SCHEMBL196248

SCHEMBL196248

CS(=O)(=O)Oc1ccccc1Cl

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NFE2L2 Q16236 5/20 0.47
LMNA P02545 2/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
PTGS2 P35354 2/20 0.43
PTGS1 P23219 1/20 0.43
KDM4E B2RXH2 2/20 0.41
ALDH1A1 P00352 1/20 0.41
MAPT P10636 1/20 0.41
MAPK1 P28482 1/20 0.41
NPSR1 Q6W5P4 1/20 0.41
HSD11B1 P28845 1/20 0.40
ELANE P08246 1/20 0.39
KCNH2 Q12809 1/20 0.39
HPGD P15428 1/20 0.39
CYP1A2 P05177 1/20 0.38
GAA P10253 1/20 0.38
CYP2C19 P33261 1/20 0.38
TDP1 Q9NUW8 1/20 0.38
SLC6A2 P23975 1/20 0.38
SLC6A4 P31645 1/20 0.38

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
SCHEMBL27740459 0.98 NFE2L2 (0.46) NFE2L2LMNASMN1; SMN2PTGS2PTGS1
SCHEMBL11577997 0.96 NFE2L2 (0.45) NFE2L2LMNASMN1; SMN2PTGS2PTGS1
SCHEMBL3839152 0.84 NFE2L2 (0.42) NFE2L2SMN1; SMN2PTGS2KDM4EALDH1A1
SCHEMBL27669602 0.83 ALDH1A1 (0.45) NFE2L2SMN1; SMN2PTGS2KDM4EALDH1A1
SCHEMBL19275104 0.82 EPAS1 (0.43) NFE2L2LMNAPTGS2PTGS1KDM4E
SCHEMBL27669603 0.82 ALDH1A1 (0.44) NFE2L2SMN1; SMN2PTGS2KDM4EALDH1A1
SCHEMBL10559419 0.80 LMNA (0.45) NFE2L2LMNASMN1; SMN2PTGS2PTGS1
SCHEMBL28479379 0.80 ELANE (0.61) NFE2L2LMNASMN1; SMN2PTGS2PTGS1
SCHEMBL10582499 0.79 NFE2L2 (0.45) NFE2L2LMNASMN1; SMN2PTGS2PTGS1
SCHEMBL27752732 0.79 NFE2L2 (0.45) NFE2L2KDM4EALDH1A1KCNH2HPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025132148-A1 ADJUVANT COMPOSITIONS FOR AGROCHEMICAL APPLICATIONS BAYER AKTIENGESELLSCHAFT (DE) 2025-06-26 WO disclosed
US-20240158424-A1 METHOD FOR PRODUCING DIPHOSPHINE MONOXIDE TAKASAGO INTERNATIONAL CORPORATION (JP) 2024-05-16 US disclosed
EP-4361162-A2 METHOD FOR PRODUCING DIPHOSPHINE MONOXIDE Takasago International Corporation (JP) 2024-05-01 EP disclosed
CN-116742135-A High-voltage electrolyte for lithium battery 浙江大学 2023-09-12 CN disclosed
CN-112839505-B Phenylpyrazole compound and method for controlling plant disease 住友化学株式会社 2023-06-06 CN disclosed
EP-3679035-A1 NOVEL FUNGICIDAL HETEROCYCLIC COMPOUNDS PI Industries Ltd. (IN) 2020-07-15 EP disclosed
WO-2019048989-A1 NOVEL FUNGICIDAL HETEROCYCLIC COMPOUNDS PI INDUSTRIES LTD. (IN) 2019-03-14 WO disclosed
WO-2018193387-A1 HETEROCYCLIC COMPOUNDS WITH MICROBIOCIDAL PROPERTIES PI INDUSTRIES LTD. (IN) 2018-10-25 WO disclosed
WO-2014124850-A1 SUBSTITUTED [1,2,4]TRIAZOLE AND IMIDAZOLE COMPOUNDS BASF SE (DE) 2014-08-21 WO disclosed
US-8293905-B2 Bipyridine compound, transition metal complex, and method for production of conjugated aromatic compound using the transition metal complex SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2012-10-23 US disclosed
US-8088883-B2 Transition metal complex and process for producing conjugated aromatic compound using the transition metal complex SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2012-01-03 US disclosed
US-20110046336-A1 TRANSITION METAL COMPLEX AND PROCESS FOR PRODUCING CONJUGATED AROMATIC COMPOUND USING THE TRANSITION METAL COMPLEX SUMITOMO CHEMICAL COMPANY, LIMITED 2011-02-24 US disclosed
US-20100184978-A1 BIPYRIDINE COMPOUND, TRANSITION METAL COMPLEX, AND METHOD FOR PRODUCTION OF CONJUGATED AROMATIC COMPOUND USING THE TRANSITION METAL COMPLEX SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2010-07-22 US disclosed
EP-2192124-A1 TRANSITION METAL COMPLEX AND PROCESS FOR PRODUCING CONJUGATED AROMATIC COMPOUND WITH THE TRANSITION METAL COMPLEX Sumitomo Chemical Company, Limited (JP) 2010-06-02 EP disclosed
EP-2172470-A1 BIPYRIDINE COMPOUND, TRANSITION METAL COMPLEX, AND METHOD FOR PRODUCTION OF CONJUGATED AROMATIC COMPOUND USING THE TRANSITION METAL COMPLEX Sumitomo Chemical Company, Limited (JP) 2010-04-07 EP 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 (3 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-20240158424-A1 METHOD FOR PRODUCING DIPHOSPHINE MONOXIDE TDO2, SCO2, DUOX1 NFE2L2 842/4885LMNA 4739/4885SMN1; SMN2 3749/4885
US-20110046336-A1 TRANSITION METAL COMPLEX AND PROCESS FOR PRODUCING CONJUGATED AROMATIC COMPOUND USING THE TRANSITION METAL COMPLEX C9, C5, AP1M1 NFE2L2 77/4885LMNA 2664/4885SMN1; SMN2 3838/4885
US-20100184978-A1 BIPYRIDINE COMPOUND, TRANSITION METAL COMPLEX, AND METHOD FOR PRODUCTION OF CONJUGATED AROMATIC COMPOUND USING THE TRANSITION METAL COMPLEX C9, C5, AP2M1 NFE2L2 380/4885LMNA 3345/4885SMN1; SMN2 4123/4885

“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.