SCHEMBL245938

SCHEMBL245938

C1=CC2=C(c3ccncc3)C3=NC(=C(c4ccncc4)C4=NC(=C(c5ccncc5)C5=NC(=C(c6ccncc6)C1=N2)C=C5)C=C4)C=C3

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ MAPT P10636 4/20 0.43
▸ LMNA P02545 1/20 0.43
▸ NOTUM Q6P988 1/20 0.37
▸ HDAC8 Q9BY41 1/20 0.35
▸ TP53 P04637 2/20 0.33
▸ PKM P14618 1/20 0.33
▸ DDAH1 O94760 1/20 0.33
▸ NOS1 P29475 1/20 0.33
▸ SMN1; SMN2 Q16637 2/20 0.32
▸ NPC1 O15118 1/20 0.32
▸ ALDH1A1 P00352 1/20 0.32
▸ RAB9A P51151 1/20 0.32
▸ MAPK10 P53779 1/20 0.32
▸ HSD17B10 Q99714 1/20 0.32
▸ KIF11 P52732 2/20 0.32
▸ KDM4E B2RXH2 1/20 0.32
▸ CYP1A2 P05177 1/20 0.32
▸ CYP3A4 P08684 1/20 0.32
▸ CYP2D6 P10635 1/20 0.32
▸ CYP2C9 P11712 1/20 0.32

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
SCHEMBL14080751 0.92 NOTUM (0.52) MAPTLMNANOTUMTP53SMN1; SMN2
SCHEMBL27838898 0.92 NOTUM (0.52) MAPTLMNANOTUMTP53SMN1; SMN2
SCHEMBL6493307 0.89 NPC1 (0.40) MAPTLMNATP53SMN1; SMN2NPC1
SCHEMBL9582303 0.89 RPS6KA3 (0.43) MAPTLMNATP53PKMSMN1; SMN2
SCHEMBL8187863 0.89 NPC1 (0.40) MAPTLMNATP53SMN1; SMN2NPC1
SCHEMBL7247277 0.89 CYP3A4 (0.42) MAPTLMNATP53SMN1; SMN2NPC1
SCHEMBL7050896 0.86 LMNA (0.32) MAPTLMNAMAPK14
SCHEMBL6766121 0.86 LMNA (0.32) MAPTLMNAMAPK14
SCHEMBL6763644 0.86 LMNA (0.32) MAPTLMNAMAPK14
SCHEMBL7258058 0.80 P2RY6 (0.35) —

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 116 patents — showing the first 20. 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
EP-4288415-A1 PYRIDINIUM DERIVATIVES MADE BY HYDROTHERMAL SYNTHESIS FOR USE AS ANOLYTES IN ELECTROCHEMICAL CELLS Wisconsin Alumni Research Foundation (US) 2023-12-13 — — EP claimed
US-20230060532-A1 METAL-ORGANIC FRAMEWORK COATED ORGANIC FIELD EFFECT TRANSISTOR BASED NO2 SENSOR AND METHOD KING ABDULLAH UNIVERSITY OF SCIENCE AND TECHNOLOGY (SA) 2023-03-02 — — US claimed
US-20220363663-A1 PYRIDINIUM DERIVATIVES MADE BY HYDROTHERMAL SYNTHESIS FOR USE AS ANOLYTES IN ELECTROCHEMICAL CELLS WISCONSIN ALUMNI RESEARCH FOUNDATION 2022-11-17 — — US claimed
WO-2022236241-A1 PYRIDINIUM DERIVATIVES MADE BY HYDROTHERMAL SYNTHESIS FOR USE AS ANOLYTES IN ELECTROCHEMICAL CELLS WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 2022-11-10 — — WO 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
WO-2021156733-A1 METAL-ORGANIC FRAMEWORK COATED ORGANIC FIELD EFFECT TRANSISTOR BASED NO2 SENSOR AND CORRESPONDING FABRICATION METHOD KING ABDULLAH UNIVERSITY OF SCIENCE AND TECHNOLOGY (SA) 2021-08-12 — — WO claimed
US-20170143633-A1 NANOPARTICLES, METHOD OF PREPARING THE SAME AND THEIR USE CITY UNIVERSITY OF HONG KONG (HK) 2017-05-25 — — US claimed
US-9287568-B2 High performance, high durability non-precious metal fuel cell catalysts 3M INNOVATIVE PROPERTIES COMPANY (US) 2016-03-15 — — US claimed
US-20110319257-A1 HIGH PERFORMANCE, HIGH DURABILITY NON-PRECIOUS METAL FUEL CELL CATALYSTS 3M INNOVATIVE PROPERTIES COMPANY 2011-12-29 — — US claimed
US-4987226-A CATALYSTS FOR EPOXIDATION OF OLEFINS WITH HYDROGEN PEROXIDE DEGUSSA AKTIENGESELLSCHAFT (DE) 1991-01-22 — — US claimed
US-4973718-A RHENIUM PROPHYRIN CATALYST DEGUSSA AKTIENGESELLSCHAFT (DE) 1990-11-27 — — US claimed
EP-0308791-B1 PROCESS FOR THE CATALYTIC EPOXYDATION OF OLEFINS WITH HYDROGEN PEROXIDE Degussa Aktiengesellschaft (DE) 1990-11-14 — — EP claimed
EP-0283753-B1 PROCESS FOR THE CATALYTIC EPOXIDATION OF OLEFINS WITH HYDROGEN PEROXIDE Degussa Aktiengesellschaft (DE) 1990-09-19 — — EP claimed
US-4845252-A COMPLEX TUNGSTEN CATALYST DEGUSSA AKTIENGESELLSCHAFT (DE) 1989-07-04 — — US claimed
EP-0308790-A2 Rhenium-oxo-porphyrin complexes Degussa Aktiengesellschaft (DE) 1989-03-29 — — EP claimed
EP-0308791-A1 Process for the catalytic epoxydation of olefins with hydrogen peroxide Degussa Aktiengesellschaft (DE) 1989-03-29 — — EP claimed
EP-0283753-A1 Process for the catalytic epoxidation of olefins with hydrogen peroxide Degussa Aktiengesellschaft (DE) 1988-09-28 — — EP claimed
EP-0283754-A2 Tungsten oxo-porphyrin complexes Degussa Aktiengesellschaft (DE) 1988-09-28 — — EP claimed
EP-0222167-A2 Process for the catalytic epoxidation of olefines with hydrogen peroxide Degussa Aktiengesellschaft (DE) 1987-05-20 — — EP claimed

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-20220363663-A1 PYRIDINIUM DERIVATIVES MADE BY HYDROTHERMAL SYNTHESIS FOR USE AS ANOLYTES IN ELECTROCHEMICAL CELLS PDXK, PNPO, ANO2 MAPT 2168/4885LMNA 2300/4885NOTUM 1455/4885
US-12565426-B2 Photothermal catalytic method for production of hydrogen peroxide without sacrificial reagents on basis of porphyrin-based supermolecule TPO, PPOX, THPO MAPT 2755/4885LMNA 3735/4885NOTUM 2842/4885

“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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