SCHEMBL5490808

SCHEMBL5490808

COc1cc(/C=C2\SC(=O)NC2=O)ccc1-c1cc2c(cc1C)C(C)(C)CCC2(C)C

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PIM1 P11309 4/20 0.60
PIM2 Q9P1W9 4/20 0.60
PIM3 Q86V86 2/20 0.60
PDE4B Q07343 2/20 0.60
GSK3B P49841 3/20 0.57
CDC7 O00311 1/20 0.57
DAPK3 O43293 1/20 0.57
DYRK3 O43781 1/20 0.57
MAP4K4 O95819 1/20 0.57
PHKG2 P15735 1/20 0.57
RPS6KB1 P23443 1/20 0.57
CSNK1D P48730 1/20 0.57
CLK2 P49760 1/20 0.57
GSK3A P49840 1/20 0.57
NEK4 P51957 1/20 0.57
CSNK2A1 P68400 1/20 0.57
CSNK1G2 P78368 1/20 0.57
CAMK2D Q13557 1/20 0.57
DYRK1A Q13627 1/20 0.57
MINK1 Q8N4C8 1/20 0.57

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
SCHEMBL5490812 1.00 PIM1 (0.60) PIM1PIM2PIM3PDE4BGSK3B
SCHEMBL5486196 0.92 PIM1 (0.60) PIM1PIM2PIM3PDE4BGSK3B
SCHEMBL5486192 0.92 PIM1 (0.60) PIM1PIM2PIM3PDE4BGSK3B
SCHEMBL14492584 0.92 PIM1 (0.60) PIM1PIM2PIM3PDE4BGSK3B
SCHEMBL7458015 0.89 PIM1 (0.52) PIM1PIM2PIM3PDE4BGSK3B
SCHEMBL7458010 0.89 PIM1 (0.52) PIM1PIM2PIM3PDE4BGSK3B
SCHEMBL7461962 0.89 IGF1R (0.59) PIM1PIM2PIM3PDE4BIGF1R
SCHEMBL7461958 0.89 IGF1R (0.59) PIM1PIM2PIM3PDE4BIGF1R
SCHEMBL7461652 0.89 PIM1 (0.48) PIM1PIM2PIM3PDE4BGSK3B
SCHEMBL7461650 0.89 PIM1 (0.48) PIM1PIM2PIM3PDE4BGSK3B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7226940-B2 Substituted heterocycles for the treatment of diabetes and other diseases INCYTE SAN DIEGO, INC. (US) 2007-06-05 US disclosed
US-7226940-B2 Substituted heterocycles for the treatment of diabetes and other diseases INCYTE SAN DIEGO, INC. (US) 2007-06-05 US disclosed
US-7226940-B2 Substituted heterocycles for the treatment of diabetes and other diseases INCYTE SAN DIEGO, INC. (US) 2007-06-05 US disclosed
US-20060004059-A1 Substituted heterocycles for the treatment of diabetes and other diseases PFAHL MAGNUS 2006-01-05 US disclosed
US-6515003-B1 Useful in the treatment of diseases related to lipid and carbohydrate metabolism MAXIA PHARMACEUTICALS, INC. 2003-02-04 US disclosed
EP-1214305-A1 BENZYLIDENE-THIAZOLIDINEDIONES AND ANALOGUES AND THEIR USE IN THE TREATMENT OF INFLAMMATION Maxia Pharmaceuticals, Inc. (US) 2002-06-19 EP disclosed
EP-1214304-A1 BENZYLIDENE-THIAZOLIDINEDIONES AND ANALOGUES AND THEIR USE IN THE TREATMENT OF DIABETES Maxia Pharmaceuticals, Inc. (US) 2002-06-19 EP disclosed
WO-2001016122-A1 BENZYLIDENE-THIAZOLIDINEDIONES AND ANALOGUES AND THEIR USE IN THE TREATMENT OF DIABETES MAXIA PHARMACEUTICALS, INC. (US) 2001-03-08 WO disclosed
WO-2001016123-A1 BENZYLIDENE-THIAZOLIDINEDIONES AND ANALOGUES AND THEIR USE IN THE TREATMENT OF INFLAMMATION MAXIA PHARMACEUTICALS, INC. (US) 2001-03-08 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-20060004059-A1 Substituted heterocycles for the treatment of diabetes and other diseases FABP4, HPGDS, GPR119 PIM1 2383/4885PIM2 1465/4885PIM3 2785/4885

“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.