SCHEMBL2460873

SCHEMBL2460873

CN1CCN(S(=O)(=O)c2ccc([C@@H](CC3CCCC3)C(=O)O)cc2)CC1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GCK P35557 1/20 0.56
APOBEC3A P31941 2/20 0.51
APOBEC3G Q9HC16 2/20 0.51
LMNA P02545 1/20 0.49
SMN1; SMN2 Q16637 2/20 0.48
USP2 O75604 1/20 0.48
POLB P06746 2/20 0.48
TSHR P16473 1/20 0.47
CYP2C9 P11712 1/20 0.46
ALDH1A1 P00352 1/20 0.46
RECQL P46063 1/20 0.46
ATM Q13315 2/20 0.46
KMT2A Q03164 1/20 0.45
HDAC3 O15379 1/20 0.45
HDAC4 P56524 1/20 0.45
HDAC1 Q13547 1/20 0.45
HDAC7 Q8WUI4 1/20 0.45
HDAC2 Q92769 1/20 0.45
HDAC10 Q969S8 1/20 0.45
HDAC11 Q96DB2 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
SCHEMBL2460877 1.00 GCK (0.56) GCKAPOBEC3AAPOBEC3GLMNASMN1; SMN2
Hydrochloric Acid SCHEMBL2654484 0.99 GCK (0.55) GCKAPOBEC3AAPOBEC3GLMNASMN1; SMN2
SCHEMBL14679685 0.88 ATM (0.48) GCKSMN1; SMN2ALDH1A1ATMKMT2A
SCHEMBL2465061 0.87 CYP2C9 (0.57) GCKAPOBEC3AAPOBEC3GLMNASMN1; SMN2
SCHEMBL13168453 0.83 TGM2 (0.50) GCKSMN1; SMN2ATM
SCHEMBL18677581 0.81 GCK (0.46) GCKUSP2KMT2A
SCHEMBL1865136 0.80 GCK (0.58) GCKKMT2A
SCHEMBL1865137 0.80 GCK (0.58) GCKKMT2A
SCHEMBL28764307 0.80 GCK (0.40) GCKALDH1A1
SCHEMBL3566516 0.79 GCK (0.56) GCKSMN1; SMN2ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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
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-20080103167-A1 Sulfonamide-Thiazolpyridine Derivatives As Glucokinase Activators Useful The Treatment Of Type 2 Diabetes NOVARTIS AG (CH) 2008-05-01 US disclosed
EP-1735322-A1 SULFONAMIDE-THIAZOLPYRIDINE DERIVATIVES AS GLUCOKINASE ACTIVATORS USEFUL THE TREATMENT OF TYPE 2 DIABETES Novartis AG (CH) 2006-12-27 EP disclosed
WO-2005095418-A1 SULFONAMIDE-THIAZOLPYRIDINE DERIVATIVES AS GLUCOKINASE ACTIVATORS USEFUL THE TREATMENT OF TYPE 2 DIABETES NOVARTIS AG (CH) 2005-10-13 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 (1 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-20080103167-A1 Sulfonamide-Thiazolpyridine Derivatives As Glucokinase Activators Useful The Treatment Of Type 2 Diabetes GCKR, GCK, SLC5A2 GCK 2/4885APOBEC3A 4650/4885APOBEC3G 4463/4885

“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.