SCHEMBL117939

SCHEMBL117939

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

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ BLM P54132 1/20 0.57
▸ LMNA P02545 1/20 0.56
▸ PTPN1 P18031 3/20 0.55
▸ KDM1A O60341 1/20 0.44
▸ MEN1 O00255 1/20 0.41
▸ CYP3A4 P08684 1/20 0.41
▸ ALOX15 P16050 1/20 0.41
▸ KMT2A Q03164 1/20 0.41
▸ CA1 P00915 2/20 0.39
▸ ALDH1A1 P00352 2/20 0.39
▸ PTGS1 P23219 1/20 0.39
▸ PDE4A P27815 1/20 0.39
▸ SNCA P37840 1/20 0.39
▸ PDE3A Q14432 1/20 0.39
▸ TDP1 Q9NUW8 1/20 0.39
▸ TRPV1 Q8NER1 1/20 0.39
▸ ACHE P22303 1/20 0.38
▸ PAOX Q6QHF9 1/20 0.38
▸ PTPN2 P17706 1/20 0.37
▸ CDC25B P30305 1/20 0.37

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
SCHEMBL7944875 1.00 BLM (0.57) BLMLMNAPTPN1KDM1AMEN1
SCHEMBL15825692 1.00 BLM (0.57) BLMLMNAPTPN1KDM1AMEN1
SCHEMBL6822195 1.00 BLM (0.57) BLMLMNAPTPN1KDM1AMEN1
SCHEMBL7943009 1.00 BLM (0.57) BLMLMNAPTPN1KDM1AMEN1
SCHEMBL14249242 1.00 BLM (0.57) BLMLMNAPTPN1KDM1AMEN1
SCHEMBL15824542 1.00 BLM (0.57) BLMLMNAPTPN1KDM1AMEN1
SCHEMBL8908184 1.00 BLM (0.57) BLMLMNAPTPN1KDM1AMEN1
SCHEMBL716506 1.00 BLM (0.57) BLMLMNAPTPN1KDM1AMEN1
SCHEMBL7942967 1.00 BLM (0.57) BLMLMNAPTPN1KDM1AMEN1
SCHEMBL6822085 1.00 BLM (0.57) BLMLMNAPTPN1KDM1AMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120004806-A Functionalized alkaline ionic liquid compound, synthesis method thereof and application thereof in alkynylation reaction 山东新和成精化科技有限公司 2025-05-16 — — CN claimed
EP-4549617-A1 PREPARATION OF SATURATED OR ETHYLENICALLY UNSATURATED (CYCLO)ALIPHATIC COMPOUNDS BY HYDROGENATION OF ETHYLENICALLY OR ACETYLENICALLY UNSATURATED (CYCLO)ALIPHATIC COMPOUNDS USING HYDROGEN WITH LOW DEUTERIUM CONTENT BASF SE (DE) 2025-05-07 — — EP claimed
CN-119191942-A Alkynylation method of ketone compound 万华化学集团股份有限公司 2024-12-27 — — CN claimed
US-20240189737-A1 COMPOSITIONS FOR LOW-TEMPERATURE DISTILLATION OF HIGH-BOILING-POINT MOLECULES Natural Extraction Systems, LLC 2024-06-13 — — US claimed
WO-2024073146-A2 COMPOSITIONS FOR LOW-TEMPERATURE DISTILLATION OF HIGH-BOILING-POINT MOLECULES Natural Extraction Systems, LLC (US) 2024-04-04 — — WO claimed
WO-2024073147-A1 COMPOSITIONS FOR LOW-TEMPERATURE DISTILLATION OF HIGH-BOILING-POINT MOLECULES Natural Extraction Systems, LLC (US) 2024-04-04 — — WO claimed
WO-2022212898-A1 COMPOSITIONS FOR LOW-TEMPERATURE DISTILLATION OF HIGH-BOILING-POINT MOLECULES Natural Extraction Systems, LLC (US) 2022-10-06 — — WO claimed
CN-110467519-B Ethynylation method 万华化学集团股份有限公司 2022-08-05 — — CN claimed
CN-112409147-B Method for preparing aldehyde or ketone by cracking acetylene still residual liquid 万华化学集团股份有限公司 2022-08-05 — — CN claimed
CN-110511127-B Method for preparing alpha-hydroxy ketone by using ethynylation reaction by-product 万华化学集团股份有限公司 2022-08-05 — — CN claimed
EP-0816321-B1 Process for producing 6-methyl-2-heptanone analogues, and process for producing phyton and isophytol KURARAY CO (JP) 2002-06-05 — — EP claimed
US-6380437-B1 REACTING A TERTIARY PROPARGYL ALCOHOL WITH ALKENYL ALKYL ETHER OR KETAL; HEATING, PRESSURIZATION IN PRESENCE OF SULFONIC ACID DEGUSSA AG (DE) 2002-04-30 — — US claimed
WO-2002020449-A1 PROCESS FOR THE PRODUCTION OF 6-METHYL HEPTANONE DEGUSSA AG (DE) 2002-03-14 — — WO claimed
EP-1164119-A2 Process for the preparation of higher ketones from unsaturated aldehydes BASF AKTIENGESELLSCHAFT (DE) 2001-12-19 — — 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
EP-1092700-A1 Process for the preparation of unsaturated 4,5-allene ketones, 3,5-dienketones and the corresponding saturated ketones Degussa-Hüls Aktiengesellschaft (DE) 2001-04-18 — — EP claimed
US-5955636-A CROSS ALDOL CONDENSATION OF BRANCHED ALDEHYDE AND ACETONE; AQUEOUS ALKALI; HYDROGENATION CATALYST KURARAY CO., LTD. (JP) 1999-09-21 — — US 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-5600015-A USING RUTHENIUM COMPLEX OF OPTICALLY ACTIVE ATROPISOMERIC DIPHOSPHINE LIGAND AS HYDROGENATION CATALYST HOFFMANN-LA ROCHE INC. (US) 1997-02-04 — — US claimed
US-4032588-A REACTING KETONE WITH ACETYLENE, HYDROCRACKING SHISEIDO CO., LTD. (JA) 1977-06-28 — — US claimed
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