SCHEMBL2994567

SCHEMBL2994567

O=C(OCc1ccccc1)C1CC2C=CC1C2

nearest known ligand 0.64

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 9/20 0.64
KMT2A Q03164 4/20 0.64
RAB9A P51151 1/20 0.54
TDP1 Q9NUW8 3/20 0.49
POLB P06746 2/20 0.49
HSD17B10 Q99714 2/20 0.49
L3MBTL1 Q9Y468 2/20 0.49
APEX1 P27695 1/20 0.49
RECQL P46063 1/20 0.49
BLM P54132 1/20 0.49
ESR2 Q92731 1/20 0.49
HPGD P15428 1/20 0.49
KDM4E B2RXH2 2/20 0.45
MEN1 O00255 1/20 0.45
ALOX15 P16050 1/20 0.45
TSHR P16473 1/20 0.45
HTT P42858 1/20 0.45
FABP7 O15540 1/20 0.44
FABP5 Q01469 1/20 0.44
CA1 P00915 1/20 0.44

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
SCHEMBL10532151 1.00 ALDH1A1 (0.64) ALDH1A1KMT2ARAB9ATDP1POLB
SCHEMBL22604708 0.89 ALDH1A1 (0.56) ALDH1A1KMT2ARAB9ATDP1POLB
SCHEMBL11950286 0.89 ALDH1A1 (0.52) ALDH1A1KMT2ARAB9AL3MBTL1TSHR
SCHEMBL21895675 0.87 ALDH1A1 (0.53) ALDH1A1KMT2ARAB9ATDP1POLB
SCHEMBL21895372 0.87 ALDH1A1 (0.53) ALDH1A1KMT2ARAB9ATDP1POLB
SCHEMBL21895660 0.86 ALDH1A1 (0.53) ALDH1A1KMT2ARAB9ATDP1POLB
SCHEMBL18559849 0.86 ALDH1A1 (0.52) ALDH1A1KMT2ARAB9ATDP1POLB
SCHEMBL21895667 0.86 ALDH1A1 (0.68) ALDH1A1KMT2ARAB9ATDP1POLB
SCHEMBL3294863 0.85 ALDH1A1 (0.49) ALDH1A1KMT2ARAB9ATDP1POLB
SCHEMBL21895379 0.84 ALDH1A1 (0.51) ALDH1A1KMT2ARAB9ATDP1POLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115340441-B Synthesis method of chiral cyclobutyl alcohol compound, chiral cyclobutyl alcohol and application 复旦大学 2024-04-26 CN claimed
WO-2025059577-A1 SUBSTITUTED AMINOPYRIDINE COMPOUNDS FOR USE AS AKT1 INHIBITORS ATAVISTIK BIO, INC. (US) 2025-03-20 WO disclosed
US-11886119-B2 Material for forming underlayer film, resist underlayer film, method of producing resist underlayer film, and laminate MITSUI CHEMICALS, INC. (JP) 2024-01-30 US disclosed
US-20230185195-A1 MATERIAL FOR FORMING UNDERLAYER FILM, RESIST UNDERLAYER FILM, METHOD OF PRODUCING RESIST UNDERLAYER FILM, AND LAMINATE MITSUI CHEMICALS, INC. (JP) 2023-06-15 US disclosed
US-11599025-B2 Resin material for forming underlayer film, resist underlayer film, method of producing resist underlayer film, and laminate MITSUI CHEMICALS, INC. (JP) 2023-03-07 US disclosed
CN-111057088-B Process for producing silicon compound and silicon compound 信越化学工业株式会社 2023-02-17 CN disclosed
CN-115210219-A Oxime ester photoinitiators 巴斯夫欧洲公司 2022-10-18 CN disclosed
EP-3640255-B1 METHOD FOR PRODUCING SILICON COMPOUND, AND SILICON COMPOUND SHINETSU CHEMICAL CO (JP) 2021-10-13 EP disclosed
EP-3640255-B1 METHOD FOR PRODUCING SILICON COMPOUND, AND SILICON COMPOUND SHINETSU CHEMICAL CO (JP) 2021-10-13 EP disclosed
CN-113316744-A Oxime ester photoinitiators with specific aroyl chromophores 巴斯夫欧洲公司 2021-08-27 CN disclosed
EP-1622916-A2 HETEROCYCLIC CYCLOPENTYL TETRAHYDROISOQUINOLINE AND TETRAHYDROPYRIDOPYRIDINE MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY Merck & Co., Inc. (US) 2006-02-08 EP disclosed
US-20050085606-A1 Method for polymerizing cycloolefin polymer containing polar functional groups and electronic devices employing the polymerized cycloolefins LG CHEM, LTD (KR) 2005-04-21 US disclosed
WO-2004094371-A2 HETEROCYCLIC CYCLOPENTYL TETRAHYDROISOQUINOLINE AND TETRAHYDROPYRIDOPYRIDINE MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY MERCK & CO., INC. (US) 2004-11-04 WO disclosed
EP-1468027-A1 METHOD FOR POLYMERIZING CYCLOOLEFIN POLYMER CONTAINING POLAR FUNCTIONAL GROUPS AND ELECTRONIC DEVICES EMPLOYING THE POLYMERIZED CYCLOOLEFINS LG Chem, Ltd. (KR) 2004-10-20 EP disclosed
WO-2004050726-A1 METHOD FOR POLYMERIZING CYCLOOLEFIN POLYMER CONTAINING POLAR FUNCTIONAL GROUPS AND ELECTRONIC DEVICES EMPLOYING THE POLYMERIZED CYCLOOLEFINS LG CHEM, LTD. (KR) 2004-06-17 WO disclosed
US-5936048-A Method for preparing modified resins and their applications MITSUI CHEMICALS, INC. (JP) 1999-08-10 US disclosed
EP-0698620-B1 Method for preparing modified resins and their applications MITSUI CHEMICALS INC (JP) 1998-12-09 EP disclosed
US-5792814-A REACTING A RESIN WITH A 5-((4,6-DIAMINO-S-TRIAZIN-2-YL)-NORBORN-2-ENE AND REACTING WITH AN EPOXIDE; FIREPROOFING; MOLDING MATERIALS MITSUI CHEMICALS, INC. (JP) 1998-08-11 US disclosed
US-5674947-A HEATING RESIN WITH FUNCTIONALIZED NORBORNENE COMPOUND IN ABSENCE OF REACTION CATALYST OR INITIATOR MITSUI TOATSU CHEMICALS, INC. (JP) 1997-10-07 US disclosed
EP-0698620-A1 Method for preparing modified resins and their applications MITSUI TOATSU CHEMICALS, Inc. (JP) 1996-02-28 EP disclosed