SCHEMBL3676635

SCHEMBL3676635

CCCC1(C)C(=O)C(C)(CCC)C1=O

nearest known ligand 0.36

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
NPC1 O15118 1/20 0.36
MTOR P42345 1/20 0.36
RAB9A P51151 1/20 0.36
HSD17B10 Q99714 1/20 0.34
POLB P06746 1/20 0.33
HSD11B1 P28845 2/20 0.32

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
SCHEMBL3677973 0.73 LMNA (0.38)
SCHEMBL15212094 0.73 LMNA (0.48) HSD17B10HSD11B1
SCHEMBL15536998 0.69 ALDH1A1 (0.32) HSD11B1
SCHEMBL11605060 0.67
SCHEMBL29165349 0.66 HSD11B1 (0.33) HSD17B10POLBHSD11B1
SCHEMBL13917523 0.65
SCHEMBL3682464 0.62 LMNA (0.35)
SCHEMBL11721680 0.61 ALDH1A1 (0.48) HSD17B10HSD11B1
SCHEMBL3683990 0.61 HDAC1 (0.32)
SCHEMBL27853773 0.61 KDM4E (0.33) HSD11B1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250109245-A1 PREPARATION OF UNSATURATED POLYESTERS EASTMAN CHEMICAL COMPANY (US) 2025-04-03 US disclosed
EP-4473036-A1 PREPARATION OF UNSATURATED POLYESTERS Eastman Chemical Company (US) 2024-12-11 EP disclosed
CN-118613528-A Preparation of unsaturated polyesters 伊士曼化工公司 2024-09-06 CN disclosed
WO-2023147330-A1 PREPARATION OF UNSATURATED POLYESTERS EASTMAN CHEMICAL COMPANY (US) 2023-08-03 WO disclosed
EP-3353228-B1 POLYMERS CONTAINING CYCLOBUTANEDIOL AND 2,2-BIS(HYDROXYMETHYL)ALKYLCARBOXYLIC ACID EASTMAN CHEM CO (US) 2022-09-14 EP disclosed
EP-2912095-B1 COPOLYESTERS CONTAINING NEOPENTYL GLYCOL AND 2,2,4,4-TETRAALKYL-1,3-CYCLOBUTANEDIOL EASTMAN CHEM CO (US) 2018-11-14 EP disclosed
EP-3353228-A1 POLYMERS CONTAINING CYCLOBUTANEDIOL AND 2,2-BIS(HYDROXYMETHYL)ALKYLCARBOXYLIC ACID Eastman Chemical Company (US) 2018-08-01 EP disclosed
US-20180002482-A1 POLYMERS CONTAINING CYCLOBUTANEDIOL AND 2,2-BIS(HYDROXYMETHYL)ALKYLCARBOXYLIC ACID EASTMAN CHEMICAL COMPANY (US) 2018-01-04 US disclosed
WO-2017053379-A1 POLYMERS CONTAINING CYCLOBUTANEDIOL AND 2,2-BIS(HYDROXYMETHYL)ALKYLCARBOXYLIC ACID EASTMAN CHEMICAL COMPANY (US) 2017-03-30 WO disclosed
US-20170088665-A1 POLYMERS CONTAINING CYCLOBUTANEDIOL AND 2,2 BIS(HYDROXYMETHYL) AlKYLCARBOXYLIC ACID EASTMAN CHEMICAL COMPANY (US) 2017-03-30 US disclosed
US-7838707-B2 for a specific cis:trans isomer ratio in order to control glass transition temperatures and/or crystallization rates in copolyesters; hydrogenation of a 2,2,4,4-tetraalkylcyclobutane-1,3-dione from the pyrolysis of isobutyric anhydride and dimerization of the resulting dimethylketene EASTMAN CHEMICAL COMPANY (US) 2010-11-23 US disclosed
US-7582804-B2 by hydrogenation of a 2,2,4,4-tetraalkylcyclobutane-1,3-dione; cesium and cobalt promoters; specific cis/trans isomer ratio in order to control glass transition temperatures and/or crystallization rates in copolyesters EASTMAN CHEMICAL COMPANY (US) 2009-09-01 US disclosed
US-7560600-B2 by hydrogenation of a 2,2,4,4-tetraalkylcyclobutane-1,3-dione in the presence of an zirconium-promoted nickel-based catalyst; specific cis/trans isomer ratio in order to control glass transition temperatures and/or crystallization rates in copolyesters EASTMAN CHEMICAL COMPANY (US) 2009-07-14 US disclosed
US-7524994-B2 by hydrogenation of a 2,2,4,4-tetraalkylcyclobutane-1,3-dione; specific cis/trans isomer ratio in order to control glass transition temperatures and/or crystallization rates in copolyesters EASTMAN CHEMICAL COMPANY (US) 2009-04-28 US disclosed
US-7521583-B2 Process for the preparation of tetraalkylcyclobutane-1,3-diol in the presence of a cobalt-based catalyst EASTMAN CHEMICAL COMPANY (US) 2009-04-21 US disclosed
US-20080154069-A1 for a specific cis:trans isomer ratio in order to control glass transition temperatures and/or crystallization rates in copolyesters; hydrogenation of a 2,2,4,4-tetraalkylcyclobutane-1,3-dione from the pyrolysis of isobutyric anhydride and dimerization of the resulting dimethylketene EASTMAN CHEMICAL COMPANY (US) 2008-06-26 US disclosed
US-20080132742-A1 by hydrogenation of a 2,2,4,4-tetraalkylcyclobutane-1,3-dione; cesium and cobalt promoters; specific cis/trans isomer ratio in order to control glass transition temperatures and/or crystallization rates in copolyesters EASTMAN CHEMICAL COMPANY (US) 2008-06-05 US disclosed
US-20080132738-A1 by hydrogenation of a 2,2,4,4-tetraalkylcyclobutane-1,3-dione in the presence of an zirconium-promoted nickel-based catalyst; specific cis/trans isomer ratio in order to control glass transition temperatures and/or crystallization rates in copolyesters EASTMAN CHEMICAL COMPANY (US) 2008-06-05 US disclosed
US-20080132737-A1 by hydrogenation of a 2,2,4,4-tetraalkylcyclobutane-1,3-dione; specific cis/trans isomer ratio in order to control glass transition temperatures and/or crystallization rates in copolyesters EASTMAN CHEMICAL COMPANY (US) 2008-06-05 US disclosed
US-20080132739-A1 PROCESS FOR THE PREPARATION OF TETRAALKYLCYCLOBUTANE-1,3-DIOL IN THE PRESENCE OF A COBALT-BASED CATALYST EASTMAN CHEMICAL COMPANY (US) 2008-06-05 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (5 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20080132739-A1 PROCESS FOR THE PREPARATION OF TETRAALKYLCYCLOBUTANE-1,3-DIOL IN THE PRESENCE OF A COBALT-BASED CATALYST TET1, TET3, HPD NPC1 3415/4885MTOR 3532/4885RAB9A 3984/4885
US-20080132738-A1 by hydrogenation of a 2,2,4,4-tetraalkylcyclobutane-1,3-dione in the presence of an zirconium-promoted nickel-based catalyst; specific cis/trans isomer ratio in order to control glass transition temperatures and/or crystallization rates in copolyesters ZRANB2, RCC1, TELO2 NPC1 1034/4885MTOR 3853/4885RAB9A 1464/4885
US-20080132742-A1 by hydrogenation of a 2,2,4,4-tetraalkylcyclobutane-1,3-dione; cesium and cobalt promoters; specific cis/trans isomer ratio in order to control glass transition temperatures and/or crystallization rates in copolyesters CA3, TELO2, CA1 NPC1 2892/4885MTOR 4435/4885RAB9A 3427/4885
US-20080154069-A1 for a specific cis:trans isomer ratio in order to control glass transition temperatures and/or crystallization rates in copolyesters; hydrogenation of a 2,2,4,4-tetraalkylcyclobutane-1,3-dione from the pyrolysis of isobutyric anhydride and dimerization of the resulting dimethylketene CA3, CA1, CA2 NPC1 4343/4885MTOR 2907/4885RAB9A 2543/4885
US-20080132737-A1 by hydrogenation of a 2,2,4,4-tetraalkylcyclobutane-1,3-dione; specific cis/trans isomer ratio in order to control glass transition temperatures and/or crystallization rates in copolyesters TELO2, CA3, CA1 NPC1 3282/4885MTOR 3743/4885RAB9A 2406/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.