SCHEMBL10013764

SCHEMBL10013764

CCN(CC)C(=O)Cc1ccccc1OC

nearest known ligand 0.78

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 2/20 0.78
CYP2D6 P10635 2/20 0.78
CYP2C19 P33261 2/20 0.78
CYP3A4 P08684 1/20 0.78
TSHR P16473 3/20 0.65
TSPO P30536 1/20 0.54
SIGMAR1 Q99720 2/20 0.52
KMT2A Q03164 4/20 0.52
MEN1 O00255 3/20 0.52
KDM4E B2RXH2 1/20 0.51
GAA P10253 1/20 0.51
CYP2C9 P11712 1/20 0.51
MAPT P10636 1/20 0.49
LMNA P02545 1/20 0.49
SMN1; SMN2 Q16637 1/20 0.49
TTR P02766 1/20 0.48
TAAR1 Q96RJ0 1/20 0.48

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
SCHEMBL18050816 0.84 CYP1A2 (0.58) CYP1A2CYP2D6CYP2C19CYP3A4TSHR
SCHEMBL8567854 0.83 TSHR (0.60) CYP1A2CYP2D6CYP2C19CYP3A4TSHR
SCHEMBL18050796 0.83 CYP1A2 (0.57) CYP1A2CYP2D6CYP2C19CYP3A4TSHR
SCHEMBL13226266 0.79 CYP1A2 (0.56) CYP1A2CYP2D6CYP2C19CYP3A4TSHR
SCHEMBL13206752 0.79 TSHR (0.56) CYP1A2CYP2D6CYP2C19CYP3A4TSHR
SCHEMBL28118170 0.78 ATM (0.58) CYP1A2CYP2D6CYP2C19CYP3A4TSHR
SCHEMBL1792326 0.78 TSHR (0.55) CYP1A2CYP2D6CYP2C19CYP3A4TSHR
SCHEMBL4556502 0.78 TSHR (0.55) CYP1A2CYP2D6CYP2C19CYP3A4TSHR
SCHEMBL17276760 0.78 TSPO (0.59) CYP1A2CYP2D6CYP2C19CYP3A4TSHR
SCHEMBL2550830 0.77 AKR1B1 (0.57) CYP1A2CYP2D6CYP2C19CYP3A4TSPO

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8168833-B2 Schwartz reagents: methods of in situ generation and use QUEEN'S UNIVERSITY AT KINGSTON (CA) 2012-05-01 US disclosed
US-20100145060-A1 Schwartz Reagents: Methods of In Situ Generation and Use QUEEN'S UNIVERSITY AT KINGSTON (CA) 2010-06-10 US disclosed
US-4305717-A P-PHENYLENEDIAMINE OXIDIZING BASE AND COUPLER TO FORM INDAMINES L'OREAL (FR) 1981-12-15 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-20100145060-A1 Schwartz Reagents: Methods of In Situ Generation and Use CBR3, CBR1, ZFR CYP1A2 597/4885CYP2D6 3048/4885CYP2C19 2203/4885

“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.