SCHEMBL753461

SCHEMBL753461

CC(C)(C)c1cc(CCC(=O)OCCCOCCCOCCCOC(=O)CCc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)cc(C(C)(C)C)c1O

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GAA P10253 7/20 0.52
KMT2A Q03164 4/20 0.49
MEN1 O00255 3/20 0.44
ALOX5 P09917 1/20 0.43
HTT P42858 2/20 0.43
PKM P14618 1/20 0.43
APP P05067 1/20 0.41
TDP1 Q9NUW8 1/20 0.41
ALDH1A1 P00352 3/20 0.40
TSHR P16473 2/20 0.40
USP2 O75604 1/20 0.40
CYP1A2 P05177 1/20 0.40
CYP3A4 P08684 1/20 0.40
CYP2D6 P10635 1/20 0.40
MAPT P10636 1/20 0.40
MAPK1 P28482 1/20 0.40
BLM P54132 1/20 0.40
ATM Q13315 1/20 0.40
HIF1A Q16665 1/20 0.40
NPSR1 Q6W5P4 1/20 0.40

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
SCHEMBL11997809 0.96 GAA (0.51) GAAKMT2AMEN1ALOX5HTT
SCHEMBL10449059 0.96 GAA (0.56) GAAKMT2AMEN1ALOX5HTT
SCHEMBL858491 0.93 GAA (0.56) GAAKMT2AMEN1ALOX5HTT
SCHEMBL11813027 0.93 GAA (0.56) GAAKMT2AMEN1ALOX5HTT
SCHEMBL10399184 0.93 GAA (0.56) GAAKMT2AMEN1ALOX5HTT
SCHEMBL808431 0.93 GAA (0.56) GAAKMT2AMEN1ALOX5HTT
SCHEMBL756228 0.92 GAA (0.45) GAAKMT2AMEN1ALOX5HTT
SCHEMBL20390738 0.92 GAA (0.55) GAAKMT2AMEN1ALOX5HTT
SCHEMBL20461221 0.92 GAA (0.55) GAAKMT2AMEN1ALOX5HTT
SCHEMBL30331 0.92 GAA (0.55) GAAKMT2AMEN1ALOX5HTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240217923-A1 A DIISOCYANATE STABILIZER, USE THEREOF, AND DIISOCYANATE COMPOSITION BASF (CHINA) COMPANY LIMITED (CN) 2024-07-04 US claimed
EP-4382588-A1 ADDITIVES FOR IMPROVING THERMAL STABILITY OF FUELS BASF SE (DE) 2024-06-12 EP claimed
EP-4330226-A1 A DIISOCYANATE STABILIZER, USE THEREOF, AND DIISOCYANATE COMPOSITION BASF SE (DE) 2024-03-06 EP claimed
US-20240217923-A1 A DIISOCYANATE STABILIZER, USE THEREOF, AND DIISOCYANATE COMPOSITION BASF (CHINA) COMPANY LIMITED (CN) 2024-07-04 US disclosed
EP-4382588-A1 ADDITIVES FOR IMPROVING THERMAL STABILITY OF FUELS BASF SE (DE) 2024-06-12 EP disclosed
EP-3906245-B1 MULTIFUNCTIONAL ORGANOSILICON COMPOUND AND RELATED METHODS, COMPOUNDS, AND COMPOSITIONS DOW SILICONES CORP (US) 2024-05-29 EP disclosed
US-11820846-B2 Composition, method of preparing copolymer, and methods and end uses thereof DOW SILICONES CORPORATION (US) 2023-11-21 US disclosed
WO-2023201146-A1 PREPARATION OF ORGANOSILICON COMPOUNDS WITH VINYLESTER FUNCTIONALITY DOW GLOBAL TECHNOLOGIES LLC (US) 2023-10-19 WO disclosed
US-20230295193-A1 PREPARATION OF MULTIFUNCTIONAL ORGANOSILICON COMPOUNDS DOW GLOBAL TECHNOLOGIES LLC 2023-09-21 US disclosed
WO-2023069844-A1 METHOD FOR PROMOTING HYDROSILYLATION REACTION TO PREPARE ESTER-FUNCTIONAL SILOXANE OLIGOMERS DOW GLOBAL TECHNOLOGIES LLC (US) 2023-04-27 WO disclosed
US-20220119420-A1 METHOD OF PREPARING ACRYLOXY-FUNCTIONAL ORGANOSILICON COMPOUNDS DOW GLOBAL TECHNOLOGIES LLC 2022-04-21 US disclosed
US-20060020078-A1 (Meth) acrylic esters of polyalkoxylated trimethylolpropane BASF AKTIENGESELLSCHAFT (DE) 2006-01-26 US disclosed
US-20050261523-A1 Preparation of (METH) acrylic acid and (METH) acrylic esters BASF AKTIENGESELLSCHAFT (DE) 2005-11-24 US disclosed
US-20050215752-A1 (Meth)acrylic esters of polyalkoxylated trimethylolpropane BASF AKTIENGESELLSCHAFT A GERMAN CORPORATION (DE) 2005-09-29 US disclosed
US-20050176910-A1 Method for the production of esters of polyalcohols BASF AKTIENGESELLSCHAFT (DE) 2005-08-11 US disclosed
US-20050165208-A1 free-radical crosslinkers for polymers (superabsorbents); high hydrolysis stability; Acrylic Ester BASF AKTIENGESELLSCHAFT (DE) 2005-07-28 US disclosed
WO-2005030907-A1 RADICAL INTERCEPTORS AS STABILIZERS OF POLYMERIZABLE COMPOUNDS BASF AKTIENGESELLSCHAFT (DE) 2005-04-07 WO disclosed
US-6818792-B2 PREPARATION AND/OR WORKING-UP OF POLYMERIZABLE COMPOUNDS USING AT LEAST ONE LIQUID RING PUMP, WHEREIN WORKING LIQUID WHICH CONTAINS A MATERIAL STREAM FROM PREPARATION AND/OR WORKING-UP OFPOLYMERIZABLE COMPOUND IS USED LIQUID RING PUMP BASF AKTIENGESELLSCHAFT (DE) 2004-11-16 US disclosed
US-20040050679-A1 Method for producing (meth) acrylic acid BASF AKTIENGESELLSCHAFT (DE) 2004-03-18 US disclosed
US-20030060654-A1 Preparation of polymerizable compounds BASF AKIENGESELLSCHAFT (DE) 2003-03-27 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-20060020078-A1 (Meth) acrylic esters of polyalkoxylated trimethylolpropane ALKBH3, CHRM2, PAM GAA 3446/4885KMT2A 423/4885MEN1 548/4885
US-11820846-B2 Composition, method of preparing copolymer, and methods and end uses thereof BRS3, OXSR1, OXER1 GAA 3426/4885KMT2A 4700/4885MEN1 348/4885
US-20230295193-A1 PREPARATION OF MULTIFUNCTIONAL ORGANOSILICON COMPOUNDS SI, CEL, VIP GAA 34/4885KMT2A 1970/4885MEN1 239/4885
US-20240217923-A1 A DIISOCYANATE STABILIZER, USE THEREOF, AND DIISOCYANATE COMPOSITION TST, DDT, PAH GAA 3177/4885KMT2A 1410/4885MEN1 3902/4885
US-20220119420-A1 METHOD OF PREPARING ACRYLOXY-FUNCTIONAL ORGANOSILICON COMPOUNDS MSMO1, MCM4, MCM6 GAA 2795/4885KMT2A 1706/4885MEN1 638/4885

“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.