SCHEMBL232993

SCHEMBL232993

CCOC(=O)CC(C)(C)CC(=O)OCC

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GAA P10253 2/20 0.55
MGAM O43451 1/20 0.55
SI P14410 1/20 0.55
MGAM2 Q2M2H8 1/20 0.55
ALDH1A1 P00352 4/20 0.50
TRPA1 O75762 1/20 0.50
LMNA P02545 1/20 0.43
HSD17B10 Q99714 1/20 0.43
CYP1A2 P05177 1/20 0.43
GSK3A P49840 1/20 0.42
GSK3B P49841 1/20 0.42
ALOX15 P16050 1/20 0.42
SOAT1 P35610 1/20 0.42
HSD11B1 P28845 1/20 0.41
CA12 O43570 1/20 0.39
CA1 P00915 1/20 0.39
CA2 P00918 1/20 0.39
CA9 Q16790 1/20 0.39
CYP4F2 P78329 1/20 0.36
CYP4A11 Q02928 1/20 0.36

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
SCHEMBL7841654 0.91 GAA (0.46) GAAMGAMSIMGAM2ALDH1A1
SCHEMBL11177993 0.91 GAA (0.46) GAAMGAMSIMGAM2ALDH1A1
SCHEMBL7668564 0.90 GAA (0.50) GAAMGAMSIMGAM2ALDH1A1
SCHEMBL10447420 0.90 GAA (0.50) GAAMGAMSIMGAM2ALDH1A1
SCHEMBL13399368 0.89 GAA (0.44) GAAMGAMSIMGAM2ALDH1A1
SCHEMBL20899760 0.89 GAA (0.44) GAAMGAMSIMGAM2ALDH1A1
SCHEMBL19719715 0.89 GAA (0.44) GAAMGAMSIMGAM2ALDH1A1
SCHEMBL4996013 0.88 GAA (0.48) GAAMGAMSIMGAM2ALDH1A1
SCHEMBL12226263 0.87 GAA (0.43) GAAMGAMSIMGAM2ALDH1A1
SCHEMBL3088273 0.86 KDM4E (0.50) GAAMGAMSIMGAM2ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116194520-B Butene-1 polymer compositions with short crystallization times 巴塞尔聚烯烃意大利有限公司 2025-05-13 CN disclosed
CN-113179643-B Catalyst component for olefin polymerization 巴塞尔聚烯烃意大利有限公司 2024-07-05 CN disclosed
CN-118284659-A Process for preparing polybutene compositions having increased crystallization temperature 巴塞尔聚烯烃意大利有限公司 2024-07-02 CN disclosed
US-20230287203-A1 BUTENE-1 POLYMER COMPOSITIONS HAVING A SHORT CRYSTALLIZATION TIME BASELL POLIOLEFINE ITALIA S.R.L. (IT) 2023-09-14 US disclosed
CN-116568752-A Flexible butene-1 copolymers for pipes 巴塞尔聚烯烃意大利有限公司 2023-08-08 CN disclosed
CN-116194520-A Butene-1 polymer compositions with short crystallization times 巴塞尔聚烯烃意大利有限公司 2023-05-30 CN disclosed
US-20220081497-A1 CATALYST COMPONENTS FOR THE POLYMERIZATION OF OLEFINS BASELL POLIOLEFINE ITALIA S.R.L. (IT) 2022-03-17 US disclosed
EP-3908614-A1 CATALYST COMPONENTS FOR THE POLYMERIZATION OF OLEFINS Basell Poliolefine Italia S.r.l. (IT) 2021-11-17 EP disclosed
CN-113179643-A Catalyst components for the polymerization of olefins 巴塞尔聚烯烃意大利有限公司 2021-07-27 CN disclosed
EP-2945971-B1 CATALYST COMPONENTS FOR THE POLYMERIZATION OF OLEFINS BASELL POLIOLEFINE ITALIA SRL (IT) 2020-12-02 EP disclosed
US-4262010-A THIENAMYCIN-RELATED ANTIBIOTICS MERCK & CO., INC. (US) 1981-04-14 US disclosed
US-4262011-A AMINO ACID DERIVATIVE ANTIBIOTICS MERCK & CO., INC. (US) 1981-04-14 US disclosed
US-4262009-A AMINO ACID DERIVATIVE ANTIBIOTICS MERCK & CO., INC. (US) 1981-04-14 US disclosed
US-4257858-A REACTING A CYCLOHEXA-1,3-DIONE-2-DIAZIDE WITH AN ARYL COMPOUND UNION CARBIDE CORPORATION (US) 1981-03-24 US disclosed
US-4256657-A CYCLIZATION, ACID CATALYST UNION CARBIDE CORPORATION (US) 1981-03-17 US disclosed
US-4256658-A CYCLIZATION, BASIC CATALYST UNION CARBIDE CORPORATION (US) 1981-03-17 US disclosed
US-4256659-A Method of preparing 2-aryl-1,3-cyclohexanedione compounds UNION CARBIDE CORPORATION (US) 1981-03-17 US disclosed
US-4209532-A Biocidal 2-aryl-1,3-cyclohexane dione compounds and alkali metal and ammonium salts thereof UNION CARBIDE CORPORATION (US) 1980-06-24 US disclosed
EP-0007243-A1 2-Aryl-1,3-cyclohexanedione compounds and alkali metal salts, ammonium salts and enol esters thereof, composition and method of controlling acarina ectoparasites on warmblooded animals UNION CARBIDE CORPORATION (US) 1980-01-23 EP disclosed
US-4175135-A Method of controlling acarina ectoparasites on warmblooded animals by orally administering to the animal an ectoparasitically effective amount of a 2-aryl-1,3-cyclohexanedione compound, and alkali metal salts, ammonium salts and enol esters thereof UNION CARBIDE CORPORATION (US) 1979-11-20 US disclosed