONT (US) 2006-09-20 EP disclosed
US-6723495-B2 IMAGEABLE HYDROPHILIC LAYER, LATENT BRONSTED ACID, BINDER, AND ACID ACTIVATED CROSSLINKING AGENT ARE HEATED AND DEVELOPED KODAK POLYCHROME GRAPHICS LLC 2004-04-20 US disclosed
US-20030148227-A1 IMAGEABLE HYDROPHILIC LAYER, LATENT BRONSTED ACID, BINDER, AND ACID ACTIVATED CROSSLINKING AGENT ARE HEATED AND DEVELOPED KODAK PHILIPPINES LTD. 2003-08-07 US disclosed
EP-0035886-B1 SOLID-STATE IMAGING DEVICE HAVING A COLOR FILTER ARRAY AND METHODS OF PREPARING SAME EASTMAN KODAK COMPANY (a New Jersey corporation) (US) 1985-11-27 EP disclosed
US-4357415-A Method of making a solid-state color imaging device having a color filter array using a photocrosslinkable barrier EASTMAN KODAK COMPANY (US) 1982-11-02 US disclosed
US-4315978-A Solid-state color imaging device having a color filter array using a photocrosslinkable barrier EASTMAN KODAK COMPANY (US) 1982-02-16 US disclosed
EP-0035886-A2 Solid-state imaging device having a color filter array and methods of preparing same EASTMAN KODAK COMPANY (a New Jersey corporation) (US) 1981-09-16 EP disclosed
US-4247615-A DIAZO RESIN, MORDANT FOR ANIONIC DYE EASTMAN KODAK COMPANY (US) 1981-01-27 US disclosed
US-4220700-A MORDANTS, ANIONIC DYES EASTMAN KODAK COMPANY (US) 1980-09-02 US disclosed