SCHEMBL4402154

SCHEMBL4402154

c1ccc(Oc2ccc3ccccc3c2)cc1

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LTA4H P09960 3/20 0.60
TSHR P16473 1/20 0.60
CYP1A2 P05177 1/20 0.56
CYP2A6 P11509 1/20 0.56
GAA P10253 1/20 0.55
RCE1 Q9Y256 1/20 0.55
MAOA P21397 2/20 0.53
MAOB P27338 2/20 0.53
NR1H2 P55055 1/20 0.52
BAX Q07812 1/20 0.52
ALOX5 P09917 1/20 0.52
KMT2A Q03164 3/20 0.51
MEN1 O00255 2/20 0.51
PGR P06401 1/20 0.51
L3MBTL1 Q9Y468 1/20 0.51
AGXT P21549 2/20 0.50
FLT3 P36888 1/20 0.49
HAO1 Q9UJM8 1/20 0.48
TDP1 Q9NUW8 2/20 0.48
PTPN7 P35236 1/20 0.48

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
SCHEMBL29860094 1.00 LTA4H (0.60) LTA4HTSHRCYP1A2CYP2A6GAA
SCHEMBL9515088 0.95 LTA4H (0.60) LTA4HTSHRCYP1A2CYP2A6GAA
SCHEMBL9789564 0.95 LTA4H (0.67) LTA4HTSHRCYP1A2CYP2A6GAA
SCHEMBL29366638 0.92 CYP1A2 (0.64) CYP1A2CYP2A6GAARCE1MAOA
SCHEMBL395026 0.92 CYP1A2 (0.64) CYP1A2CYP2A6GAARCE1MAOA
SCHEMBL16890178 0.90 CYP1A2 (0.56) LTA4HTSHRCYP1A2CYP2A6GAA
SCHEMBL29378143 0.90 CYP1A2 (0.61) CYP1A2CYP2A6GAARCE1MAOA
Hydrochloric Acid SCHEMBL9443225 0.90 CYP1A2 (0.61) CYP1A2CYP2A6GAARCE1MAOA
Diphenylether SCHEMBL28808049 0.87 CYP1A2 (0.79) LTA4HTSHRCYP1A2CYP2A6ALOX5
Diphenylether SCHEMBL4982232 0.87 LTA4H (0.80) LTA4HTSHRCYP2A6MAOAMAOB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118059901-A Preparation method and application of organic acid modified aluminum metaphosphate supported nickel-palladium catalyst 中国矿业大学 2024-05-24 CN claimed
US-4533766-A Process for the production of dihydroxybenzenes DEGUSSA AKTIENGESELLSCHAFT (DE) 1985-08-06 US claimed
EP-4273117-B1 NAPHTHYL PHENYL ETHER COMPOUND AND LUBRICANT COMPOSITION CONTAINING SAME MORESCO CORP (JP) 2025-09-10 EP disclosed
US-12215290-B2 Naphthyl phenyl ether compound and lubricant composition containing same MORESCO CORPORATION (JP) 2025-02-04 US disclosed
CN-118059901-A Preparation method and application of organic acid modified aluminum metaphosphate supported nickel-palladium catalyst 中国矿业大学 2024-05-24 CN disclosed
US-20240117265-A1 NAPHTHYL PHENYL ETHER COMPOUND AND LUBRICANT COMPOSITION CONTAINING SAME MORESCO CORPORATION (JP) 2024-04-11 US disclosed
US-11858953-B2 Compositions and methods for synthesis of phosphorylated molecules THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2024-01-02 US disclosed
US-11858953-B2 Compositions and methods for synthesis of phosphorylated molecules THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2024-01-02 US disclosed
EP-4273117-A1 NAPHTHYL PHENYL ETHER COMPOUND AND LUBRICANT COMPOSITION CONTAINING SAME Moresco Corporation (JP) 2023-11-08 EP disclosed
CN-116829527-A Naphthyl phenyl ether compound and lubricating oil composition containing the same 株式会社MORESCO 2023-09-29 CN disclosed
CN-109553592-B Synthetic method for converting lignin 4-O-5 model compound diaryl ether into nitrogen-containing compound 兰州大学(CN) 2023-01-13 CN disclosed
EP-0748812-A1 Novel oxaphosphorines and process for their preparation HOECHST AKTIENGESELLSCHAFT (DE) 1996-12-18 EP disclosed
CN-1117632-A Laser marking method and aqueous laser marking composition NIPPON KAYAKU KK (JP) 1996-02-28 CN disclosed
US-4978811-A Process for hydrolysis of ortho-aromatic di-aryl ethers THE DOW CHEMICAL COMPANY (US) 1990-12-18 US disclosed
EP-0363961-A2 Thermosensitive recording material MITSUBISHI PAPER MILLS, LTD. (JP) 1990-04-18 EP disclosed
US-4590305-A CATALYTIC HYDROXYLATION OF PHENOLS USING HYDROGEN PEROXIDE DEGUSSA AKTIENGESELLSCHAFT (DE) 1986-05-20 US disclosed
US-4551562-A Process for the production of dihydroxybenzenes DEGUSSA AKTIENGESELLSCHAFT (DE) 1985-11-05 US disclosed
US-4533766-A Process for the production of dihydroxybenzenes DEGUSSA AKTIENGESELLSCHAFT (DE) 1985-08-06 US disclosed
US-4174460-A Process for the hydroxylation of phenols and phenol ethers in the nucleus BAYER AKTIENGESELLSCHAFT (DE) 1979-11-13 US disclosed
US-4045496-A Process for the hydroxylation of phenols and phenol ethers in the nucleus BAYER AKTIENGESELLSCHAFT (DT) 1977-08-30 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-11858953-B2 Compositions and methods for synthesis of phosphorylated molecules PIK3CA, CHAMP1, TYMP LTA4H 3513/4885TSHR 4517/4885CYP1A2 4093/4885

“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.