Dipyridyl

Dipyridyl

SCHEMBL2245805

Cl.[Ru].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

ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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
CCR5 known ✓ P51681 3/20 0.88
HSP90AA1 known ✓ P07900 1/20 0.70
GLA known ✓ P06280 1/20 0.59
CYP19A1 known ✓ P11511 1/20 0.48
KDM4E B2RXH2 9/20 0.88
LMNA P02545 3/20 0.88
CCR1 P32246 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

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 SCHEMBL5251632 1.00 KDM4E (0.88) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL5663541 1.00 KDM4E (0.88) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL646317 1.00 KDM4E (0.88) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL7619601 1.00 KDM4E (0.88) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL8214175 0.97 KDM4E (0.82) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL5555235 0.97 KDM4E (0.82) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL6517724 0.97 KDM4E (0.82) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL608684 0.97 KDM4E (0.82) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL6496504 0.97 KDM4E (0.82) KDM4ELMNACCR1CCR5CCR8
Dipyridyl SCHEMBL6304360 0.97 KDM4E (0.82) 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 35 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2023215883-A1 PHOTOCROSSLINKABLE SYNTHETIC POLYMERS COOK BIOTECH INCORPORATED (US) 2023-11-09 WO claimed
US-20250345478-A1 PHOTOCROSSLINKABLE SYNTHETIC POLYMERS Cook Biotech Incoporated (US) 2025-11-13 US disclosed
US-20250325727-A1 PHOTOCURABLE ADHESIVES WITH FERULATED PECTIN COOK BIOTECH INCORPORATED (US) 2025-10-23 US disclosed
WO-2023215883-A1 PHOTOCROSSLINKABLE SYNTHETIC POLYMERS COOK BIOTECH INCORPORATED (US) 2023-11-09 WO disclosed
US-20160114075-A1 PHOTOACTIVATED CROSSLINKING OF A PROTEIN OR PEPTIDE COMMONWEALTH SCIENTIFIC AND INDUSTRIAL RESEARCH ORGANISATION (AU) 2016-04-28 US disclosed
US-9216235-B2 Photoactivated crosslinking of a protein or peptide COOK MEDICAL TECHNOLOGIES LLC (US) 2015-12-22 US disclosed
CN-102504802-A Metallic organic luminescent molecule and hydrotalcite compounded electrochemiluminiscent ultrathin film and method of preparing same UNIV BEIJING CHEMICAL 2012-06-20 CN disclosed
US-20110190813-A1 PHOTOACTIVATED CROSSLINKING OF A PROTEIN OR PEPTIDE ELVIN, Christopher M. (AU) 2011-08-04 US disclosed
EP-2178949-A1 PHOTOACTIVATED CROSSLINKING OF A PROTEIN OR PEPTIDE Commonwealth Scientific and Industrial Research Organisation (AU) 2010-04-28 EP disclosed
WO-2009021287-A1 PHOTOACTIVATED CROSSLINKING OF A PROTEIN OR PEPTIDE COMMONWEALTH SCIENTIFIC AND INDUSTRIAL RESEARCH ORGANISATION (AU) 2009-02-19 WO disclosed
US-6297018-B1 LOCATING SAMPLE AT EXAMINATION SITE, ILLUMINATING WITH POLARIZED LIGHT, DETECTING LIGHT EMITTED ONLY FROM VOLUME LOCATED AWAY FROM SAMPLE BOUNDARY INTERFACES, THEN ANALYZING DATA LJL BIOSYSTEMS, INC. 2001-10-02 US disclosed
WO-2000055372-A1 METHODS AND APPARATUS FOR DETECTING NUCLEIC ACID POLYMORPHISMS LJL BIOSYSTEMS, INC. (US) 2000-09-21 WO disclosed
WO-1999037203-A9 APPARATUS AND METHODS FOR IMPROVING SIGNAL RESOLUTION IN OPTICAL SPECTROSCOPY LJL BIOSYSTEMS INC (US) 1999-11-18 WO disclosed
WO-1999037203-A2 APPARATUS AND METHODS FOR IMPROVING SIGNAL RESOLUTION IN OPTICAL SPECTROSCOPY LJL BIOSYSTEMS, INC. (US) 1999-07-29 WO disclosed
US-5292409-A Electrolytically generating superoxide ion under protective layer of ion exchange material CAPE COD RESEARCH, INC. (US) 1994-03-08 US disclosed
US-4977320-A Electrospray ionization mass spectrometer with new features THE ROCKEFELLER UNIVERSITY (US) 1990-12-11 US disclosed
EP-0043251-B1 CATALYST FOR THE PHOTODECOMPOSITION OF WATER, AND A PROCESS FOR THE PREPARATION THEREOF SIBIT S.p.A. (IT) 1984-10-03 EP disclosed
US-4370263-A Catalyst for the photo-decomposition of water and process for the preparation of the catalyst SIBIT, S.P.A. (IT) 1983-01-25 US disclosed
EP-0043251-A2 Catalyst for the photodecomposition of water, and a process for the preparation thereof SIBIT S.p.A. (IT) 1982-01-06 EP disclosed
US-3964912-A Ruthenium containing photographic developers EASTMAN KODAK COMPANY (US) 1976-06-22 US disclosed