SCHEMBL1344

SCHEMBL1344

[Pd].c1ccc(P(c2ccccc2)c2ccccc2)cc1.c1ccc(P(c2ccccc2)c2ccccc2)cc1.c1ccc(P(c2ccccc2)c2ccccc2)cc1.c1ccc(P(c2ccccc2)c2ccccc2)cc1

nearest known ligand 0.92

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TDP1 Q9NUW8 3/20 0.92
CYP3A4 P08684 1/20 0.92
ESR1 P03372 4/20 0.63
ESR2 Q92731 4/20 0.63
KDM4E B2RXH2 1/20 0.48
GAA P10253 1/20 0.48
ALDH1A1 P00352 4/20 0.38
NPSR1 Q6W5P4 1/20 0.37
DRD1 P21728 2/20 0.35
TSHR P16473 4/20 0.33
CA1 P00915 2/20 0.33
CA2 P00918 2/20 0.33
CA9 Q16790 2/20 0.33
LMNA P02545 2/20 0.33
CA12 O43570 1/20 0.33
GLA P06280 1/20 0.33
CA3 P07451 1/20 0.33
CA4 P22748 1/20 0.33
CA14 Q9ULX7 1/20 0.33
ALOX12 P18054 1/20 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
SCHEMBL3710821 1.00 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
SCHEMBL1747083 1.00 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
SCHEMBL3931585 1.00 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
SCHEMBL4718125 1.00 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
SCHEMBL236600 1.00 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
SCHEMBL5968399 1.00 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
SCHEMBL224846 1.00 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
SCHEMBL201704 1.00 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
SCHEMBL22558063 1.00 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
SCHEMBL722872 1.00 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E

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

Appears in 153205 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122079294-A Method for degrading levofloxacin in wastewater based on visible light driving CMPs photocatalytic system 2026-05-26 CN claimed
CN-119101046-B 3-Naphthyl thiophene derivative, and preparation method and application thereof SHENYANG PHARMACEUTICAL UNIVERSITY (CN) 2026-05-26 CN claimed
CN-122071403-A Synthesis method of 3, 5-bis (difluoromethyl) benzoic acid 武汉誉祥医药科技有限公司 2026-05-22 CN claimed
CN-122071424-A Synthesis method of 4-cyano-2-fluoro-5-methyl benzoate 武汉誉祥医药科技有限公司 2026-05-22 CN claimed
WO-2026103415-A1 PYRIDYL-SUBSTITUTED FUSED TRIAZOLE RING COMPOUND AND PREPARATION METHOD THEREFOR, INSECTICIDAL COMPOSITION THEREOF AND USE THEREOF 青岛清原化合物有限公司 2026-05-21 WO claimed
WO-2026102563-A1 DISUBSTITUTED PYRIMIDOPYRROLE ANALOG AND USE THEREOF 深圳湾实验室坪山生物医药研发转化中心 2026-05-21 WO claimed
CN-117700352-B Aryl ketone derivative containing tetraphenyl ethylene and carbazole units, preparation method and application thereof 青海大学 2026-05-19 CN claimed
CN-122059954-A Pyridyl-substituted benzotriazole ring compound, preparation method thereof, insecticidal composition and application 青岛清原化合物有限公司 2026-05-19 CN claimed
CN-121517286-B Ring two-body monomer for preparing electrochemical corrosion resistant parylene coating, and preparation method and application thereof 苏州大学 2026-05-19 CN claimed
CN-116813670-B Large-steric-hindrance C-C coupled palladium ligand and synthesis method thereof 西安欧得光电材料有限公司 2026-05-15 CN claimed
US-4314942-A Deprotection of allylic esters, carbonates and carbamates catalyzed by palladium compounds SCHERING CORPORATION (US) 1982-02-09 US claimed
EP-0013844-B1 SUBSTITUTED PENT-2-ENYL DERIVATIVES OF MALONIC ACID; A METHOD FOR THEIR PREPARATION, AND THEIR USE IN THE SYNTHESIS OF A PRECURSOR OF CHRYSANTHEMIC ACID ROUSSEL-UCLAF (FR) 1981-11-04 EP claimed
EP-0027421-A1 Process for the preparation of unsaturated sulphones, and sulphones obtained ANVAR Agence Nationale de Valorisation de la Recherche (FR) 1981-04-22 EP claimed
EP-0013844-A1 Substituted pent-2-enyl derivatives of malonic acid; a method for their preparation, and their use in the synthesis of a precursor of chrysanthemic acid ROUSSEL-UCLAF (FR) 1980-08-06 EP claimed
US-4146738-A ACTIVATED PALLADIUM TRIARYLPHOSPHINE CATALYST CHEMISCHE WERKE HUELS, AKTIENGESELLSCHAFT (DE) 1979-03-27 US claimed
US-4051157-A Catalytic allylic alkylation WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 1977-09-27 US claimed
US-4028387-A BUTADIENE, CARBON MONOXIDE, AND HEPTADIENE-1-OL REACTANTS, PALLADIUM CATALYST KUREHA KAGAKU KOGYO KABUSHIKI KAISHA (JA) 1977-06-07 US claimed
US-3992456-A BY REACTING BUTADIENE WITH WATER IN THE PRESENCE OF A PALLADIUM CATALYST UNION CARBIDE CORPORATION (US) 1976-11-16 US claimed
US-3937857-A THERMAL DECOMPOSITION, NONCONDUCTIVE SUBSTRATE AMP INCORPORATED (US) 1976-02-10 US claimed
US-3933770-A Method of preparing transition metal complex catalysts TOKYO INSTITUTE OF TECHNOLOGY (JA) 1976-01-20 US claimed