SCHEMBL984576

SCHEMBL984576

CC[CH]OCCCCCCCCC

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
THRB P10828 2/20 0.42
TSHR P16473 1/20 0.42
MEN1 O00255 1/20 0.39
HTT P42858 1/20 0.39
KMT2A Q03164 1/20 0.39
MAPT P10636 1/20 0.39
CA1 P00915 8/20 0.38
CA2 P00918 8/20 0.38
CA9 Q16790 7/20 0.38
LPAR3 Q9UBY5 6/20 0.38
LPAR2 Q9HBW0 5/20 0.38
CA12 O43570 3/20 0.38
CA7 P43166 3/20 0.38
CA14 Q9ULX7 3/20 0.38
LPAR1 Q92633 2/20 0.38
CA3 P07451 2/20 0.38
CA4 P22748 2/20 0.38
CA6 P23280 2/20 0.38
CA5A P35218 2/20 0.38
CA5B Q9Y2D0 2/20 0.38

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
SCHEMBL980210 1.00 THRB (0.42) THRBTSHRMEN1HTTKMT2A
SCHEMBL982824 1.00 THRB (0.42) THRBTSHRMEN1HTTKMT2A
SCHEMBL983250 1.00 THRB (0.42) THRBTSHRMEN1HTTKMT2A
SCHEMBL982044 1.00 THRB (0.42) THRBTSHRMEN1HTTKMT2A
SCHEMBL982532 1.00 THRB (0.42) THRBTSHRMEN1HTTKMT2A
SCHEMBL983446 1.00 THRB (0.42) THRBTSHRMEN1HTTKMT2A
SCHEMBL134426 1.00 THRB (0.42) THRBTSHRMEN1HTTKMT2A
SCHEMBL133829 1.00 THRB (0.42) THRBTSHRMEN1HTTKMT2A
SCHEMBL982845 1.00 THRB (0.42) THRBTSHRMEN1HTTKMT2A
SCHEMBL352666 1.00 THRB (0.42) THRBTSHRMEN1HTTKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2005100373-A2 MONOSACCHARIDE DERIVATIVES AS ANTI-CANCER AND ANTI-INFLAMMATORY AGENTS RANBAXY LABORATORIES LIMITED (IN) 2005-10-27 WO claimed
US-5367062-A Disubstituted and deoxydisubstituted derivatives of α-d-lyxofuranosides having anti-inflammatory and anti-proliferative activity MEDICARB INC. (US) 1994-11-22 US claimed
CN-118302407-A Carbonyl compound, method for producing isocyanate compound, and isocyanate composition 旭化成株式会社 2024-07-05 CN disclosed
CN-118215651-A Method for producing isocyanate compound, method for producing urethane compound, method for recovering amine compound, and isocyanate composition 旭化成株式会社 2024-06-18 CN disclosed
EP-4381012-A1 PROCESS FOR MODIFYING AN AQUEOUS POLYMER LATEX BASF SE (DE) 2024-06-12 EP disclosed
WO-2023080257-A1 METHOD FOR PRODUCING ISOCYANATE COMPOUNDS, METHOD FOR PRODUCING CARBAMATE COMPOUNDS, METHOD FOR RECOVERING AMINE COMPOUNDS, AND ISOCYANATE COMPOSITION 旭化成株式会社 2023-05-11 WO disclosed
WO-2023080258-A1 CARBONYL COMPOUND, METHOD FOR PRODUCING CARBONYL COMPOUND, METHOD FOR PRODUCING ISOCYANATE COMPOUND, AND ISOCYANATE COMPOSITION 旭化成株式会社 2023-05-11 WO disclosed
WO-2023012213-A1 PROCESS FOR MODIFYING AN AQUEOUS POLYMER LATEX BASF SE (DE) 2023-02-09 WO disclosed
EP-2275406-B1 PROCESS FOR PRODUCING ISOCYANATE ASAHI CHEMICAL IND (JP) 2018-11-28 EP disclosed
US-9487519-B2 5,6-Dialkyl-7-aminotriazolopyrimidines, their preparation and their use for controlling harmful fungi, and compositions comprising these compounds BASF SE (DE) 2016-11-08 US disclosed
EP-2966702-A1 ORGANIC SEMICONDUCTOR THIN FILM PRODUCTION METHOD National University Corporation Kobe University (JP) 2016-01-13 EP disclosed
US-5367062-A Disubstituted and deoxydisubstituted derivatives of α-d-lyxofuranosides having anti-inflammatory and anti-proliferative activity MEDICARB INC. (US) 1994-11-22 US disclosed
US-5360794-A Disubstituted and deoxy disubstituted derivatives of α-D-mannofuranosides and β-L-gulofuranosides having anti-inflammatory and anti-proliferative activity MEDICARB INC. (US) 1994-11-01 US disclosed
US-5326871-A Optically active pyrimidine compound, process for producing the same and liquid crystal composition containing the same SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1994-07-05 US disclosed
WO-1994003185-A1 DISUBSTITUTED AND DEOXY DISUBSTITUTED DERIVATIVES OF α-D-MANNOFURANOSIDES AND β-L-GULOFURANOSIDES HAVING ANTI-INFLAMMATORY AND ANTI-PROLIFERATIVE ACTIVITY MEDICARB INC. (US) 1994-02-17 WO disclosed
EP-0549279-A1 Optically active pyrimidine compound, process for producing the same and liquid crystal composition containing the same SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1993-06-30 EP disclosed
EP-0385120-A1 Fiber reactive asymmetric dioxazine compounds and their use as fiber reactive dyes SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1990-09-05 EP disclosed
EP-0215058-A1 SYNTHESIS OF VINBLASTINE AND VINCRISTINE TYPE COMPOUNDS THE UNIVERSITY OF VERMONT AND STATE AGRICULTURAL COLLEGE (US) 1987-03-25 EP disclosed
EP-0206251-A1 Haloacetamide compounds, process for production thereof, and use thereof as herbicide TOKUYAMA SODA KABUSHIKI KAISHA (JP) 1986-12-30 EP disclosed
WO-1986005491-A1 SYNTHESIS OF VINBLASTINE AND VINCRISTINE TYPE COMPOUNDS THE UNIVERSITY OF VERMONT AND STATE AGRICULTURAL C (US) 1986-09-25 WO disclosed