SCHEMBL1418921

SCHEMBL1418921

CCOC(=O)C(CC1CCCC1)c1ccc([N+](=O)[O-])cc1

nearest known ligand 0.49

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 6/20 0.49
GAA P10253 1/20 0.49
AR P10275 1/20 0.48
SLC6A3 Q01959 1/20 0.46
MAPT P10636 6/20 0.46
LMNA P02545 2/20 0.46
KDM4E B2RXH2 1/20 0.46
CRHBP P24387 1/20 0.44
CRHR2 Q13324 1/20 0.44
L3MBTL1 Q9Y468 2/20 0.44
SMN1; SMN2 Q16637 2/20 0.44
POLB P06746 1/20 0.44
CASP3 P42574 1/20 0.42
KMT2A Q03164 5/20 0.42
MEN1 O00255 2/20 0.41

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
SCHEMBL3393131 0.89 ALDH1A1 (0.47) ALDH1A1GAAARSLC6A3MAPT
SCHEMBL10379316 0.83 L3MBTL1 (0.46) ALDH1A1GAASLC6A3MAPTL3MBTL1
SCHEMBL1418785 0.83 ALDH1A1 (0.44) ALDH1A1GAASLC6A3MAPTLMNA
SCHEMBL2647143 0.82 LMNA (0.43) ALDH1A1SLC6A3LMNAKDM4EL3MBTL1
SCHEMBL2646980 0.82 L3MBTL1 (0.44) SLC6A3L3MBTL1POLBKMT2AMEN1
SCHEMBL2644774 0.81 SLC6A2 (0.53) ALDH1A1GAASLC6A3LMNAKDM4E
SCHEMBL11038742 0.81 MAPT (0.54) ALDH1A1GAAARMAPTLMNA
SCHEMBL2646165 0.81 GCK (0.44) ALDH1A1SLC6A3LMNAPOLBKMT2A
SCHEMBL11932079 0.80 SLC6A3 (0.54) ALDH1A1GAASLC6A3MAPTLMNA
SCHEMBL13839179 0.79 CYP19A1 (0.47) ALDH1A1SLC6A3KDM4EPOLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2554540-A2 3-Cyclyl-2-(4-sulfamoyl-phenyl)-n-cyclyl-propionamide derivatives useful in the treatment of impaired glucose tolerance and diabetes Novartis AG (CH) 2013-02-06 EP disclosed
EP-1934180-B1 3-CYCLYL-2-(4-SULFAMOYL-PHENYL)-N-CYCLYL-PROPIONAMIDE DERIVATIVES USEFUL IN THE TREATMENT OF IMPAIRED GLUCOSE TOLERANCE AND DIABETES NOVARTIS AG (CH) 2012-12-05 EP disclosed
US-8252931-B2 Thiazolo[5,4-B]pyridine glucokinase activators NOVARTIS AG (CH) 2012-08-28 US disclosed
EP-1934233-B1 SULFONAMIDE DERIVATIVES AS GLYCOKINASE ACTIVATORS USEFUL IN THE TREATMENT OF TYPE 2 DIABETES NOVARTIS AG (CH) 2012-05-16 EP disclosed
EP-1735322-B1 SULFONAMIDE-THIAZOLPYRIDINE DERIVATIVES AS GLUCOKINASE ACTIVATORS USEFUL FOR THE TREATMENT OF TYPE 2 DIABETES NOVARTIS AG (CH) 2011-09-14 EP disclosed
EP-2298779-A1 Sulfonamide derivatives as glycokinase activators useful in the treatment of type 2 diabetes Novartis AG (CH) 2011-03-23 EP disclosed
CN-1960995-B Sulfonamide-thiazolpyridine derivatives as glucokinase activators useful in the treatment of type 2 diabetes NOVARTIS AG 2010-12-08 CN disclosed
US-7795257-B2 Organic compounds NOVARTIS AG (CH) 2010-09-14 US disclosed
US-7750020-B2 3-Cyclopentyl-2-(4-cyclopropylsulfamoyl-phenyl)-N-(5-methoxy-thiazolo[5,4-b]pyridin-2-yl)-propionamide; antidiabetic agent; insulin resistance, impaired glucose tolerance, obesity; with other hypolipidemic agent, anti-obesity and hypotensive agent NOVARTIS AG (CH) 2010-07-06 US disclosed
US-20080318948-A1 Organic Compounds NOVARTIS AG (CH) 2008-12-25 US disclosed
US-6489485-B2 INCREASES INSULIN SECRETION; TREATMENT OF TYPE II DIABETES HOFFMANN-LA ROCHE INC. 2002-12-03 US disclosed
US-6384220-B2 ANTIDIABETIC AGENTS INCREASING THE EXPRESSION OF GLUCOKINASE (GK) TO IMPROVE GLUCOSE TOLERANCE; INCREASE IN GLUCOSE EXPOSURE COUPLED THROUGH GK IN BETA-CELLS TO INCREASE INSULIN SECRETION AND IN HEPATOCYTES TO INCREASE GLYCOGEN DEPOSITION HOFFMANN-LA ROCHE INC. 2002-05-07 US disclosed
EP-1169312-A2 GLUCOKINASE ACTIVATORS F. HOFFMANN-LA ROCHE AG (CH) 2002-01-09 EP disclosed
US-20020002190-A1 Para-aryl or heterocyclic substituted phenyl glucokinase activators HOFFMANN-LA ROCHE INC. 2002-01-03 US disclosed
US-20010051731-A1 Para-amine substituted phenylamide glucokinase activators HOFFMANN-LA ROCHE INC. 2001-12-13 US disclosed
US-6320050-B1 2-SUBSTITUTED PHENYL-3-CYCLOALKYL SUBSTITUTED N-HETEROAROMATIC PROPIONAMIDES; USED TO INCREASE INSULIN SECRETION IN THE TREATMENT OF TYPE II DIABETES. HOFFMANN-LA ROCHE INC. 2001-11-20 US disclosed
WO-2001085707-A1 PARA-AMINE SUBSTITUTED PHENYLAMIDE GLUCOKINASE ACTIVATORS F. HOFFMANN-LA ROCHE AG (CH) 2001-11-15 WO disclosed
WO-2001085706-A1 SUBSTITUTED PHENYLACETAMIDES AND THEIR USE AS GLUCOKINASE ACTIVATORS F. HOFFMANN-LA ROCHE AG (CH) 2001-11-15 WO disclosed
US-20010039344-A1 Heteroaromatic glucokinase activators HOFFMANN-LA ROCHE INC. 2001-11-08 US disclosed
WO-2000058293-A2 GLUCOKINASE ACTIVATORS F. HOFFMANN-LA ROCHE AG (CH) 2000-10-05 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 (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-20020002190-A1 Para-aryl or heterocyclic substituted phenyl glucokinase activators GCKR, GCK, PDXK ALDH1A1 2470/4885GAA 103/4885AR 2492/4885
US-20080318948-A1 Organic Compounds GCK, GCKR, SLC2A2 ALDH1A1 236/4885GAA 83/4885AR 3449/4885
US-20010051731-A1 Para-amine substituted phenylamide glucokinase activators GCKR, GCK, PDXK ALDH1A1 3015/4885GAA 82/4885AR 3186/4885
US-20010039344-A1 Heteroaromatic glucokinase activators GCKR, GCK, PDXK ALDH1A1 3111/4885GAA 384/4885AR 1917/4885

“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.