SCHEMBL331007

SCHEMBL331007

CC(C)C(=O)Cc1ccccc1

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 1/20 0.57
CES1 P23141 2/20 0.56
CES2 O00748 1/20 0.56
AKR1B1 P15121 1/20 0.56
CYP1A2 P05177 2/20 0.49
POLB P06746 1/20 0.49
KMT2A Q03164 3/20 0.48
MEN1 O00255 2/20 0.48
HDAC8 Q9BY41 1/20 0.48
HDAC6 Q9UBN7 1/20 0.48
CNR2 P34972 2/20 0.47
NPC1 O15118 1/20 0.47
RAB9A P51151 1/20 0.47
FNTA P49354 1/20 0.47
FNTB P49356 1/20 0.47
CYP2D6 P10635 1/20 0.46
CYP2C9 P11712 1/20 0.46
CYP2C19 P33261 1/20 0.46
ITGA4 P13612 1/20 0.46
ITGB7 P26010 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
Phosphonic Acid SCHEMBL11615478 0.92 TSHR (0.50) TSHRCES1CES2AKR1B1CYP1A2
SCHEMBL13197240 0.88 POLB (0.45) TSHRCES1CES2AKR1B1CYP1A2
SCHEMBL2625190 0.88 LMNA (0.62) TSHRCYP1A2KMT2AMEN1CYP2D6
SCHEMBL21099952 0.84 ITGA4 (0.48) TSHRCES1CES2AKR1B1CYP1A2
SCHEMBL4725179 0.84 TSHR (0.55) TSHRCES1CES2AKR1B1CYP1A2
SCHEMBL107178 0.84 TSHR (0.55) TSHRCES1CES2AKR1B1CYP1A2
SCHEMBL10137814 0.84 CA2 (0.56) TSHRAKR1B1POLBKMT2AMEN1
SCHEMBL12908027 0.84 TSHR (0.50) TSHRCES1CES2AKR1B1CYP1A2
SCHEMBL12267745 0.83 PTGS2 (0.51) ITGA4ITGB7
SCHEMBL14462168 0.83 MAPT (0.48) TSHRCYP1A2POLBKMT2AMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250163014-A1 PRODUCTION METHOD FOR EPISULFIDE COMPOUND MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2025-05-22 US claimed
EP-4491621-A1 PRODUCTION METHOD FOR EPISULFIDE COMPOUND MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2025-01-15 EP claimed
CN-118829634-A Method for producing episulfide compound 三菱瓦斯化学株式会社 2024-10-22 CN claimed
WO-2023171591-A1 PRODUCTION METHOD FOR EPISULFIDE COMPOUND 三菱瓦斯化学株式会社 2023-09-14 WO claimed
CN-108929400-B Nickel catalyst system, high-performance polybutadiene and preparation method thereof 北京化工大学 2023-03-14 CN claimed
US-11528912-B2 Bacillus methylotrophicus strain DR-08 producing natural volatile compound and having antibacterial activity, and use thereof GLOBAL AGRO CO., LTD. (KR) 2022-12-20 US claimed
US-20190166849-A1 BACILLUS METHYLOTROPHICUS STRAIN DR-08 PRODUCING NATURAL VOLATILE COMPOUND AND HAVING ANTIBACTERIAL ACTIVITY, AND USE THEREOF GLOBAL AGRO CO., LTD. (KR) 2019-06-06 US claimed
EP-3492580-A1 BACILLUS METHYLOTROPHICUS STRAIN DR-08 PRODUCING NATURAL VOLATILE COMPOUND AND HAVING ANTIBACTERIAL ACTIVITY, AND USE THEREOF Global Agro Co., Ltd. (KR) 2019-06-05 EP claimed
CN-108929400-A A kind of nickel catalyst system, high-performance polybutadiene and preparation method thereof 北京化工大学 2018-12-04 CN claimed
US-20250163014-A1 PRODUCTION METHOD FOR EPISULFIDE COMPOUND MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2025-05-22 US disclosed
EP-4547683-A2 CYCLIC-DISULFIDE MODIFIED PHOSPHATE BASED OLIGONUCLEOTIDE PRODRUGS Alnylam Pharmaceuticals, Inc. (US) 2025-05-07 EP disclosed
EP-4491621-A1 PRODUCTION METHOD FOR EPISULFIDE COMPOUND MITSUBISHI GAS CHEMICAL COMPANY, INC. (JP) 2025-01-15 EP disclosed
EP-4462501-A2 SLURRY FOR FORMING NEGATIVE ELECTRODE ACTIVE MATERIAL LAYER SLURRY, NEGATIVE ELECTRODE ACTIVE MATERIAL LAYER, AND SOLID-STATE BATTERY TOYOTA JIDOSHA KABUSHIKI KAISHA (JP) 2024-11-13 EP disclosed
US-20240368001-A1 SALT RECOVERY SOLUTION AND PROCESSES OF USE THEREOF AQUAFORTUS TECHNOLOGIES LIMITED (NZ) 2024-11-07 US disclosed
EP-0325130-A2 Substituted pyridines BAYER AG (DE) 1989-07-26 EP disclosed
EP-0317845-A2 Substituted hydroxyl amines BAYER AG (DE) 1989-05-31 EP disclosed
EP-0300278-A2 Process for the preparation of 2-substituted pyrroles BAYER AG (DE) 1989-01-25 EP disclosed
EP-0267794-A2 Process for preparing polyolefins Nippon Petrochemicals Co., Ltd. (JP) 1988-05-18 EP disclosed
US-3975373-A CYCLOPENTANONE HELVETICOSIDE JOHANN A. WULFING FABRIK PHARMAZEUTISCHER PRAPARATE (DT) 1976-08-17 US disclosed
US-3951946-A Cardioglycoside derivatives of the strophanthidin type, a process for their manufacture and medicinal preparations containing these compounds JOHANN A. WULFING FABRIK PHARMAZEUTISCHER PRAPARATE (DT) 1976-04-20 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 (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-20250163014-A1 PRODUCTION METHOD FOR EPISULFIDE COMPOUND SULT1E1, ESR2, MRPL21 TSHR 2688/4885CES1 526/4885CES2 709/4885

“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.