SCHEMBL13096263

SCHEMBL13096263

CCNC(=O)OC1=C(c2c(CC)cc(C)cc2CC)C(=O)NC12CCC(C)CC2

nearest known ligand 0.35

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
THRB P10828 2/20 0.35
LMNA P02545 1/20 0.34
FPR2 P25090 1/20 0.34
PKM P14618 1/20 0.33
ALDH1A1 P00352 1/20 0.33
HTT P42858 2/20 0.33
L3MBTL1 Q9Y468 2/20 0.33
MAPT P10636 2/20 0.31
ACHE P22303 1/20 0.30
KDM4E B2RXH2 1/20 0.30
MEN1 O00255 1/20 0.30
POLB P06746 1/20 0.30
GAA P10253 1/20 0.30
BLM P54132 1/20 0.30
KMT2A Q03164 1/20 0.30

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
SCHEMBL13096244 0.86 THRB (0.36) THRBLMNAFPR2PKMALDH1A1
SCHEMBL13096254 0.85 THRB (0.33) THRBLMNAFPR2PKMHTT
SCHEMBL13288550 0.84 KMT2A (0.34) THRBLMNAL3MBTL1MAPTKDM4E
SCHEMBL14490563 0.82 KMT2A (0.31) THRBLMNAKMT2A
SCHEMBL14372094 0.82 ACACB (0.38) ACHE
SCHEMBL13071297 0.82 LMNA (0.35) LMNAALDH1A1MEN1KMT2A
SCHEMBL13244221 0.81 KMT2A (0.30) KMT2A
SCHEMBL13096258 0.79 THRB (0.33) THRBHTT
SCHEMBL13096248 0.78 ACACB (0.39) THRBLMNAFPR2PKMALDH1A1
SCHEMBL13096247 0.78 ACACB (0.38)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8383853-B2 Method for preparing 2,6-diethyl-4-methylphenylacetic acid BAYER CROPSCIENCE AG (DE) 2013-02-26 US disclosed
US-8383853-B2 Method for preparing 2,6-diethyl-4-methylphenylacetic acid BAYER CROPSCIENCE AG (DE) 2013-02-26 US disclosed
US-20100261934-A1 Method for Preparing 2,6-Diethyl-4-Methylphenylacetic Acid BAYER CROPSCIENCE AG (DE) 2010-10-14 US disclosed
US-20100261934-A1 Method for Preparing 2,6-Diethyl-4-Methylphenylacetic Acid BAYER CROPSCIENCE AG (DE) 2010-10-14 US disclosed
EP-2218710-A1 Procedure for the preparation of 2,6-diethyl-4-methylphenylacetic acid Bayer CropScience AG (DE) 2010-08-18 EP disclosed
US-20080318776-A1 2,6-Diethyl-4-Methylphenyl-Substituted Tetramic Acid Derivatives BAYER CROPSCIENCE AG (DE) 2008-12-25 US disclosed
US-20080318776-A1 2,6-Diethyl-4-Methylphenyl-Substituted Tetramic Acid Derivatives BAYER CROPSCIENCE AG (DE) 2008-12-25 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 (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-20100261934-A1 Method for Preparing 2,6-Diethyl-4-Methylphenylacetic Acid DDT, TET1, DDC THRB 754/4885LMNA 4009/4885FPR2 4596/4885
US-20080318776-A1 2,6-Diethyl-4-Methylphenyl-Substituted Tetramic Acid Derivatives DDT, TET1, TET3 THRB 288/4885LMNA 4223/4885FPR2 4683/4885

“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.