SCHEMBL1959286

SCHEMBL1959286

CC(C)Cn1c(N)c(N=O)c(=O)n(C)c1=S

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CASP6 P55212 1/20 0.61
ALDH1A1 P00352 6/20 0.39
LMNA P02545 5/20 0.39
SMN1; SMN2 Q16637 4/20 0.39
HTT P42858 3/20 0.39
MAPK1 P28482 3/20 0.34
CFTR P13569 2/20 0.34
TSHR P16473 2/20 0.34
PDE2A O00408 2/20 0.34
PDE1A P54750 2/20 0.34
PDE1B Q01064 2/20 0.34
PDE1C Q14123 2/20 0.34
PDE5A O76074 2/20 0.34
PDE4A P27815 2/20 0.34
PDE4B Q07343 2/20 0.34
PDE4C Q08493 2/20 0.34
PDE4D Q08499 2/20 0.34
CYP1A2 P05177 1/20 0.34
CYP3A4 P08684 1/20 0.34
ADORA1 P30542 1/20 0.34

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
SCHEMBL1545988 0.78 ALDH1A1 (0.47) CASP6ALDH1A1LMNASMN1; SMN2HTT
SCHEMBL9849014 0.78 ALDH1A1 (0.42) CASP6ALDH1A1LMNASMN1; SMN2HTT
SCHEMBL1546524 0.74 SIRT1 (0.41) CASP6ALDH1A1LMNASMN1; SMN2HTT
SCHEMBL1962737 0.73 SMN1; SMN2 (0.41) CASP6ALDH1A1LMNASMN1; SMN2HTT
SCHEMBL1946869 0.69 KDM4E (0.56) ALDH1A1LMNASMN1; SMN2L3MBTL1MEN1
SCHEMBL7321137 0.68 CASP6 (0.50) CASP6ALDH1A1LMNASMN1; SMN2HTT
SCHEMBL1963344 0.67 ALDH1A1 (0.71) ALDH1A1LMNASMN1; SMN2HTTMAPK1
SCHEMBL11606963 0.66 CASP6 (0.44) CASP6ALDH1A1LMNASMN1; SMN2HTT
SCHEMBL1546783 0.66 ALDH1A1 (0.42) ALDH1A1LMNASMN1; SMN2HTTMAPK1
SCHEMBL4193697 0.65 CASP6 (0.66) CASP6ALDH1A1LMNAHTTTDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8236951-B2 Thioxanthine derivatives as myeloperoxidase inhibitors ASTRAZENECA AB (SE) 2012-08-07 US disclosed
EP-2332541-A1 Use of thioxanthine derivatives as MPO inhibitors AstraZeneca AB (SE) 2011-06-15 EP disclosed
US-20080293748-A1 Thioxanthine Derivatives as Myeloperoxidase Inhibitors ASTRAZENECA AB (SE) 2008-11-27 US disclosed
US-7425560-B2 Thioxanthine derivatives as myeloperoxidase inhibitors ASTRAZENECA AB (SE) 2008-09-16 US disclosed
US-20050234036-A1 Thioxanthine derivatives as myeloperoxidase inhibitors ASTRAZENECA AB (SE) 2005-10-20 US disclosed
EP-1499613-A1 THIOXANTHINE DERIVATIVES AS MYELOPEROXIDASE INHIBITORS AstraZeneca AB (SE) 2005-01-26 EP disclosed
WO-2003089430-A1 THIOXANTHINE DERIVATIVES AS MYELOPEROXIDASE INHIBITORS ASTRAZENECA AB (SE) 2003-10-30 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 (2 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-20080293748-A1 Thioxanthine Derivatives as Myeloperoxidase Inhibitors MPO, XDH, EPX CASP6 2484/4885ALDH1A1 178/4885LMNA 3917/4885
US-20050234036-A1 Thioxanthine derivatives as myeloperoxidase inhibitors MPO, XDH, EPX CASP6 2484/4885ALDH1A1 178/4885LMNA 3917/4885

“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.