Phosphoric Acid

Phosphoric Acid

SCHEMBL143339

NC(CO)CO.O=P(O)(O)O

nearest known ligand 0.42

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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 13)

geneUniProtsupporting neighboursconfidence
ANPEP P15144 5/20 0.41
ERAP2 Q6P179 1/20 0.41
LAP3 P28838 4/20 0.39
ENPEP Q07075 2/20 0.39
ERAP1 Q9NZ08 1/20 0.36
ALDH1A1 P00352 2/20 0.33
FDPS P14324 1/20 0.33
TDP1 Q9NUW8 1/20 0.33
METAP1 P53582 1/20 0.33
S1PR2 O95136 2/20 0.32
S1PR1 P21453 2/20 0.32
S1PR3 Q99500 2/20 0.32
S1PR4 O95977 1/20 0.32

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 SCHEMBL9843904 0.83 LAP3 (0.50) ANPEPERAP2LAP3ERAP1METAP1
SCHEMBL74076 0.82
SCHEMBL2354479 0.82 LMNA (0.36) ALDH1A1TDP1
SCHEMBL3420157 0.79
Hydrochloric Acid SCHEMBL45666 0.78
L-Alaninol SCHEMBL182784 0.78 ALDH1A1 (0.48) ANPEPERAP2LAP3ERAP1ALDH1A1
L-Alaninol SCHEMBL182786 0.78 ALDH1A1 (0.48) ANPEPERAP2LAP3ERAP1ALDH1A1
SCHEMBL5065179 0.75 ENPEP (0.64) ANPEPENPEPALDH1A1TDP1S1PR2
SCHEMBL5496452 0.75 ANPEP (0.39) ANPEPERAP2LAP3ENPEPERAP1
Hypochlorous Acid SCHEMBL25425590 0.74

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109321610-B Efficient preparation of 2-amino-1, 3-propanediol by microbial fermentation method 上海交通大学 2022-11-04 CN claimed
WO-2026106979-A1 PROCESSES AND SYSTEMS FOR FERMENTATIVE ALCOHOL PRODUCTION AND RECOVERY GEVO, INC. (US) 2026-05-21 WO disclosed
US-20260132429-A1 PROCESSES AND SYSTEMS FOR FERMENTATIVE ALCOHOL PRODUCTION AND RECOVERY GEVO INC (US) 2026-05-14 US disclosed
CN-109321610-B Efficient preparation of 2-amino-1, 3-propanediol by microbial fermentation method 上海交通大学 2022-11-04 CN disclosed
EP-2906706-B1 PROCESSES AND SYSTEMS FOR THE PRODUCTION OF FERMENTATION PRODUCTS BUTAMAX ADVANCED BIOFUELS LLC (US) 2020-02-26 EP disclosed
US-10308910-B2 Partial adaption for butanol production BUTAMAX ADVANCED BIOFUELS LLC (US) 2019-06-04 US disclosed
US-10280438-B2 Method for the production of yeast BUTAMAX ADVANCED BIOFUELS LLC (US) 2019-05-07 US disclosed
EP-2970863-B1 GLYCEROL 3- PHOSPHATE DEHYDROGENASE FOR BUTANOL PRODUCTION DU PONT (US) 2019-04-24 EP disclosed
CN-109321610-A Microbe fermentation method efficiently prepares 2- amino -1,3- propylene glycol 上海交通大学 2019-02-12 CN disclosed
US-9962623-B2 Process to remove product alcohols from fermentation broth BUTAMAX ADVANCED BIOFUELS LLC (US) 2018-05-08 US disclosed
CN-101080234-A Certain aminoalkyl glucosaminide phosphate compounds and their use CORIXA CORP (US) 2007-11-28 CN disclosed
WO-2007130518-A2 FERMENTIVE PRODUCTION OF FOUR CARBON ALCOHOLS E. I. DU PONT DE NEMOURS AND COMPANY (US) 2007-11-15 WO disclosed
WO-2007130521-A2 FERMENTIVE PRODUCTION OF FOUR CARBON ALCOHOLS E. I. DU PONT DE NEMOURS AND COMPANY (US) 2007-11-15 WO disclosed
US-20070259410-A1 FERMENTIVE PRODUCTION OF FOUR CARBON ALCOHOLS GEVO, INC. 2007-11-08 US disclosed
CN-101010328-A Certain aminoalkyl glucosaminide phosphate compounds and their use CORIXA CORP (US) 2007-08-01 CN disclosed
EP-1776375-A2 CERTAIN AMINOALKYL GLUCOSAMINIDE PHOSPHATE COMPOUNDS AND THEIR USE CORIXA CORPORATION (US) 2007-04-25 EP disclosed
WO-2006016997-A2 CERTAIN AMINOALKYL GLUCOSAMINIDE PHOSPHATE COMPOUNDS AND THEIR USE CORIXA CORPORATION (US) 2006-02-16 WO disclosed
EP-1589934-A2 CERTAIN AMINOALKYL GLUCOSAMINIDE PHOSPHATE COMPOUNDS AND THEIR USE CORIXA CORPORATION (US) 2005-11-02 EP disclosed
US-20050227943-A1 Certain aminoalkyl glucosaminide phosphate compounds and their use CORIXA CORPORATION (US) 2005-10-13 US disclosed
WO-2004062599-A2 CERTAIN AMINOALKYL GLUCOSAMINIDE PHOSPHATE COMPOUNDS AND THEIR USE CORIXA CORPORATION (US) 2004-07-29 WO 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 (2 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-20260132429-A1 PROCESSES AND SYSTEMS FOR FERMENTATIVE ALCOHOL PRODUCTION AND RECOVERY GK, ADH1C, ADH5 ANPEP 4717/4885ERAP2 4706/4885LAP3 3616/4885
US-20050227943-A1 Certain aminoalkyl glucosaminide phosphate compounds and their use IFNG, CD68, IL2 ANPEP 63/4885ERAP2 339/4885LAP3 708/4885

“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.