SCHEMBL319906

SCHEMBL319906

CC(C)(C)Oc1ccc(CO)cc1

nearest known ligand 0.63

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PPARA Q07869 4/20 0.63
PPARG P37231 3/20 0.63
LTA4H P09960 1/20 0.48
ACACB O00763 3/20 0.42
TSHR P16473 1/20 0.39
ELANE P08246 1/20 0.38
NOS3 P29474 1/20 0.36
NOS1 P29475 1/20 0.36
HRH3 Q9Y5N1 1/20 0.36
EPHX2 P34913 1/20 0.36
PRSS1 P07477 1/20 0.35
PRSS2 P07478 1/20 0.35
PRSS3 P35030 1/20 0.35
TRPV1 Q8NER1 1/20 0.35
SLC6A2 P23975 1/20 0.35
SLC6A4 P31645 1/20 0.35
SLC6A3 Q01959 1/20 0.35
VHL P40337 1/20 0.34
ELOC Q15369 1/20 0.34
ELOB Q15370 1/20 0.34

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
Alcohol SCHEMBL28244815 0.83 PPARA (0.44) PPARAPPARGACACBTSHRTRPV1
SCHEMBL934447 0.83 PPARA (0.59) PPARAPPARGLTA4HTSHRELANE
SCHEMBL6667517 0.83 PPARA (0.66) PPARAPPARGACACBTSHRHRH3
SCHEMBL11054493 0.83 PPARG (0.59) PPARAPPARGLTA4HTSHRELANE
SCHEMBL197077 0.81 ELANE (0.50) PPARAPPARGLTA4HACACBTSHR
SCHEMBL26746 0.80 SLC6A2 (0.44) PPARAPPARGACACBTSHRELANE
SCHEMBL3451212 0.79 PPARA (0.68) PPARAPPARGLTA4HACACBEPHX2
SCHEMBL1126574 0.79 SMN1; SMN2 (0.42) PPARAPPARGACACBTSHR
SCHEMBL19755194 0.78 PPARG (0.42) PPARAPPARGACACBELANEEPHX2
SCHEMBL9996916 0.78 PPARG (1.00) PPARAPPARG

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 74 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119504372-A Method for synthesizing 4-tert-butoxy styrene 西安近代化学研究所 2025-02-25 CN claimed
EP-0059372-A1 Process for the preparation of 4-tert.-butoxybenzyl alcohol BASF Aktiengesellschaft (DE) 1982-09-08 EP claimed
CN-119504372-A Method for synthesizing 4-tert-butoxy styrene 西安近代化学研究所 2025-02-25 CN disclosed
CN-119504372-A Method for synthesizing 4-tert-butoxy styrene 西安近代化学研究所 2025-02-25 CN disclosed
CN-117263778-A Preparation method of styrene series compound for 248nm photoresist 河北凯诺中星科技有限公司 2023-12-22 CN disclosed
US-11440884-B2 Compounds, salts thereof and methods for treatment of diseases ACADIA PHARMACEUTICALS INC. (US) 2022-09-13 US disclosed
US-8772226-B2 Methods and compositions for the detection of cancer THE JOHNS HOPKINS UNIVERSITY (US) 2014-07-08 US disclosed
EP-2612858-A1 STAT3/5 activation inhibitor OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2013-07-10 EP disclosed
EP-2585068-A1 PROKINETICIN 1 RECEPTOR ANTAGONISTS FOR THE TREATMENT OF PAIN Janssen Pharmaceutica, N.V. (BE) 2013-05-01 EP disclosed
EP-1866290-B1 PROKINETICIN 1 RECEPTOR ANTAGONISTS JANSSEN PHARMACEUTICA NV (BE) 2013-05-01 EP disclosed
US-8362247-B2 Prokineticin 1 receptor antagonists JANSSEN PHARMACEUTICA N.V. (BE) 2013-01-29 US disclosed
EP-0256763-A1 Process for azetidinones THE UNIVERSITY OF NOTRE DAME DU LAC (US) 1988-02-24 EP disclosed
EP-0240609-A2 Antibiotic A 40926 N-acylaminoglucuronyl aglycons and antibiotic A 40926 aglycon GRUPPO LEPETIT S.p.A. (IT) 1987-10-14 EP disclosed
US-4629781-A STRONG ACIDOLYSIS CONTROLLED BY THE USE OF SOLVENT, ACID, CONCENTRATION AND HEATING GRUPPO LEPETIT S.P.A. (IT) 1986-12-16 US disclosed
EP-0146053-A2 Chemical process for preparing antibiotic L 17392 (Deglucoteicoplanin) and its salts GRUPPO LEPETIT S.p.A. (IT) 1985-06-26 EP disclosed
EP-0059373-B1 PROCESS FOR THE PREPARATION OF BENZYL ALCOHOLS BASF Aktiengesellschaft (DE) 1984-05-23 EP disclosed
EP-0059372-A1 Process for the preparation of 4-tert.-butoxybenzyl alcohol BASF Aktiengesellschaft (DE) 1982-09-08 EP disclosed
EP-0059372-A1 Process for the preparation of 4-tert.-butoxybenzyl alcohol BASF Aktiengesellschaft (DE) 1982-09-08 EP disclosed
EP-0059372-A1 Process for the preparation of 4-tert.-butoxybenzyl alcohol BASF Aktiengesellschaft (DE) 1982-09-08 EP disclosed
EP-0059373-A1 Process for the preparation of benzyl alcohols BASF Aktiengesellschaft (DE) 1982-09-08 EP 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-11440884-B2 Compounds, salts thereof and methods for treatment of diseases SLC10A1, VHL, CYP11B2 PPARA 423/4885PPARG 275/4885LTA4H 980/4885

“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.