SCHEMBL10193165

SCHEMBL10193165

CO/C(N)=N\C(c1ccc(OC)cc1)c1cccc(NC(=O)c2cnc(C)cn2)c1

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
AURKA O14965 3/20 0.48
RPS6KB1 P23443 2/20 0.48
MAPT P10636 4/20 0.47
SMN1; SMN2 Q16637 4/20 0.47
NPC1 O15118 3/20 0.47
RAB9A P51151 3/20 0.47
LMNA P02545 1/20 0.47
ALDH1A1 P00352 4/20 0.46
TDP1 Q9NUW8 1/20 0.46
MEN1 O00255 2/20 0.46
KMT2A Q03164 2/20 0.46
HPGD P15428 2/20 0.45
CYP1A2 P05177 1/20 0.45
POLB P06746 1/20 0.45
CYP3A4 P08684 1/20 0.45
CYP2C9 P11712 1/20 0.45
CYP2C19 P33261 1/20 0.45
ATM Q13315 1/20 0.45
L3MBTL1 Q9Y468 1/20 0.45
ACKR3 P25106 1/20 0.45

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
SCHEMBL10193227 0.91 SMN1; SMN2 (0.51) AURKARPS6KB1MAPTSMN1; SMN2NPC1
SCHEMBL10193841 0.91 AURKA (0.52) AURKASMN1; SMN2MEN1KMT2AKDM4E
SCHEMBL10193271 0.88 BACE1 (0.46) MAPTSMN1; SMN2NPC1RAB9AALDH1A1
SCHEMBL10193157 0.84 BACE1 (0.45) AURKARPS6KB1SMN1; SMN2BACE1GRM4
SCHEMBL10193854 0.83 AURKA (0.52) AURKABACE1
SCHEMBL10193160 0.81 BACE1 (0.48) SMN1; SMN2LMNAALDH1A1MEN1KMT2A
SCHEMBL10193694 0.81 SMN1; SMN2 (0.48) MAPTSMN1; SMN2NPC1RAB9ALMNA
SCHEMBL10193013 0.81 AURKA (0.50) AURKAMAPTSMN1; SMN2NPC1RAB9A
SCHEMBL10194093 0.79 BACE1 (0.42) AURKASMN1; SMN2NPC1RAB9ALMNA
SCHEMBL10193776 0.78 AURKA (0.44) AURKAMEN1KMT2AKDM4EBACE1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20120015961-A1 ISOTHIOUREA DERIVATIVES OR ISOUREA DERIVATIVES HAVING BACE1 INHIBITORY ACTIVITY SHIONOGI & CO., LTD. (JP) 2012-01-19 US 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-20120015961-A1 ISOTHIOUREA DERIVATIVES OR ISOUREA DERIVATIVES HAVING BACE1 INHIBITORY ACTIVITY BACE1, BACE2, APP AURKA 4453/4885RPS6KB1 2384/4885MAPT 40/4885

“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.