SCHEMBL2516997

SCHEMBL2516997

Cc1ccc(S(=O)(=O)Nc2ccccc2-c2ccccc2)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ LMNA P02545 4/20 1.00
▸ MCOLN3 Q8TDD5 3/20 1.00
▸ CA2 P00918 3/20 1.00
▸ CA9 Q16790 3/20 1.00
▸ CA12 O43570 2/20 1.00
▸ ALDH1A1 P00352 2/20 0.81
▸ L3MBTL1 Q9Y468 2/20 0.81
▸ CYP2C9 P11712 2/20 0.81
▸ CYP2C19 P33261 2/20 0.81
▸ MAPT P10636 2/20 0.81
▸ USP2 O75604 1/20 0.81
▸ POLB P06746 1/20 0.81
▸ NOD2 Q9HC29 1/20 0.81
▸ SMN1; SMN2 Q16637 2/20 0.64
▸ KEAP1 Q14145 1/20 0.61
▸ NFE2L2 Q16236 1/20 0.61
▸ CA1 P00915 2/20 0.60
▸ CA4 P22748 1/20 0.60
▸ CA7 P43166 1/20 0.60
▸ CKS1B P61024 1/20 0.59

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
SCHEMBL31207793 1.00 LMNA (1.00) LMNAMCOLN3CA2CA9CA12
SCHEMBL9902123 0.95 LMNA (0.91) LMNAMCOLN3CA2CA9CA12
SCHEMBL8659813 0.94 LMNA (0.88) LMNAMCOLN3CA2CA9CA12
SCHEMBL5410713 0.88 MCOLN3 (0.78) LMNAMCOLN3CA2CA9CA12
SCHEMBL27431915 0.87 LMNA (0.76) LMNAMCOLN3CA2CA9CA12
SCHEMBL9901414 0.85 LMNA (0.74) LMNAMCOLN3CA2CA9CA12
SCHEMBL11785265 0.84 LMNA (0.77) LMNAMCOLN3CA2CA9CA12
SCHEMBL2068526 0.84 LMNA (0.82) LMNAMCOLN3CA2CA9CA12
SCHEMBL27826958 0.84 MCOLN3 (0.72) LMNAMCOLN3CA2CA9CA12
SCHEMBL23057287 0.83 LMNA (0.71) LMNAMCOLN3CA2CA9CA12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113004248-B Method for synthesizing carbazole compound by catalyzing hydrocarbon amination reaction with cobalt 绍兴文理学院 2022-11-18 — — CN disclosed
CN-113004248-A Method for synthesizing carbazole compound by catalyzing hydrocarbon amination reaction with cobalt 绍兴文理学院 2021-06-22 — — CN disclosed
US-20140088066-A1 PLATINUM COMPOUNDS, COMPOSITIONS AND METHODS FOR THE TREATMENT OF CANCER BLEND THERAPEUTICS (US) 2014-03-27 — — US disclosed
US-8034827-B2 Phenanthridine derivatives as bradykinin antagonists Richter Gegeon Nyrt. (HU) 2011-10-11 — — US disclosed
US-20090270411-A1 PHENANTHRIDINE DERIVATIVES AS BRADYKININ ANTAGONISTS RICHTER GEDEON NYRT. (HU) 2009-10-29 — — US disclosed
EP-1966142-A2 NEW PHENANTHRIDINE DERIVATIVES AS BRADYKININ ANTAGONISTS Richter Gedeon NYRT (HU) 2008-09-10 — — EP disclosed
WO-2007072092-A2 NEW PHENANTHRIDINE DERIVATIVES AS BRADYKININ ANTAGONISTS RICHTER GEDEON NYRT. (HU) 2007-06-28 — — WO 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-20140088066-A1 PLATINUM COMPOUNDS, COMPOSITIONS AND METHODS FOR THE TREATMENT OF CANCER APEX1, DPYD, VHL LMNA 1847/4885MCOLN3 1806/4885CA2 2195/4885
US-20090270411-A1 PHENANTHRIDINE DERIVATIVES AS BRADYKININ ANTAGONISTS BDKRB2, BDKRB1, HRH2 LMNA 2729/4885MCOLN3 1510/4885CA2 855/4885

“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.

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