SCHEMBL2884396

SCHEMBL2884396

COc1ccc(P(Cl)Cl)c(OC)c1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA12 O43570 1/20 0.56
CA1 P00915 1/20 0.56
CA2 P00918 1/20 0.56
CA7 P43166 1/20 0.56
CA9 Q16790 1/20 0.56
CA14 Q9ULX7 1/20 0.56
ALDH1A1 P00352 5/20 0.48
CYP1A1 P04798 5/20 0.48
CYP1A2 P05177 5/20 0.48
CYP1B1 Q16678 5/20 0.48
CYP3A4 P08684 2/20 0.48
MAPT P10636 4/20 0.47
HPGD P15428 3/20 0.47
RAD52 P43351 1/20 0.47
NPC1 O15118 1/20 0.44
GAA P10253 1/20 0.44
CYP2E1 P05181 1/20 0.44
CYP2C8 P10632 1/20 0.44
CYP2D6 P10635 1/20 0.44
CYP2A6 P11509 1/20 0.44

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
SCHEMBL29509911 1.00 CA12 (0.56) CA12CA1CA2CA7CA9
SCHEMBL8029752 0.88 CA12 (0.56) CA12CA1CA2CA7CA9
SCHEMBL5154770 0.83 CA12 (0.56) CA12CA1CA2CA7CA9
SCHEMBL31240957 0.83 CA12 (0.60) CA12CA1CA2CA7CA9
SCHEMBL667942 0.83 CA12 (0.60) CA12CA1CA2CA7CA9
SCHEMBL9838572 0.81 CA12 (0.58) CA12CA1CA2CA7CA9
SCHEMBL18855065 0.81 CA12 (0.58) CA12CA1CA2CA7CA9
SCHEMBL17377389 0.79 CA12 (0.56) CA12CA1CA2CA7CA9
SCHEMBL11788741 0.79 ACHE (0.56) ALDH1A1CYP1A2CYP3A4MAPTHPGD
SCHEMBL11789375 0.79 GAA (0.41) CA12CA1CA2CA7CA9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3853172-B1 METHODS FOR PREPARING ARYLPHOSPHINE-BORANE COMPLEXES DOW GLOBAL TECHNOLOGIES LLC (US) 2023-07-05 EP claimed
EP-3601303-B1 METHODS FOR FORMING 1,3,5,7-TETRAALKYL-6-(2,4-DIMETHOXYPHENYL)-2,4,8-TRIOXA-6-PHOSPHAADAMANTANE DOW GLOBAL TECHNOLOGIES LLC (US) 2022-04-13 EP claimed
US-20210380613-A1 METHODS FOR PREPARING ARYLPHOSPHINE-BORANE COMPLEXES DOW GLOBAL TECHNOLOGIES LLC (US) 2021-12-09 US claimed
US-11111260-B2 Methods for forming 1,3,5,7-tetraalkyl-6-(2,4-dimethoxyphenyl)-2,4,8-trioxa-6-phosphaadamantane DOW GLOBAL TECHNOLOGIES LLC (US) 2021-09-07 US claimed
EP-3853172-A1 METHODS FOR PREPARING ARYLPHOSPHINE-BORANE COMPLEXES Dow Global Technologies LLC (US) 2021-07-28 EP claimed
WO-2020061151-A1 METHODS FOR PREPARING ARYLPHOSPHINE-BORANE COMPLEXES DOW GLOBAL TECHNOLOGIES LLC (US) 2020-03-26 WO claimed
EP-3601303-A1 METHODS FOR FORMING 1,3,5,7-TETRAALKYL-6-(2,4-DIMETHOXYPHENYL)-2,4,8-TRIOXA-6-PHOSPHAADAMANTANE Dow Global Technologies LLC (US) 2020-02-05 EP claimed
US-20200010494-A1 METHODS FOR FORMING 1,3,5,7-TETRAALKYL-6-(2,4-DIMETHOXYPHENYL)-2,4,8-TRIOXA-6-PHOSPHAADAMANTANE DOW GLOBAL TECHNOLOGIES LLC (US) 2020-01-09 US claimed
WO-2018175671-A1 METHODS FOR FORMING 1,3,5,7-TETRAALKYL-6-(2,4-DIMETHOXYPHENYL)-2,4,8-TRIOXA-6-PHOSPHAADAMANTANE DOW GLOBAL TECHNOLOGIES LLC (US) 2018-09-27 WO claimed
EP-1354886-B1 Process for the preparation of tertiary phosphines SALTIGO GMBH (DE) 2009-08-26 EP claimed
US-7230136-B2 Reacting phosphorus halide with organomagnesium compound in presence of copper compound LANXESS DEUTSCHLAND GMBH (DE) 2007-06-12 US claimed
US-20030229240-A1 Reacting phosphorus halide with organomagnesium compound in presence of copper compound LANXESS DEUTSCHLAND GMBH (DE) 2003-12-11 US claimed
EP-1354886-A1 Process for the preparation of tertiary phosphines Bayer Aktiengesellschaft (DE) 2003-10-22 EP claimed
US-11999674-B2 Butadiene telomerization catalyst preparation and use thereof DOW GLOBAL TECHNOLOGIES LLC (US) 2024-06-04 US disclosed
US-20230331643-A1 BUTADIENE TELOMERIZATION CATALYST PREPARATION AND USE THEREOF DOW GLOBAL TECHNOLOGIES LLC (US) 2023-10-19 US disclosed
US-11713286-B2 Butadiene telomerization catalyst preparation and use thereof DOW GLOBAL TECHNOLOGIES LLC (US) 2023-08-01 US disclosed
US-20070299273-A1 prepared by reacting phosphorus halide with organomagnesium compound in presence of copper compound; di(tert-butyl)phenylphosphonium tetrafluoroborate, for example LANXESS DEUTSCHLAND GMBH (DE) 2007-12-27 US disclosed
US-7230136-B2 Reacting phosphorus halide with organomagnesium compound in presence of copper compound LANXESS DEUTSCHLAND GMBH (DE) 2007-06-12 US disclosed
US-20030229240-A1 Reacting phosphorus halide with organomagnesium compound in presence of copper compound LANXESS DEUTSCHLAND GMBH (DE) 2003-12-11 US disclosed
EP-1354886-A1 Process for the preparation of tertiary phosphines Bayer Aktiengesellschaft (DE) 2003-10-22 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 (5 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-11713286-B2 Butadiene telomerization catalyst preparation and use thereof TELO2, TERT, TPR CA12 4546/4885CA1 4173/4885CA2 4531/4885
US-20200010494-A1 METHODS FOR FORMING 1,3,5,7-TETRAALKYL-6-(2,4-DIMETHOXYPHENYL)-2,4,8-TRIOXA-6-PHOSPHAADAMANTANE LPAR6, DDX6, AS3MT CA12 2368/4885CA1 441/4885CA2 629/4885
US-20230331643-A1 BUTADIENE TELOMERIZATION CATALYST PREPARATION AND USE THEREOF TELO2, TERT, TPR CA12 4546/4885CA1 4173/4885CA2 4531/4885
US-11111260-B2 Methods for forming 1,3,5,7-tetraalkyl-6-(2,4-dimethoxyphenyl)-2,4,8-trioxa-6-phosphaadamantane LPAR6, DDX6, AS3MT CA12 2368/4885CA1 441/4885CA2 629/4885
US-11999674-B2 Butadiene telomerization catalyst preparation and use thereof TELO2, TERT, TPR CA12 4546/4885CA1 4173/4885CA2 4531/4885

“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.