SCHEMBL254903

SCHEMBL254903

Cc1cccc(-c2ccccn2)n1

nearest known ligand 0.71

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 6/20 0.71
CCR1 P32246 4/20 0.71
CCR8 P51685 4/20 0.71
TP53 P04637 4/20 0.71
LMNA P02545 3/20 0.71
CCR5 P51681 3/20 0.71
SMN1; SMN2 Q16637 3/20 0.71
TDP1 Q9NUW8 3/20 0.71
ALPL P05186 2/20 0.71
ALOX15 P16050 2/20 0.71
HTT P42858 2/20 0.71
L3MBTL1 Q9Y468 2/20 0.71
HSP90AA1 P07900 1/20 0.71
ALPI P09923 1/20 0.71
ALPG P10696 1/20 0.71
MAPK1 P28482 1/20 0.71
POLB P06746 2/20 0.61
CYP1A2 P05177 1/20 0.61
METAP1 P53582 1/20 0.61
BLM P54132 1/20 0.61

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
SCHEMBL29595637 1.00 KDM4E (0.71) KDM4ECCR1CCR8TP53LMNA
SCHEMBL14255745 0.98 KDM4E (0.75) KDM4ECCR1CCR8TP53LMNA
Dipyridyl SCHEMBL28273724 0.93 KDM4E (0.67) KDM4ECCR1CCR8TP53LMNA
SCHEMBL1456375 0.92 KDM4E (0.67) KDM4ECCR1CCR8TP53LMNA
SCHEMBL19009236 0.84 CCR1 (0.54) KDM4ECCR1CCR8TP53LMNA
Terpyridine SCHEMBL30610403 0.84 KDM4E (0.90) KDM4ECCR1CCR8TP53LMNA
SCHEMBL7964803 0.84 KDM4E (1.00) KDM4ECCR1CCR8TP53LMNA
Hydrochloric Acid SCHEMBL2410509 0.84 CCR1 (0.89) KDM4ECCR1CCR8TP53LMNA
Terpyridine SCHEMBL57442 0.84 KDM4E (1.00) KDM4ECCR1CCR8TP53LMNA
SCHEMBL30172832 0.84 KDM4E (1.00) KDM4ECCR1CCR8TP53LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230167144-A1 PREPARATION AND ITS APPLICATION OF A CYANIDE-BRIDGED METAL ORGANIC COMPOUND WITH INTRAMOLECULAR MAGNETIC TRANSFORMATION Hubei Jingmen Industrial Technology Research Institute Co., Ltd. (CN) 2023-06-01 US claimed
CN-112500411-B Preparation method of 1,1 '-ethylene-2, 2' -bipyridyl dichloride salt 南京红太阳生物化学有限责任公司 2023-03-14 CN claimed
CN-115595634-A Cyanide-free gold plating solution containing Ru coordination compound and gold plating method 广东工业大学(CN) 2023-01-13 CN claimed
CN-112500411-A Preparation method of 1,1 '-ethylene-2, 2' -bipyridyl dichloride salt 南京红太阳生物化学有限责任公司 2021-03-16 CN claimed
CN-110416586-B Iron-based flow battery, positive and negative electrolyte thereof and preparation method 江西理工大学 2020-09-11 CN claimed
CN-111518145-A Cyanide-bridged metal organic compound with intramolecular magnetic transformation, and preparation method and application thereof 荆楚理工学院 2020-08-11 CN claimed
CN-110416586-A Iron-based flow battery and its positive and negative anodes electrolyte and preparation method UNIV JIANGXI SCI & TECHNOLOGY 2019-11-05 CN claimed
CN-105669689-B A kind of preparation and application of the mercury ion fluorescence probe compound based on rhodamine B 济南大学 2017-12-12 CN claimed
CN-105669689-A Preparation and application of mercury ion fluorescent probe compound based on rhodamine B 济南大学 2016-06-15 CN claimed
EP-2586893-A2 Copper plating bath and method Rohm and Haas Electronic Materials LLC (US) 2013-05-01 EP claimed
US-20250223418-A1 VALUE CHAIN RETURN PROCESS FOR THE RECOVERY OF PHOSPHOROUS ESTER-BASED FLAME RETARDANTS FROM POLYURETHANE RIGID FOAMS BASF SE (DE) 2025-07-10 US disclosed
US-20240376044-A1 METHOD FOR PREPARING AROMATIC AMINO ACID DERIVATIVE CHUGAI PHARMACEUTICAL CO LTD (JP) 2024-11-14 US disclosed
US-12071396-B2 Method for preparing aromatic amino acid derivative CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2024-08-27 US disclosed
WO-2024132695-A1 CONVERSION OF A BIOMASS-DERIVED HYDROCARBON FEEDSTOCK TO PRODUCE ADIPIC ACID IFP Energies Nouvelles (FR) 2024-06-27 WO disclosed
CN-114436996-B Beta-form2Process for the preparation of amino acid derivatives 华中科技大学 2024-05-10 CN disclosed
US-6187928-B1 TREATING FUNGAL DISEASES THE ROCKEFELLER UNIVERSITY 2001-02-13 US disclosed
US-6087510-A Method of use of imidazolium cations THE ROCKEFELLER UNIVERSITY (US) 2000-07-11 US disclosed
US-5969150-A FLUORESCENT COMPOUNDS FOR MEDICAL DIAGNOSIS, DRUGS AND LABELS OR FUNGICIDES AND VIRICIDES THE ROCKEFELLER UNIVERSITY (US) 1999-10-19 US disclosed
US-5874587-A FLUORESCENCE THE ROCKEFELLER UNIVERSITY (US) 1999-02-23 US disclosed
EP-0423866-A1 Phosphorous compounds SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) 1991-04-24 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 (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-20250223418-A1 VALUE CHAIN RETURN PROCESS FOR THE RECOVERY OF PHOSPHOROUS ESTER-BASED FLAME RETARDANTS FROM POLYURETHANE RIGID FOAMS HNRNPC, RFC2, PUF60 KDM4E 1100/4885CCR1 1969/4885CCR8 1053/4885
US-20240376044-A1 METHOD FOR PREPARING AROMATIC AMINO ACID DERIVATIVE DDC, AADAT, TYR KDM4E 626/4885CCR1 4144/4885CCR8 3602/4885
US-12071396-B2 Method for preparing aromatic amino acid derivative DDC, AADAT, TYR KDM4E 626/4885CCR1 4144/4885CCR8 3602/4885

“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.