Dipyridyl

Dipyridyl

SCHEMBL1237608

[Cl-].[Cl-].[Cl-].[Cl-].[Ru+4].c1ccc(-c2ccccn2)nc1.c1ccc(-c2ccccn2)nc1.c1ccc(-c2ccccn2)nc1

nearest known ligand 0.93

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEBDKRB2CHRM1CHRM2CHRM3CHRNA1CHRNB1CHRNDCHRNECHRNGGUCY1A1GUCY1A2GUCY1B1GUCY1B2NAMPTPTAFRSLC10A2SLC6A2SLC6A3TACR1dacAdacBdacCftsImrcAmrcBmrdA

The experimentally established mechanism targets of Dipyridyl. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

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 SCHEMBL15136892 1.00 KDM4E (0.93) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL3799914 1.00 KDM4E (0.93) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL2371023 1.00 KDM4E (0.93) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL18065641 1.00 KDM4E (0.93) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL497901 1.00 KDM4E (0.93) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL8716183 1.00 KDM4E (0.93) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL7909040 1.00 KDM4E (0.93) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL6749371 0.97 KDM4E (0.88) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL28482248 0.97 KDM4E (0.88) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL29115681 0.97 KDM4E (0.88) 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 96 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108794432-B Method for preparing gamma lactone by photosensitization catalysis 山东新和成药业有限公司 2020-04-21 CN claimed
EP-1192448-B1 PROCESS OF USING A SENSOR PLATFORM NOVARTIS AG (CH) 2006-09-27 EP claimed
US-6771376-B2 ANALYSING SAMPLES, AFFINITY SENSING, DNA, PROTEIN, PEPTIDE AND ANTIBODY CHIP TECHNOLOGY NOVARTIS AG (CH) 2004-08-03 US claimed
US-20040115825-A1 Substrate with thin, optical transparent layer; variations in refractive index; corrugated structure BUDACH WOLFGANG ERNST GUSTAV (DE) 2004-06-17 US claimed
US-20040115826-A1 Detector on substrate; variations in refractive index BUDACH WOLFGANG ERNST GUSTAV (DE) 2004-06-17 US claimed
US-6469785-B1 Optical detection device based on semi-conductor laser array ZEPTOSENS AG (CH) 2002-10-22 US claimed
US-20020135780-A1 Sensor platform, apparatus incorporating the platform, and process using the platform NOVARTIS AG (CH) 2002-09-26 US claimed
EP-1192448-A1 SENSOR PLATFORM, APPARATUS INCORPORATING THE PLATFORM, AND PROCESS USING THE PLATFORM Novartis AG (CH) 2002-04-03 EP claimed
WO-2001002839-A1 SENSOR PLATFORM, APPARATUS INCORPORATING THE PLATFORM, AND PROCESS USING THE PLATFORM NOVARTIS AG (CH) 2001-01-11 WO claimed
EP-0918984-A1 OPTICAL DETECTOR Novartis AG (CH) 1999-06-02 EP claimed
WO-1998008077-A1 OPTICAL DETECTOR NOVARTIS AG (CH) 1998-02-26 WO claimed
EP-0824684-A1 SENSOR PLATFORM AND METHOD FOR THE PARALLEL DETECTION OF A PLURALITY OF ANALYTES USING EVANESCENTLY EXCITED LUMINESCENCE Novartis AG (CH) 1998-02-25 EP claimed
WO-1996035940-A1 SENSOR PLATFORM AND METHOD FOR THE PARALLEL DETECTION OF A PLURALITY OF ANALYTES USING EVANESCENTLY EXCITED LUMINESCENCE NOVARTIS AG (CH) 1996-11-14 WO claimed
WO-2025233239-A1 PROCESSES FOR PRODUCING OPTICAL EFFECT LAYERS SICPA HOLDING SA (CH) 2025-11-13 WO disclosed
US-11926697-B2 Fluorine-containing liquid crystal elastomer and preparation method and use thereof SOOCHOW UNIVERSITY (CN) 2024-03-12 US disclosed
US-20220119589-A1 FLUORINE-CONTAINING LIQUID CRYSTAL ELASTOMER AND PREPARATION METHOD AND USE THEREOF SOOCHOW UNIVERSITY (CN) 2022-04-21 US disclosed
WO-1996035940-A1 SENSOR PLATFORM AND METHOD FOR THE PARALLEL DETECTION OF A PLURALITY OF ANALYTES USING EVANESCENTLY EXCITED LUMINESCENCE NOVARTIS AG (CH) 1996-11-14 WO disclosed
WO-1995033197-A1 PROCESS FOR DETECTING EVANESCENTLY EXCITED LUMINESCENCE CIBA-GEIGY AG (CH) 1995-12-07 WO disclosed
WO-1995033198-A1 PROCESS FOR DETECTING EVANESCENTLY EXCITED LUMINESCENCE CIBA-GEIGY AG (CH) 1995-12-07 WO disclosed
WO-1993014104-A1 PHOTOCLEAVAGE OF DNA USING ORGANIC OXYRADICALS EASTMAN KODAK COMPANY (US) 1993-07-22 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 (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-20220119589-A1 FLUORINE-CONTAINING LIQUID CRYSTAL ELASTOMER AND PREPARATION METHOD AND USE THEREOF PFN1, FSCN1, FLNA KDM4E 2323/4885LMNA 1157/4885CCR1 748/4885
US-11926697-B2 Fluorine-containing liquid crystal elastomer and preparation method and use thereof PFN1, FSCN1, FLNA KDM4E 2323/4885LMNA 1157/4885CCR1 748/4885

“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.