4-Chloro-Benzoic Acid

4-Chloro-Benzoic Acid

SCHEMBL9493322

O=C([O-])c1ccc(Cl)cc1.[K+]

nearest known ligand 0.95

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of 4-Chloro-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 12)

geneUniProtsupporting neighboursconfidence
CA2 P00918 12/20 0.95
CA1 P00915 11/20 0.95
CES2 O00748 2/20 0.59
CES1 P23141 2/20 0.59
ALOX15 P16050 1/20 0.56
TSHR P16473 1/20 0.56
SRD5A2 P31213 1/20 0.50
GSK3B P49841 1/20 0.50
MAPK1 P28482 1/20 0.50
CA4 P22748 1/20 0.50
ERCC5 P28715 1/20 0.48
FEN1 P39748 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
4-Chloro-Benzoic Acid SCHEMBL9316882 0.95 CA2 (0.95) CA2CA1CES2CES1ALOX15
4-Chloro-Benzoic Acid SCHEMBL11173039 0.95 CA2 (0.95) CA2CA1CES2CES1ALOX15
4-Chloro-Benzoic Acid SCHEMBL11710684 0.95 CA2 (0.95) CA2CA1CES2CES1ALOX15
4-Chloro-Benzoic Acid SCHEMBL9316878 0.95 CA2 (0.95) CA2CA1CES2CES1ALOX15
4-Chloro-Benzoic Acid SCHEMBL9149742 0.95 CA2 (0.95) CA2CA1CES2CES1ALOX15
4-Chloro-Benzoic Acid SCHEMBL8024002 0.95 CA2 (1.00) CA2CA1CES2CES1ALOX15
4-Chloro-Benzoic Acid SCHEMBL2918289 0.95 CA2 (0.95) CA2CA1CES2CES1ALOX15
4-Chloro-Benzoic Acid SCHEMBL10603885 0.95 CA2 (0.95) CA2CA1CES2CES1ALOX15
4-Chloro-Benzoic Acid SCHEMBL2918296 0.95 CA2 (0.95) CA2CA1CES2CES1ALOX15
4-Chloro-Benzoic Acid SCHEMBL379138 0.95 CA2 (0.95) CA2CA1CES2CES1ALOX15

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250243137-A1 METHOD FOR PREPARING 3-CHLOROBICYCLO[3.2.1]-3-OCTEN-2-OL SHANDONG WEIFANG RAINBOW CHEMICAL CO.,LTD (CN) 2025-07-31 US claimed
WO-2024152641-A1 PREPARATION METHOD FOR 3-CHLOROBICYCLO[3.2.1]-3-OCTEN-2-OL 山东潍坊润丰化工股份有限公司 2024-07-25 WO claimed
CN-112679384-B Preparation method of p-cyanobenzoic acid 国药集团化学试剂有限公司 2023-04-07 CN claimed
CN-112679384-A Preparation method of p-cyanobenzoic acid 国药集团化学试剂有限公司 2021-04-20 CN claimed
CN-111574322-A Preparation method of difluoromethyl aromatic compound 南京工业大学 2020-08-25 CN claimed
JP-57124349-A None JP disclosed
US-20250243137-A1 METHOD FOR PREPARING 3-CHLOROBICYCLO[3.2.1]-3-OCTEN-2-OL SHANDONG WEIFANG RAINBOW CHEMICAL CO.,LTD (CN) 2025-07-31 US disclosed
CN-116514635-B Process for preparing 3-chlorobicyclo [3.2.1] -3-octen-2-ol 山东潍坊润丰化工股份有限公司 2025-02-14 CN disclosed
CN-115974697-B Method for catalytic synthesis of 4' -chloro-2-nitrobiphenyl 南京工业大学 2024-11-05 CN disclosed
WO-2024152641-A1 PREPARATION METHOD FOR 3-CHLOROBICYCLO[3.2.1]-3-OCTEN-2-OL 山东潍坊润丰化工股份有限公司 2024-07-25 WO disclosed
CN-116514635-A Process for preparing 3-chlorobicyclo [3.2.1] -3-octen-2-ol 山东潍坊润丰化工股份有限公司 2023-08-01 CN disclosed
CN-115784837-B Process for preparing 3-chlorobicyclo [3.2.1] -3-octen-2-ol 山东潍坊润丰化工股份有限公司 2023-04-25 CN disclosed
US-20160046577-A1 N-Haloalkylindoline Intermediates, Their Process And Use In Preparation of Silodosin And its Derivatives MANKIND PHARMA LTD (IN) 2016-02-18 US disclosed
EP-2984070-A1 N-HALOALKYLINDOLINE INTERMEDIATES, THEIR PROCESS AND USE IN PREPARATION OF SILODOSIN AND ITS DERIVATIVES Mankind Research Centre (IN) 2016-02-17 EP disclosed
WO-2014167507-A1 N-HALOALKYLINDOLINE INTERMEDIATES, THEIR PROCESS AND USE IN PREPARATION OF SILODOSIN AND ITS DERIVATIVES MANKIND RESEARCH CENTRE (IN) 2014-10-16 WO disclosed
CN-101407510-A Preparation of duloxetine hydrochloride intermediate ZHEJIANG HUAHAI PHARM CO LTD (CN) 2009-04-15 CN disclosed
US-5185471-A Reacting 5-halo-2-nitrobenzotrifluorides with inorganic base to form 1,1*-oxy-Bis(3-trifluoromethyl-4-nitrobenzen using benzoate catalyst OCCIDENTAL CHEMICAL CORPORATION (US) 1993-02-09 US disclosed
EP-0509241-A2 A novel method for ether formation OCCIDENTAL CHEMICAL CORPORATION (US) 1992-10-21 EP disclosed
US-4723016-A Preparation of anhydrous organic acid salts E. I. DU PONT DE NEMOURS AND COMPANY (US) 1988-02-02 US disclosed
JP-S57124349-A IMAGE FORMATION METHOD KIMOTO & CO LTD 1982-08-03 JP 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-20250243137-A1 METHOD FOR PREPARING 3-CHLOROBICYCLO[3.2.1]-3-OCTEN-2-OL OSTC, HAO2, ODC1 CA2 71/4885CA1 728/4885CES2 302/4885
US-20160046577-A1 N-Haloalkylindoline Intermediates, Their Process And Use In Preparation of Silodosin And its Derivatives ADRA1D, ADRA1A, ADRB1 CA2 2966/4885CA1 4507/4885CES2 1397/4885

“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.