SCHEMBL4315032

SCHEMBL4315032

N#Cc1ccc(Oc2ccc(O)cc2)cc1

nearest known ligand 0.73

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CA12 O43570 1/20 0.73
▸ CA2 P00918 1/20 0.73
▸ CA3 P07451 1/20 0.73
▸ CA6 P23280 1/20 0.73
▸ CA9 Q16790 1/20 0.73
▸ CA14 Q9ULX7 1/20 0.73
▸ MMP3 P08254 1/20 0.64
▸ MEN1 O00255 2/20 0.64
▸ KMT2A Q03164 2/20 0.64
▸ ESR1 P03372 1/20 0.64
▸ ESR2 Q92731 1/20 0.64
▸ PARP10 Q53GL7 2/20 0.58
▸ PARP15 Q460N3 1/20 0.58
▸ PARP2 Q9UGN5 1/20 0.58
▸ KDM4E B2RXH2 1/20 0.56
▸ LMNA P02545 1/20 0.56
▸ POLB P06746 1/20 0.56
▸ MAPT P10636 1/20 0.56
▸ PKM P14618 1/20 0.56
▸ MAPK1 P28482 1/20 0.56

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
P-Cresol SCHEMBL29176413 0.90 ALDH1A1 (0.59) CA12CA2CA3CA6CA9
Mequinol SCHEMBL6185858 0.90 LTA4H (0.70) CA12CA2CA3CA6CA9
SCHEMBL7041250 0.88 PARP15 (0.63) CA12CA2CA3CA6CA9
SCHEMBL8852392 0.88 PARP15 (0.63) CA12CA2CA3CA6CA9
SCHEMBL28781661 0.86 PARP10 (0.63) CA12CA2CA3CA6CA9
4-Cyanophenol SCHEMBL50814 0.85 — —
4-Cyanophenol SCHEMBL27294505 0.85 CA2 (1.00) CA12CA2CA3CA6CA9
4-Cyanophenol SCHEMBL28811803 0.85 CA2 (1.00) CA12CA2CA3CA6CA9
SCHEMBL1897244 0.85 CA12 (0.52) CA12CA2CA3CA6CA9
4-Cyanophenol SCHEMBL7393582 0.83 CA2 (0.94) CA12CA2CA3CA6CA9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-59020292-A — — None — — JP disclosed
CN-115536586-B Pyrazole amide compound as well as preparation method and application thereof 华东理工大学 2024-08-09 — — CN disclosed
CN-118290298-A Benzoyl hydrazine compound and synthetic method and application thereof 南京农业大学 2024-07-05 — — CN disclosed
CN-115536586-A Pyrazole amide compounds and preparation method and application thereof 华东理工大学 2022-12-30 — — CN disclosed
CN-101312948-B Biaryl substituted heterocycle inhibitors of lTA4H for treating inflammation DECODE GENETICS EHF 2015-01-14 — — CN disclosed
EP-1926708-B1 BIARYL SUBSTITUTED HETEROCYCLE INHIBITORS OF LTA4H FOR TREATING INFLAMMATION DECODE GENETICS EHF (IS) 2014-06-18 — — EP disclosed
US-8598359-B2 Biaryl substituted heterocycle inhibitors of LTA4H for treating inflammation DECODE GENETICS EHF (IS) 2013-12-03 — — US disclosed
US-20090163462-A1 BIARYL SUBSTITUTED HETEROCYCLE INHIBITORS OF LTA4H FOR TREATING INFLAMMATION DECODE GENETICS, EHF (IS) 2009-06-25 — — US disclosed
US-7402684-B2 Biaryl substituted heterocycle inhibitors of LTA4H for treating inflammation DECODE GENECTICS EHF. (IS) 2008-07-22 — — US disclosed
EP-1926708-A1 BIARYL SUBSTITUTED HETEROCYCLE INHIBITORS OF LTA4H FOR TREATING INFLAMMATION Decode Chemistry, Inc. (US) 2008-06-04 — — EP disclosed
US-20040006057-A1 Triaryl-oxy-aryloxy-pyrimidine-2,4,6-trione metalloproteinase inhibitors PFIZER PRODUCTS INC. 2004-01-08 — — US disclosed
WO-2003090752-A1 TRIARYL-OXY-ARYLOXY-PYRIMIDINE-2,4,6-TRIONE METALLOPROTEINASE INHIBITORS PFIZER PRODUCTS INC. (US) 2003-11-06 — — WO disclosed
US-6242654-B1 REACTING A PHENOLATE COMPOUND WITH AN ORGANIC FLUORINATING AGENT TO PREPARE A FLUORINE SUBSTITUTED AROMATIC COMPOUND MITSUI CHEMICALS, INC. (JP) 2001-06-05 — — US disclosed
EP-1013629-A1 Preparation process of fluorine subsituted aromatic compound Mitsui Chemicals, Inc. (JP) 2000-06-28 — — EP disclosed
EP-0303415-B1 Herbicidally active phenoxy-alkanecarboxylic acid derivatives SUNTORY LTD (JP) 1994-11-30 — — EP disclosed
US-5205855-A Postemergence, preemergence herbicides SUNTORY LIMITED (JP) 1993-04-27 — — US disclosed
US-4976773-A SELECTIVITY BETWEEN MONOCOYLEDON PLANTS SUNTORY LIMITED (JP) 1990-12-11 — — US disclosed
EP-0303415-A2 Herbicidally active phenoxy-alkanecarboxylic acid derivatives SUNTORY LIMITED (JP) 1989-02-15 — — EP disclosed
US-4608081-A SELECTIVITY AGAINST GRASSES KANESHO COMPANY LIMITED (JP) 1986-08-26 — — US disclosed
JP-S5920292-A ORGANIC PHOSPHORIC ESTER COMPOUND, ITS PREPARATION, INSECTICIDE AND ACARICIDE CONTAINING IT AS ACTIVE INGREDIENT KANESHO KK 1984-02-01 — — JP 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-20040006057-A1 Triaryl-oxy-aryloxy-pyrimidine-2,4,6-trione metalloproteinase inhibitors MMP8, MMP9, MMP1 CA12 3394/4885CA2 848/4885CA3 1719/4885
US-20090163462-A1 BIARYL SUBSTITUTED HETEROCYCLE INHIBITORS OF LTA4H FOR TREATING INFLAMMATION LTA4H, LTB4R, LTC4S CA12 4856/4885CA2 4722/4885CA3 4715/4885

“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.

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