Benzoic Acid

Benzoic Acid

SCHEMBL2679685

Cc1c(O)cccc1O.O=C(O)c1ccccc1.O=C(O)c1ccccc1

nearest known ligand 0.61

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Known targets — ChEMBL curated mechanism

CACNA1CCACNA1DCACNA1FCACNA1SDPP4HTR1BHTR1D

The experimentally established mechanism targets of Benzoic 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
NAPRT Q6XQN6 2/20 0.61
TSHR P16473 2/20 0.61
DAO P14920 1/20 0.61
CES2 O00748 3/20 0.52
CES1 P23141 3/20 0.52
SRD5A2 P31213 2/20 0.52
CA12 O43570 4/20 0.48
CA1 P00915 4/20 0.48
CA2 P00918 4/20 0.48
CA9 Q16790 4/20 0.48
CA6 P23280 3/20 0.48
CA7 P43166 3/20 0.48
CA14 Q9ULX7 3/20 0.48
ALDH1A1 P00352 3/20 0.48
SMN1; SMN2 Q16637 2/20 0.48
TRPA1 O75762 1/20 0.48
ATM Q13315 1/20 0.48
CA4 P22748 2/20 0.46
KDM4E B2RXH2 2/20 0.46
HMGB1 P09429 1/20 0.46

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
Benzoic Acid SCHEMBL11069756 1.00 NAPRT (0.61) NAPRTTSHRDAOCES2CES1
Benzoic Acid SCHEMBL27577743 0.90 TRPA1 (0.65) NAPRTTSHRDAOCES2CES1
Benzoic Acid SCHEMBL6463794 0.89 TSHR (0.64) NAPRTTSHRDAOCES2CES1
Benzoic Acid SCHEMBL28621884 0.88 ALDH1A1 (0.55) NAPRTTSHRDAOCES2CES1
Benzoic Acid SCHEMBL7669891 0.84 TSHR (0.78) NAPRTTSHRDAOCES2CES1
Benzoic Acid SCHEMBL2019528 0.84 TSHR (0.78) NAPRTTSHRDAOCES2CES1
Benzoic Acid SCHEMBL28096536 0.83 NAPRT (0.61) NAPRTTSHRDAOCES2CES1
Benzoic Acid SCHEMBL3827683 0.82 TSHR (0.67) NAPRTTSHRDAOCES2CES1
Benzoic Acid SCHEMBL28232473 0.82 TRPA1 (0.65) NAPRTTSHRDAOCES2CES1
Benzoic Acid SCHEMBL23212125 0.80 NAPRT (0.64) NAPRTTSHRDAOCES2CES1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4478876-A BLEND OF ACRYLATE MONOMER, COLLOIDAL SILICA, ACRYLOXY FUNCTIONAL SILANE, AND PHOTOINITIATORS GENERAL ELECTRIC COMPANY (US) 1984-10-23 US claimed
CN-102421856-B UV-curable protective layer for thermoplastic substrates BAYER MATERIALSCIENCE AG 2014-08-27 CN disclosed
US-8753739-B2 UV-curing protective layer for thermoplastic substrates BAYER MATERIALSCIENCE AG (DE) 2014-06-17 US disclosed
CN-101466805-B UV-curable protective layer for thermoplastic substrates BAYER MATERIALSCIENCE AG 2013-08-07 CN disclosed
US-20120114933-A1 UV-CURING PROTECTIVE LAYER FOR THERMOPLASTIC SUBSTRATES BAYER MATERIALSCIENCE AG (DE) 2012-05-10 US disclosed
CN-102421856-A UV-curable protective layer for thermoplastic substrates BAYER MATERIALSCIENCE AG 2012-04-18 CN disclosed
EP-1500098-B1 METHOD FOR MAKING LIMITED PLAY DATA STORAGE MEDIA GEN ELECTRIC (US) 2009-06-24 EP disclosed
CN-101466805-A UV-curable protective layer for thermoplastic substrates BAYER MATERIALSCIENCE AG (DE) 2009-06-24 CN disclosed
EP-1371059-B1 LIMITED PLAY DATA STORAGE MEDIA AND METHOD FOR LIMITING ACCESS TO DATA THEREON GEN ELECTRIC (US) 2009-01-07 EP disclosed
EP-1969595-A2 STORAGE MEDIA AND ASSOCIATED METHOD GENERAL ELECTRIC COMPANY (US) 2008-09-17 EP disclosed
EP-0565310-B1 Method of making a UV-curable hardcoat compositions GEN ELECTRIC (US) 1996-08-14 EP disclosed
US-5468789-A Devolatilization under inert atmosphere mixture containing specified anaerobic gelation inhibitors; weatherproofing thermoplastic substrates GENERAL ELECTRIC COMPANY (US) 1995-11-21 US disclosed
US-5466491-A Polymer substrate with curable coating and gelation inhibitor sensitive to radiation GENERAL ELECTRIC COMPANY (US) 1995-11-14 US disclosed
US-5318850-A A mixture consisting of silica, hydrolysis product of an alkoxysilyl acrylate, acrylate monomer having hexanediol diacrylate, isobornyl acrylate or cyclohexyl acrylate and a photoinitiators GENERAL ELECTRIC COMPANY (US) 1994-06-07 US disclosed
EP-0576247-A2 Radiation curable hardcoat compositions GENERAL ELECTRIC COMPANY (US) 1993-12-29 EP disclosed
EP-0565310-A1 Method of making a UV-curable hardcoat compositions GENERAL ELECTRIC COMPANY (US) 1993-10-13 EP disclosed
US-5242719-A Reaction of multifunctional acrylate and silyl functional acrylate and silicon dioxide GENERAL ELECTRIC COMPANY (US) 1993-09-07 US disclosed
EP-0544465-A1 UV curable abrasion-resistant coatings GENERAL ELECTRIC COMPANY (US) 1993-06-02 EP disclosed
US-4491508-A Method of preparing curable coating composition from alcohol, colloidal silica, silylacrylate and multiacrylate monomer GENERAL ELECTRIC COMPANY (US) 1985-01-01 US disclosed
US-4455205-A ULTRAVIOLET RADIATION, WEAR RESISTANCE COATINGS GENERAL ELECTRIC COMPANY (US) 1984-06-19 US disclosed