SCHEMBL234057

SCHEMBL234057

CCOP(=O)(CC(=O)OC(C)(C)C)OCC

nearest known ligand 0.48

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
TSHR P16473 2/20 0.43
PPARD Q03181 2/20 0.42
TP53 P04637 1/20 0.33
TDP1 Q9NUW8 1/20 0.33
CA12 O43570 1/20 0.32
CA1 P00915 1/20 0.32
CA2 P00918 1/20 0.32
CA9 Q16790 1/20 0.32
L3MBTL1 Q9Y468 1/20 0.31
MAPT P10636 2/20 0.31
CYP3A4 P08684 1/20 0.31
CYP2C9 P11712 1/20 0.31
CYP2C19 P33261 1/20 0.31
HTT P42858 1/20 0.30
MAPK1 P28482 1/20 0.30
CYP2D6 P10635 1/20 0.30

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
SCHEMBL16978350 0.85 TSHR (0.40) TSHRPPARDTP53TDP1CA12
SCHEMBL15438714 0.83 TSHR (0.43) TSHRPPARDTP53TDP1CA12
SCHEMBL805146 0.82 TSHR (0.34) TSHRPPARDTP53TDP1CA12
SCHEMBL23457672 0.81 TSHR (0.34) TSHRPPARDCA12CA1CA2
SCHEMBL6823520 0.81 PPARD (0.48) TSHRPPARDTP53TDP1CA12
SCHEMBL27617158 0.81 L3MBTL1 (0.30) L3MBTL1
SCHEMBL25582825 0.81 TSHR (0.35) TSHRPPARDTP53TDP1CA12
SCHEMBL15438678 0.80 TSHR (0.41) TSHRPPARD
SCHEMBL421908 0.79 DGAT1 (0.35) CA12CA2L3MBTL1CYP2D6
SCHEMBL16047 0.77 TSHR (0.48) TSHRPPARDTP53TDP1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250206703-A1 PROCESS FOR PREPARING ((1S,2S)-2-(5-METHYLPYRIDIN-2-YL)CYCLOPROPYL)METHANOL MERCK SHARP & DOHME LLC (US) 2025-06-26 US claimed
CN-120119112-A Method for recovering aluminum matrix from aluminum target containing indium-tin solder 新疆众和股份有限公司 2025-06-10 CN claimed
EP-4504703-A1 PROCESS FOR PREPARING ((1S,2S)-2-(5-METHYLPYRIDIN-2-YL)CYCLOPROPYL)METHANOL Merck Sharp & Dohme LLC (US) 2025-02-12 EP claimed
WO-2023192170-A1 PROCESS FOR PREPARING ((1S,2S)-2-(5-METHYLPYRIDIN-2-YL)CYCLOPROPYL)METHANOL MERCK SHARP & DOHME LLC (US) 2023-10-05 WO claimed
CN-112384493-B Process for preparing fused tricyclic gamma-amino acid derivatives and intermediates 四川海思科制药有限公司 2023-06-06 CN claimed
US-20220025424-A1 COMPOSITIONS AND METHODS FOR PRODUCING STEREOISOMERICALLY PURE AMINOCYCLOPROPANES IMAGO BIOSCIENCES, INC. 2022-01-27 US claimed
WO-2020029762-A1 PREPARATION METHOD FOR FUSED TRICYCLIC γ-AMINO ACID DERIVATIVE AND INTERMEDIATE THEREOF 四川海思科制药有限公司 2020-02-13 WO claimed
CN-109824645-A Warfarin haptens and artificial antigen and the preparation method and application thereof 中国农业大学 2019-05-31 CN claimed
WO-2018035249-A1 COMPOSITIONS AND METHODS FOR PRODUCING STEREOISOMERICALLY PURE AMINOCYCLOPROPANES IMAGO BIOSCIENCES, INC. (US) 2018-02-22 WO claimed
CN-103789055-B M15 methanol gasoline vapor pressure stabilizer GANSU SANGTIAN CLEAN ENERGY DEV CO LTD 2015-06-17 CN claimed
US-20130158075-A1 HETEROCYCLIC COMPOUNDS AS DGAT1 INHIBITORS Piramal Enterprises Limited (IN) 2013-06-20 US claimed
US-7265229-B2 Method for synthesizing macrosphelides LEAD CHEMICAL CO., LTD. (JP) 2007-09-04 US claimed
US-20060030720-A1 Method for synthesizing macrosphelides LEAD CHEMICAL CO., LTD. (JP) 2006-02-09 US claimed
JP-57200396-A None JP disclosed
US-20260137680-A1 NOVEL COMPOUNDS SITRYX THERAPEUTICS LTD (GB) 2026-05-21 US disclosed
US-20260138973-A1 SUBSTITUTED PYRIDINES FOR USE IN TREATING OR PREVENTING INFLAMMATORY DISEASES OR DISEASES ASSOCIATED WITH AN UNDESIRABLE IMMUNE RESPONSE SITRYX THERAPEUTICS LTD (GB) 2026-05-21 US disclosed
EP-0405116-A2 Phenylalkan(en)oic acids ONO PHARMACEUTICAL CO., LTD. (JP) 1991-01-02 EP disclosed
JP-S57200396-A PREPARATION OF ALPHA-AMINOPHOSPHONOACETATES KYOWA HAKKO KOGYO CO LTD 1982-12-08 JP disclosed
US-4130659-A Polyprenyl carboxylic acid compound and hypotensive agent containing it as active ingredient EISAI CO., LTD. (JP) 1978-12-19 US disclosed
US-4107193-A HYPOTENSIVE EISAI CO., LTD. (JP) 1978-08-15 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-20260137680-A1 NOVEL COMPOUNDS CCR1, CCR4, CCR3 TSHR 3430/4885PPARD 2857/4885TP53 2073/4885
US-20060030720-A1 Method for synthesizing macrosphelides ADH1C, HPD, HSD17B12 TSHR 1594/4885PPARD 278/4885TP53 4220/4885
US-20260138973-A1 SUBSTITUTED PYRIDINES FOR USE IN TREATING OR PREVENTING INFLAMMATORY DISEASES OR DISEASES ASSOCIATED WITH AN UNDESIRABLE IMMUNE RESPONSE CCR1, CCR2, CBR1 TSHR 2729/4885PPARD 2093/4885TP53 3186/4885
US-20250206703-A1 PROCESS FOR PREPARING ((1S,2S)-2-(5-METHYLPYRIDIN-2-YL)CYCLOPROPYL)METHANOL ADH1C, ADH1A, CYP2S1 TSHR 2880/4885PPARD 2043/4885TP53 3903/4885
US-20130158075-A1 HETEROCYCLIC COMPOUNDS AS DGAT1 INHIBITORS DGAT1, DGAT2, SOAT1 TSHR 3592/4885PPARD 480/4885TP53 1654/4885

“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.