SCHEMBL224149

SCHEMBL224149

O=C(Cl)Cc1ccc(OCc2ccccc2)cc1

nearest known ligand 0.71

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALOX5 P09917 7/20 0.65
NR4A1 P22736 1/20 0.62
NR4A2 P43354 1/20 0.62
NR4A3 Q92570 1/20 0.62
FFAR1 O14842 1/20 0.61
FFAR4 Q5NUL3 1/20 0.61
PTGS1 P23219 2/20 0.59
PTGS2 P35354 2/20 0.59
LMNA P02545 1/20 0.59
CYP1A2 P05177 1/20 0.59
SLC6A2 P23975 1/20 0.59
CYP2C19 P33261 1/20 0.59
SLC6A3 Q01959 1/20 0.59
HIF1A Q16665 1/20 0.59
HDAC6 Q9UBN7 1/20 0.59
MAOB P27338 1/20 0.58
PARP10 Q53GL7 1/20 0.58
LTB4R Q15722 1/20 0.57
LTB4R2 Q9NPC1 1/20 0.57
SRD5A2 P31213 1/20 0.57

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
SCHEMBL1066614 0.86 FFAR1 (0.70) ALOX5NR4A1NR4A2NR4A3FFAR1
SCHEMBL3501067 0.85 NR4A2 (0.64) NR4A2FFAR1MAOBPARP10HRH3
Ammonia Solution, Strong SCHEMBL27788257 0.84 FFAR1 (0.68) ALOX5NR4A1NR4A2NR4A3FFAR1
Hydrochloric Acid SCHEMBL10622121 0.84 FFAR1 (0.68) ALOX5NR4A1NR4A2NR4A3FFAR1
SCHEMBL3054083 0.84 PLA2G4B (0.64) ALOX5NR4A1NR4A2NR4A3FFAR1
SCHEMBL4222632 0.84 FFAR1 (0.68) ALOX5NR4A1NR4A2NR4A3FFAR1
Benzylphenylether SCHEMBL27549280 0.83 NR4A2 (0.67) NR4A1NR4A2NR4A3FFAR1FFAR4
SCHEMBL1796796 0.83 FFAR1 (0.77) ALOX5NR4A1NR4A2NR4A3FFAR1
SCHEMBL2790268 0.83 NR4A2 (0.62) NR4A2FFAR1MAOBLTB4RLTB4R2
SCHEMBL6169826 0.83 ALOX5 (0.61) ALOX5NR4A1NR4A2NR4A3FFAR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-101613335-B Natural product 5,7-dimethoxy-4'-hydroxyisoflavone preparation method UNIV DONGHUA 2011-07-20 CN claimed
CN-101613335-A Natural product 5, the preparation method of 7-dimethoxy-4 ' '-hydroxy-isoflavone UNIV DONGHUA 2009-12-30 CN claimed
US-20240408092-A1 PEPTIDE AND SMALL MOLECULE AGONISTS OF EPHA AND THEIR USES UNIV CASE WESTERN RESERVE (US) 2024-12-12 US disclosed
CN-115536584-B Synthesis method of norlinderane hydrochloride 珠海润都制药股份有限公司 2024-07-05 CN disclosed
US-11944624-B2 Peptide and small molecule agonists of EphA and their uses CASE WESTERN RESERVE UNIVERSITY (US) 2024-04-02 US disclosed
CN-112521395-B Preparation method of galanthamine 鲁南制药集团股份有限公司 2023-09-05 CN disclosed
CN-115536584-A Synthetic method of higenamine hydrochloride 珠海润都制药股份有限公司 2022-12-30 CN disclosed
CN-112521395-A Preparation method of galanthamine 鲁南制药集团股份有限公司 2021-03-19 CN disclosed
US-20200222405-A1 PEPTIDE AND SMALL MOLECULE AGONISTS OF EPHA AND THEIR USES CASE WESTERN RESERVE UNIVERSITY 2020-07-16 US disclosed
US-20200222405-A1 PEPTIDE AND SMALL MOLECULE AGONISTS OF EPHA AND THEIR USES CASE WESTERN RESERVE UNIVERSITY 2020-07-16 US disclosed
EP-3648766-A1 PEPTIDE AND SMALL MOLECULE AGONISTS OF EPHA AND THEIR USES Case Western Reserve University (US) 2020-05-13 EP disclosed
US-4733000-A OLIGOPEPTIDES FOR HYPOTENSIVES KYOWA HAKKO KOGYO CO., LTD. (JP) 1988-03-22 US disclosed
US-4681879-A 11-substituted 5H,11H-pyrrolo[2,1-c][1,4]benzoxazepines as antipsychotic and analgesic agents HOECHST-ROUSSEL PHARMACEUTICALS INC. (US) 1987-07-21 US disclosed
US-4608374-A 11-substituted 5H,11H-pyrrolo[2,1-c][1,4]benzoxazepines as antipsychotic and analgesic agents HOECHST-ROUSSEL PHARMACEUTICALS INC. (US) 1986-08-26 US disclosed
EP-0061172-B1 PHOSPHORUS-CONTAINING OLIGOPEPTIDES, PROCESSES FOR PREPARATION THEREOF AND A PHARMACEUTICAL COMPOSITION CONTAINING THE SAME KYOWA HAKKO KOGYO CO., LTD. (JP) 1985-06-19 EP disclosed
EP-0144729-A1 11-Substituted 5H,11H-pyrrolo[2,1-c][1,4]benzoxazepines, a process for their preparation and their use in medicaments HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED (US) 1985-06-19 EP disclosed
US-4421763-A HYPOTENSIVE AGENTS EISAI CO., LTD. (JP) 1983-12-20 US disclosed
EP-0061172-A1 Phosphorus-containing oligopeptides, processes for preparation thereof and a pharmaceutical composition containing the same KYOWA HAKKO KOGYO CO., LTD. (JP) 1982-09-29 EP disclosed
US-4350705-A HYPOTENSIVE AGENTS EISAI CO., LTD. (JP) 1982-09-21 US disclosed
EP-0017195-A1 Derivatives of 2,5-disubstituted-cyclohexane-1,3-diones, process for preparation thereof and pharmaceutical composition containing them Eisai Co., Ltd. (JP) 1980-10-15 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 (3 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-20200222405-A1 PEPTIDE AND SMALL MOLECULE AGONISTS OF EPHA AND THEIR USES EPHA1, EPHA7, EPHA3 ALOX5 2693/4885NR4A1 1465/4885NR4A2 1483/4885
US-11944624-B2 Peptide and small molecule agonists of EphA and their uses EPHA1, EPHA7, EPHA3 ALOX5 2693/4885NR4A1 1465/4885NR4A2 1483/4885
US-20240408092-A1 PEPTIDE AND SMALL MOLECULE AGONISTS OF EPHA AND THEIR USES EPHA1, EPHA7, EPHA3 ALOX5 2693/4885NR4A1 1465/4885NR4A2 1483/4885

“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.