Phenanthroline

Phenanthroline

SCHEMBL29521774

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

nearest known ligand 0.67

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
LMNA P02545 5/20 0.67
CCR1 P32246 3/20 0.67
CCR5 P51681 3/20 0.67
CCR8 P51685 3/20 0.67
KDM4E B2RXH2 3/20 0.67
TDP1 Q9NUW8 3/20 0.67
MAPT P10636 2/20 0.67
HTT P42858 2/20 0.67
SMN1; SMN2 Q16637 2/20 0.67
MMP2 P08253 2/20 0.67
TSHR P16473 2/20 0.67
GMNN O75496 1/20 0.67
TP53 P04637 1/20 0.67
HSP90AA1 P07900 1/20 0.67
CYP3A4 P08684 1/20 0.67
CYP2D6 P10635 1/20 0.67
MMP9 P14780 1/20 0.67
ALOX15 P16050 1/20 0.67
NFKB1 P19838 1/20 0.67
MMP8 P22894 1/20 0.67

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 SCHEMBL3408768 1.00 LMNA (0.67) LMNACCR1CCR5CCR8KDM4E
Phenanthroline SCHEMBL22401704 0.98 LMNA (0.70) LMNACCR1CCR5CCR8KDM4E
Phenanthroline SCHEMBL4881417 0.98 LMNA (0.70) LMNACCR1CCR5CCR8KDM4E
Phenanthroline SCHEMBL29278213 0.96 LMNA (0.67) LMNACCR1CCR5CCR8KDM4E
Phenanthroline SCHEMBL28097109 0.91 LMNA (0.73) LMNACCR1CCR5CCR8KDM4E
Phenanthroline SCHEMBL27878295 0.87 KDM4E (0.80) LMNACCR1CCR5CCR8KDM4E
Phenanthroline SCHEMBL28776402 0.86 LMNA (0.59) LMNACCR1CCR5CCR8KDM4E
Phenanthroline SCHEMBL2532986 0.86 KDM4E (0.64) LMNACCR1CCR5CCR8KDM4E
Phenanthroline SCHEMBL29278214 0.86 KDM4E (0.64) LMNACCR1CCR5CCR8KDM4E
Phenanthroline SCHEMBL29188565 0.86 KDM4E (0.64) LMNACCR1CCR5CCR8KDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250207163-A1 METHODS AND APPARATUS FOR SYNTHESIZING NUCLEIC ACIDS TRILINK BIOTECHNOLOGIES, LLC 2025-06-26 US disclosed
CN-115959987-B Catalyst composition for preparing unsaturated carboxylate by carbon dioxide and ethylene 华东理工大学 2025-05-09 CN disclosed
CN-119916644-A Photosensitive resin composition containing alkynyl anthracene photosensitizer and application thereof 湖南初源新材料股份有限公司 2025-05-02 CN disclosed
EP-4499824-A1 METHODS AND APPARATUS FOR SYNTHESIZING NUCLEIC ACIDS Molecular Assemblies, Inc. (US) 2025-02-05 EP disclosed
EP-4121407-B1 CATALYTIC PROCESS FOR PREPARING AN ALPHA, BETA-ETHYLENICALLY UNSATURATED CARBOXYLIC ACID SALT BASF SE (DE) 2024-03-06 EP disclosed
WO-2023183569-A1 METHODS AND APPARATUS FOR SYNTHESIZING NUCLEIC ACIDS Molecular Assemblies, Inc. (US) 2023-09-28 WO disclosed
US-20230138524-A1 CATALYTIC PROCESS FOR PREPARING AN a,ß-ETHYLENICALLY UNSATURATED CARBOXYLIC ACID SALT BASF SE (DE) 2023-05-04 US disclosed
CN-115959987-A Catalyst composition for preparing unsaturated carboxylate from carbon dioxide and ethylene 华东理工大学 2023-04-14 CN disclosed
EP-4121407-A1 Catalytic process for preparing an alpha, Beta-ethylenically unsaturated carboxylic acid salt BASF SE (DE) 2023-01-25 EP disclosed
CN-108884010-B Process for preparing unsaturated carboxylic acid salts 巴斯夫欧洲公司 2022-11-08 CN disclosed
CN-115298157-A Catalytic process for preparing alpha, beta-ethylenically unsaturated carboxylic acid salts 巴斯夫欧洲公司 2022-11-04 CN disclosed
CN-106458823-B Process for preparing unsaturated carboxylic acid salts 巴斯夫欧洲公司 2022-04-19 CN 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-20230138524-A1 CATALYTIC PROCESS FOR PREPARING AN a,ß-ETHYLENICALLY UNSATURATED CARBOXYLIC ACID SALT ADH1C, ADH1A, COASY LMNA 1590/4885CCR1 1086/4885CCR5 1819/4885
US-20250207163-A1 METHODS AND APPARATUS FOR SYNTHESIZING NUCLEIC ACIDS RNGTT, POLRMT, POLN LMNA 698/4885CCR1 4545/4885CCR5 4386/4885

“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.