Phenanthroline

Phenanthroline

SCHEMBL2532986

CC(=O)[O-].CC(=O)[O-].[Pd+2].c1cnc2c(c1)ccc1cccnc12

nearest known ligand 0.64

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA2AADRA2BADRA2CADRB2AGTR1AVPR1AAVPR1BAVPR2BDKRB2CALCRCHRNA3CHRNB4ESR1ESR2GHSRGNRHRGSC1HSPA8MALT1MC1RMC4RNOS1NOS2NOS3OPRK1OXTRRAMP1RAMP2RAMP3SCN5ASSTR1SSTR2SSTR3SSTR4SSTR5dacAdacBdacCfolPftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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
KDM4E B2RXH2 4/20 0.64
LMNA P02545 4/20 0.64
HSP90AA1 P07900 4/20 0.64
TDP1 Q9NUW8 3/20 0.64
CCR1 P32246 3/20 0.64
CCR5 P51681 3/20 0.64
CCR8 P51685 3/20 0.64
MAPT P10636 2/20 0.64
HTT P42858 2/20 0.64
SMN1; SMN2 Q16637 2/20 0.64
MMP2 P08253 2/20 0.64
TSHR P16473 2/20 0.64
GMNN O75496 1/20 0.64
TP53 P04637 1/20 0.64
CYP3A4 P08684 1/20 0.64
CYP2D6 P10635 1/20 0.64
MMP9 P14780 1/20 0.64
ALOX15 P16050 1/20 0.64
NFKB1 P19838 1/20 0.64
MMP8 P22894 1/20 0.64

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 SCHEMBL16192743 1.00 KDM4E (0.64) KDM4ELMNAHSP90AA1TDP1CCR1
Phenanthroline SCHEMBL29278214 0.96 KDM4E (0.64) KDM4ELMNAHSP90AA1TDP1CCR1
Phenanthroline SCHEMBL29188565 0.96 KDM4E (0.64) KDM4ELMNAHSP90AA1TDP1CCR1
Phenanthroline SCHEMBL28227266 0.96 KDM4E (0.64) KDM4ELMNAHSP90AA1TDP1CCR1
Phenanthroline SCHEMBL28097109 0.90 LMNA (0.73) KDM4ELMNAHSP90AA1TDP1CCR1
Phenanthroline SCHEMBL22401704 0.88 LMNA (0.70) KDM4ELMNAHSP90AA1TDP1CCR1
Phenanthroline SCHEMBL4881417 0.88 LMNA (0.70) KDM4ELMNAHSP90AA1TDP1CCR1
Acetic Acid SCHEMBL8883463 0.86 HSP90AA1 (0.52) KDM4ELMNAHSP90AA1TDP1CCR1
Acetic Acid SCHEMBL8883458 0.86 KDM4E (0.52) KDM4ELMNAHSP90AA1TDP1CCR1
Phenanthroline SCHEMBL29521774 0.86 LMNA (0.67) KDM4ELMNAHSP90AA1TDP1CCR1

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 15 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025068206-A1 PERFUME COMPOSITIONS GIVAUDAN SA (CH) 2025-04-03 WO disclosed
CN-109715593-B Method for removing or recovering 2-alkoxyethanol and method for producing (2-alkoxyethyl) vinyl ether 丸善石油化学株式会社 2022-05-31 CN disclosed
US-11247961-B2 Me 1 hod for removing or collecting 2-alkoxyethanol, and method for producing (2-alkoxyethyl) vinyl ether MARUZEN PETROCHEMICAL CO., LTD. (JP) 2022-02-15 US disclosed
EP-3514133-B1 METHOD FOR REMOVING OR COLLECTING 2-ALKOXYETHANOL, AND METHOD FOR PRODUCING (2-ALKOXYETHYL) VINYL ETHER MARUZEN PETROCHEM CO LTD (JP) 2020-11-25 EP disclosed
EP-3514133-A1 METHOD FOR REMOVING OR COLLECTING 2-ALKOXYETHANOL, AND METHOD FOR PRODUCING (2-ALKOXYETHYL) VINYL ETHER Maruzen Petrochemical Co., Ltd. (JP) 2019-07-24 EP disclosed
US-20190210949-A1 METHOD FOR REMOVING OR COLLECTING 2-ALKOXYETHANOL, AND METHOD FOR PRODUCING (2-ALKOXYETHYL) VINYL ETHER MARUZEN PETROCHEMICAL CO., LTD. (JP) 2019-07-11 US disclosed
EP-3245191-A1 QUINOLINES AND PROCESS FOR THE PREPARATION THEREOF Council of Scientific & Industrial Research (IN) 2017-11-22 EP disclosed
WO-2016113759-A1 QUINOLINES AND PROCESS FOR THE PREPARATION THEREOF COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH (IN) 2016-07-21 WO disclosed
EP-2256170-B1 Tunable fluorescent UV curable gel inks containing fluorescent monomers for food packaging applications XEROX CORP (US) 2014-12-24 EP disclosed
US-8334026-B2 Tunable fluorescent UV curable gel inks containing fluorescent monomers for food packaging applications XEROX CORPORATION (US) 2012-12-18 US disclosed
US-8039663-B2 Acrylate resins with the dimethanocyclopenta naphthalene in the backbone; reducing cure-induced shrinkage; semiconductor packages and microelectronic devices DESIGNER MOLECULES, INC. (US) 2011-10-18 US disclosed
US-20100304040-A1 TUNABLE FLUORESCENT UV CURABLE GEL INKS CONTAINING FLUORESCENT MONOMERS FOR FOOD PACKAGING APPLICATIONS XEROX CORPORATION (US) 2010-12-02 US disclosed
EP-2256170-A1 Tunable fluorescent UV curable gel inks containing fluorescent monomers for food packaging applications Xerox Corporation (US) 2010-12-01 EP disclosed
US-20100249465-A1 PROCESS FOR PRODUCTION OF HIGH-PURITY VINYL ETHER MARUZEN PETROCHEMICAL CO., LTD. (JP) 2010-09-30 US disclosed
US-20080257493-A1 MONOMERS DERIVED FROM PENTACYCLOPENTADECANE DIMETHANOL DESIGNER MOLECULES, INC. 2008-10-23 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 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-20080257493-A1 MONOMERS DERIVED FROM PENTACYCLOPENTADECANE DIMETHANOL TELO2, MSMO1, TMT1A KDM4E 920/4885LMNA 4137/4885HSP90AA1 3259/4885
US-20100249465-A1 PROCESS FOR PRODUCTION OF HIGH-PURITY VINYL ETHER ADH1A, ADH1C, VMP1 KDM4E 821/4885LMNA 3597/4885HSP90AA1 1097/4885

“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.