SCHEMBL2024847

SCHEMBL2024847

Cc1ccccc1CC(C)c1ccccc1O

nearest known ligand 0.58

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
TSHR P16473 1/20 0.58
GABRA1 P14867 2/20 0.48
GABRB2 P47870 2/20 0.48
POLB P06746 2/20 0.41
MAPK1 P28482 2/20 0.41
MAPT P10636 3/20 0.40
MEN1 O00255 2/20 0.40
KMT2A Q03164 2/20 0.40
ALDH1A1 P00352 1/20 0.40
HTT P42858 1/20 0.40
TP53 P04637 1/20 0.38
GAA P10253 1/20 0.38
HSD17B10 Q99714 1/20 0.38
HSPA5 P11021 1/20 0.38
TAAR1 Q96RJ0 1/20 0.37
TRPA1 O75762 2/20 0.36
ATM Q13315 1/20 0.36
PPARG P37231 1/20 0.36
PPARA Q07869 1/20 0.36

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
SCHEMBL2023255 0.88 TSHR (0.53) TSHRGABRA1GABRB2POLBMAPK1
SCHEMBL188373 0.87 TSHR (0.64) TSHRGABRA1GABRB2POLBMAPK1
SCHEMBL30455902 0.87 TSHR (0.64) TSHRGABRA1GABRB2POLBMAPK1
SCHEMBL1838330 0.87 TSHR (0.43) TSHRGABRA1GABRB2POLBMAPK1
SCHEMBL1954000 0.86 TSHR (0.48) TSHRGABRA1GABRB2POLBMAPK1
SCHEMBL6547208 0.85 ESR1 (0.43) TSHRTAAR1PPARGPPARA
SCHEMBL18076591 0.84 TSHR (0.46) TSHRGABRA1GABRB2POLBMAPK1
SCHEMBL2022076 0.82 TSHR (0.63) TSHRGABRA1GABRB2POLBMAPK1
SCHEMBL1954596 0.81 MAPT (0.49) TSHRGABRA1GABRB2POLBMAPK1
SCHEMBL2016335 0.81 TSHR (0.53) TSHRGABRA1GABRB2POLBMAPK1

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-20110160476-A1 N-Substituted Carbamic Acid Ester Production Method and Isocyanate Production Method Using the N-Substituted Carbamic Acid Ester ASAHI KASEI CHEMICALS CORPORATION (JP) 2011-06-30 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-20110160476-A1 N-Substituted Carbamic Acid Ester Production Method and Isocyanate Production Method Using the N-Substituted Carbamic Acid Ester ALKBH3, CPS1, APEH TSHR 2998/4885GABRA1 1573/4885GABRB2 1720/4885

“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.