SCHEMBL6924285

SCHEMBL6924285

Cc1ccc(S(=O)(=O)OCCNC(=O)OCc2ccccc2)cc1

nearest known ligand 0.59

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.59
SMN1; SMN2 Q16637 1/20 0.59
L3MBTL1 Q9Y468 2/20 0.56
MAPT P10636 2/20 0.52
HTT P42858 1/20 0.50
CA2 P00918 4/20 0.48
CA1 P00915 3/20 0.48
MMP2 P08253 3/20 0.47
MMP9 P14780 3/20 0.47
CTSK P43235 1/20 0.46
P2RX7 Q99572 1/20 0.46
GAA P10253 1/20 0.46
MMP3 P08254 2/20 0.46
MMP14 P50281 2/20 0.46
MMP1 P03956 1/20 0.46
MMP7 P09237 1/20 0.46
TGM2 P21980 1/20 0.45
CA5A P35218 1/20 0.45

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
SCHEMBL23573712 0.93 LMNA (0.64) LMNASMN1; SMN2L3MBTL1MAPTHTT
SCHEMBL23636489 0.93 LMNA (0.64) LMNASMN1; SMN2L3MBTL1MAPTHTT
SCHEMBL23636429 0.93 LMNA (0.64) LMNASMN1; SMN2L3MBTL1MAPTHTT
SCHEMBL23636477 0.93 LMNA (0.64) LMNASMN1; SMN2L3MBTL1MAPTHTT
SCHEMBL23636502 0.93 LMNA (0.64) LMNASMN1; SMN2L3MBTL1MAPTHTT
SCHEMBL25363728 0.93 LMNA (0.64) LMNASMN1; SMN2L3MBTL1MAPTHTT
SCHEMBL6245784 0.93 HTT (0.54) LMNASMN1; SMN2L3MBTL1MAPTHTT
SCHEMBL26813921 0.91 TGM2 (0.53) LMNASMN1; SMN2L3MBTL1MAPTHTT
SCHEMBL591226 0.84 L3MBTL1 (0.47) LMNASMN1; SMN2L3MBTL1MAPTHTT
SCHEMBL31122455 0.83 P2RX7 (0.45) LMNASMN1; SMN2L3MBTL1MAPTCA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4590673-A1 FLUORESCENT PROBES FOR MAGL F. Hoffmann-La Roche AG (CH) 2025-07-30 EP disclosed
WO-2024061853-A1 FLUORESCENT PROBES FOR MAGL F. HOFFMANN-LA ROCHE AG (CH) 2024-03-28 WO disclosed
WO-2017089890-A1 CONJUGATES COMPRISING SELF-IMMOLATIVE GROUPS AND METHODS RELATED THERETO LEGOCHEM BIOSCIENCES, INC. (KR) 2017-06-01 WO disclosed
WO-2017089895-A1 ANTIBODY-DRUG CONJUGATES COMPRISING BRANCHED LINKERS AND METHODS RELATED THERETO LEGOCHEM BIOSCIENCES, INC. (KR) 2017-06-01 WO disclosed
US-6737416-B2 THROMBOLYTIC AGENT HAVING HIGHER SAFETY MEIJI SEIKA KAISHA LTD. (JP) 2004-05-18 US disclosed
US-20030207804-A1 Modified peptide nucleic acids ISIS PHARMACEUTICALS, INC. 2003-11-06 US disclosed
US-6620848-B2 Antiarthritic agents, antihistamines, headaches SMITHKLINE BEECHAM CORPORATION 2003-09-16 US disclosed
US-20030119787-A1 Phosphonic acid derivative having inhibitory activity against carboxypeptidase B MEIJI SEIKA KAISHA LTD. (JP) 2003-06-26 US disclosed
US-6576627-B1 Such as 7-amino-2-((2-methyl-1-(3-phenylpropanoylamino)-propyl)hydroxyphosphinoyl) -methylheptanoic acid; thrombotic disease MEIJI SEIKA KAISHA LTD. (JP) 2003-06-10 US disclosed
EP-1152004-B1 Phosphonic acid derivatives having carboxypeptidase B inhibitory action MEIJI SEIKA KAISHA (JP) 2003-05-07 EP disclosed
US-6369272-B1 ENZYME INHIBITORS OF AMIDINE ALKYL SULFIDE AMINOACIDS GLAXOSMITHKLINE 2002-04-09 US disclosed
US-20020010366-A1 Nitric oxide synthase inhibitors SMITHKLINE BEECHAM CORPORATION 2002-01-24 US disclosed
EP-1174434-A1 Phosphonic acid derivative having inhibitory activity against carboxypeptidase B MEIJI SEIKA KAISHA LTD. (JP) 2002-01-23 EP disclosed
EP-0958277-B1 NITRIC OXIDE SYNTHASE INHIBITORS GLAXO GROUP LTD (GB) 2001-11-21 EP disclosed
EP-1152004-A1 PHOSPHONIC ACID DERIVATIVES HAVING CARBOXYPEPTIDASE B INHIBITORY ACTIVITY MEIJI SEIKA KAISHA LTD. (JP) 2001-11-07 EP disclosed
EP-0958277-A1 NITRIC OXIDE SYNTHASE INHIBITORS GLAXO GROUP LIMITED (GB) 1999-11-24 EP disclosed
WO-1998030537-A1 NITRIC OXIDE SYNTHASE INHIBITORS GLAXO GROUP LIMITED (GB) 1998-07-16 WO disclosed
EP-0389437-B1 Luciferin derivatives NIPPON ZOKI PHARMACEUTICAL CO (JP) 1995-05-24 EP disclosed
US-5128069-A Luciferin derivatives NIPPON ZOKI PHARMACEUTICAL CO., LTD. (JP) 1992-07-07 US disclosed
EP-0389437-A1 Luciferin derivatives NIPPON ZOKI PHARMACEUTICAL CO. LTD. (JP) 1990-09-26 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-20030119787-A1 Phosphonic acid derivative having inhibitory activity against carboxypeptidase B CPB1, RNPEP, CPN1 LMNA 2640/4885SMN1; SMN2 4505/4885L3MBTL1 440/4885
US-20030207804-A1 Modified peptide nucleic acids NGLY1, PARN, NPPA LMNA 628/4885SMN1; SMN2 1515/4885L3MBTL1 943/4885
US-20020010366-A1 Nitric oxide synthase inhibitors NOS1, NOS2, NOS3 LMNA 2211/4885SMN1; SMN2 2062/4885L3MBTL1 4794/4885

“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.