SCHEMBL6519601

SCHEMBL6519601

Cc1ccc(S(=O)(=O)N2CCC(C(=O)O)CC2)cc1

nearest known ligand 0.72

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 9/20 0.72
NPC1 O15118 1/20 0.70
RAB9A P51151 1/20 0.70
GAA P10253 3/20 0.67
KDM4E B2RXH2 1/20 0.67
TSHR P16473 1/20 0.67
LMNA P02545 4/20 0.66
SMN1; SMN2 Q16637 2/20 0.66
USP2 O75604 2/20 0.64
EPHX2 P34913 1/20 0.64
APEX1 P27695 1/20 0.62
MEN1 O00255 1/20 0.60
KMT2A Q03164 1/20 0.60
ATM Q13315 1/20 0.60

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
SCHEMBL7458911 0.91 AKR1C3 (0.64) ALDH1A1NPC1RAB9AGAAKDM4E
SCHEMBL8290497 0.86 NPC1 (0.68) ALDH1A1NPC1RAB9AGAALMNA
SCHEMBL29256038 0.85 NPC1 (0.67) ALDH1A1NPC1RAB9AGAAKDM4E
SCHEMBL2285784 0.85 ALDH1A1 (0.76) ALDH1A1NPC1GAAKDM4ELMNA
SCHEMBL4801328 0.84 MEN1 (0.68) ALDH1A1GAAKDM4ETSHRLMNA
SCHEMBL2636523 0.84 MAPT (0.70) ALDH1A1GAAKDM4ETSHRLMNA
SCHEMBL6955039 0.84 ALDH1A1 (0.68) ALDH1A1GAAKDM4ETSHRLMNA
SCHEMBL10568862 0.84 POLB (0.57) ALDH1A1NPC1RAB9AGAATSHR
SCHEMBL4799931 0.84 PKM (0.78) ALDH1A1NPC1RAB9AGAATSHR
SCHEMBL29145909 0.84 PKM (0.78) ALDH1A1NPC1RAB9ALMNAEPHX2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-102491941-B Preparation method of N-methoxy-N-methyl-1-p-toluenesulfonyl piperidine-4-amide UNIV NORTHWEST NORMAL 2014-01-22 CN claimed
EP-2475644-B1 HSL INHIBITORS USEFUL IN THE TREATMENT OF DIABETES HOFFMANN LA ROCHE (CH) 2014-01-08 EP claimed
US-8258158-B2 HSL inhibitors useful in the treatment of diabetes HOFFMANN-LA ROCHE INC. (US) 2012-09-04 US claimed
EP-2475644-A1 HSL INHIBITORS USEFUL IN THE TREATMENT OF DIABETES F. Hoffmann-La Roche AG (CH) 2012-07-18 EP claimed
WO-2011029808-A1 HSL INHIBITORS USEFUL IN THE TREATMENT OF DIABETES F. HOFFMANN-LA ROCHE AG (CH) 2011-03-17 WO claimed
US-20110065707-A1 NEW HSL INHIBITORS USEFUL IN THE TREATMENT OF DIABETES HOFFMANN-LA ROCHE, INC. 2011-03-17 US claimed
US-20040058877-A1 Somatostatin antagonists and agonists that act at the sst subtype 2 receptor PFIZER INC 2004-03-25 US claimed
US-20020128206-A1 Somatostatin antagonists and agonists that act at the sst subtype 2 receptor HAY BRUCE A (US) 2002-09-12 US claimed
US-20020016298-A1 Somatostatin antagonists and agonists that act at the sst subtype 2 receptor PFIZER INC. 2002-02-07 US claimed
EP-1086947-A1 Somatostatin antagonists and agonists that act at the SST subtype 2 receptor Pfizer Products Inc. (US) 2001-03-28 EP claimed
CN-115141138-B Method for constructing fluoride by decarboxylation of alkyl carboxylic acid 中山大学 2023-11-28 CN disclosed
CN-115141138-A Method for constructing fluoride by decarboxylation of alkyl carboxylic acid 中山大学 2022-10-04 CN disclosed
CN-112028814-B Method for preparing amine compound based on novel catalytic Curtius rearrangement reaction 南京大学 2022-03-15 CN disclosed
WO-2020252457-A1 PROCESSES AND COMPOUNDS FOR THE DECARBOXYLATIVE AMINATION OF REDOX-ACTIVE ESTERS WITH DIAZIRINES H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. (US) 2020-12-17 WO disclosed
CN-112028814-A Method for preparing amine compound based on novel catalytic Curtius rearrangement reaction 南京大学 2020-12-04 CN disclosed
US-6696418-B1 ANIMAL GROWTH REGULATORS SUCH AS 6-AMINO-2-(2-((1-BENZENE SULFONYL-PIPERIDINE-4-CARBONYL)-AMINO)-3-(1H-INDOL-3-YL)-PROPIONYLAMINO) -HEXANOIC ACID TERT-BUTYL ESTER, ADMINISTERED TO MODULATE CELL DIFFERENTIATION PFIZER INC. 2004-02-24 US disclosed
US-20020128206-A1 Somatostatin antagonists and agonists that act at the sst subtype 2 receptor HAY BRUCE A (US) 2002-09-12 US disclosed
US-20020016298-A1 Somatostatin antagonists and agonists that act at the sst subtype 2 receptor PFIZER INC. 2002-02-07 US disclosed
EP-1086947-A1 Somatostatin antagonists and agonists that act at the SST subtype 2 receptor Pfizer Products Inc. (US) 2001-03-28 EP disclosed
EP-0520336-A2 Aldehyde derivatives and their use as calpain inhibitors FUJIREBIO Inc. (JP) 1992-12-30 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 (4 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-20020128206-A1 Somatostatin antagonists and agonists that act at the sst subtype 2 receptor GHSR, SSTR1, GHRHR ALDH1A1 3407/4885NPC1 1706/4885RAB9A 3088/4885
US-20020016298-A1 Somatostatin antagonists and agonists that act at the sst subtype 2 receptor GHSR, SSTR1, GHRHR ALDH1A1 3284/4885NPC1 1804/4885RAB9A 3102/4885
US-20040058877-A1 Somatostatin antagonists and agonists that act at the sst subtype 2 receptor GHSR, SSTR1, GHRHR ALDH1A1 3284/4885NPC1 1804/4885RAB9A 3102/4885
US-20110065707-A1 NEW HSL INHIBITORS USEFUL IN THE TREATMENT OF DIABETES LIPE, PNLIP, LPL ALDH1A1 721/4885NPC1 447/4885RAB9A 3818/4885

“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.