SCHEMBL3717147

SCHEMBL3717147

NNC(=O)CNC(=O)c1cccc(Cl)c1

nearest known ligand 0.60

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 5/20 0.60
MEN1 O00255 4/20 0.60
GPR139 Q6DWJ6 2/20 0.60
ATM Q13315 1/20 0.60
ALDH1A1 P00352 3/20 0.54
CYP1A2 P05177 1/20 0.54
CYP2D6 P10635 1/20 0.54
CYP2C9 P11712 1/20 0.54
CYP2C19 P33261 1/20 0.54
LMNA P02545 1/20 0.53
SMN1; SMN2 Q16637 1/20 0.53
CA1 P00915 1/20 0.52
CA2 P00918 1/20 0.52
MAPT P10636 1/20 0.52

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
SCHEMBL31242942 0.85 KDM4E (0.63) KMT2AMEN1ATMALDH1A1LMNA
SCHEMBL316626 0.85 KDM4E (0.63) KMT2AMEN1ATMALDH1A1LMNA
SCHEMBL13331944 0.84 PARP1 (0.58) KMT2AMEN1GPR139ATMALDH1A1
Hydrochloric Acid SCHEMBL15137104 0.83 KDM4E (0.61) KMT2AMEN1ATMALDH1A1LMNA
SCHEMBL2984329 0.82 KMT2A (0.60) KMT2AMEN1GPR139ATMALDH1A1
SCHEMBL15906174 0.81 KMT2A (0.60) KMT2AMEN1GPR139ATMALDH1A1
SCHEMBL47363 0.80 CA1 (0.57) KMT2AMEN1GPR139ALDH1A1CYP1A2
Cyanide SCHEMBL29178066 0.80 KDM4E (0.58) KMT2AMEN1ATMALDH1A1LMNA
SCHEMBL7674509 0.80 GAA (0.59) KMT2AMEN1GPR139SMN1; SMN2MAPT
SCHEMBL8858800 0.79 KMT2A (0.61) KMT2AMEN1GPR139ATMALDH1A1

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
US-8791299-B2 Compounds for the inhibition of herpes viruses UNIVERSITE LAVAL (CA) 2014-07-29 US disclosed
US-8791299-B2 Compounds for the inhibition of herpes viruses UNIVERSITE LAVAL (CA) 2014-07-29 US disclosed
US-20120157538-A1 Compounds for the Inhibition of Herpes Viruses UNIVERSITE LAVAL (CA) 2012-06-21 US disclosed
US-20120157538-A1 Compounds for the Inhibition of Herpes Viruses UNIVERSITE LAVAL (CA) 2012-06-21 US disclosed
WO-2010132992-A1 COMPOUNDS FOR THE INHIBITION OF HERPESVIRUSES UNIVERSITé LAVAL (CA) 2010-11-25 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-20120157538-A1 Compounds for the Inhibition of Herpes Viruses NOS3, NOS1, DNA2 KMT2A 523/4885MEN1 1837/4885GPR139 1473/4885

“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.