SCHEMBL6910192

SCHEMBL6910192

COC(=O)c1ccc(C2=C3C=CC(=N3)C(c3ccc(C(=O)OC)cc3)=C3C=CC(=N3)C(c3ccc(C(=O)OC)cc3)=C3C=CC(=N3)C(c3ccc(C(=O)OC)cc3)=C3C=CC2=N3)cc1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CA1 P00915 4/20 0.46
▸ CA2 P00918 4/20 0.46
▸ CA12 O43570 3/20 0.46
▸ CA9 Q16790 3/20 0.46
▸ CA14 Q9ULX7 3/20 0.46
▸ TDP1 Q9NUW8 1/20 0.46
▸ CA7 P43166 1/20 0.46
▸ ALDH1A1 P00352 7/20 0.45
▸ KDM4E B2RXH2 5/20 0.45
▸ SETD7 Q8WTS6 1/20 0.45
▸ ERN1 O75460 1/20 0.43
▸ TSHR P16473 1/20 0.43
▸ MAPT P10636 5/20 0.42
▸ LMNA P02545 2/20 0.42
▸ MEN1 O00255 1/20 0.42
▸ GAA P10253 1/20 0.42
▸ KMT2A Q03164 1/20 0.42
▸ HPGD P15428 4/20 0.42
▸ SMN1; SMN2 Q16637 4/20 0.42
▸ LOXL2 Q9Y4K0 1/20 0.41

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
SCHEMBL19718104 0.94 TSHR (0.42) CA1CA2CA12CA9CA14
SCHEMBL6686810 0.94 TSHR (0.50) ALDH1A1KDM4ETSHRMAPTLMNA
SCHEMBL80100 0.87 TDP1 (0.42) CA1CA2CA12CA9CA14
SCHEMBL1410169 0.84 SMN1; SMN2 (0.44) TDP1ALDH1A1KDM4ESETD7TSHR
SCHEMBL18039303 0.83 SETD7 (0.39) CA1CA2CA12CA9CA14
SCHEMBL2318543 0.83 MAPT (0.43) ALDH1A1MAPTMEN1KMT2ASMN1; SMN2
SCHEMBL2342869 0.83 MAPT (0.43) ALDH1A1MAPTMEN1KMT2ASMN1; SMN2
SCHEMBL1517330 0.82 ALDH1A1 (0.38) CA1CA2CA12CA9CA14
SCHEMBL28349555 0.81 SETD7 (0.40) ALDH1A1KDM4ESETD7TSHRMAPT
SCHEMBL19718139 0.80 MAPK1 (0.54) CA1CA2ALDH1A1KDM4ELMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12565426-B2 Photothermal catalytic method for production of hydrogen peroxide without sacrificial reagents on basis of porphyrin-based supermolecule JIANGNAN UNIVERSITY (CN) 2026-03-03 — — US claimed
US-20220340423-A1 Photothermal Catalytic Method for Production of Hydrogen Peroxide without Sacrificial Reagents on Basis of Porphyrin-based Supermolecule JIANGNAN UNIVERSITY (CN) 2022-10-27 — — US claimed
US-12565426-B2 Photothermal catalytic method for production of hydrogen peroxide without sacrificial reagents on basis of porphyrin-based supermolecule JIANGNAN UNIVERSITY (CN) 2026-03-03 — — US disclosed
US-20220340423-A1 Photothermal Catalytic Method for Production of Hydrogen Peroxide without Sacrificial Reagents on Basis of Porphyrin-based Supermolecule JIANGNAN UNIVERSITY (CN) 2022-10-27 — — US disclosed
CN-106432366-A Preparation and application of nano metal-organic framework material PCN-223 based on porphyrin ligand 哈尔滨理工大学 2017-02-22 — — CN disclosed
WO-2016135180-A1 PHOTOSENSITIZER UNIVERSITEIT VAN AMSTERDAM (NL) 2016-09-01 — — WO disclosed
EP-3061762-A1 PHOTOSENSITIZERS Universiteit van Amsterdam (NL) 2016-08-31 — — EP disclosed
WO-2015177511-A1 METHOD OF PREPARING A METAL ORGANIC FRAMEWORK THE TEXAS A&M UNIVERSITY SYSTEM (US) 2015-11-26 — — WO disclosed
US-20040076585-A1 Nanoparticles of cyclic tetrapyrrolic compounds as gene and drug delivery carriers GONG XIANCHANG (US) 2004-04-22 — — 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 (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-12565426-B2 Photothermal catalytic method for production of hydrogen peroxide without sacrificial reagents on basis of porphyrin-based supermolecule TPO, PPOX, THPO CA1 1180/4885CA2 1133/4885CA12 2189/4885
US-20040076585-A1 Nanoparticles of cyclic tetrapyrrolic compounds as gene and drug delivery carriers CCDC6, CCDC47, ABCB1 CA1 717/4885CA2 372/4885CA12 952/4885

“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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