SCHEMBL4939397

SCHEMBL4939397

O=P(I)(c1ccccc1)c1ccccc1

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA2 P00918 1/20 0.52
CA4 P22748 1/20 0.52
CA5A P35218 1/20 0.52
CFTR P13569 1/20 0.46
ALDH1A1 P00352 4/20 0.44
GAA P10253 2/20 0.44
L3MBTL1 Q9Y468 2/20 0.44
MAPT P10636 2/20 0.44
TDP1 Q9NUW8 1/20 0.44
ALPG P10696 1/20 0.44
ALOX12 P18054 1/20 0.44
NPY1R P25929 1/20 0.44
HTT P42858 1/20 0.44
NPY2R P49146 1/20 0.44
NPSR1 Q6W5P4 1/20 0.44
TSHR P16473 2/20 0.42
ALOX15 P16050 1/20 0.42
USP2 O75604 1/20 0.42
ESR1 P03372 1/20 0.42
MEN1 O00255 2/20 0.41

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
SCHEMBL19737701 0.81 CA2 (0.52) CA2CA4CA5ACFTRALDH1A1
SCHEMBL18935759 0.80 ESR1 (0.38) CA2CA4CA5ACFTRALDH1A1
SCHEMBL13081158 0.79 CA2 (0.65) CA2CA4CA5ACFTRALDH1A1
SCHEMBL19732114 0.77 ESR1 (0.50) CA2CA4CA5ACFTRALDH1A1
Hydrochloric Acid SCHEMBL28465544 0.77 CA2 (0.48) CA2CA4CA5ACFTRALDH1A1
SCHEMBL7079874 0.75 CA2 (0.52) CA2CA4CA5ACFTRALDH1A1
SCHEMBL27430905 0.73 CA2 (0.43) CA2CA4CA5ACFTRALDH1A1
Triphenylphosphine Oxide SCHEMBL513223 0.73 CA2 (0.58) CA2CA4CA5ACFTRALDH1A1
SCHEMBL10309470 0.73 CA2 (0.58) CA2CA4CA5ACFTRALDH1A1
Triphenylphosphine Oxide SCHEMBL3949 0.73 CA2 (0.58) CA2CA4CA5ACFTRALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230295198-A1 VANILLIN-DERIVED FLAME RETARDANT MONOMERS, RESINS, PREPOLYMERS, AND POLYMERS THE GOVERNING COUNCIL OF THE UNIVERSITY OF TORONTO (CA) 2023-09-21 US disclosed
EP-3932965-A1 BLOCK COPOLYMER STRUCTURE AND THE PREPARING METHOD THEREOF National Tsing Hua University (TW) 2022-01-05 EP disclosed
WO-2020016233-A1 COMPOUND AND ORGANIC SEMICONDUCTING LAYER, ORGANIC ELECTRONIC DEVICE, DISPLAY DEVICE AND LIGHTING DEVICE COMPRISING THE SAME NOVALED GMBH (DE) 2020-01-23 WO disclosed
US-10305046-B2 Heterocyclic compound and organic light-emitting device including the same SAMSUNG DISPLAY CO., LTD. (KR) 2019-05-28 US disclosed
US-10280260-B2 Phosphorus-containing polyphenylene oxide resin, its preparation method, method for preparing prepolymer of phosphorus-containing polyphenylene oxide, resin composition and its application Elite Material Co., Ltd. (TW) 2019-05-07 US disclosed
EP-3333168-A1 CONDENSED CYCLIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME Samsung Display Co., Ltd. (KR) 2018-06-13 EP disclosed
EP-2980877-B1 ORGANIC ELECTROLUMINESCENT ELEMENT KYULUX INC (JP) 2017-11-29 EP disclosed
US-20170338419-A1 HETEROCYCLIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME SAMSUNG DISPLAY CO., LTD. (KR) 2017-11-23 US disclosed
US-20170088669-A1 PHOSPHORUS-CONTAINING POLYPHENYLENE OXIDE RESIN, ITS PREPARATION METHOD, METHOD FOR PREPARING PREPOLYMER OF PHOSPHORUS-CONTAINING POLYPHENYLENE OXIDE, RESIN COMPOSITION AND ITS APPLICATION Elite Material Co., Ltd. (TW) 2017-03-30 US disclosed
US-7470762-B2 Living radical polymerization of acrylic monomers and the formation of block copolymers therefrom UNIVERSITY OF PENNSYLVANIA (US) 2008-12-30 US disclosed
EP-1853638-A1 LIVING RADICAL POLYMERIZATION OF HALOGEN-CONTAINING AND ACRYLIC MONOMERS AND THE FORMATION OF BLOCK COPOLYMERS THEREFROM The University of Pennsylvania (US) 2007-11-14 EP disclosed
US-20070073065-A1 Substituted optically active disphosphine compound TAKASAGO INTERNATIONAL CORPORATION (JP) 2007-03-29 US disclosed
WO-2006080928-A1 LIVING RADICAL POLYMERIZATION OF HALOGEN-CONTAINING AND ACRYLIC MONOMERS AND THE FORMATION OF BLOCK COPOLYMERS THEREFROM UNIVERSITY OF PENNSYLVANIA (US) 2006-08-03 WO disclosed
US-7026420-B2 Aqueous room temperature living radical polymerization of vinyl halides UNIVERSITY OF PENNSYLVANIA (US) 2006-04-11 US disclosed
US-20050148734-A1 Aqueous room temperature living radical polymerization of vinyl halides UNIVERSITY OF PENNSYLVANIA 2005-07-07 US disclosed
US-6911515-B2 Aqueous room temperature living radical polymerization of vinyl halides UNIVERSITY OF PENNSYLVANIA (US) 2005-06-28 US disclosed
US-20050131186-A1 Living radical polymerization of halogen-containing and acrylic monomers and the formation of block copolymers therefrom PENNSYLVANIA, UNIVERSITY OF 2005-06-16 US disclosed
EP-1406935-A1 RADICAL POLYMERIZATION OF VINYL HALIDE The University of Pennsylvania (US) 2004-04-14 EP disclosed
US-20030078353-A1 Aqueous room temperature living radical polymerization of vinyl halides UNIVERSITY OF PENNSYLVANIA 2003-04-24 US disclosed
WO-2003002621-A1 RADICAL POLYMERIZATION OF VINYL HALIDE UNIVERSITY OF PENNSYLVANIA (US) 2003-01-09 WO 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 (4 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-10305046-B2 Heterocyclic compound and organic light-emitting device including the same CYP1A1, CRY1, CCNA1 CA2 1947/4885CA4 2088/4885CA5A 3601/4885
US-20170338419-A1 HETEROCYCLIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME CYP1A1, CRY1, CCNA1 CA2 1947/4885CA4 2088/4885CA5A 3601/4885
US-20230295198-A1 VANILLIN-DERIVED FLAME RETARDANT MONOMERS, RESINS, PREPOLYMERS, AND POLYMERS PNN, PFAS, POLN CA2 2095/4885CA4 2438/4885CA5A 2549/4885
US-20070073065-A1 Substituted optically active disphosphine compound DHPS, DOHH, DHODH CA2 690/4885CA4 866/4885CA5A 253/4885

“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.