Dipyridyl

Dipyridyl

SCHEMBL608685

O.O.O.O.O.O.[Cl-].[Cl-].[Ru+2].c1ccc(-c2ccccn2)nc1.c1ccc(-c2ccccn2)nc1.c1ccc(-c2ccccn2)nc1

nearest known ligand 0.88

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABCC9ABL1ACEACHEACVR1ADORA1ADORA2AADORA2BADORA3ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALOX5ATP4AATP4BBCRBTKCACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGCRBNCUL4ACXCR1CXCR2DDB1DDCDHFRDPP4DRD2DRD3DRD4EGFRERBB2ERBB4ESR1ESR2FDPSFKBP1AFLT1FLT3FLT4GARTGHSRGRIA1GRIA2GRIA3GRIA4GRIK1GRIK2GRIK3GRIK4GRIK5GRIN2AGSK3AGSK3BHDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IDH1IDH2IMPA1ITGA2BITGB3JAK1JAK2JAK3KCNJ11KCNK3KCNK9KDRKITMEN1METMMP1MMP13MMP7MMP8NANOD2NS5bODC1OPG057OPRD1OPRK1OPRM1PPARP1PARP2PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PKLRPPARDPPATPTGS1PTGS2RBX1ROCK1ROCK2RRM1RRM2RRM2BSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC10A2SLC5A2SLC6A2SLC6A3SLC6A4SLC9A3SYKTACR1THRATHRBTOP1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYK2TYMSVDRampCblablaT-3blaT-4blaT-5blaT-6blaUOE-1dacAdacBdacCfolAfolPftsIgyrAgyrBileSmecAmrcAmrcBmrdAparCparEpbp2pbp4pbpApbpFrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUthyAykgMykgO

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 0.88
LMNA P02545 3/20 0.88
CCR1 P32246 3/20 0.88
CCR5 P51681 3/20 0.88
CCR8 P51685 3/20 0.88
CYP1A2 P05177 1/20 0.88
POLB P06746 1/20 0.88
METAP1 P53582 1/20 0.88
BLM P54132 1/20 0.88
HIF1A Q16665 1/20 0.88
DOHH Q9BU89 1/20 0.88
P4HTM Q9NXG6 1/20 0.88
NPC1 O15118 6/20 0.70
TP53 P04637 4/20 0.70
RAB9A P51151 4/20 0.70
ALOX15 P16050 3/20 0.70
SMN1; SMN2 Q16637 3/20 0.70
L3MBTL1 Q9Y468 3/20 0.70
HTT P42858 2/20 0.70
TDP1 Q9NUW8 2/20 0.70

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 SCHEMBL8214178 1.00 KDM4E (0.88) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL6496507 1.00 KDM4E (0.88) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL6496678 1.00 KDM4E (0.88) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL7107765 1.00 KDM4E (0.88) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL6300635 1.00 KDM4E (0.88) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL8083419 1.00 KDM4E (0.88) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL5555244 1.00 KDM4E (0.88) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL8962334 0.97 KDM4E (0.93) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL11114417 0.97 KDM4E (0.93) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL5147238 0.97 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 186 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111077208-A Method for electrocatalytic detection of thymol based on polypyridine ruthenium complex 蚌埠学院 2020-04-28 CN claimed
EP-2872876-B1 OPTO-CHEMICAL SENSOR AND ITS USE JOANNEUM RES FORSCHUNGSGMBH (AT) 2020-02-19 EP claimed
US-10011587-B2 Multivalent ligands targeting VEGFR THE METHODIST HOSPITAL SYSTEM (US) 2018-07-03 US claimed
US-8409869-B2 Hydrogen sensor, hydrogen detecting system and method NATIONAL TSING HUA UNIVERSITY (TW) 2013-04-02 US claimed
US-20120040469-A1 HYDROGEN SENSOR, HYDROGEN DETECTING SYSTEM AND METHOD NATIONAL TSING HUA UNIVERSITY (TW) 2012-02-16 US claimed
US-20080251393-A1 Comprising system of electrodes operating inside reaction chamber intended to contain system of reagents in solution, system of electrodes comprising at least one working nanoelectrode series, one counter electrode and one reference electrode; for detection of biological molecules NANO-SIMS S.R.L. (IT) 2008-10-16 US claimed
EP-1964933-A1 Electrochemical sensor, kit comprising said sensor and process for the production thereof Nano-Sims S.r.l. (IT) 2008-09-03 EP claimed
US-7338778-B2 Luminescent method for determining cell oxygen consumption BECTON, DICKINSON AND COMPANY (US) 2008-03-04 US claimed
US-6991918-B2 Methods for improving sensitivity of oxygen biosensors BECTON DICKINSON AND CO., (US) 2006-01-31 US claimed
US-6967086-B2 Method for determining the presence or absence of respiring cells on a three-dimensional scaffold BECTON DICKINSON AND COMPANY (US) 2005-11-22 US claimed
US-20020155424-A1 Device for monitoring cells PITNER J BRUCE (US) 2002-10-24 US claimed
US-6432697-B1 SAMPLING CONTAINERS WITH CLOSURES FOR PURE SAMPLES BECTON, DICKINSON AND COMPANY 2002-08-13 US claimed
US-6432665-B1 CONTAINERS FOR SAMPLING, RADIATION, FLUORESCENCE AND DETECTION BECTON, DICKINSON AND COMPANY 2002-08-13 US claimed
US-6395506-B1 MONITORING ACTIVITY OF DRUGS ON MAMMALIAN OR INSECT CELLS; PREPARE BROTH, INCUBATE WITH LUMINESECENT COMPOUND AND DRUG, IRRADIATE DETECT VISIBILE ADJUSTMENT IN LUMINESCENT ACTIVITY, COMPARE TO CONTROL, ADJUSTMENT IN ACTIVITY INDICATES TOXICITY BECTON, DICKINSON AND COMPANY 2002-05-28 US claimed
EP-1165746-A1 TRANSPARENT SAMPLE CONTAINER Becton, Dickinson and Company (US) 2002-01-02 EP claimed
WO-2001057179-A1 TRANSPARENT SAMPLE CONTAINER BECTON, DICKINSON AND COMPANY (US) 2001-08-09 WO claimed
EP-1021557-A1 MICROBIAL MONITORING DEVICE Becton, Dickinson and Company (US) 2000-07-26 EP claimed
WO-1998012348-A1 MICROBIAL MONITORING DEVICE BECTON, DICKINSON AND COMPANY (US) 1998-03-26 WO claimed
US-5567598-A DETECTIING PRESENCE OF RESPIRING MICOORGANISM USING FLUORESCENT SENSOR BECTON DICKINSON AND COMPANY (US) 1996-10-22 US claimed
EP-0509791-A1 Microbial monitoring device Becton, Dickinson and Company (US) 1992-10-21 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 (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-10011587-B2 Multivalent ligands targeting VEGFR KDR, FLT4, FLT1 KDM4E 2044/4885LMNA 4586/4885CCR1 590/4885

“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.