SCHEMBL863102

SCHEMBL863102

COCC(=O)c1ccc(O)cc1

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ESR2 Q92731 1/20 0.59
NPC1 O15118 2/20 0.58
RAB9A P51151 2/20 0.58
ALDH1A1 P00352 2/20 0.58
MAPT P10636 1/20 0.58
HSD17B3 P37058 3/20 0.55
PTPN1 P18031 1/20 0.54
CA12 O43570 1/20 0.54
CA1 P00915 1/20 0.54
CA2 P00918 1/20 0.54
CA7 P43166 1/20 0.54
CA9 Q16790 1/20 0.54
CA14 Q9ULX7 1/20 0.54
KDM4E B2RXH2 1/20 0.52
ABL1 P00519 1/20 0.52
POLB P06746 1/20 0.52
ALPI P09923 1/20 0.52
GAA P10253 1/20 0.52
ALPG P10696 1/20 0.52
APEX1 P27695 1/20 0.52

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
SCHEMBL5460100 0.83 NPC1 (0.45) ESR2NPC1RAB9AALDH1A1MAPT
SCHEMBL2064455 0.83 NPC1 (0.58) NPC1RAB9AALDH1A1MAPTPOLB
SCHEMBL7290567 0.83 CA1 (0.54) NPC1RAB9AALDH1A1MAPTCA12
SCHEMBL14735749 0.82 NPC1 (0.58) ESR2NPC1RAB9AALDH1A1MAPT
SCHEMBL841978 0.81 ESR2 (0.50) ESR2NPC1RAB9AALDH1A1MAPT
SCHEMBL246263 0.81 HDAC3 (0.66) ESR2NPC1RAB9AALDH1A1MAPT
SCHEMBL10796669 0.81 HAO1 (0.46) ESR2NPC1RAB9AALDH1A1MAPT
SCHEMBL3833913 0.81 LMNA (0.50) ESR2NPC1RAB9AALDH1A1MAPT
SCHEMBL7290231 0.81 GSK3B (0.41) ESR2NPC1RAB9AALDH1A1MAPT
SCHEMBL20135229 0.81 MAPT (0.62) ESR2NPC1RAB9AALDH1A1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119019231-A Preparation method of p-methoxyethylphenol 常州瑞明药业有限公司 2024-11-26 CN claimed
CN-107382683-A A kind of synthetic method for preparing Metoprolol intermediate 荆门医药工业技术研究院 2017-11-24 CN claimed
US-5107034-A Bromination of 4-hydroxyacetophenone, treating with methoxide to produce alpha-methoxy-4-hydroxyacetophenone, reduction HOECHST CELANESE CORPORATION (US) 1992-04-21 US claimed
EP-0449602-A1 Method for producing 4-(2'-methoxyethyl) phenol HOECHST CELANESE CORPORATION (US) 1991-10-02 EP claimed
EP-0041295-B1 PROCESS FOR THE PREPARATION OF 1-ISOPROPYLAMINO-3-(4-(2-METHOXY-ETHYL)-PHENOXY)-2-PROPANOL Aktiebolaget Hässle (SE) 1984-01-04 EP claimed
EP-0041295-A1 Process for the preparation of 1-isopropylamino-3-(4-(2-methoxy-ethyl)-phenoxy)-2-propanol Aktiebolaget Hässle (SE) 1981-12-09 EP claimed
JP-4221334-A None JP disclosed
US-20250171427-A1 THERAPEUTIC COMPOUNDS SANOFI (FR) 2025-05-29 US disclosed
WO-2025104230-A1 BENZOXAZOLES AS MODULATORS OF IL-17A SANOFI (FR) 2025-05-22 WO disclosed
CN-119019231-A Preparation method of p-methoxyethylphenol 常州瑞明药业有限公司 2024-11-26 CN disclosed
WO-2024115926-A1 FORMULATION COMPRISING APOCYNIN AND PAEONOL AKL RESEARCH & DEVELOPMENT LTD (GB) 2024-06-06 WO disclosed
CN-116999417-A Liquid preparation containing paeonol and apocynin AKL研究发展有限公司 2023-11-07 CN disclosed
US-20230330017-A1 LIQUID FORMULATION COMPRISING PAEONOL AND APOCYNIN AKL RES & DEVELOPMENT LTD (GB) 2023-10-19 US disclosed
EP-0113236-B1 SUBSTITUTED IMIDAZOPYRIMIDINES-PYRAZINES, AND -TRIAZINES ELI LILLY AND COMPANY (US) 1987-04-22 EP disclosed
US-4636502-A Methods of producing a positive inotropic effect or vasodilation by administration of 2-phenyl imidazo pyrimidines and pyrazines ELI LILLY AND COMPANY (US) 1987-01-13 US disclosed
US-4537889-A PHENYL SUBSTITUTED IMIDAZO COMPOUNDS ELI LILLY AND COMPANY (US) 1985-08-27 US disclosed
EP-0113236-A1 Substituted imidazopyrimidines-pyrazines, and -triazines ELI LILLY AND COMPANY (US) 1984-07-11 EP disclosed
EP-0041295-B1 PROCESS FOR THE PREPARATION OF 1-ISOPROPYLAMINO-3-(4-(2-METHOXY-ETHYL)-PHENOXY)-2-PROPANOL Aktiebolaget Hässle (SE) 1984-01-04 EP disclosed
EP-0041295-A1 Process for the preparation of 1-isopropylamino-3-(4-(2-methoxy-ethyl)-phenoxy)-2-propanol Aktiebolaget Hässle (SE) 1981-12-09 EP disclosed
EP-0041295-A1 Process for the preparation of 1-isopropylamino-3-(4-(2-methoxy-ethyl)-phenoxy)-2-propanol Aktiebolaget Hässle (SE) 1981-12-09 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 (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-20230330017-A1 LIQUID FORMULATION COMPRISING PAEONOL AND APOCYNIN LPL, PNLIP, LPO ESR2 4024/4885NPC1 1163/4885RAB9A 4416/4885
US-20250171427-A1 THERAPEUTIC COMPOUNDS IL17A, IL2, IL36G ESR2 360/4885NPC1 461/4885RAB9A 818/4885

“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.