SCHEMBL563975

SCHEMBL563975

O=P(O)(O)c1ccccc1-c1ccccc1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
POLB P06746 3/20 0.47
KDM4E B2RXH2 1/20 0.47
CA2 P00918 1/20 0.46
CA4 P22748 1/20 0.46
CA5A P35218 1/20 0.46
ALDH1A1 P00352 2/20 0.44
HPGD P15428 1/20 0.44
BCL2L1 Q07817 1/20 0.44
HSD17B10 Q99714 1/20 0.44
HDAC4 P56524 1/20 0.43
HDAC2 Q92769 1/20 0.43
HDAC8 Q9BY41 1/20 0.43
HDAC6 Q9UBN7 1/20 0.43
PTK2B Q14289 2/20 0.43
ALPG P10696 1/20 0.43
BCAT2 O15382 1/20 0.42
GPR84 Q9NQS5 1/20 0.42
NPC1 O15118 2/20 0.41
CHRNB2 P17787 1/20 0.41
CHRNB4 P30926 1/20 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
SCHEMBL30729584 0.96 ACP3 (0.47) POLBKDM4ECA2CA4CA5A
Propane SCHEMBL28351173 0.92 POLB (0.42) POLBKDM4ECA2CA4CA5A
SCHEMBL6889688 0.91 POLB (0.44) POLBKDM4ECA2CA4CA5A
SCHEMBL1965079 0.86 ALDH1A1 (0.44) POLBKDM4ECA2CA4CA5A
SCHEMBL4956835 0.85 CA2 (0.48) POLBKDM4ECA2CA4CA5A
SCHEMBL22499728 0.85 ABL1 (0.48) POLBKDM4EALDH1A1HPGDBCL2L1
SCHEMBL3360430 0.84 HNF4A (0.43) POLBKDM4ECA2CA4CA5A
SCHEMBL4956839 0.84 POLB (0.42) POLBKDM4ECA2CA4CA5A
SCHEMBL874792 0.84 HNF4A (0.43) POLBKDM4ECA2CA4CA5A
SCHEMBL29169364 0.84 HDAC4 (0.52) POLBKDM4ECA2CA4CA5A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112441974-A Chiral o-diamine compound and chiral N-heterocyclic carbene compound, and preparation methods and applications thereof 中国科学院化学研究所 2021-03-05 CN claimed
US-7626051-B2 Method for preparing a biphenylphosphonate compound CHUNG SHAN INSTITUTE OF SCIENCE & TECHNOLOGY (TW) 2009-12-01 US claimed
US-20070213551-A1 Method for preparing a Biphenylphosphonate compound CHUNG SHAN INSTITUTE OF SCIENCE & TECHNOLOGY (TW) 2007-09-13 US claimed
US-7232921-B2 Method for preparing a biphenylphosphonate compound CHUNG SHAN INSTITUTE OF SCIENCE & TECHNOLOGY (TW) 2007-06-19 US claimed
US-20050101793-A1 Method for preparing a biphenylphosphonate compound CHUNG SHAN INSTITUTE OF SCIENCE & TECHNOLOGY (TW) 2005-05-12 US claimed
EP-1110988-B1 CATALYST FOR POLYESTER PRODUCTION AND PROCESS FOR PRODUCING POLYESTER WITH THE SAME TEIJIN LTD (JP) 2005-04-27 EP claimed
US-6593447-B1 Reaction product of titanium alkoxide, aromatic polycarboxylic acid, and organophosphonic acid TEIJIN LIMITED (JP) 2003-07-15 US claimed
EP-1110988-A1 CATALYST FOR POLYESTER PRODUCTION AND PROCESS FOR PRODUCING POLYESTER WITH THE SAME TEIJIN LIMITED (JP) 2001-06-27 EP claimed
EP-0736539-B1 Mesoporous crystalline acid composition of a diphosphonate-phosphite of a tetravalent metal which can be used as a catalyst ENITECNOLOGIE SPA (IT) 2000-12-20 EP claimed
US-5892080-A Mesoporous crystalline acid composition of a diphosphonate-phosphite of a tetravalent metal which can be used as a catalyst ENIRICERCHE S.P.A. (IT) 1999-04-06 US claimed
EP-0736539-A2 Mesoporous crystalline acid composition of a diphosphonate-phosphite of a tetravalent metal which can be used as a catalyst ENIRICERCHE S.p.A. (IT) 1996-10-09 EP claimed
US-5246901-A POLYSULFONIC ACIDS CATALYTICA, INC. (US) 1993-09-21 US claimed
EP-0416000-A4 POLYSULFONIC ACIDS 1991-12-04 EP claimed
EP-0416000-A1 POLYSULFONIC ACIDS CATALYTICA ASSOCIATES (US) 1991-03-13 EP claimed
WO-1989011485-A1 POLYSULFONIC ACIDS CATALYTICA ASSOCIATES (US) 1989-11-30 WO claimed
US-4423270-A HYDROPHOBIC, PHOSPHONIC ACID PEARSON DONALD E 1983-12-27 US claimed
US-12597441-B2 Magnetic recording medium including fatty ester and fatty acid ester Sony Group Corporation (JP) 2026-04-07 US disclosed
US-20260065932-A1 MAGNETIC RECORDING MEDIUM SONY GROUP CORP (JP) 2026-03-05 US disclosed
EP-0199997-A2 Process for preparing diaryl-pentaerythritol ADEKA ARGUS CHEMICAL CO., Ltd. (JP) 1986-11-05 EP disclosed
EP-0019702-A2 Distyrylebiphenyles, process for their preparation and their use for the optical brightening of organic materials, as well as detergent compositions, textile treating compositions and products for the after-treatment of laundry containing them CIBA-GEIGY AG (CH) 1980-12-10 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 (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-12597441-B2 Magnetic recording medium including fatty ester and fatty acid ester ELOVL1, MEF2D, ELOVL3 POLB 3001/4885KDM4E 1088/4885CA2 325/4885
US-20260065932-A1 MAGNETIC RECORDING MEDIUM RAB10, RAB29, RAB1A POLB 4440/4885KDM4E 2128/4885CA2 1816/4885
US-20050101793-A1 Method for preparing a biphenylphosphonate compound POF1B, AOC2, AOC3 POLB 112/4885KDM4E 3098/4885CA2 1473/4885
US-20070213551-A1 Method for preparing a Biphenylphosphonate compound POF1B, AOC2, AOC3 POLB 112/4885KDM4E 3098/4885CA2 1473/4885

“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.