SCHEMBL5403788

SCHEMBL5403788

Nc1ccccc1P(c1ccccc1)c1ccccc1

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP3A4 P08684 5/20 0.52
TDP1 Q9NUW8 2/20 0.52
ALOX15 P16050 2/20 0.43
SMN1; SMN2 Q16637 2/20 0.43
CASP1 P29466 1/20 0.43
CASP7 P55210 1/20 0.43
ESR1 P03372 2/20 0.41
ESR2 Q92731 2/20 0.41
DRD1 P21728 2/20 0.40
ALDH1A1 P00352 5/20 0.38
L3MBTL1 Q9Y468 2/20 0.38
HSD17B10 Q99714 3/20 0.37
GAA P10253 3/20 0.37
KDM4E B2RXH2 3/20 0.37
TSHR P16473 4/20 0.35
MEN1 O00255 3/20 0.33
MAPT P10636 3/20 0.33
KMT2A Q03164 3/20 0.33
NPC1 O15118 2/20 0.33
CYP1A2 P05177 2/20 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
SCHEMBL29620625 1.00 CYP3A4 (0.52) CYP3A4TDP1ALOX15SMN1; SMN2CASP1
Iodide SCHEMBL8511390 0.98 CYP3A4 (0.50) CYP3A4TDP1ALOX15SMN1; SMN2CASP1
Bromide SCHEMBL17963057 0.98 CYP3A4 (0.50) CYP3A4TDP1ALOX15SMN1; SMN2CASP1
SCHEMBL9324946 0.95 CYP3A4 (0.52) CYP3A4TDP1ALOX15SMN1; SMN2CASP1
SCHEMBL31193487 0.84 CYP3A4 (0.46) CYP3A4TDP1ALOX15SMN1; SMN2CASP1
SCHEMBL3064055 0.84 CYP3A4 (0.53) CYP3A4TDP1ALOX15SMN1; SMN2CASP1
SCHEMBL30842821 0.82 ALDH1A1 (0.54) CYP3A4TDP1ALOX15SMN1; SMN2CASP1
SCHEMBL30842815 0.82 ALDH1A1 (0.54) CYP3A4TDP1ALOX15SMN1; SMN2CASP1
SCHEMBL29230460 0.82 ALDH1A1 (0.54) CYP3A4TDP1ALOX15SMN1; SMN2CASP1
SCHEMBL150139 0.81 TDP1 (0.69) CYP3A4TDP1ESR1ESR2DRD1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116199716-A Chiral P, N, N ligand and preparation and application thereof 中国科学院大连化学物理研究所 2023-06-02 CN claimed
US-8436111-B2 Nickel catalyst system for the preparation of high CIS polybutadiene BRIDGESTONE CORPORATION (JP) 2013-05-07 US claimed
CN-116199716-A Chiral P, N, N ligand and preparation and application thereof 中国科学院大连化学物理研究所 2023-06-02 CN disclosed
CN-116199716-A Chiral P, N, N ligand and preparation and application thereof 中国科学院大连化学物理研究所 2023-06-02 CN disclosed
EP-3700914-A1 HYDROGENATION OF CARBONYLS WITH TETRADENTATE PNNP LIGAND RUTHENIUM COMPLEXES Firmenich SA (CH) 2020-09-02 EP disclosed
CN-111417644-A Hydrogenation of carbonyl groups using tetradentate PNNP ligand ruthenium complexes 弗门尼舍有限公司 2020-07-14 CN disclosed
CN-107207546-B Ligand component, related reaction product, activated reaction product, composition containing same and preparation method thereof 美国陶氏有机硅公司 2020-06-09 CN disclosed
CN-108794527-B Bidentate phosphine ligand and application thereof in hydroformylation reaction 南京诚志清洁能源有限公司 2020-05-12 CN disclosed
CN-108586530-B Bidentate phosphine ligand and its application in hydroformylation reaction 南京诚志清洁能源有限公司 2020-05-12 CN disclosed
WO-2019175158-A1 HYDROGENATION OF CARBONYLS WITH TETRADENTATE PNNP LIGAND RUTHENIUM COMPLEXES FIRMENICH SA (CH) 2019-09-19 WO disclosed
US-10179331-B2 Ligand based chromium catalyst and application in catalyzing ethylene oligomerization CHINA PETROLEUM & CHEIMCAL CORPORATION (CN) 2019-01-15 US disclosed
EP-1426385-A1 CATALYST FOR POLYMERIZATION OR COPOLYMERIZATION OF OLEFINS, PREPARATION AND USE OF THE SAME SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY, CHINESE ACADEMY OF SCIENCES (CN) 2004-06-09 EP disclosed
CN-1098269-C Process for synthesizing water-soluble P-N bidental ligand and its application in preparing high-carbon aldehyde CHINA PETROCHEMICAL CORP (CN) 2003-01-08 CN disclosed
CN-1332182-A Catalyst for polymerization and copolymerization of olefine and its synthesis and use SHANGHAI INST ORGANIC CHEM (CN) 2002-01-23 CN disclosed
US-6307067-B1 Palladium and boron co-catalyzed addition of oxygen nucleophiles to vinyl epoxides THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY 2001-10-23 US disclosed
EP-1112240-A1 THE ADDITION OF OXYGEN NUCLEOPHILES TO VINYL EPOXIDES The Board of Trustees of The Leland S. Stanford Junior University (US) 2001-07-04 EP disclosed
CN-1283626-A Process for synthesizing water-soluble P-N bidental ligand and its application in preparing high-carbon aldehyde CHINA PETROCHEMICAL CORP (CN) 2001-02-14 CN disclosed
WO-2000014033-A1 THE ADDITION OF OXYGEN NUCLEOPHILES TO VINYL EPOXIDES THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY (US) 2000-03-16 WO disclosed
EP-0218100-B1 CONJUGATED ALKADIENE TELOMERIZATION TO ORGANO-OXYALKADIENES QUANTUM CHEMICAL CORPORATION (a Virginia corp.) (US) 1989-11-29 EP disclosed
EP-0218100-A1 Conjugated alkadiene telomerization to organo-oxyalkadienes QUANTUM CHEMICAL CORPORATION (a Virginia corp.) (US) 1987-04-15 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-10179331-B2 Ligand based chromium catalyst and application in catalyzing ethylene oligomerization CHRNE, NOD2, NOD1 CYP3A4 2033/4885TDP1 1443/4885ALOX15 2800/4885

“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.