SCHEMBL97495

SCHEMBL97495

O=C(/C=C\c1ccccc1)/C=C/c1ccccc1.[Pd]

nearest known ligand 0.95

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 4/20 0.95
CYP2C9 P11712 3/20 0.95
F3 P13726 3/20 0.95
CYP1A2 P05177 3/20 0.95
PLIN1 O60240 2/20 0.95
LMNA P02545 2/20 0.95
RECQL P46063 2/20 0.95
PLIN5 Q00G26 2/20 0.95
ABHD5 Q8WTS1 2/20 0.95
CYP2D6 P10635 2/20 0.95
ALDH1A1 P00352 2/20 0.95
SMN1; SMN2 Q16637 1/20 0.95
HDAC3 O15379 2/20 0.70
HDAC4 P56524 2/20 0.70
HDAC1 Q13547 2/20 0.70
HDAC2 Q92769 2/20 0.70
HDAC8 Q9BY41 2/20 0.70
HDAC6 Q9UBN7 2/20 0.70
TNKS O95271 1/20 0.70
HCAR2 Q8TDS4 1/20 0.70

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
SCHEMBL546073 1.00 MAPT (0.95) MAPTCYP2C9F3CYP1A2PLIN1
SCHEMBL7512289 1.00 MAPT (0.95) MAPTCYP2C9F3CYP1A2PLIN1
SCHEMBL509571 1.00 MAPT (0.95) MAPTCYP2C9F3CYP1A2PLIN1
SCHEMBL1646390 1.00 MAPT (0.95) MAPTCYP2C9F3CYP1A2PLIN1
SCHEMBL5111 1.00 MAPT (0.95) MAPTCYP2C9F3CYP1A2PLIN1
SCHEMBL14832106 1.00 MAPT (0.95) MAPTCYP2C9F3CYP1A2PLIN1
SCHEMBL2438441 1.00 MAPT (0.95) MAPTCYP2C9F3CYP1A2PLIN1
SCHEMBL18039478 1.00 MAPT (0.95) MAPTCYP2C9F3CYP1A2PLIN1
SCHEMBL187662 1.00 MAPT (0.95) MAPTCYP2C9F3CYP1A2PLIN1
SCHEMBL21879664 1.00 MAPT (0.95) MAPTCYP2C9F3CYP1A2PLIN1

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 1041 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12233087-B2 Palladium hyaluronic acid particles and methods of managing cancer or angiogenic conditions EMORY UNIVERSITY (US) 2025-02-25 US claimed
CN-119191949-A Biaryl compound and synthesis method thereof 海南大学 2024-12-27 CN claimed
CN-118530144-A Paen Jia preparation method of beach 中国医学科学院药物研究所 2024-08-23 CN claimed
CN-118406075-A Silicon-containing polycyclic chromone skeleton compound, preparation method and application thereof 遵义医科大学 2024-07-30 CN claimed
CN-118271166-A Preparation method of 1, n-diol diacid ester compound 中国科学院上海有机化学研究所 2024-07-02 CN claimed
CN-117924343-A New skeleton silicon heterocyclic benzo six-membered compound containing silicon chiral center, and preparation method and application thereof 杭州师范大学 2024-04-26 CN claimed
CN-117756950-A Bio-based carbonylation reagent and application thereof 东北林业大学 2024-03-26 CN claimed
CN-117186150-A Preparation method of LFA-1 inhibitor 维眸生物科技(上海)有限公司 2023-12-08 CN claimed
CN-117186077-A 3-triazolylmethyl-1, 3, 5-triazine-2, 4-dione compound and preparation method and application thereof 陕西盘龙药业集团股份有限公司 2023-12-08 CN claimed
CN-114478582-B Conjugated fused macrocyclic material containing phenothiazine, and preparation method and application thereof 复旦大学 2023-10-10 CN claimed
US-5847117-A Reagent and catalytic process useful for cleaving a protected functional group RHONE-POULENC CHIMIE (FR) 1998-12-08 US claimed
EP-0649831-B1 Process for the preparation of 3-(p-fluorphenyle)-2-methylepropionic acid and of derivatives of 3-(p-fluorphenyle)-2-methylepropionic acid HOECHST AG (DE) 1998-10-14 EP claimed
US-5675034-A Process for preparing 2-(p-fluorophenyl)-2 methyl-propionic acid and 3-(p-fluorophenyl)-2-methylpropionic acid derivatives HOECHST AKTIENGESELLSCHAFT (DE) 1997-10-07 US claimed
EP-0553668-B1 Process for making arylacrylic acids and their esters GIVAUDAN ROURE INT (CH) 1997-04-16 EP claimed
US-5045436-A Which thermally decomposes to catalytically active palladium metal, coated on plastic surface to catalyze metallization reactions, printed circuits CIBA-GEIGY CORPORATION (US) 1991-09-03 US claimed
EP-0378463-A1 Process for the desallylation of N-allylanilines and N,N-diallylanilines with metals RHONE-POULENC CHIMIE (FR) 1990-07-18 EP claimed
US-4879398-A Process for producing 2,6-disubstituted tyrosine MONSANTO COMPANY (US) 1989-11-07 US claimed
EP-0233145-B1 POLYMERIC COMPOSITIONS CONTAINING A DISSOLVED DIBENZAL ACETONE PALLADIUM COMPLEX CIBA-GEIGY AG (CH) 1989-10-18 EP claimed
US-4814489-A ALKYLATION MONSANTO COMPANY (US) 1989-03-21 US claimed
US-4042603-A SUBSTITUTED DIBENZOFURAN OR 9-FLUORENONE FROM A DIPHENYL ETHER OR BENZOPHENONE UBE INDUSTRIES, LTD. (JA) 1977-08-16 US claimed