Phenanthroline

Phenanthroline

SCHEMBL725644

Cl.c1cnc2c(c1)ccc1cccnc12

nearest known ligand 0.94

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 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
CCR5 known ✓ P51681 3/20 0.94
HSP90AA1 known ✓ P07900 1/20 0.94
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
CA2 known ✓ P00918 1/20 0.48
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
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

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 SCHEMBL4901390 1.00 CCR1 (0.94) CCR1CCR8LMNACCR5KDM4E
Phenanthroline SCHEMBL31040598 1.00 CCR1 (0.94) CCR1CCR8LMNACCR5KDM4E
Phenanthroline SCHEMBL28973442 1.00 CCR1 (0.94) CCR1CCR8LMNACCR5KDM4E
Phenanthroline SCHEMBL30165588 0.97 CCR1 (0.89) CCR1CCR8LMNACCR5KDM4E
Phenanthroline SCHEMBL8324317 0.97 CCR1 (0.89) CCR1CCR8LMNACCR5KDM4E
Phenanthroline SCHEMBL996092 0.97 CCR1 (0.89) CCR1CCR8LMNACCR5KDM4E
Phenanthroline SCHEMBL1237620 0.97 CCR1 (0.89) CCR1CCR8LMNACCR5KDM4E
Phenanthroline SCHEMBL29354015 0.97 CCR1 (1.00) CCR1CCR8LMNACCR5KDM4E
Phenanthroline SCHEMBL29367277 0.97 CCR1 (1.00) CCR1CCR8LMNACCR5KDM4E
Phenanthroline SCHEMBL8845760 0.97 CCR1 (1.00) 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 88 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111218270-A Preparation method of modified time-resolved fluorescent microspheres 长沙美牛生物科技有限公司 2020-06-02 CN claimed
CN-110010912-A A kind of catalyst of fuel cell and its preparation method and application 中国石油大学(北京) 2019-07-12 CN claimed
US-9970121-B2 Composite material, method for forming the composite material, electrode plated with the composite material, and connection structure having the composite material DENSO CORPORATION (JP) 2018-05-15 US claimed
CN-104588003-B A kind of heterogeneous metal catalyst and its application in isobutanol is prepared by methanol and ethanol water 中国科学院青岛生物能源与过程研究所 2017-11-07 CN claimed
US-20160201211-A1 COMPOSITE MATERIAL, METHOD FOR FORMING THE COMPOSITE MATERIAL, ELECTRODE PLATED WITH THE COMPOSITE MATERIAL, AND CONNECTION STRUCTURE HAVING THE COMPOSITE MATERIAL DENSO CORPORATION (JP) 2016-07-14 US claimed
CN-102276604-A Preparation method of o-phenanthroline hydrochloride 2011-12-14 CN claimed
EP-2237029-A1 Pumping electrode of gas sensor, method of manufacturing conductive paste, and gas sensor NGK Insulators, Ltd. (JP) 2010-10-06 EP claimed
US-20100243447-A1 PUMPING ELECTRODE OF GAS SENSOR, METHOD OF MANUFACTURING CONDUCTIVE PASTE, AND GAS SENSOR NGK INSULATORS, LTD. (JP) 2010-09-30 US claimed
US-20080300133-A1 Oxygen Scavenger/Indicator FRAUNHOFER-GESELLSCHAFT ZUR FORDERUNG DER ANGEWANDTEN FORSCHUNG E.V. (DE) 2008-12-04 US claimed
CN-119997942-A Compounds for the treatment of cancer 埃维克斯塔生物公司 2025-05-13 CN disclosed
CN-119463850-A Silicon-coated color fluorescent microsphere and mild preparation method and application thereof 南京理工大学 2025-02-18 CN disclosed
CN-117186872-B Method for preparing color time-resolved fluorescent microsphere by one-step method 南京立顶医疗科技有限公司 2024-05-10 CN disclosed
WO-2024075780-A1 METHOD FOR CULTURING DEHALOCOCCOIDES GENUS BACTERIA AND METHOD FOR PURIFYING CHLORINATED ETHYLENES 株式会社テクノスルガ・ラボ 2024-04-11 WO disclosed
CN-116585530-B Chloroplast composite hydrogel capable of efficiently producing oxygen and preparation method and application thereof 暨南大学 2024-02-02 CN disclosed
WO-1989003434-A1 SUPPORTED HETEROPOLYCYCLIC COMPOUNDS IN THE SEPARATION AND REMOVAL OF LATE TRANSITION METALS MACEDO, PEDRO, B. (US) 1989-04-20 WO disclosed
EP-0078544-A1 Reagent and process for the detection of a critical water content in hydraulic fluids, especially brake fluids LUCAS INDUSTRIES public limited company (GB) 1983-05-11 EP disclosed
EP-0040722-B1 PROCESS FOR THE PREPARATION OF SYNTHETIC LEPIDOCROCITE BASF Aktiengesellschaft (DE) 1983-03-23 EP disclosed
EP-0040722-A1 Process for the preparation of synthetic lepidocrocite BASF Aktiengesellschaft (DE) 1981-12-02 EP disclosed
US-4275031-A A CUVETTE WITH REAGENT EMBEDDED IN A CLEAR POLYMER COATING MERCK PATENT GESELLSCHAFT MIT BESCHRANKTER HAFTUNG (DE) 1981-06-23 US disclosed
US-3978096-A Production of 1-chloroanthraquinone BASF AKTIENGESELLSCHAFT (DT) 1976-08-31 US disclosed