SCHEMBL2155309

SCHEMBL2155309

COc1cccc([PH](=O)c2cccc(OC)c2)c1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ACHE P22303 1/20 0.50
CES2 O00748 1/20 0.48
CES1 P23141 1/20 0.48
CA1 P00915 1/20 0.48
CA2 P00918 1/20 0.48
CA7 P43166 1/20 0.48
CA9 Q16790 1/20 0.48
ALDH1A1 P00352 1/20 0.48
CYP3A4 P08684 1/20 0.48
PARP1 P09874 1/20 0.46
PRSS1 P07477 1/20 0.46
PRSS2 P07478 1/20 0.46
PRSS3 P35030 1/20 0.46
MGLL Q99685 1/20 0.44
ENPP2 Q13822 1/20 0.44
LMNA P02545 1/20 0.43
MEN1 O00255 1/20 0.43
POLB P06746 1/20 0.43
KMT2A Q03164 1/20 0.43
CHRM5 P08912 1/20 0.42

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
SCHEMBL31327793 1.00 ACHE (0.50) ACHECES2CES1CA1CA2
SCHEMBL2153528 0.94 CA4 (0.48) ACHECES2CES1CA1CA2
SCHEMBL28433395 0.83 ACHE (0.47) ACHECES2CES1CA1CA2
SCHEMBL13081390 0.83 CES2 (0.50) ACHECES2CES1CA1CA2
SCHEMBL2859493 0.79 ALDH1A1 (0.61) CA1CA2CA7CA9ALDH1A1
SCHEMBL2155175 0.78 KIF11 (0.38) ALDH1A1CYP3A4LMNAMEN1POLB
SCHEMBL2155513 0.78 TP53 (0.53) ALDH1A1CYP3A4LMNAMEN1KMT2A
SCHEMBL2154958 0.78 RXRA (0.46) CA2ALDH1A1PRSS1LMNAMEN1
SCHEMBL13970485 0.77 ALDH1A1 (0.43) ACHECES2CES1CA1CA2
SCHEMBL8637786 0.76 NFE2L2 (0.49) ALDH1A1LMNAMEN1POLBKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110669070-B Synthesis method of O- (dialkyl phosphinic group) ketoxime 成都理工大学 2021-08-27 CN claimed
CN-110669070-A Synthesis method of O- (dialkyl phosphinic group) ketoxime 成都理工大学 2020-01-10 CN claimed
CN-120004942-A Method for synthesizing phosphorothioate compound by using manganese acetate dihydrate 苏州大学 2025-05-16 CN disclosed
CN-118996447-A Phosphine-oxide substituted quinoxaline quinazolinone compound, preparation method and application thereof 南阳师范学院 2024-11-22 CN disclosed
CN-115403623-B Method for preparing 2-pyrrolyl substituted phosphine oxide compound 湖南理工学院 2024-10-29 CN disclosed
CN-116836198-A Synthesis method of 2-aryl-4-phosphono-4H-chromene compound 成都大学 2023-10-03 CN disclosed
CN-116462706-A Synthesis method of organic phosphonyl fluoride compound 湖南科技大学 2023-07-21 CN disclosed
CN-116237068-A Preparation method of 2-phosphonomethyl phenol compound 广西中烟工业有限责任公司 2023-06-09 CN disclosed
CN-115322222-A Photocatalytic preparation method of ((alkylamino) methyl) diphenyl phosphine oxide compound 河南师范大学 2022-11-11 CN disclosed
CN-110669070-B Synthesis method of O- (dialkyl phosphinic group) ketoxime 成都理工大学 2021-08-27 CN disclosed
CN-110669070-A Synthesis method of O- (dialkyl phosphinic group) ketoxime 成都理工大学 2020-01-10 CN disclosed
US-9120826-B1 Olefin hydroboration CHEVRON PHILLIPS CHEMICAL COMPANY LP (US) 2015-09-01 US disclosed
WO-2015094207-A1 PHOSPHINYL FORMAMIDINE COMPOUNDS, METAL COMPLEXES, CATALYST SYSTEMS, AND THEIR USE TO OLIGOMERIZE OR POLYMERIZE OLEFINS CHEVRON PHILLIPS CHEMICAL COMPANY LP (US) 2015-06-25 WO disclosed
US-8865610-B2 Phosphinyl guanidine compounds, metal salt complexes, catalyst systems, and their use to oligomerize or polymerize olefins CHEVRON PHILLIPS CHEMICAL COMPANY LP (US) 2014-10-21 US disclosed
US-20140221645-A1 Phosphinyl Amidine Compounds, Metal Complexes, Catalyst Systems, and Their Use to Oligomerize or Polymerize Olefins CHEVRON PHILLIPS CHEMICAL COMPANY LP (US) 2014-08-07 US disclosed
US-8680003-B2 Phosphinyl amidine compounds, metal complexes, catalyst systems, and their use to oligomerize or polymerize olefins CHEVRON PHILLIPS CHEMICAL COMPANY LP (US) 2014-03-25 US disclosed
US-20130331629-A1 Phosphinyl Guanidine Compounds, Metal Salt Complexes, Catalyst Systems, and Their Use to Oligomerize or Polymerize Olefins CHEVRON PHILLIPS CHEMICAL COMPANY LP (US) 2013-12-12 US disclosed
US-20120309965-A1 Phosphinyl Amidine Compounds, Metal Complexes, Catalyst Systems, and Their Use to Oligomerize or Polymerize Olefins CHEVRON PHILLIPS CHEMICAL COMPANY LP (US) 2012-12-06 US disclosed
EP-2519532-A1 PHOSPHINYL AMIDINE COMPOUNDS, METAL COMPLEXES, CATALYST SYSTEMS, AND THEIR USE TO OLIGOMERIZE OR POLYMERIZE OLEFINS Chevron Phillips Chemical Company LP (US) 2012-11-07 EP disclosed
WO-2011082192-A1 PHOSPHINYL AMIDINE COMPOUNDS, METAL COMPLEXES, CATALYST SYSTEMS, AND THEIR USE TO OLIGOMERIZE OR POLYMERIZE OLEFINS CHEVRON PHILLIPS CHEMICAL COMPANY LP (US) 2011-07-07 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 (3 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-20120309965-A1 Phosphinyl Amidine Compounds, Metal Complexes, Catalyst Systems, and Their Use to Oligomerize or Polymerize Olefins NIT2, NCLN, NPM1 ACHE 1107/4885CES2 4230/4885CES1 4516/4885
US-20140221645-A1 Phosphinyl Amidine Compounds, Metal Complexes, Catalyst Systems, and Their Use to Oligomerize or Polymerize Olefins NIT2, NCLN, NPM1 ACHE 1107/4885CES2 4230/4885CES1 4516/4885
US-20130331629-A1 Phosphinyl Guanidine Compounds, Metal Salt Complexes, Catalyst Systems, and Their Use to Oligomerize or Polymerize Olefins GMPS, ITPA, GEMIN4 ACHE 1474/4885CES2 4072/4885CES1 4729/4885

“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.