SCHEMBL51072

SCHEMBL51072

CC1(C)CC(OC(=O)c2ccccc2)CC(C)(C)N1[O]

nearest known ligand 0.70

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 2/20 0.70
GAA P10253 2/20 0.66
KMT2A Q03164 3/20 0.62
MEN1 O00255 1/20 0.54
CHRNA7 P36544 2/20 0.52
HTR3E A5X5Y0 1/20 0.52
HTR3B O95264 1/20 0.52
HTR3A P46098 1/20 0.52
HTR3D Q70Z44 1/20 0.52
HTR3C Q8WXA8 1/20 0.52
APOBEC3A P31941 1/20 0.48
APOBEC3G Q9HC16 1/20 0.48
HTT P42858 1/20 0.47
SCN1A P35498 1/20 0.47
SCN2A Q99250 1/20 0.47
SCN3A Q9NY46 1/20 0.47
CARM1 Q86X55 1/20 0.46
PRMT6 Q96LA8 1/20 0.46
ALDH1A1 P00352 1/20 0.46
ESR1 P03372 1/20 0.46

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
SCHEMBL4797939 0.88 TSHR (0.60) TSHRGAAKMT2AMEN1CHRNA7
SCHEMBL294975 0.88 TSHR (0.70) TSHRGAAKMT2AMEN1CHRNA7
SCHEMBL243559 0.88 TSHR (0.70) TSHRGAAKMT2AMEN1CHRNA7
SCHEMBL19720352 0.86 TSHR (0.68) TSHRGAAKMT2AMEN1CHRNA7
SCHEMBL7857242 0.85 TSHR (0.67) TSHRGAAKMT2AMEN1CHRNA7
SCHEMBL27690100 0.85 TSHR (0.67) TSHRGAAKMT2AMEN1CHRNA7
SCHEMBL1138721 0.85 KMT2A (0.84) TSHRGAAKMT2AMEN1CHRNA7
SCHEMBL28108099 0.85 TSHR (0.67) TSHRGAAKMT2AMEN1CHRNA7
SCHEMBL9657743 0.85 TSHR (0.71) TSHRGAAKMT2AMEN1CHRNA7
SCHEMBL7533362 0.85 TSHR (0.75) TSHRGAAKMT2AMEN1CHRNA7

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 1027 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119661466-A Preparation method of imidazopyridine compound intermediate 武汉瑞晟药业有限公司 2025-03-21 CN claimed
US-20250042832-A1 METHOD OF PREPARING GLUCARIC ACID FROM GLUCOSE USING NITROXIDE RADICAL-MEDIATED ORGANOCATALYST AND METHOD OF SEPARATING GLUCARIC ACID SEOUL NATIONAL UNIVERSITY R&DB FOUNDATION (KR) 2025-02-06 US claimed
US-12110271-B2 Manufacturing method for 4-methoxypyrrole derivatives DAEWOONG PHARMACEUTICAL CO., LTD. (KR) 2024-10-08 US claimed
US-20240327324-A1 METHOD FOR PRODUCING FATTY ALDEHYDES AND DERIVATIVES THEREOF FMC Agricultural Solutions A/S (DK) 2024-10-03 US claimed
CN-118439936-A Method for preparing anisic aldehyde by using p-methoxybenzyl chloride 山东新和成药业有限公司 2024-08-06 CN claimed
EP-4380916-A1 METHOD FOR PRODUCING FATTY ALDEHYDES AND DERIVATIVES THEREOF FMC Agricultural Solutions A/S (DK) 2024-06-12 EP claimed
CN-118146075-A Method for preparing anisaldehyde by utilizing anisyl alcohol kettle residual liquid 山东新和成药业有限公司 2024-06-07 CN claimed
CN-117897373-A Process for producing fatty aldehyde and derivative thereof FMC农业解决方案股份有限公司 2024-04-16 CN claimed
WO-2023229323-A1 METHOD FOR PREPARING 6-METHOXYPYRIDIN-3-YL DERIVATIVE 일동제약(주) 2023-11-30 WO claimed
WO-2023012151-A1 METHOD FOR PRODUCING FATTY ALDEHYDES AND DERIVATIVES THEREOF BIOPHERO APS (DK) 2023-02-09 WO claimed
EP-1737872-B1 METHOD FOR THE PRODUCTION OF ORGANOSILICON COMPOUNDS COMPRISING CARBOXY RADICALS WACKER CHEMIE AG (DE) 2007-08-15 EP claimed
US-20070129520-A1 High yield of 2-formylethyldimethylsilanol-modified polydimethylsiloxane obtained by the continuous process of oxidizing 3-hydroxypropyldimethylsilanol-modified corresponding polymer using Tempoas an oxidation catalyst and air or oxygen as oxidizer in an aqueous dispersion; industrial scale; low cost WACKER CHEMIE AG (DE) 2007-06-07 US claimed
EP-1590312-A4 BROMINE FREE TEMPO BASED CATALYST SYSTEM FOR OXIDATION OF PRIMARY AND SECONDARY ALCOHOLS USING NAOCI AS AN OXIDANT. NUTRASWEET CO (US) 2006-08-23 EP claimed
EP-1674440-A1 Process for transition metal free catalytic aerobic oxidation of alcohols under mild conditions using stable free nitroxyl radicals Degussa GmbH (DE) 2006-06-28 EP claimed
US-7030279-B1 Process for transition metal free catalytic aerobic oxidation of alcohols under mild conditions using stable free nitroxyl radicals DEGUSSA AG (DE) 2006-04-18 US claimed
EP-1590383-A2 PRESSURE-SENSITIVE ADHESIVE TAPE FOR THE ADHESION OF PRINTING PLATES AND METHOD FOR THE PRODUCTION THEREOF Tesa AG (DE) 2005-11-02 EP claimed
EP-1590312-A2 BROMINE FREE TEMPO BASED CATALYST SYSTEM FOR OXIDATION OF PRIMARY AND SECONDARY ALCOHOLS USING NAOCI AS AN OXIDANT. The NutraSweet Company (US) 2005-11-02 EP claimed
US-6825384-B1 3,3-DIMETHYLBUTYRALDEHYDE FROM 3,3-DIMETHYLBUTANOL/1-/; CATALYST SELECTIVITY; 2,2,6,6,-TETRAMETHYLPIPERIDINYLOXY CATALYSTS AND OXYMETAL SALT COCATALYST THE NUTRASWEET COMPANY 2004-11-30 US claimed
WO-2004067484-A2 BROMINE FREE TEMPO BASED CATALYST SYSTEM FOR OXIDATION OF PRIMARY AND SECONDARY ALCOHOLS USING NAOCI AS AN OXIDANT. THE NUTRASWEET COMPANY (US) 2004-08-12 WO claimed
WO-2004067661-A2 TWO-STAGE FREE-RADICAL POLYMERIZATION METHOD FOR THE PRODUCTION OF PRESSURE-SENSITIVE ADHESIVES FOR PRESSURE-SENSITIVE ADHESIVE TAPES USED FOR BONDING PRINTING PLATES TESA AG (DE) 2004-08-12 WO claimed

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

For each of this compound's patents that has machine-readable text (1 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-12110271-B2 Manufacturing method for 4-methoxypyrrole derivatives COMT, TH, HPD TSHR 3504/4885GAA 1321/4885KMT2A 616/4885

“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.