Phosphoric Acid

Phosphoric Acid

SCHEMBL6946760

CC(C)O.O=P([O-])([O-])O.[K+].[K+]

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
SLC34A1 Q06495 1/20 0.53
LMNA P02545 3/20 0.43
ALDH1A1 P00352 1/20 0.43
CA2 P00918 2/20 0.38
LAP3 P28838 3/20 0.36
CA12 O43570 1/20 0.33
CA1 P00915 1/20 0.33
MMP1 P03956 1/20 0.33
MMP2 P08253 1/20 0.33
MMP9 P14780 1/20 0.33
MMP8 P22894 1/20 0.33
CA9 Q16790 1/20 0.33
ANPEP P15144 3/20 0.32
ERAP1 Q9NZ08 1/20 0.32
KDM4E B2RXH2 1/20 0.32
CYP2C19 P33261 1/20 0.32
KMT2A Q03164 1/20 0.32
TP53 P04637 1/20 0.32
GABBR2 O75899 2/20 0.31
GABBR1 Q9UBS5 2/20 0.31

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 SCHEMBL27767980 0.86 SLC34A1 (0.53) SLC34A1LMNAALDH1A1CA2LAP3
Phosphoric Acid SCHEMBL6906000 0.85 SLC34A1 (0.50) SLC34A1LMNAALDH1A1CA2LAP3
Phosphoric Acid SCHEMBL27995441 0.83 SLC34A1 (0.50) SLC34A1LMNAALDH1A1CA2LAP3
Propylene Glycol SCHEMBL27676897 0.82 TDP1 (0.56) SLC34A1ALDH1A1LAP3ANPEPERAP1
Phosphoric Acid SCHEMBL27518794 0.82 SLC34A1 (0.50) SLC34A1LMNAALDH1A1CA2LAP3
Phosphoric Acid SCHEMBL28353739 0.81 LMNA (0.46) SLC34A1LMNAALDH1A1CA2LAP3
Phosphoric Acid SCHEMBL29090802 0.81 LMNA (0.46) SLC34A1LMNAALDH1A1CA2LAP3
Phosphoric Acid SCHEMBL5479745 0.81 ALDH1A1 (0.55) LMNAALDH1A1CA2LAP3CA12
Phosphoric Acid SCHEMBL3869841 0.81
Phosphoric Acid SCHEMBL28218504 0.81

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106946692-B A method of using ketoglutaric acid in aqueous two-phase extraction fermentation liquid 四川理工学院 2019-06-18 CN claimed
CN-106946692-B A method of using ketoglutaric acid in aqueous two-phase extraction fermentation liquid 四川理工学院 2019-06-18 CN disclosed
CN-106946692-A A kind of method of ketoglutaric acid in use aqueous two-phase extraction zymotic fluid 四川理工学院 2017-07-14 CN disclosed
EP-1351960-A1 IMPROVED PREPARATION OF (4R, 5S, 6S)-3-[[(2R,3R)-2-[[[(S)-2-AMINO-3-METHYL-1-OXOBUTYL]METHYL]TETRAHYDRO-3-FURANYL]THIO]-6-[(R)-1-HYDROXYETHYL]-4-METHYL-7-OXO-1-AZABICYCLO[3.2.0]HEPT-2-ENE-2-CARBOXYLIC ACID Wyeth (US) 2003-10-15 EP disclosed
WO-2002006283-A1 IMPROVED PREPARATION OF (4R, 5S, 6S)-3-(((2R,3R)-2-((((S)-2-AMINO-3-METHYL-1-OXOBUTYL)METHYL)TETRAHYDRO-3-FURANYL)THIO)-6-((R)-1-HYDROXYETHYL)-4-METHYL-7-OXO-1-AZABICYCLO(3.2.0)HEPT-2-ENE-2-CARBOXYLIC ACID WYETH (US) 2002-01-24 WO disclosed
EP-0478874-A2 Novel 2-substituted alkyl-3-carboxy carbapenems as antibiotics and a method of producing them AMERICAN CYANAMID COMPANY (US) 1992-04-08 EP disclosed
EP-0062840-B1 PROCESS FOR THE PREPARATION OF (2S)-TETRAHYDRO-2ALPHA-METHYL-6-OXO-4BETA-AMINO-2H-PYRAN-3ALPHA-CARBOXYLIC ACID ESTERS MERCK & CO. INC. (US) 1987-12-16 EP disclosed
EP-0235823-A2 Carbapenem antibiotics, a process for preparing them and pharmaceutical compositions containing them Bristol-Myers Squibb Company (US) 1987-09-09 EP disclosed
US-4344885-A Intermediate for the preparation of thienamycin MERCK & CO., INC. (US) 1982-08-17 US disclosed
US-4341791-A 6-, 2- and 1,1-Disubstituted-1-carbadethiapen-2-em-3-carboxylic acid S-oxides MERCK & CO., INC. (US) 1982-07-27 US disclosed
EP-0032400-A1 (3SR, 4RS)-3-((RS)-1-hydroxyethyl)- and -((RS)-1-acyloxyethyl)-2-oxo-4-azetidineacetic acid compounds and a process for preparing the same MERCK & CO. INC. (US) 1981-07-22 EP disclosed