Phosphoric Acid

Phosphoric Acid

SCHEMBL2214342

O=P(O)(O)O.Oc1ccc(-c2ccccc2)cc1

nearest known ligand 0.75

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
MMP3 P08254 1/20 0.75
BCL2L1 Q07817 1/20 0.75
MEN1 O00255 3/20 0.56
KMT2A Q03164 3/20 0.56
RAB9A P51151 2/20 0.56
LMNA P02545 1/20 0.56
MAPT P10636 1/20 0.56
ESR1 P03372 6/20 0.55
ESR2 Q92731 3/20 0.55
DEGS1 O15121 1/20 0.55
ACP3 P15309 2/20 0.54
PTPN5 P54829 1/20 0.52
HSD17B1 P14061 1/20 0.50
HSD17B2 P37059 1/20 0.50
NPC1 O15118 1/20 0.50
CTDSP1 Q9GZU7 1/20 0.50
UQCRB P14927 1/20 0.48
MMP8 P22894 1/20 0.48
MMP14 P50281 1/20 0.48
CA14 Q9ULX7 1/20 0.48

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 SCHEMBL34467592 1.00 MMP3 (0.75) MMP3BCL2L1MEN1KMT2ARAB9A
Phenol SCHEMBL28986147 0.98 MMP3 (0.71) MMP3BCL2L1MEN1KMT2ARAB9A
Biphenyl SCHEMBL28415908 0.97 MMP3 (0.70) MMP3BCL2L1MEN1KMT2ARAB9A
Phenol SCHEMBL6430425 0.95 MMP3 (0.67) MMP3BCL2L1MEN1KMT2ARAB9A
Biphenyl SCHEMBL16782901 0.92 MMP3 (0.62) MMP3BCL2L1MEN1KMT2ARAB9A
Phosphoric Acid SCHEMBL28234425 0.89 BCL2L1 (0.58) MMP3BCL2L1MEN1KMT2ARAB9A
Hydroquinone SCHEMBL21291909 0.87 CA2 (0.65) MMP3BCL2L1MEN1KMT2ARAB9A
SCHEMBL38273 0.87 MMP3 (1.00) MMP3BCL2L1MEN1KMT2ARAB9A
SCHEMBL7865208 0.87 MMP3 (1.00) MMP3BCL2L1MEN1KMT2ARAB9A
Biphenyl SCHEMBL263925 0.87 ALDH1A1 (0.60) MMP3BCL2L1RAB9AACP3PTPN5

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1254252-A4 NOVEL STABILIZED FORMULATIONS FOR CHEMILUMINESCENT ASSAYS GIRI BRIJ P (US) 2006-06-07 EP claimed
US-6602679-B2 Substrate of an oxidant, stabilizer and buffer with an extended shelf life is useful with enzyme based probes; detecting DNA fragments in DNA sequencing GIRI BRIJ (US) 2003-08-05 US claimed
US-20010046688-A1 Novel stabilized formulations for chemiluminescent assays GIRI BRIJ PAL (US) 2001-11-29 US claimed
WO-2001055446-A1 NOVEL STABILIZED FORMULATIONS FOR CHEMILUMINESCENT ASSAYS GIRI BRIJ PAL (US) 2001-08-02 WO claimed
EP-3494396-B1 CHEMILUMINESCENT AND FLUORESCENT SUBSTRATE PADS AND USES THEREOF PIERCE BIOTECHNOLOGY INC (US) 2025-06-11 EP disclosed
US-10722882-B2 Chemiluminescent and fluorescent substrate pads and uses thereof PIERCE BIOTECHNOLOGY, INC. (US) 2020-07-28 US disclosed
EP-3494396-A1 CHEMILUMINESCENT AND FLUORESCENT SUBSTRATE PADS AND USES THEREOF Pierce Biotechnology, Inc. (US) 2019-06-12 EP disclosed
US-20180043355-A1 CHEMILUMINESCENT AND FLUORESCENT SUBSTRATE PADS AND USES THEREOF PIERCE BIOTECHNOLOGY, INC. 2018-02-15 US disclosed
WO-2018027004-A1 CHEMILUMINESCENT AND FLUORESCENT SUBSTRATE PADS AND USES THEREOF PIERCE BIOTECHNOLOGY, INC. (US) 2018-02-08 WO disclosed
US-20110178182-A1 ENRICHED NANOSTRUCTURE COMPOSITION DO-COOP TECHNOLOGIES LTD. 2011-07-21 US disclosed
US-20100086929-A1 DETECTION OF ANALYTES DO-COOP TECHNOLOGIES LTD. (IL) 2010-04-08 US disclosed
EP-2122350-A2 DETECTION OF ANALYTES Do-Coop Technologies Ltd (IL) 2009-11-25 EP disclosed
WO-2006076034-A2 STABILIZED TWO COMPONENT SYSTEM FOR CHEMILUMIESCENT ASSAY IN IMMUNODIAGNOSTICS BHANU, KALRA (US) 2006-07-20 WO disclosed
US-20050272108-A1 Stabilized two component system for chemiluminescent assay in immunodiagnostics KALRA BHANU 2005-12-08 US disclosed
EP-0778947-B1 CHEMILUMINESCENT DETECTION OF HYDROLYTIC ENZYMES USING AN ACRIDAN LUMIGEN INC (US) 2004-05-12 EP disclosed
US-6602679-B2 Substrate of an oxidant, stabilizer and buffer with an extended shelf life is useful with enzyme based probes; detecting DNA fragments in DNA sequencing GIRI BRIJ (US) 2003-08-05 US disclosed
US-20010046688-A1 Novel stabilized formulations for chemiluminescent assays GIRI BRIJ PAL (US) 2001-11-29 US disclosed
EP-0516948-B1 Chemiluminescent method and compositions LUMIGEN INC (US) 2000-05-31 EP disclosed
US-5686258-A Chemiluminescent detection of hydrolytic enzymes using an acridan LUMIGEN, INC. (US) 1997-11-11 US disclosed
EP-0516948-A1 Chemiluminescent method and compositions LUMIGEN, INC. (US) 1992-12-09 EP disclosed