SCHEMBL492763

SCHEMBL492763

O=C(O)c1nc(-c2cccs2)no1

nearest known ligand 0.64

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 6/20 0.64
LMNA P02545 3/20 0.64
NPC1 O15118 8/20 0.63
RAB9A P51151 8/20 0.63
DAGLA Q9Y4D2 1/20 0.60
MCL1 Q07820 1/20 0.59
KMT2A Q03164 2/20 0.59
MAPT P10636 5/20 0.56
ATM Q13315 2/20 0.56
TP53 P04637 1/20 0.56
PKM P14618 2/20 0.51
KDM4E B2RXH2 2/20 0.50
HDAC1 Q13547 2/20 0.50
HPGD P15428 1/20 0.50
HDAC4 P56524 1/20 0.50
HDAC6 Q9UBN7 1/20 0.50
POLB P06746 1/20 0.49
HTT P42858 1/20 0.49
ALDH1A1 P00352 1/20 0.49
L3MBTL1 Q9Y468 1/20 0.49

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
SCHEMBL29518033 0.86 NPC1 (0.61) SMN1; SMN2LMNANPC1RAB9ADAGLA
SCHEMBL2162193 0.83 NPC1 (0.70) SMN1; SMN2LMNANPC1RAB9ADAGLA
SCHEMBL31036198 0.82 SMN1; SMN2 (0.72) SMN1; SMN2LMNANPC1RAB9ADAGLA
SCHEMBL493604 0.81 SMN1; SMN2 (0.74) SMN1; SMN2LMNANPC1RAB9ADAGLA
SCHEMBL28816256 0.79 MAPT (0.64) SMN1; SMN2LMNANPC1RAB9ADAGLA
SCHEMBL16437799 0.79 SMN1; SMN2 (0.75) SMN1; SMN2LMNANPC1RAB9ADAGLA
SCHEMBL493260 0.79 SMN1; SMN2 (0.75) SMN1; SMN2LMNANPC1RAB9ADAGLA
SCHEMBL9911656 0.78 SMN1; SMN2 (0.62) SMN1; SMN2LMNANPC1RAB9ADAGLA
SCHEMBL3664535 0.77 MCL1 (0.56) SMN1; SMN2LMNANPC1RAB9ADAGLA
SCHEMBL19380258 0.77 RAB9A (0.73) SMN1; SMN2LMNANPC1RAB9ADAGLA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8058475-B2 Substituted cyclohexylmethyl compounds GRUENENTHAL GMBH (DE) 2011-11-15 US claimed
EP-1989174-B1 SUBSTITUTED CYCLOHEXYLMETHYL DERIVATIVES GRUENENTHAL GMBH (DE) 2011-08-03 EP claimed
EP-2139851-A2 SUBSTITUTED AMIDE DERIVATIVES Grünenthal GmbH (DE) 2010-01-06 EP claimed
US-20090286833-A1 Substituted Cyclohexylmethyl Compounds GRUENENTHAL GMBH (DE) 2009-11-19 US claimed
US-20080306084-A1 Substituted Amide Compounds GRUENENTHAL GMBH (DE) 2008-12-11 US claimed
WO-2008131946-A2 SUBSTITUTED AMIDE DERIVATIVES Grünenthal GmbH (DE) 2008-11-06 WO claimed
US-8106055-B2 Substituted amide compounds GRUENENTHAL GMBH (DE) 2012-01-31 US disclosed
US-8058475-B2 Substituted cyclohexylmethyl compounds GRUENENTHAL GMBH (DE) 2011-11-15 US disclosed
EP-2139851-A2 SUBSTITUTED AMIDE DERIVATIVES Grünenthal GmbH (DE) 2010-01-06 EP disclosed
US-20090286833-A1 Substituted Cyclohexylmethyl Compounds GRUENENTHAL GMBH (DE) 2009-11-19 US disclosed
US-20080306084-A1 Substituted Amide Compounds GRUENENTHAL GMBH (DE) 2008-12-11 US disclosed
WO-2008131946-A2 SUBSTITUTED AMIDE DERIVATIVES Grünenthal GmbH (DE) 2008-11-06 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-20080306084-A1 Substituted Amide Compounds OPRK1, NAA50, ACMSD SMN1; SMN2 1729/4885LMNA 2485/4885NPC1 519/4885
US-20090286833-A1 Substituted Cyclohexylmethyl Compounds CNR1, H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, C1R SMN1; SMN2 1867/4885LMNA 1432/4885NPC1 112/4885

“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.