SCHEMBL6035356

SCHEMBL6035356

CCOC(=O)C1=C2C=CC(=N2)C(C(=O)OCC)=C2C=CC(=N2)C(C(=O)OCC)=C2C=CC(=N2)C(C(=O)OCC)=C2C=CC1=N2

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CYP1A2 P05177 2/20 0.42
▸ TSHR P16473 1/20 0.41
▸ MAPT P10636 3/20 0.41
▸ MEN1 O00255 2/20 0.41
▸ KMT2A Q03164 2/20 0.41
▸ FGFR1 P11362 1/20 0.40
▸ FLT1 P17948 1/20 0.40
▸ FGFR3 P22607 1/20 0.40
▸ CA12 O43570 3/20 0.39
▸ CA1 P00915 3/20 0.39
▸ CA2 P00918 3/20 0.39
▸ CA7 P43166 3/20 0.39
▸ CA9 Q16790 3/20 0.39
▸ CA14 Q9ULX7 3/20 0.39
▸ ESR1 P03372 1/20 0.39
▸ ESR2 Q92731 1/20 0.39
▸ LMNA P02545 2/20 0.38
▸ NR1H2 P55055 1/20 0.38
▸ NR1H3 Q13133 1/20 0.38
▸ CYP3A4 P08684 1/20 0.38

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
SCHEMBL7413745 0.86 ALDH1A1 (0.44) CYP1A2TSHRMAPTESR1LMNA
SCHEMBL7415710 0.83 TSHR (0.47) CYP1A2TSHRESR1LMNANR1H2
SCHEMBL6421365 0.79 NPSR1 (0.38) TSHRMAPTFGFR1FGFR3CA12
SCHEMBL7411501 0.74 ALDH1A1 (0.35) TSHRMAPTESR1LMNAALDH1A1
SCHEMBL7418768 0.73 TSHR (0.38) CYP1A2TSHRESR1LMNANR1H2
SCHEMBL6687802 0.69 RARA (0.51) CYP1A2TSHRMAPTMEN1KMT2A
SCHEMBL6439546 0.68 — —
SCHEMBL9626490 0.66 ALDH1A1 (0.49) CYP1A2TSHRMAPTMEN1KMT2A
SCHEMBL4921789 0.63 CYP1A2 (0.46) CYP1A2TSHRMEN1KMT2ACA12
SCHEMBL11008658 0.62 ALDH1A1 (0.62) TSHRMAPTKMT2ACA12CA1

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 13 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10646595-B2 Porphyrin compounds and their use as MRI contrast agents THE GOVERNING COUNCIL OF THE UNIVERSITY OF TORONTO (CA) 2020-05-12 — — US disclosed
US-20160235866-A1 MRI CONTRAST AGENTS FOR CELL LABELING THE GOVERNING COUNCIL OF THE UNIVERSITY OF TORONTO (CA) 2016-08-18 — — US disclosed
WO-2015048912-A1 MRI CONTRAST AGENTS FOR CELL LABELING THE GOVERNING COUNCIL OF THE UNIVERSITY OF TORONTO (CA) 2015-04-09 — — WO disclosed
US-20140227196-A1 PORPHYRIN COMPOUNDS AND THEIR USE AS MRI CONTRAST AGENTS THE HOSPITAL FOR SICK CHILDREN (CA) 2014-08-14 — — US disclosed
US-20060128944-A1 Molecular linkers suitable for crystallization and structural analysis of molecules of interest, method of using same, and methods of purifying g protein-coupled receptors YEDA RESEARCH AND DEVELOPMENT CO. LTD. AT THE WEIZMANN INSTRITUTE OF SCIENCE 2006-06-15 — — US disclosed
EP-1071474-B1 SUBSTITUTED PORPHYRINS UNIV DUKE (US) 2005-11-30 — — EP disclosed
EP-1478658-A2 MOLECULAR LINKERS SUITABLE FOR CRYSTALLIZATION AND STRUCTURAL ANALYSIS OF MOLECULES OF INTEREST, METHOD OF USING SAME, AND METHODS OF PURIFYING G PROTEIN-COUPLED RECEPTORS YEDA RESEARCH AND DEVELOPMENT Co. LTD. (IL) 2004-11-24 — — EP disclosed
WO-2003016330-A2 MOLECULAR LINKERS SUITABLE FOR CRYSTALLIZATION AND STRUCTURAL ANALYSIS OF MOLECULES OF INTEREST, METHOD OF USING SAME, AND METHODS OF PURIFYING G PROTEIN-COUPLED RECEPTORS YEDA RESEARCH AND DEVELOPMENT CO. LTD. (IL) 2003-02-27 — — WO disclosed
US-6479477-B1 SUITABLE FOR USE IN MODULATING INTRA- AND EXTRACELLULAR PROCESSES IN WHICH SUPEROXIDE RADICALS, OR OTHER OXIDANTS SUCH AS HYDROGEN PEROXIDE OR PEROXYNITRITE, ARE A PARTICIPANT DUKE UNIVERSITY 2002-11-12 — — US disclosed
EP-1071474-A4 SUBSTITUTED PORPHYRINS UNIV DUKE (US) 2002-10-24 — — EP disclosed
EP-1071474-A1 SUBSTITUTED PORPHYRINS DUKE UNIVERSITY (US) 2001-01-31 — — EP disclosed
WO-1999055388-A9 SUBSTITUTED PORPHYRINS UNIV DUKE (US) 2000-01-27 — — WO disclosed
WO-1999055388-A1 SUBSTITUTED PORPHYRINS DUKE UNIVERSITY (US) 1999-11-04 — — 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 (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-20160235866-A1 MRI CONTRAST AGENTS FOR CELL LABELING MPI, HMBS, TSPO CYP1A2 1483/4885TSHR 3333/4885MAPT 3289/4885
US-20140227196-A1 PORPHYRIN COMPOUNDS AND THEIR USE AS MRI CONTRAST AGENTS PML, HMBS, PPOX CYP1A2 2669/4885TSHR 4312/4885MAPT 211/4885
US-10646595-B2 Porphyrin compounds and their use as MRI contrast agents PML, HMBS, PPOX CYP1A2 2669/4885TSHR 4312/4885MAPT 211/4885

“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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