Phenanthroline

Phenanthroline

SCHEMBL1730256

[Cl-].[Cl-].[Ru+2].c1cnc2c(c1)ccc1cccnc12.c1cnc2c(c1)ccc1cccnc12.c1cnc2c(c1)ccc1cccnc12

nearest known ligand 0.94

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEBDKRB2CHRM1CHRM2CHRM3CHRNA1CHRNB1CHRNDCHRNECHRNGGUCY1A1GUCY1A2GUCY1B1GUCY1B2NAMPTPTAFRSLC10A2SLC6A2SLC6A3TACR1dacAdacBdacCftsImrcAmrcBmrdA

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
CHRM1 known ✓ P11229 1/20 0.58
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
CYP3A4 P08684 1/20 0.94
CYP2D6 P10635 1/20 0.94
MMP9 P14780 1/20 0.94
ALOX15 P16050 1/20 0.94
NFKB1 P19838 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 SCHEMBL29467763 1.00 CCR1 (0.94) CCR1CCR8LMNACCR5KDM4E
Phenanthroline SCHEMBL7765519 1.00 CCR1 (0.94) CCR1CCR8LMNACCR5KDM4E
Phenanthroline SCHEMBL7904213 1.00 CCR1 (0.94) CCR1CCR8LMNACCR5KDM4E
Phenanthroline SCHEMBL29506434 1.00 CCR1 (0.94) CCR1CCR8LMNACCR5KDM4E
Phenanthroline SCHEMBL30649310 1.00 CCR1 (0.94) CCR1CCR8LMNACCR5KDM4E
Phenanthroline SCHEMBL31300436 1.00 CCR1 (0.94) CCR1CCR8LMNACCR5KDM4E
Phenanthroline SCHEMBL8686807 1.00 CCR1 (0.94) CCR1CCR8LMNACCR5KDM4E
Phenanthroline SCHEMBL5465049 1.00 CCR1 (0.94) CCR1CCR8LMNACCR5KDM4E
Phenanthroline SCHEMBL999010 0.97 CCR1 (0.89) CCR1CCR8LMNACCR5KDM4E
Phenanthroline SCHEMBL8685731 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 27 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110075927-B Synthesis method of chloroethylene 浙江工业大学 2021-12-21 CN claimed
EP-1788392-A1 Biosensor and its use Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. (DE) 2007-05-23 EP claimed
EP-1206288-B1 TARGETED FIBERLESS RADIATIVE EFFECTORS UNIV MICHIGAN (US) 2007-01-10 EP claimed
US-11739022-B2 Functionalised bimodal periodic mesoporous organosilicates (PMOS) and method for producing same using pseudomorphic transformation Sentronic GmbH Gesellschaft für optische Meßsysteme (DE) 2023-08-29 US disclosed
US-20220144692-A1 FUNCTIONALISED BIMODAL PERIODIC MESOPOROUS ORGANOSILICATES (PMOS) AND METHOD FOR PRODUCING SAME USING PSEUDOMORPHIC TRANSFORMATION Sentronic GmbH Gesellschaft für optische Meßsysteme (DE) 2022-05-12 US disclosed
US-11261126-B2 Functionalised bimodal periodic mesoporous organosilicates (PMOs) and method for producing same using pseudomorphic transformation Sentronic GmbH Gesellschaft für optische Meßsysteme (DE) 2022-03-01 US disclosed
CN-110075927-B Synthesis method of chloroethylene 浙江工业大学 2021-12-21 CN disclosed
US-20210311068-A1 METHODS AND COMPOSITIONS RELATED TO MODIFIED GREEN FLUORESCENT PROTEIN (GFP) WITH AN EMBEDDED FOREIGN PEPTIDE UNIVERSITY OF SOUTH FLORIDA 2021-10-07 US disclosed
CN-107057454-B Ink for manufacturing luminous layer, preparation method and application 上海幂方电子科技有限公司 2021-04-13 CN disclosed
CN-109521073-B Method for detecting content of bisphenol A by using electrochemical luminescence aptamer sensor 中国农业科学院农业质量标准与检测技术研究所 2021-02-26 CN disclosed
US-20210032157-A1 FUNCTIONALISED BIMODAL PERIODIC MESOPOROUS ORGANOSILICATES (PMOS) AND METHOD FOR PRODUCING SAME USING PSEUDOMORPHIC TRANSFORMATION Sentronic GmbH Gesellschaft für optische Meßsysteme (DE) 2021-02-04 US disclosed
US-20070111251-A1 Chemical address tags REGENTS OF THE UNIVERSITY OF MICHIGAN, THE 2007-05-17 US disclosed
EP-1206288-B1 TARGETED FIBERLESS RADIATIVE EFFECTORS UNIV MICHIGAN (US) 2007-01-10 EP disclosed
WO-2005022362-A2 CHEMICAL ADDRESS TAGS THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2005-03-10 WO disclosed
US-20050042753-A1 Artificial micelles comprising magnetic nanoparticle and therapeutic composition for use in tissue targeted therapy and side effect reduction THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2005-02-24 US disclosed
WO-2004026252-A2 GLIOMA TREATMENTS THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2004-04-01 WO disclosed
EP-1206288-A2 TARGETED FIBERLESS RADIATIVE EFFECTORS THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2002-05-22 EP disclosed
EP-0870189-B1 OPTICAL TEMPERATURE SENSORS AND OPTICAL-CHEMICAL SENSORS WITH OPTICAL TEMPERATURE COMPENSATION MAX PLANCK GESELLSCHAFT (DE) 2002-04-10 EP disclosed
WO-2001008660-A2 TARGETED FIBERLESS RADIATIVE EFFECTORS THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2001-02-08 WO disclosed
WO-1994010553-A1 FIBRE-OPTIC PROBE FOR THE MEASUREMENT OF FLUID PARAMETERS OPTEX BIOMEDICAL, INC. (US) 1994-05-11 WO disclosed