SCHEMBL4437129

SCHEMBL4437129

C=CC(C)(O)CCCC(C)CCCC(C)C

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
ALOX15 P16050 3/20 1.00
MEN1 O00255 1/20 1.00
CYP3A4 P08684 1/20 1.00
KMT2A Q03164 1/20 1.00
LMNA P02545 1/20 0.48
PTPN1 P18031 3/20 0.44
PTPN2 P17706 1/20 0.44
CDC25B P30305 1/20 0.44
BLM P54132 1/20 0.41
PTGS1 P23219 1/20 0.31
PDE4A P27815 1/20 0.31
SNCA P37840 1/20 0.31
PDE3A Q14432 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
SCHEMBL8082488 1.00 ALOX15 (1.00) ALOX15MEN1CYP3A4KMT2ALMNA
SCHEMBL21429 1.00 ALOX15 (1.00) ALOX15MEN1CYP3A4KMT2ALMNA
SCHEMBL17239377 1.00 ALOX15 (1.00) ALOX15MEN1CYP3A4KMT2ALMNA
SCHEMBL29659795 1.00 ALOX15 (1.00) ALOX15MEN1CYP3A4KMT2ALMNA
SCHEMBL8079400 1.00 ALOX15 (1.00) ALOX15MEN1CYP3A4KMT2ALMNA
SCHEMBL15824175 1.00 ALOX15 (1.00) ALOX15MEN1CYP3A4KMT2ALMNA
Alcohol SCHEMBL11523426 0.95 ALOX15 (0.90) ALOX15MEN1CYP3A4KMT2ALMNA
SCHEMBL722489 0.92 ALOX15 (0.85) ALOX15MEN1CYP3A4KMT2ALMNA
SCHEMBL30492702 0.92 ALOX15 (0.85) ALOX15MEN1CYP3A4KMT2ALMNA
SCHEMBL28826305 0.90 ALOX15 (0.81) ALOX15MEN1CYP3A4KMT2ALMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119775909-A Antistatic TAC high-permeability silica gel protective film and preparation method thereof 东莞市墨田科技实业有限公司 2025-04-08 CN claimed
CN-118725309-A Modified silicone oil, preparation method thereof and hydrogen fuel cell sealant using modified silicone oil 惠州市杜科新材料有限公司 2024-10-01 CN claimed
CN-116462578-B Method for synthesizing delta-methyl ketone by one-pot method 万华化学集团股份有限公司 2024-04-09 CN claimed
CN-116462578-A Method for synthesizing delta-methyl ketone by one-pot method 万华化学集团股份有限公司 2023-07-21 CN claimed
EP-2935177-B1 (6R,10R)-6,10,14-TRIMETYLPENTADECAN-2-ONE PREPARED FROM 6,10-DIMETYLUNDEC-5-EN-2-ONE OR 6,10-DIMETYLUNDECA-5,9-DIEN-2-ONE DSM IP ASSETS BV (NL) 2019-07-24 EP claimed
EP-2935190-B1 (6R,10R)-6,10,14-TRIMETYLPENTADECAN-2-ONE PREPARED FROM 6,10-DIMETYLUNDECA-3,5,9-TRIEN-2-ONE DSM IP ASSETS BV (NL) 2018-09-19 EP claimed
EP-2935191-B1 PREPARATION OF (6R,10R)-6,10,14-TRIMETYLPENTADECAN-2-ONE FROM 3,7-DIMETYLOCT-2-ENAL OR 3,7-DIMETYLOCTA-2,6-DIENAL DSM IP ASSETS BV (NL) 2018-08-01 EP claimed
EP-2935176-B1 (6R,10R)-6,10,14-TRIMETYLPENTADECAN-2-ONE PREPARED FROM (R)-3,7-DIMETYLOCT-6-ENAL DSM IP ASSETS BV (NL) 2018-08-01 EP claimed
US-7411098-B2 Method for the production of tetrahydrogeranylacetone BASF SE (DE) 2008-08-12 US claimed
US-20070167655-A1 Method for the production of tetrahydrogeranylacetone BASF AKTIENGESELLSCHAFT (DE) 2007-07-19 US claimed
US-20010039368-A1 Preparation of C10-C30-alkenes by partial hydrogenation of alkynes over fixed-bed supported palladium catalysts BASF AKTIENGESELLSCHAFT (DE) 2001-11-08 US claimed
US-6300524-B1 REACTING ALPHA,BETA-UNSATURATED ALCOHOL WITH ALKYL ACETOACETATE IN PRESENCE OF ORGANIC ALUMINUM COMPOUND AS CATALYST WITH ELIMINATION AND CONTINUOUS REMOVAL BY DISTILLATION OF CARBON DIOXIDE AND ALCOHOL FORMED BASF AKTIENGESELLSCHAFT (DE) 2001-10-09 US claimed
EP-1110932-A2 Process for the preparation of C10-C30-alkenes by partial hydrogenation of alkynes on fixed-bed palladium-supported catalysts BASF AKTIENGESELLSCHAFT (DE) 2001-06-27 EP claimed
US-6232506-B1 SUBJECTING ISOVALERALDEHYDE AND ACETONE TO CROSS ALDOL CONDENSATION CARRIED OUT WHILE CONTINUOUSLY ADDING TO ACETONE BOTH ISOVALERALDEHYDE AND AQUEOUS ALKALI CONTAINING ALKALINE SUBSTANCE TO GIVE 6-METHYL-3-HEPTEN-2-ONE KURARAY CO., LYD. (JP) 2001-05-15 US claimed
US-6184420-B1 REACTING ALLYL ALCOHOLS OR PROPARGYL ALCOHOLS WITH ISOPROPENYL ETHERS WITH THE FORMATION OF KETALS OF ACETONE AS A BYPRODUCT, THE ISOPROPENYL ETHERS BEING PREPARED BY REACTING KETALS OF ACETONE WITH PROPYNE OR ALLENE BASF AKTIENGESELLSCHAFT (DE) 2001-02-06 US claimed
EP-1000922-A1 Process for the preparation of higher unsaturated ketones BASF AKTIENGESELLSCHAFT (DE) 2000-05-17 EP claimed
CN-1217316-A Preparation for unsaturated ketone BASF AG (DE) 1999-05-26 CN claimed
EP-0902001-A1 Process for the preparation of unsaturated ketones BASF AKTIENGESELLSCHAFT (DE) 1999-03-17 EP claimed
EP-0816321-A1 Process for producing 6-methyl-3-hepten-2-one and 6-methyl-2-heptanone analogues, and process for producing phyton or isophytol KURARAY CO., LTD. (JP) 1998-01-07 EP claimed
US-3975446-A FROM UNSATURATED ALCOHOL, TERTIARY AMINE SHINETSU CHEMICAL COMPANY (JA) 1976-08-17 US claimed