SCHEMBL5043820

SCHEMBL5043820

COc1ccc(-c2nc(-c3cc(C(=O)NCC(C)C)c(C)n3Cc3ccco3)cs2)cc1

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KLKB1 P03952 5/20 0.48
SMN1; SMN2 Q16637 4/20 0.45
NPC1 O15118 3/20 0.45
RAB9A P51151 3/20 0.45
HPGD P15428 2/20 0.45
MEN1 O00255 5/20 0.44
KMT2A Q03164 5/20 0.44
ALDH1A1 P00352 8/20 0.43
LMNA P02545 5/20 0.43
TP53 P04637 4/20 0.43
TSHR P16473 2/20 0.43
CASP1 P29466 2/20 0.43
CASP7 P55210 2/20 0.43
MAPT P10636 6/20 0.42
KDM4E B2RXH2 3/20 0.42
GLA P06280 2/20 0.42
NPSR1 Q6W5P4 2/20 0.42
IDH1 O75874 1/20 0.42
GAA P10253 1/20 0.42
RUNX1 Q01196 1/20 0.42

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
SCHEMBL5043669 0.89 KLKB1 (0.54) KLKB1SMN1; SMN2NPC1RAB9AHPGD
SCHEMBL5047785 0.89 SMN1; SMN2 (0.45) KLKB1SMN1; SMN2NPC1RAB9AMEN1
SCHEMBL5048727 0.89 ALDH1A1 (0.47) KLKB1SMN1; SMN2NPC1RAB9AHPGD
SCHEMBL5046920 0.89 KLKB1 (0.46) KLKB1SMN1; SMN2NPC1RAB9AHPGD
SCHEMBL5039266 0.88 NPC1 (0.51) KLKB1SMN1; SMN2NPC1RAB9AHPGD
SCHEMBL5039868 0.88 ALDH1A1 (0.48) SMN1; SMN2NPC1RAB9AMEN1KMT2A
SCHEMBL5039574 0.88 ALDH1A1 (0.42) KLKB1SMN1; SMN2NPC1RAB9AHPGD
SCHEMBL5044164 0.87 KLKB1 (0.51) KLKB1SMN1; SMN2NPC1RAB9AHPGD
SCHEMBL5039244 0.86 KLKB1 (0.46) KLKB1SMN1; SMN2NPC1RAB9AMEN1
SCHEMBL5043787 0.85 ALDH1A1 (0.51) KLKB1SMN1; SMN2NPC1RAB9AHPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1583762-B1 PYRROLYL-THIAZOLES AND THEIR USE AS CB 1 RECEPTOR INVERSE AGONISTS HOFFMANN LA ROCHE (CH) 2008-07-09 EP claimed
US-7135488-B2 Pyrrolyl-thiazole derivatives HOFFMANN-LA ROCHE INC. (US) 2006-11-14 US claimed
EP-1583762-A1 PYRROLYL-THIAZOLES AND THEIR USE AS CB 1 RECEPTOR INVERSE AGONISTS F. HOFFMANN-LA ROCHE AG (CH) 2005-10-12 EP claimed
US-20040147572-A1 Novel pyrrolyl-thiazole derivatives HOFFMAN-LA ROCHE INC. 2004-07-29 US claimed
WO-2004060888-A1 NOVEL CB 1 RECEPTOR INVERSE AGONISTS F. HOFFMANN-LA ROCHE AG (CH) 2004-07-22 WO claimed
EP-1583762-B1 PYRROLYL-THIAZOLES AND THEIR USE AS CB 1 RECEPTOR INVERSE AGONISTS HOFFMANN LA ROCHE (CH) 2008-07-09 EP disclosed
US-7135488-B2 Pyrrolyl-thiazole derivatives HOFFMANN-LA ROCHE INC. (US) 2006-11-14 US disclosed
EP-1583762-A1 PYRROLYL-THIAZOLES AND THEIR USE AS CB 1 RECEPTOR INVERSE AGONISTS F. HOFFMANN-LA ROCHE AG (CH) 2005-10-12 EP disclosed
US-20040147572-A1 Novel pyrrolyl-thiazole derivatives HOFFMAN-LA ROCHE INC. 2004-07-29 US disclosed
WO-2004060888-A1 NOVEL CB 1 RECEPTOR INVERSE AGONISTS F. HOFFMANN-LA ROCHE AG (CH) 2004-07-22 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-20040147572-A1 Novel pyrrolyl-thiazole derivatives CNR1, CNR2, NPY1R KLKB1 3949/4885SMN1; SMN2 3330/4885NPC1 500/4885

“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.