SCHEMBL969484

SCHEMBL969484

Cc1cc(C)cc(P(=O)(O)c2cc(C)cc(C)c2)c1

nearest known ligand 0.56

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
TSHR P16473 4/20 0.56
LMNA P02545 1/20 0.56
PGK1 P00558 3/20 0.44
PGK2 P07205 3/20 0.44
ALDH1A1 P00352 3/20 0.42
CYP3A4 P08684 1/20 0.42
MAPK1 P28482 1/20 0.42
TDP1 Q9NUW8 1/20 0.42
TPMT P51580 1/20 0.40
SRC P12931 1/20 0.38
HPGD P15428 1/20 0.35
GAA P10253 1/20 0.34
SELL P14151 1/20 0.33
SELP P16109 1/20 0.33
SELE P16581 1/20 0.33
ACHE P22303 1/20 0.33
THRB P10828 1/20 0.33

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
SCHEMBL2470616 0.87 TSHR (0.56) TSHRLMNAPGK1PGK2ALDH1A1
SCHEMBL3353801 0.83 PGK1 (0.44) TSHRLMNAPGK1PGK2ALDH1A1
Phosphoric Acid SCHEMBL15475844 0.82 PGK1 (0.52) TSHRLMNAPGK1PGK2ALDH1A1
Phosphoric Acid SCHEMBL29023595 0.82 PGK1 (0.52) TSHRLMNAPGK1PGK2ALDH1A1
Phosphoric Acid SCHEMBL31047197 0.79 PGK1 (0.50) TSHRLMNAPGK1PGK2ALDH1A1
SCHEMBL1203845 0.77 TSHR (0.46) TSHRLMNAPGK1PGK2ALDH1A1
SCHEMBL12230093 0.75 TSHR (0.41) TSHRLMNAPGK1PGK2ALDH1A1
SCHEMBL971683 0.75 LMNA (0.54) TSHRLMNATDP1HPGDACHE
SCHEMBL6671376 0.74 TSHR (0.44) TSHRLMNAPGK1PGK2ALDH1A1
SCHEMBL15147577 0.74 TSHR (0.44) TSHRLMNAPGK1PGK2ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108293284-A The luminescent layer ionic compound of electrochemical luminescence unit, the luminescent layer formation composition of electrochemical luminescence unit and electrochemical luminescence unit 日本化学工业株式会社 2018-07-17 CN disclosed
US-9822425-B2 Processes for recovering metals from aqueous solutions CYTEC TECHNOLOGY CORP. (US) 2017-11-21 US disclosed
US-9725552-B2 HMF-based phenol formaldehyde resin INDUSTRIAL TECHNOLOGY RESEARCH INSTITUTE (TW) 2017-08-08 US disclosed
US-20160102165-A1 HMF-BASED PHENOL FORMALDEHYDE RESIN INDUSTRIAL TECHNOLOGY RESEARCH INSTITUTE (TW) 2016-04-14 US disclosed
US-20150135903-A1 PROCESSES FOR RECOVERING METALS FROM AQUEOUS SOLUTIONS CYTEC TECHNOLOGY CORP. (US) 2015-05-21 US disclosed
US-8968698-B2 Processes for recovering metals from aqueous solutions CYTEC TECHNOLOGY CORP. (US) 2015-03-03 US disclosed
US-8859110-B2 Cyclic phosphazene compounds and use thereof in organic light emitting diodes BASF SE (DE) 2014-10-14 US disclosed
US-8859110-B2 Cyclic phosphazene compounds and use thereof in organic light emitting diodes BASF SE (DE) 2014-10-14 US disclosed
US-8859110-B2 Cyclic phosphazene compounds and use thereof in organic light emitting diodes BASF SE (DE) 2014-10-14 US disclosed
US-20140127095-A1 PROCESSES FOR RECOVERING METALS FROM AQUEOUS SOLUTIONS CYTEC TECHNOLOGY CORP. (US) 2014-05-08 US disclosed
US-20110172423-A1 CYCLIC PHOSPHAZENE COMPOUNDS AND USE THEREOF IN ORGANIC LIGHT EMITTING DIODES BASF SE (DE) 2011-07-14 US disclosed
US-20110172423-A1 CYCLIC PHOSPHAZENE COMPOUNDS AND USE THEREOF IN ORGANIC LIGHT EMITTING DIODES BASF SE (DE) 2011-07-14 US disclosed
EP-2301091-A1 CYCLIC PHOSPHAZENE COMPOUNDS AND USE THEREOF IN ORGANIC LIGHT EMITTING DIODES BASF SE (DE) 2011-03-30 EP disclosed
WO-2011005736-A2 PROCESSES FOR RECOVERING METALS FROM AQUEOUS SOLUTIONS CYTEC TECHNOLOGY CORP. (US) 2011-01-13 WO disclosed
US-20110005354-A1 PROCESSES FOR RECOVERING METALS FROM AQUEOUS SOLUTIONS CYTEC TECHNOLOGY CORP. (US) 2011-01-13 US disclosed
WO-2009153276-A1 CYCLIC PHOSPHAZENE COMPOUNDS AND USE THEREOF IN ORGANIC LIGHT EMITTING DIODES BASF SE (DE) 2009-12-23 WO disclosed
WO-2009153276-A1 CYCLIC PHOSPHAZENE COMPOUNDS AND USE THEREOF IN ORGANIC LIGHT EMITTING DIODES BASF SE (DE) 2009-12-23 WO disclosed
EP-0444930-B1 Compounds containing 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl and catalytic metal complexes thereof TAKASAGO PERFUMERY CO LTD (JP) 1994-11-30 EP disclosed
US-5223632-A 2,2'-BIS(DI-(3,5-DIALKYLPHENYL)PHOSPHINO)-1,1'-BINAPHTHYL AND TRANSITION METAL COMPLEX CONTAINING THE SAMD LIGAND TAKASAGO INTERNATIONAL CORPORATION (JP) 1993-06-29 US disclosed
EP-0444930-A1 Compounds containing 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl and catalytic metal complexes thereof Takasago International Corporation (JP) 1991-09-04 EP 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 (1 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-20110172423-A1 CYCLIC PHOSPHAZENE COMPOUNDS AND USE THEREOF IN ORGANIC LIGHT EMITTING DIODES PHOSPHO1, PDE6B, PDE6C TSHR 3087/4885LMNA 3580/4885PGK1 1339/4885

“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.