Phenanthroline

Phenanthroline

SCHEMBL44857

O.c1cnc2c(c1)ccc1cccnc12

nearest known ligand 0.94

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of Phenanthroline. 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
MMP8 known ✓ P22894 1/20 0.94
MMP13 known ✓ P45452 1/20 0.94
CHRM1 known ✓ P11229 1/20 0.58
ADRA1A known ✓ P35348 1/20 0.58
HDAC8 known ✓ Q9BY41 1/20 0.58
PARP1 known ✓ P09874 1/20 0.48
CCR1 P32246 5/20 0.94
CCR8 P51685 5/20 0.94
LMNA P02545 4/20 0.94
CCR5 P51681 3/20 0.94
KDM4E B2RXH2 3/20 0.94
MMP2 P08253 2/20 0.94
TSHR P16473 2/20 0.94
MAPT P10636 2/20 0.94
HTT P42858 2/20 0.94
SMN1; SMN2 Q16637 2/20 0.94
TDP1 Q9NUW8 2/20 0.94
GMNN O75496 1/20 0.94
TP53 P04637 1/20 0.94
HSP90AA1 P07900 1/20 0.94

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
Phenanthroline SCHEMBL27616640 1.00 CCR1 (0.94) CCR1CCR8LMNACCR5KDM4E
Phenanthroline SCHEMBL28662342 1.00 CCR1 (0.94) CCR1CCR8LMNACCR5KDM4E
Phenanthroline SCHEMBL30477083 1.00 CCR1 (0.94) CCR1CCR8LMNACCR5KDM4E
Phenanthroline SCHEMBL28519994 1.00 CCR1 (0.94) CCR1CCR8LMNACCR5KDM4E
Phenanthroline SCHEMBL15397666 0.97 CCR1 (0.89) CCR1CCR8LMNACCR5KDM4E
Phenanthroline SCHEMBL999010 0.97 CCR1 (0.89) CCR1CCR8LMNACCR5KDM4E
Phenanthroline SCHEMBL31091571 0.97 CCR1 (0.89) CCR1CCR8LMNACCR5KDM4E
Phenanthroline SCHEMBL996092 0.97 CCR1 (0.89) CCR1CCR8LMNACCR5KDM4E
Phenanthroline SCHEMBL1449977 0.97 CCR1 (0.89) CCR1CCR8LMNACCR5KDM4E
Phenanthroline SCHEMBL30165588 0.97 CCR1 (0.89) CCR1CCR8LMNACCR5KDM4E

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 1022 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119372704-A Nickel-oxygen modified carbon black catalyst for electrocatalytic synthesis of hydrogen peroxide and preparation method and application thereof 东南大学 2025-01-28 CN claimed
CN-119330715-A Preparation of high-purity and high-crystallinity CaLa2S4Method for preparing infrared ceramic powder 江苏师范大学 2025-01-21 CN claimed
US-12066437-B2 Method for determining Escherichia coli AQSENS HEALTH OY (FI) 2024-08-20 US claimed
CN-117987147-A Complexing agent for ferrous ions needed by plants and preparation method and application thereof 武汉工程大学 2024-05-07 CN claimed
CN-117510507-A Palladium-catalyzed indoline quinoline derivative synthesized by intramolecular dearomatization of indole and preparation method thereof 河北工业大学 2024-02-06 CN claimed
CN-117423843-A Separation type vapor deposition method for preparing ultralow noble metal alloy supported M-N-C hybrid catalyst and application thereof 厦门大学 2024-01-19 CN claimed
CN-116914164-A Electrocatalytic oxygen reduction catalytic material based on MOF (metal oxide fiber) derivatization and preparation method thereof 浙江工业大学 2023-10-20 CN claimed
CN-116870909-A Monoatomic iron-loaded graphene Fenton catalyst, and preparation method and application thereof 温州大学 2023-10-13 CN claimed
CN-116815204-A Application and preparation method of porous carbon supported Ni-N-C catalytic electrode 中国能源建设股份有限公司 2023-09-29 CN claimed
CN-114284512-B Preparation method of carbon molecular sieve-cobalt monoatomic catalyst for zinc-air battery 吉林大学 2023-09-19 CN claimed
US-20090029480-A1 Testing device VERITEQUE USA, INC. 2009-01-29 US claimed
EP-1896605-A2 STIMULATION OF PANCREATIC B CELL PROLIFERATION The Rockefeller University (US) 2008-03-12 EP claimed
EP-1844321-A1 TESTING DEVICE System Two Pty Ltd (AU) 2007-10-17 EP claimed
WO-2006133333-A2 STIMULATION OF PANCREATIC B CELL PROLIFERATION THE ROCKEFELLER UNIVERSITY (US) 2006-12-14 WO claimed
WO-2006079167-A1 TESTING DEVICE SYSTEM TWO PTY LTD (AU) 2006-08-03 WO claimed
US-20050277130-A1 Removing aurintricarboxylic acid (ATA), a reverse transcriptase inhibitor, from a blood sample containing ATA and a chaotropic salt for nucleic acid extraction by using urea at a pH of about 8.0; high speed analysis by creating a fibrin aggregate to confine pathogens to facilitate pathogen DNA extraction UNIVERSITY OF SOUTH FLORIDA 2005-12-15 US claimed
US-6066505-A INCREASING EFFICIENCY OF MEASUREMENT OF A COMPOUND PRESENT IN SAMPLE USING FLUORESCENCE TESTING; INCUBATION OF COMPOUND WITH SECOND COMPOUND WHICH REDUCES INTERFERENCE FROM SUBSTANCES ENDOGENOUS TO SAMPLE ROCHE DIAGNOSTICS CORPORATION (US) 2000-05-23 US claimed
EP-0892865-A1 METHOD FOR BLEACHING OF LIGNOCELLULOSIC FIBERS Jaschinski, Thomas (DE) 1999-01-27 EP claimed
WO-1997039179-A1 METHOD FOR BLEACHING OF LIGNOCELLULOSIC FIBERS JASCHINSKI THOMAS (DE) 1997-10-23 WO claimed
US-5580681-A SOLID ELECTROLYTE, ORGANIC ANODE, SOLID CATHODE E.C.R.-ELECTRO-CHEMICAL RESEARCH LTD. (IL) 1996-12-03 US claimed