Dipyridyl

Dipyridyl

SCHEMBL498031

[Pt].c1ccc(-c2ccccn2)nc1

nearest known ligand 0.93

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 9/20 0.93
LMNA P02545 3/20 0.93
CCR1 P32246 3/20 0.93
CCR5 P51681 3/20 0.93
CCR8 P51685 3/20 0.93
CYP1A2 P05177 1/20 0.93
POLB P06746 1/20 0.93
METAP1 P53582 1/20 0.93
BLM P54132 1/20 0.93
HIF1A Q16665 1/20 0.93
DOHH Q9BU89 1/20 0.93
P4HTM Q9NXG6 1/20 0.93
NPC1 O15118 6/20 0.74
TP53 P04637 4/20 0.74
RAB9A P51151 4/20 0.74
ALOX15 P16050 3/20 0.74
SMN1; SMN2 Q16637 3/20 0.74
L3MBTL1 Q9Y468 3/20 0.74
HTT P42858 2/20 0.74
TDP1 Q9NUW8 2/20 0.74

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
Dipyridyl SCHEMBL8944330 1.00 KDM4E (0.93) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL28007615 0.97 KDM4E (0.88) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL29351528 0.97 KDM4E (1.00) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL29907716 0.97 KDM4E (1.00) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL5922 0.97 KDM4E (1.00) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL3711450 0.97 KDM4E (1.00) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL4577373 0.93 KDM4E (0.93) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL11114417 0.93 KDM4E (0.93) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL497901 0.93 KDM4E (0.93) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL2340917 0.93 KDM4E (0.93) KDM4ELMNACCR1CCR5CCR8

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114349794-B Platinum bisphosphonate complex and synthesis method and application thereof 南京医科大学 2023-11-24 CN claimed
CN-112110959-A Preparation method of [ (S) - (-) -2, 2-bis (di-p-tolylphosphine) -1, 1-binaphthyl ] platinum dichloride 西安凯立新材料股份有限公司 2020-12-22 CN claimed
CN-108864199-A The metal supermolecular gel rubber material and its synthetic method of a kind of temperature control variations in light and application 中山大学 2018-11-23 CN claimed
US-20120269728-A1 Methods and compositions for detecting one or more target agents using tracking components ANTARA BIOSCIENCES INC. (US) 2012-10-25 US claimed
US-7939703-B2 Method for photocatalytic isomerization of 1,2-diphenylethylene analogues Technical Institute of Physics and Chemistry of Chinese Academy of Science (CN) 2011-05-10 US claimed
US-20090156872-A1 METHOD FOR PHOTOCATALYTIC ISOMERIZATION OF 1,2-DIPHENYLETHYLENE ANALOGUES Technical Institute of Physics and Chemistry of the Chinese Academy of Sciences (CN) 2009-06-18 US claimed
US-20090036315-A1 Device and methods for detecting and quantifying one or more target agents ANTARA BIOSCIENCES INC. (US) 2009-02-05 US claimed
WO-2007092552-A2 DEVICE AND METHODS FOR DETECTING AND QUANTIFYING ONE OR MORE TARGET AGENTS ANTARA BIOSCIENCES INC. (US) 2007-08-16 WO claimed
US-7223851-B2 Nucleic acid-binding polymers GENERAL DYNAMICS ADVANCED INFORMATION SYSTEMS, INC. (US) 2007-05-29 US claimed
US-20070111025-A1 Use of platinum ll complexes as luminescent materials in organic light-emitting diodes (oleds) BASF AKTIENGESELLSCHAFT (DE) 2007-05-17 US claimed
EP-1692244-B1 USE OF PLATINUM II COMPLEXES AS LUMINESCENT MATERIALS IN ORGANIC LIGHT-EMITTING DIODES (OLEDS) BASF AG (DE) 2007-04-11 EP claimed
US-20040157217-A1 Nucleic acid-binding polymers VERIDIAN SYSTEMS DIVISION 2004-08-12 US claimed
CN-117899941-A Diatomic catalyst, preparation method and application 北京工业大学 2024-04-19 CN disclosed
CN-117463405-A Ferroferric oxide loaded bidentate chelating platinum catalyst and preparation method and application thereof 江西省科学院应用化学研究所 2024-01-30 CN disclosed
CN-117417533-A Preparation method of organosilicon polymer 江西省科学院应用化学研究所 2024-01-19 CN disclosed
CN-114349794-B Platinum bisphosphonate complex and synthesis method and application thereof 南京医科大学 2023-11-24 CN disclosed
US-4980473-A Cobalt or ruthenium complexes of 1,10-phenanthroline or derivatives THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK (US) 1990-12-25 US disclosed
US-4721669-A METAL 1,10-PHENANTHROLINE COMPLEXES THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK (US) 1988-01-26 US disclosed
EP-0211043-A1 CHEMICAL PROBES FOR LEFT-HANDED DNA AND CHIRAL METAL COMPLEXES AS Z-SPECIFIC ANTITUMOR AGENTS THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK (US) 1987-02-25 EP disclosed
WO-1986004244-A1 CHEMICAL PROBES FOR LEFT-HANDED DNA AND CHIRAL METAL COMPLEXES AS Z-SPECIFIC ANTITUMOR AGENTS THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF (US) 1986-07-31 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 (1 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-20090156872-A1 METHOD FOR PHOTOCATALYTIC ISOMERIZATION OF 1,2-DIPHENYLETHYLENE ANALOGUES PIN1, PPOX, DDT KDM4E 2659/4885LMNA 3986/4885CCR1 888/4885

“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.