SCHEMBL5074372

SCHEMBL5074372

COc1ccc(C(=O)c2ccc(C)cc2)cc1OC

nearest known ligand 0.81

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 2/20 0.81
CYP2C19 P33261 2/20 0.81
CYP3A4 P08684 1/20 0.81
CYP2C9 P11712 1/20 0.81
TSHR P16473 1/20 0.81
ALDH1A1 P00352 5/20 0.74
GAA P10253 1/20 0.74
CTNNB1 P35222 1/20 0.68
WNT3A P56704 1/20 0.68
MAPT P10636 2/20 0.64
CA12 O43570 1/20 0.61
CA1 P00915 1/20 0.61
CA2 P00918 1/20 0.61
CA4 P22748 1/20 0.61
CA6 P23280 1/20 0.61
CA7 P43166 1/20 0.61
TPMT P51580 1/20 0.61
CA9 Q16790 1/20 0.61
CA14 Q9ULX7 1/20 0.61
SLC22A6 Q4U2R8 1/20 0.59

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
SCHEMBL9364577 0.92 CYP1A2 (0.96) CYP1A2CYP2C19CYP3A4CYP2C9TSHR
SCHEMBL1493250 0.90 CYP1A2 (1.00) CYP1A2CYP2C19CYP3A4CYP2C9TSHR
SCHEMBL11805654 0.87 CYP1A2 (0.61) CYP1A2CYP2C19CYP3A4CYP2C9TSHR
SCHEMBL15100716 0.87 CYP1A2 (0.61) CYP1A2CYP2C19CYP3A4CYP2C9TSHR
SCHEMBL7867471 0.86 TUBB4A (0.69) CYP1A2CYP2C19CYP3A4CYP2C9TSHR
SCHEMBL7373760 0.86 SLC22A6 (0.83) CYP1A2CYP2C19CYP3A4CYP2C9TSHR
SCHEMBL6872165 0.85 TSHR (0.81) CYP1A2CYP2C19CYP3A4CYP2C9TSHR
SCHEMBL2601961 0.85 CYP1A2 (0.81) CYP1A2CYP2C19CYP3A4CYP2C9TSHR
SCHEMBL4818731 0.85 ALDH1A1 (1.00) CYP1A2CYP2C19CYP3A4CYP2C9TSHR
SCHEMBL1333620 0.85 CYP1A2 (0.81) CYP1A2CYP2C19CYP3A4CYP2C9TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0855379-A1 Methods for the preparation of benzophenones derivatives F. HOFFMANN-LA ROCHE AG (CH) 1998-07-29 EP claimed
JP-10204021-A None JP disclosed
US-20230192908-A1 BIOMASS-DERIVED PHOTOINITIATORS BOWLING GREEN STATE UNIVERSITY (US) 2023-06-22 US disclosed
WO-2021236563-A1 BIOMASS-DERIVED PHOTOINITIATORS BOWLING GREEN STATE UNIVERSITY (US) 2021-11-25 WO disclosed
EP-1361210-B1 Novel immunotherapeutic agents and their use in the reduction of cytokine levels CELGENE CORP (US) 2008-12-24 EP disclosed
US-7019030-B2 Cyano and carboxy derivatives of substituted styrenes; inhibitors of tumor necrosis factor alpha, nuclear factor kappa B, and phosphodiesterase CELGENE CORPORATION (US) 2006-03-28 US disclosed
US-20040019106-A1 Novel immunotherapeutic agents MULLER GEORGE W (US) 2004-01-29 US disclosed
EP-1361210-A2 Novel immunotherapeutic agents and their use in the reduction of cytokine levels CELGENE CORPORATION (US) 2003-11-12 EP disclosed
EP-0918746-B1 IMMUNOTHERAPEUTIC AGENTS AND THEIR USE IN THE REDUCTION OF CYTOKINE LEVELS CELGENE CORP (US) 2003-04-09 EP disclosed
US-20030045726-A1 Novel immunotherapeutic agents MULLER GEORGE W (US) 2003-03-06 US disclosed
US-20010056107-A1 Novel immunotherapeutic agents MULLER GEORGE W (US) 2001-12-27 US disclosed
EP-0855379-B1 Methods for the preparation of benzophenone derivatives HOFFMANN LA ROCHE (CH) 2001-09-05 EP disclosed
US-6262101-B1 ALPHA-PYRROLIDINE, IMIDAZOLE AND THIOPHENE-SUBSTITUTED STYRENE DERIVATIVES; INHIBITORS OF TUMOR NECROSIS FACTOR ALPHA, NUCLEAR FACTOR KAPPA B, AND PHOSPHODIESTERASE CELGENE CORPORATION 2001-07-17 US disclosed
US-6130226-A Immunotherapeutic agents CELGENE CORPORATION (US) 2000-10-10 US disclosed
US-5929117-A COMPOUNDS WHICH MEDIATE ACTION OF PHOSPHODIESTERASE AND FORMATION OF TUMOR NECROSIS FACTOR AND NUCLEAR FACTORS CELGENE CORPORATION (US) 1999-07-27 US disclosed
EP-0918746-A1 IMMUNOTHERAPEUTIC AGENTS AND THEIR USE IN THE REDUCTION OF CYTOKINE LEVELS CELGENE CORPORATION (US) 1999-06-02 EP disclosed
US-5877353-A Process for the preparation of benzophenone derivatives HOFFMANN-LA ROCHE INC. (US) 1999-03-02 US disclosed
JP-H10204021-A PRODUCTION OF BENZOPHENONE DERIVATIVE F HOFFMANN LA ROCHE AG 1998-08-04 JP disclosed
EP-0855379-A1 Methods for the preparation of benzophenones derivatives F. HOFFMANN-LA ROCHE AG (CH) 1998-07-29 EP disclosed
WO-1998006692-A1 NOVEL IMMUNOTHERAPEUTIC AGENTS AND THEIR USE IN THE REDUCTION OF CYTOKINE LEVELS CELGENE CORPORATION (US) 1998-02-19 WO 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 (4 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-20030045726-A1 Novel immunotherapeutic agents NFKBIA, RELA, IKBKG CYP1A2 3471/4885CYP2C19 4166/4885CYP3A4 3495/4885
US-20230192908-A1 BIOMASS-DERIVED PHOTOINITIATORS BLVRB, CYP1B1, GLB1 CYP1A2 39/4885CYP2C19 148/4885CYP3A4 30/4885
US-20040019106-A1 Novel immunotherapeutic agents NFKBIA, RELA, IKBKG CYP1A2 3471/4885CYP2C19 4166/4885CYP3A4 3495/4885
US-20010056107-A1 Novel immunotherapeutic agents NFKBIA, RELA, IKBKG CYP1A2 3471/4885CYP2C19 4166/4885CYP3A4 3495/4885

“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.