SCHEMBL257223

SCHEMBL257223

COCC1CC2C=CC1C2

nearest known ligand 0.46

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 12/20 0.46
ALDH1A1 P00352 4/20 0.46
MEN1 O00255 3/20 0.37
KMT2A Q03164 3/20 0.37
HTT P42858 1/20 0.37
TSHR P16473 1/20 0.37
POLB P06746 1/20 0.35
ALOX15 P16050 1/20 0.35
TDP1 Q9NUW8 1/20 0.32
MAPT P10636 1/20 0.31
PKM P14618 1/20 0.31
MAPK1 P28482 1/20 0.31
LMNA P02545 1/20 0.31
CYP1A2 P05177 1/20 0.30
CYP3A4 P08684 1/20 0.30
CYP2D6 P10635 1/20 0.30
CYP2C19 P33261 1/20 0.30
ATM Q13315 1/20 0.30

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
SCHEMBL8402107 0.83 KDM4E (0.40) KDM4EALDH1A1MEN1KMT2AHTT
SCHEMBL415514 0.82 KDM4E (0.44) KDM4EALDH1A1MEN1KMT2AHTT
SCHEMBL19380644 0.81 KDM4E (0.39) KDM4EALDH1A1MEN1KMT2AHTT
SCHEMBL123013 0.81 KDM4E (0.39) KDM4EALDH1A1MEN1KMT2AHTT
SCHEMBL122796 0.81 KDM4E (0.39) KDM4EALDH1A1MEN1KMT2AHTT
SCHEMBL1548023 0.81 KDM4E (0.41) KDM4EALDH1A1MEN1KMT2AHTT
SCHEMBL12028597 0.80 KDM4E (0.38) KDM4EALDH1A1MEN1KMT2AHTT
SCHEMBL4787657 0.79 KDM4E (0.43) KDM4EALDH1A1MEN1KMT2AHTT
SCHEMBL10447558 0.79 KDM4E (0.47) KDM4EALDH1A1MEN1KMT2AHTT
SCHEMBL24796703 0.78 KDM4E (0.42) KDM4EALDH1A1MEN1KMT2AHTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114507251-B Double-silicon-center chiral heteroaryl silane and preparation method thereof 南方科技大学 2023-08-22 CN claimed
US-4080491-A CATALYST CONTAINS ORGANOMETALLIC COMPOUND AND THE REACTION PRODUCT OF TUNGSTEN OR MOLYBDENUM OXIDE AND A PHOSPHOROUS HALIDE OR OXYHALIDE SHOWA DENKO K.K. (JA) 1978-03-21 US claimed
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
CN-114507251-B Double-silicon-center chiral heteroaryl silane and preparation method thereof 南方科技大学 2023-08-22 CN disclosed
CN-113820920-B Photosensitive resin composition, method for producing cured relief pattern, and semiconductor device 旭化成株式会社 2023-07-04 CN disclosed
WO-2023112921-A1 FLEXIBLE WAVEGUIDE 三井化学株式会社 2023-06-22 WO 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-110088680-B Double-layer photosensitive layer roll 旭化成株式会社 2022-12-30 CN disclosed
CN-115185157-A Photosensitive resin composition, method for producing cured relief pattern, and semiconductor device 旭化成株式会社 2022-10-14 CN disclosed
CN-109313388-B Negative photosensitive composition 住友电木株式会社 2022-06-21 CN disclosed
US-7163982-B2 Process for preparing fluorine-containing polymer and method of forming fine pattern using same DAIKI INDUSTRIES, LTD. (JP) 2007-01-16 US disclosed
US-6794459-B2 PHOTOLITHOGRAPHY SUMITOMO BAKELITE CO., LTD. (JP) 2004-09-21 US disclosed
EP-1060206-B1 MODIFIED POLYCYCLIC POLYMERS SUMITOMO BAKELITE CO (JP) 2004-04-14 EP disclosed
US-20030018153-A1 Modified polycyclic polymers THE B.F.GOODRICH COMPANY 2003-01-23 US disclosed
US-6486263-B2 INCREASING THE RATE OF REACTION OF THE HYDROGENATION STEP OF THE RING-OPENING METATHESIS POLYMERIZATION (ROMP) WITH CARBENE CONTAINING CATALYST BY ADDING A NON-INERT SOLVENT SUCH AS METHANOL; MULTIPLE CYCLES WITHOUT ADDITIONAL CATALYST UNIVERSITY OF OTTAWA (CA) 2002-11-26 US disclosed
US-6451945-B1 CONTAINING PENDANT ACID LABILE FUNCTIONAL GROUP AND A FUNCTIONAL GROUP CONTAINING A METHYL CARBONYL OR SILYL PROTECTED HYDROXYL MOIETY THE B.F. GOODRICH COMPANY 2002-09-17 US disclosed
US-20020040109-A1 Method for producing saturated polymers and saturated or unsaturated blends OTTAWA, UNIVERSITY OF (CA) 2002-04-04 US disclosed
EP-1060206-A1 MODIFIED POLYCYCLIC POLYMERS The B.F.Goodrich Co. (US) 2000-12-20 EP disclosed
WO-1999042510-A1 MODIFIED POLYCYCLIC POLYMERS THE B.F. GOODRICH COMPANY (US) 1999-08-26 WO disclosed