SCHEMBL541710

SCHEMBL541710

Cc1ccccc1P(Cl)c1ccccc1C

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 4/20 0.47
ACHE P22303 3/20 0.47
ALDH1A1 P00352 4/20 0.38
CA1 P00915 2/20 0.38
CA2 P00918 2/20 0.38
CA7 P43166 2/20 0.38
CA9 Q16790 2/20 0.38
CYP3A4 P08684 1/20 0.36
TDP1 Q9NUW8 1/20 0.36
ALKBH5 Q6P6C2 1/20 0.35
FTO Q9C0B1 1/20 0.35
CYP1A2 P05177 2/20 0.35
CYP2A6 P11509 2/20 0.35
MAPT P10636 1/20 0.32
HTT P42858 1/20 0.32
ESR1 P03372 1/20 0.32
LMNA P02545 1/20 0.32
ALOX12 P18054 1/20 0.32
TAAR1 Q96RJ0 1/20 0.31
HSD17B10 Q99714 1/20 0.31

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
SCHEMBL31258279 1.00 TSHR (0.47) TSHRACHEALDH1A1CA1CA2
SCHEMBL2154271 0.85 ACHE (0.39) TSHRACHEALDH1A1CA1CA2
SCHEMBL258502 0.83 TSHR (0.47) TSHRACHEALDH1A1CA1CA2
SCHEMBL12311876 0.83 CA1 (0.44) TSHRACHEALDH1A1CA1CA2
Hydrochloric Acid SCHEMBL15845273 0.81 TSHR (0.45) TSHRACHEALDH1A1CA1CA2
SCHEMBL9326405 0.79 TSHR (0.43) TSHRACHEALDH1A1CA1CA2
SCHEMBL11079984 0.79 TRPA1 (0.42) TSHRACHEALDH1A1CA1CA2
SCHEMBL1176479 0.79 TSHR (0.43) TSHRACHEALDH1A1CA1CA2
SCHEMBL8647690 0.78 TSHR (0.47) TSHRACHEALDH1A1CA1CA2
SCHEMBL4480 0.77 TSHR (0.53) TSHRACHEALDH1A1CA1CA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1598053-B1 Use of a composition containing at least one phosphine as majority reducing agent to remove the artificial colour of keratinic fibres OREAL (FR) 2006-12-20 EP claimed
EP-1598053-A1 Use of a composition containing at least one phosphine as majority reducing agent to remove the artificial colour of keratinic fibres L'OREAL (FR) 2005-11-23 EP claimed
US-20050251928-A1 Method for stripping artificial color from keratin fibers L'OREAL (FR) 2005-11-17 US claimed
US-20250368598-A1 CATALYTIC CARBOXYCARBONYLATION OF ALKENES TO FORM ANHYDRIDES BHATTACHARYA SHRABANTI (US) 2025-12-04 US disclosed
EP-4543841-A2 CATALYTIC CARBOXYCARBONYLATION OF ALKENES TO FORM ANHYDRIDES The University of North Carolina at Chapel Hill (US) 2025-04-30 EP disclosed
US-12162001-B2 Magnetic-nanoparticle-supported catalyst and method of making KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) 2024-12-10 US disclosed
US-12157114-B2 Method for making Fe3O4 magnetic catalysts KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) 2024-12-03 US disclosed
US-12107264-B2 Anode active material comprising metal phosphide coating on surface of carbon material, preparation method therefor, nonaqueous lithium secondary battery comprising anode active material, and manufacturing method therefor KOREA ELECTROTECHNOLOGY RESEARCH INSTITUTE (KR) 2024-10-01 US disclosed
US-20240293807-A1 METHOD FOR MAKING Fe3O4 MAGNETIC CATALYSTS KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) 2024-09-05 US disclosed
US-20240286121-A1 MAGNETIC-NANOPARTICLE-SUPPORTED CATALYST AND METHOD OF MAKING KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) 2024-08-29 US disclosed
US-20240286120-A1 SONICATION METHOD FOR MAKING MAGNETIC SUPPORTED CATALYSTS KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS (SA) 2024-08-29 US disclosed
EP-1191030-A2 Phosphinite-oxazolines and metal complexes Solvias AG (CH) 2002-03-27 EP disclosed
EP-0683786-B1 PROCESS FOR THE PREPARATION OF LITHIUM DIARYLPHOSPHIDES AND ALKYLATED DERIVATIVES THEREOF EASTMAN CHEM CO (US) 1996-12-18 EP disclosed
US-5354894-A Treating triarylphosphine with lithium and a primary or secondary amine EASTMAN CHEMICAL COMPANY (US) 1994-10-11 US disclosed
US-5288912-A Hydrohalogenation of a triarylphosphine; alkylation; using lithium diarylphosphine as chemical intermediate EASTMAN KODAK COMPANY (US) 1994-02-22 US disclosed
EP-0340985-B1 PROCESS FOR PREPARING TRANS-2,2-DIMETHYL-3-(2,2-DIHALOVINYL)-CYCLOPROPANE CARBOXYLIC ACID HALIDE SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1992-07-08 EP disclosed
US-4954651-A Process for preparing trans-2,2-dimethyl-3-(2,2-dihalovinyl)-cyclopropane carboxylic acid halide SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1990-09-04 US disclosed
US-4902833-A Bisphosphine dioxides UNION CARBIDE CHEMICALS AND PLASTICS COMPANY INC. (US) 1990-02-20 US disclosed
EP-0340985-A1 Process for preparing trans-2,2-dimethyl-3-(2,2-dihalovinyl)-cyclopropane carboxylic acid halide SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1989-11-08 EP disclosed
US-RE29523-E Olefinic polymers stabilized with thioacyl trivalent phosphorus compounds BORG-WARNER CORPORATION (US) 1978-01-24 US 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 (2 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-20250368598-A1 CATALYTIC CARBOXYCARBONYLATION OF ALKENES TO FORM ANHYDRIDES CA4, CA12, CA14 TSHR 4615/4885ACHE 2398/4885ALDH1A1 688/4885
US-20050251928-A1 Method for stripping artificial color from keratin fibers KRT18, DSG1, JUP TSHR 4245/4885ACHE 704/4885ALDH1A1 4512/4885

“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.