SCHEMBL654370

SCHEMBL654370

Pc1ccccc1C1CCCCC1

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ PTGDR2 Q9Y5Y4 1/20 0.42
▸ PTGS2 P35354 1/20 0.41
▸ BCHE P06276 1/20 0.38
▸ ACHE P22303 1/20 0.38
▸ HTR1A P08908 1/20 0.38
▸ HTR7 P34969 1/20 0.38
▸ POLB P06746 1/20 0.37
▸ CASP3 P42574 1/20 0.37
▸ SENP7 Q9BQF6 1/20 0.37
▸ SENP6 Q9GZR1 1/20 0.37
▸ CEL P19835 1/20 0.36
▸ HTR2C P28335 2/20 0.35
▸ CYP11B2 P19099 1/20 0.35
▸ NOS1 P29475 1/20 0.35
▸ PTPRC P08575 1/20 0.35
▸ PTPRF P10586 1/20 0.35
▸ PTPN1 P18031 1/20 0.35
▸ CDC25B P30305 1/20 0.35
▸ HTR1D P28221 1/20 0.35
▸ HTR1B P28222 1/20 0.35

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
Hydrochloric Acid SCHEMBL29208047 0.98 PTGDR2 (0.41) PTGDR2PTGS2BCHEACHEHTR1A
SCHEMBL15286193 0.98 PTGDR2 (0.40) PTGDR2PTGS2BCHEACHEHTR1A
SCHEMBL15285957 0.93 HTR2C (0.36) PTGDR2PTGS2HTR1AHTR7HTR2C
SCHEMBL15285534 0.88 HTR2C (0.39) HTR1AHTR2C
SCHEMBL42781 0.83 PTGDR2 (0.48) PTGDR2PTGS2BCHEACHECEL
SCHEMBL301162 0.81 HTR1A (0.38) PTGDR2PTGS2BCHEACHEHTR1A
SCHEMBL301130 0.81 HTR1A (0.38) PTGDR2PTGS2BCHEACHEHTR1A
SCHEMBL260121 0.81 HTR1A (0.38) PTGDR2PTGS2BCHEACHEHTR1A
SCHEMBL779938 0.80 CHRNB4 (0.46) PTGDR2PTGS2BCHEACHEHTR1A
SCHEMBL9634731 0.79 HTR1A (0.37) PTGDR2PTGS2BCHEACHEHTR1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111018923-B Carbohydrate monophosphines, method for the production and use thereof 东莞市均成高新材料有限公司 2024-04-19 — — CN disclosed
CN-113474383-B Free radical polymerizable composition 波林复合材料美国股份有限公司 2023-10-31 — — CN disclosed
CN-115536697-A Phosphine ligand compound, catalyst composition for preparing aldehyde by catalytic hydroformylation and method 中国石油化工股份有限公司 2022-12-30 — — CN disclosed
CN-115536698-A Phosphine ligand compound, catalyst composition for homogeneous hydroformylation reaction and method 中国石油化工股份有限公司 2022-12-30 — — CN disclosed
CN-115536695-A Asymmetric phosphine ligand containing polyethylene glycol amino and application thereof 中国石油化工股份有限公司 2022-12-30 — — CN disclosed
CN-115536694-A Symmetric phosphine ligand containing polyethylene glycol amino and application thereof 中国石油化工股份有限公司 2022-12-30 — — CN disclosed
CN-113698280-A Olefin hydroformylation method 中国石油化工股份有限公司 2021-11-26 — — CN disclosed
CN-113698281-A Hydroformylation process 中国石油化工股份有限公司 2021-11-26 — — CN disclosed
CN-113474383-A Radically polymerizable composition 波林复合材料美国股份有限公司 2021-10-01 — — CN disclosed
US-20190048274-A1 PROCESS FOR THE PRODUCTION OF ONE OR MORE PRODUCT FUELS JOHNSON MATTHEY DAVY TECHNOLOGIES LIMITED (GB) 2019-02-14 — — US disclosed
WO-2004056897-A1 CURABLE LIQUID ACRYLOYL GROUP CONTAINING RESIN COMPOSITION DAINIPPON INK AND CHEMICALS, INC. (JP) 2004-07-08 — — WO disclosed
EP-1004563-B1 Process for producing alcohols MITSUBISHI CHEM CORP (JP) 2004-04-28 — — EP disclosed
US-6455743-B1 VAPOR PHASE CATALYTIC HYDROGENATION OF ALDEHYDE MIXTURES; BY-PRODUCT INHIBITION; ESTERIFICATION; ALDOL CONDENSATION MITSUBISHI CHEMICAL CORPORATION (JP) 2002-09-24 — — US disclosed
US-6084133-A REACTING A PHOSPHINE HALIDE WITH A METAL, THEN PROTONATION RESULTING DIORGANO-SUBSTITUTED METAL PHOSPHIDE; SIMPLIFICATION, NONTOXIC, EFFICIENCY KANKYO KAGAKU CENTER CO., LTD. (JP) 2000-07-04 — — US disclosed
EP-1004563-A2 Process for producing alcohols Mitsubishi Chemical Corporation (JP) 2000-05-31 — — EP disclosed
US-5557027-A METAL COMPLEX WITH CYCLIC PHOSPHORANE LIGAND, PREPARATION OF LINEAR ALPHA-OLEFINS SHELL OIL COMPANY (US) 1996-09-17 — — US disclosed
US-5439862-A Comprising transition metal complexed with a five coordinate phosphorus compound, such as a phosphorane; producing linear ethylene oligomers SHELL OIL COMPANY 1995-08-08 — — US disclosed
US-5268492-A Optically active diphosphines, intermediates thereof, and processes for production thereof MITSUI TOATSU CHEMICALS, INC. (JP) 1993-12-07 — — US disclosed
EP-0530015-A1 Optically active diphosphines, intermediates thereof, and processes for production thereof MITSUI TOATSU CHEMICALS, Inc. (JP) 1993-03-03 — — EP disclosed
EP-0052929-A1 Sulfonated group VA ylides and process for preparing same GULF RESEARCH & DEVELOPMENT COMPANY (US) 1982-06-02 — — EP disclosed
Send feedback