Benzoyl Formic Acid

Benzoyl Formic Acid

SCHEMBL1702148

O=C([O-])C(=O)c1ccccc1.[K+]

nearest known ligand 0.68

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

AGTR1DHFRGABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTNR3C2PBP2XPTGS1PTGS2VKORC1blablaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAftsImrcAmrcBmrdApbp1apbp1bpbp2apbp2bpbp3polthyA

The experimentally established mechanism targets of Benzoyl Formic 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
CES2 O00748 14/20 0.68
CES1 P23141 13/20 0.68
CA2 P00918 2/20 0.59
CA4 P22748 2/20 0.59
TSHR P16473 2/20 0.52
DAO P14920 1/20 0.52
NAPRT Q6XQN6 1/20 0.52
ALDH1A1 P00352 1/20 0.52
POLB P06746 1/20 0.48
CYP3A4 P08684 1/20 0.48
PARP1 P09874 1/20 0.48
MAPT P10636 1/20 0.48
CYP2C19 P33261 1/20 0.48
RECQL P46063 1/20 0.48
BLM P54132 1/20 0.48
PMP22 Q01453 1/20 0.48
HSD17B10 Q99714 1/20 0.48
TDP1 Q9NUW8 1/20 0.48
L3MBTL1 Q9Y468 1/20 0.48
CA12 O43570 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
Benzoyl Formic Acid SCHEMBL1532670 0.97 CES2 (0.65) CES2CES1CA2CA4TSHR
Benzoyl Formic Acid SCHEMBL1042299 0.97 CES2 (0.65) CES2CES1CA2CA4TSHR
Benzoyl Formic Acid SCHEMBL1446195 0.97 CES2 (0.65) CES2CES1CA2CA4TSHR
Benzoyl Formic Acid SCHEMBL8623983 0.97 CES2 (0.65) CES2CES1CA2CA4TSHR
Benzoyl Formic Acid SCHEMBL3079821 0.97 CES2 (0.65) CES2CES1CA2CA4TSHR
Benzoyl Formic Acid SCHEMBL5448316 0.97 CES2 (0.65) CES2CES1CA2CA4TSHR
Benzoyl Formic Acid SCHEMBL699116 0.87 CES2 (0.52) CES2CES1CA2CA4TSHR
Benzil SCHEMBL7142843 0.82 CES2 (1.00) CES2CES1CA2CA4TSHR
Benzil SCHEMBL9517636 0.82 CES2 (1.00) CES2CES1CA2CA4TSHR
Benzil SCHEMBL2156589 0.82 CES2 (1.00) CES2CES1CA2CA4TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20140100371-A1 PROCESS FOR PREPARING AZOMETHINES FROM ALPHA-OXOCARBOXYLATES, AMINES AND ARYL BROMIDES SALTIGO GMBH (DE) 2014-04-10 US disclosed
EP-2640692-A1 PROCESS FOR PREPARING AZOMETHINES FROM ALPHA-OXOCARBOXYLATES, AMINES AND ARYL BROMIDES Saltigo GmbH (DE) 2013-09-25 EP disclosed
WO-2012066134-A1 PROCESS FOR PREPARING AZOMETHINES FROM ALPHA-OXOCARBOXYLATES, AMINES AND ARYL BROMIDES SALTIGO GMBH (DE) 2012-05-24 WO disclosed
EP-2455364-A1 Process for Preparing Azomethines from alpha-Oxocarboxylates, Amines and Aryl Bromides Saltigo GmbH (DE) 2012-05-23 EP disclosed
EP-2096101-B1 Method for producing ketones from alpha-oxocarboxylates and aryl bromides SALTIGO GMBH (DE) 2012-04-18 EP disclosed
US-8022255-B2 Process for preparing ketones from alpha-oxo carboxylates and aryl bromides SALTIGO GMBH (DE) 2011-09-20 US disclosed
US-20090221832-A1 PROCESS FOR PREPARING KETONES FROM ALPHA-OXO CARBOXYLATES AND ARYL BROMIDES SALTIGO GMBH (DE) 2009-09-03 US disclosed
EP-2096101-A1 Method for producing ketones from alpha-oxocarboxylates and aryl bromides Saltigo GmbH (DE) 2009-09-02 EP disclosed
EP-0788476-B1 STILBENE DERIVATIVES USEFUL AS CYCLOOXYGENASE-2 INHIBITORS MERCK FROSST CANADA INC (CA) 1999-10-20 EP disclosed
US-5849943-A Stilbene derivatives useful as cyclooxygenase-2 inhibitors MERCK FROSST CANADA, INC. (CA) 1998-12-15 US disclosed
EP-0788476-A1 STILBENE DERIVATIVES USEFUL AS CYCLOOXYGENASE-2 INHIBITORS MERCK FROSST CANADA INC. (CA) 1997-08-13 EP disclosed
WO-1996013483-A1 STILBENE DERIVATIVES USEFUL AS CYCLOOXYGENASE-2 INHIBITORS MERCK FROSST CANADA INC. (CA) 1996-05-09 WO disclosed
US-4638072-A POLYAMIDES, POLYIMIDES STANDARD OIL COMPANY (INDIANA) (US) 1987-01-20 US disclosed
US-4596867-A Disubstituted maleic anhydride compounds STANDARD OIL COMPANY (INDIANA) (US) 1986-06-24 US 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-20140100371-A1 PROCESS FOR PREPARING AZOMETHINES FROM ALPHA-OXOCARBOXYLATES, AMINES AND ARYL BROMIDES AOC2, AOC3, CBR1 CES2 1794/4885CES1 3293/4885CA2 542/4885
US-20090221832-A1 PROCESS FOR PREPARING KETONES FROM ALPHA-OXO CARBOXYLATES AND ARYL BROMIDES CBR1, CBR3, AKR1C3 CES2 1854/4885CES1 2032/4885CA2 2089/4885

“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.