Benzoic Acid

Benzoic Acid

SCHEMBL7413764

Fc1ncc(OCN2CCC2)cc1Br.O=C(O)c1ccccc1.O=C(O)c1ccccc1

nearest known ligand 0.37

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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 19)

geneUniProtsupporting neighboursconfidence
ESR1 P03372 1/20 0.37
ESR2 Q92731 1/20 0.37
CXCR1 P25024 1/20 0.37
LTA4H P09960 1/20 0.37
CYP2D6 P10635 1/20 0.36
CYP2C9 P11712 1/20 0.36
HIF1A Q16665 1/20 0.36
MRGPRX4 Q96LA9 1/20 0.35
KDM4E B2RXH2 5/20 0.35
ALDH1A1 P00352 4/20 0.35
HRH4 Q9H3N8 1/20 0.35
HRH3 Q9Y5N1 1/20 0.35
ABCB1 P08183 2/20 0.34
GAA P10253 2/20 0.34
POLB P06746 1/20 0.34
MAPK1 P28482 1/20 0.34
PDK2 Q15119 1/20 0.34
GRM5 P41594 1/20 0.34
SMN1; SMN2 Q16637 1/20 0.34

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 SCHEMBL7477571 0.86 ESR1 (0.39) ESR1ESR2CXCR1LTA4HCYP2D6
Benzoic Acid SCHEMBL7664241 0.81 ALOX15 (0.44) ESR1ESR2KDM4EALDH1A1GAA
Benzoic Acid SCHEMBL7480908 0.81 HCAR2 (0.42) ESR1ESR2LTA4HCYP2D6CYP2C9
Benzoic Acid SCHEMBL7409792 0.77 PPARG (0.43) ESR1ESR2CXCR1LTA4HCYP2D6
Benzoic Acid SCHEMBL7672846 0.76 NAPRT (0.44) ESR1ESR2LTA4HKDM4EALDH1A1
SCHEMBL7413854 0.69 KDM4E (0.33) CXCR1KDM4EALDH1A1HRH3POLB
Hydrochloric Acid SCHEMBL7416361 0.68 ALDH1A1 (0.40) ALDH1A1GAA
SCHEMBL487804 0.66 HCAR2 (0.47) CYP2C9KDM4EALDH1A1POLB
SCHEMBL6589690 0.66 LTA4H (0.44) LTA4HKDM4EPOLBSMN1; SMN2
SCHEMBL2300940 0.66 LTA4H (0.53) ESR1ESR2CXCR1LTA4HCYP2D6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1228024-A1 NOVEL HYDRONAPHTALENE COMPOUNDS, PREPARED BY A RHODIUM CATALYZED RING OPENING REACTION IN THE PRESENCE OF PHOSPHINE LIGAND AstraZeneca AB (SE) 2002-08-07 EP claimed
WO-2001030734-A1 NOVEL HYDRONAPHTALENE COMPOUNDS, PREPARED BY A RHODIUM CATALYZED RING OPENING REACTION IN THE PRESENCE OF PHOSPHINE LIGAND ASTRAZENECA AB (SE) 2001-05-03 WO claimed
US-6403575-B1 ANTI-INFLAMMATORIES ABBOTT LABORATORIES 2002-06-11 US disclosed
EP-1047690-A1 HETEROCYCLIC ETHER AND THIOETHER COMPOUNDS USEFUL IN CONTROLLING CHEMICAL SYNAPTIC TRANSMISSION Abbott Laboratories (US) 2000-11-02 EP disclosed
US-6133253-A NEURONAL CELL DEATH PREVENTORS AND ANTI-INFLAMMATORIES ABBOTT LABORATORIES (US) 2000-10-17 US disclosed
WO-1999032480-A1 HETEROCYCLIC ETHER AND THIOETHER COMPOUNDS USEFUL IN CONTROLLING CHEMICAL SYNAPTIC TRANSMISSION ABBOTT LABORATORIES (US) 1999-07-01 WO disclosed