SCHEMBL249200

SCHEMBL249200

Oc1cccc(C2=C3C=CC(=N3)C(c3cccc(O)c3)=C3C=CC(=N3)C(c3cccc(O)c3)=C3C=CC(=N3)C(c3cccc(O)c3)=C3C=CC2=N3)c1

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ HSD17B1 P14061 12/20 0.47
▸ HSD17B2 P37059 11/20 0.47
▸ CYP3A4 P08684 3/20 0.47
▸ CYP2C9 P11712 2/20 0.47
▸ ESR1 P03372 2/20 0.40
▸ ESR2 Q92731 2/20 0.40
▸ CYP1A2 P05177 1/20 0.40
▸ CYP2D6 P10635 1/20 0.40
▸ CYP2B6 P20813 1/20 0.40
▸ CYP2C19 P33261 1/20 0.40
▸ CA12 O43570 1/20 0.39
▸ ALDH1A1 P00352 1/20 0.39
▸ CA2 P00918 1/20 0.39
▸ LMNA P02545 1/20 0.39
▸ CA5A P35218 1/20 0.39
▸ CA9 Q16790 1/20 0.39
▸ HSD17B10 Q99714 1/20 0.39
▸ CA14 Q9ULX7 1/20 0.39
▸ CA5B Q9Y2D0 1/20 0.39
▸ PIK3CG P48736 1/20 0.39

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
SCHEMBL4412721 0.95 HSD17B1 (0.43) HSD17B1HSD17B2CYP3A4CYP2C9ESR1
SCHEMBL4411533 0.95 HSD17B1 (0.43) HSD17B1HSD17B2CYP3A4CYP2C9ESR1
SCHEMBL4411632 0.95 HSD17B1 (0.43) HSD17B1HSD17B2CYP3A4CYP2C9ESR1
SCHEMBL17651780 0.88 HSD17B1 (0.38) HSD17B1HSD17B2CYP3A4CYP2C9ESR1
SCHEMBL17651814 0.88 HSD17B1 (0.38) HSD17B1HSD17B2CYP3A4CYP2C9ESR1
SCHEMBL5100896 0.84 CHRNB4 (0.38) HSD17B1HSD17B2CYP3A4CYP2C9ESR1
SCHEMBL584790 0.83 HSD17B1 (0.37) HSD17B1HSD17B2CYP3A4CYP2C9ESR1
SCHEMBL5104039 0.82 CHRNB4 (0.38) HSD17B1HSD17B2CYP3A4CYP2C9ESR1
SCHEMBL15522569 0.80 BACE1 (0.35) —
SCHEMBL2337738 0.80 GCGR (0.40) HSD17B1HSD17B2CYP3A4ESR1ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1600766-B1 ACTIVE OXYGEN SPECIES MEASURING DEVICE YUASA MAKOTO (JP) 2019-06-26 — — EP claimed
US-9867800-B2 Method of quenching singlet and triplet excited states of pigments, such as porphyrin compounds, particularly protoporphyrin IX, with conjugated fused tricyclic compounds have electron withdrawing groups, to reduce generation of reactive oxygen species, particularly singlet oxygen HALLSTAR INNOVATIONS CORP. (US) 2018-01-16 — — US claimed
US-20150164852-A1 METHOD OF QUENCHING SINGLET AND TRIPLET EXCITED STATES OF PIGMENTS, SUCH AS PORPHYRIN COMPOUNDS, PARTICULARLY PROTOPORPHYRIN IX, WITH CONJUGATED FUSED TRICYCLIC COMPOUNDS HAVE ELECTRON WITHDRAWING GROUPS, TO REDUCE GENERATION OF REACTIVE OXYGEN SPECIES, PARTICULARLY SINGLET OXYGEN HALLSTAR INNOVATIONS CORP. (US) 2015-06-18 — — US claimed
WO-2014025370-A1 TRICYCLIC ENERGY QUENCHER COMPOUNDS FOR REDUCING SINGLET OXYGEN GENERATION HALLSTAR INNOVATIONS CORP. (US) 2014-02-13 — — WO claimed
US-8298387-B2 Reactive oxygen species measuring device YUASA MAKOTO (JP) 2012-10-30 — — US claimed
WO-2012000610-A1 COMPLEXES WITH POLYSTYRENE SULFONATE Universität des Saarlandes (DE) 2012-01-05 — — WO claimed
US-20110275686-A1 NANOPARTICLE CARRIER SYSTEMS BASED ON POLY(DL-LACTIC-CO-GLYCOLIC ACID) (PLGA) FOR PHOTODYNAMIC THERAPY (PDT) BIOLITEC, INC. 2011-11-10 — — US claimed
US-20110142948-A1 Nanoparticle Carrier Systems based on Human Serum Albumin for Photodynamic Therapy BIOLITEC, INC. 2011-06-16 — — US claimed
US-20060289313-A1 Reactive oxygen species measuring device YUASA MAKOTO 2006-12-28 — — US claimed
EP-1600766-A1 ACTIVE OXYGEN SPECIES MEASURING DEVICE Yuasa, Makoto (JP) 2005-11-30 — — EP claimed
US-12071498-B2 Radically polymerizable compositions Polynt Composites USA, Inc. (US) 2024-08-27 — — US disclosed
US-11873306-B1 Nano-sized 5,10,15,20-tetrakis (4-hydroxyphenyl)-porphyrins pd(II) complex for super medicinal applications King Faisal University (SA) 2024-01-16 — — US disclosed
EP-2856109-B1 LIGHTING SYSTEMS AND METHODS OF USING LIGHTING SYSTEMS FOR IN VITRO POTENCY ASSAY FOR PHOTOFRIN CONCORDIA LABORATORIES INC (BB) 2023-09-06 — — EP disclosed
US-20230257500-A1 RADICALLY POLYMERIZABLE COMPOSITIONS BNY MELLON CORPORATE TRUSTEE SERVICES LIMITED, AS SECURITY AGENT (GB) 2023-08-17 — — US disclosed
US-11518834-B2 Radically polymerizable compositions Polynt Composites USA, Inc. (US) 2022-12-06 — — US disclosed
WO-1994019352-A1 MESO-TETRAPHENYL PORPHYRIN COMPLEX COMPOUNDS, PROCESS FOR PREPARING THE SAME AND PHARMACEUTICALS CONTAINING THE SAME Institut für Diagnostikforschung GmbH an der Freien Universität Berlin (DE) 1994-09-01 — — WO disclosed
EP-0337601-B1 PORPHYRINS AND MEDICAMENTS FOR CANCER TREATMENT SCOTIA HOLDINGS PLC (GB) 1993-05-05 — — EP disclosed
US-5162519-A Porphyrins and cancer treatment EFAMOL HOLDINGS PLC (GB) 1992-11-10 — — US disclosed
US-4992257-A Dihydroporphyrins and method of treating tumors EFAMOL HOLDINGS PLC (GB) 1991-02-12 — — US disclosed
EP-0337601-A1 Porphyrins and medicaments for cancer treatment SCOTIA HOLDINGS PLC (GB) 1989-10-18 — — EP 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-11873306-B1 Nano-sized 5,10,15,20-tetrakis (4-hydroxyphenyl)-porphyrins pd(II) complex for super medicinal applications COX15, HMBS, MT-ND5 HSD17B1 2003/4885HSD17B2 1405/4885CYP3A4 907/4885
US-20150164852-A1 METHOD OF QUENCHING SINGLET AND TRIPLET EXCITED STATES OF PIGMENTS, SUCH AS PORPHYRIN COMPOUNDS, PARTICULARLY PROTOPORPHYRIN IX, WITH CONJUGATED FUSED TRICYCLIC COMPOUNDS HAVE ELECTRON WITHDRAWING GROUPS, TO REDUCE GENERATION OF REACTIVE OXYGEN SPECIES, PARTICULARLY SINGLET OXYGEN NOX3, CBR3, CCR3 HSD17B1 2184/4885HSD17B2 2303/4885CYP3A4 1491/4885
US-20110275686-A1 NANOPARTICLE CARRIER SYSTEMS BASED ON POLY(DL-LACTIC-CO-GLYCOLIC ACID) (PLGA) FOR PHOTODYNAMIC THERAPY (PDT) MTHFD1, DLD, HPD HSD17B1 1923/4885HSD17B2 2134/4885CYP3A4 3175/4885
US-20110142948-A1 Nanoparticle Carrier Systems based on Human Serum Albumin for Photodynamic Therapy ALB, HPN, TTR HSD17B1 3835/4885HSD17B2 3784/4885CYP3A4 1803/4885

“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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