SCHEMBL608359

SCHEMBL608359

CC1CCC(C(C)C)C([O])C1

nearest known ligand 0.56

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
TRPM8 Q7Z2W7 5/20 0.56
TRPA1 O75762 2/20 0.56
EPHX1 P07099 3/20 0.52
KCNA5 P22460 1/20 0.42
ALDH1A1 P00352 3/20 0.41
TRPV1 Q8NER1 3/20 0.38
LMNA P02545 1/20 0.38
NFE2L2 Q16236 1/20 0.37
HPGD P15428 1/20 0.36

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
SCHEMBL15564614 1.00 TRPM8 (0.56) TRPM8TRPA1EPHX1KCNA5ALDH1A1
SCHEMBL7103829 1.00 TRPM8 (0.56) TRPM8TRPA1EPHX1KCNA5ALDH1A1
SCHEMBL30604482 0.77 TRPM8 (0.62) TRPM8TRPA1EPHX1KCNA5ALDH1A1
SCHEMBL10612768 0.76 TRPM8 (0.56) TRPM8TRPA1EPHX1KCNA5ALDH1A1
SCHEMBL767051 0.76
SCHEMBL21349959 0.75 TRPM8 (0.60) TRPM8TRPA1EPHX1KCNA5ALDH1A1
SCHEMBL26770470 0.75 TRPM8 (0.60) TRPM8TRPA1EPHX1KCNA5ALDH1A1
SCHEMBL9080881 0.75 TRPM8 (0.60) TRPM8TRPA1EPHX1KCNA5ALDH1A1
SCHEMBL19719730 0.75 TRPM8 (0.60) TRPM8TRPA1EPHX1KCNA5ALDH1A1
SCHEMBL2761364 0.75 TRPM8 (0.60) TRPM8TRPA1EPHX1KCNA5ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108025001-A Gamma secretase modulators for the treatment of immune system dysfunction 安可初克公司 2018-05-11 CN claimed
US-20110144033-A1 Proteasome Inhibitors and Methods of Using the Same CEPHALON, INC. (US) 2011-06-16 US claimed
US-7915236-B2 Proteasome inhibitors and methods of using the same CEPHALON, INC. (US) 2011-03-29 US claimed
EP-1660507-B9 PROTEASOME INHIBITORS AND METHODS OF USING THE SAME CEPHALON INC (US) 2010-03-24 EP claimed
US-20090291918-A1 PROTEASOME INHIBITORS AND METHODS OF USING THE SAME CEPHALON, INC. (US) 2009-11-26 US claimed
EP-1660507-B1 PROTEASOME INHIBITORS AND METHODS OF USING THE SAME CEPHALON INC (US) 2009-08-05 EP claimed
EP-1948601-A1 FAB I INHIBITOR AND PROCESS FOR PREPARING SAME Crystalgenomics, Inc. (KR) 2008-07-30 EP claimed
US-20070135465-A1 Fab I Inhibitor and Process for Preparing Same CRYSTALGENOMICS, INC. (KR) 2007-06-14 US claimed
WO-2007043835-A1 FAB I INHIBITOR AND PROCESS FOR PREPARING SAME CRYSTALGENOMICS, INC. (KR) 2007-04-19 WO claimed
EP-1622610-B1 1-(2H-PYRAZOL-3-YL)-3-{4-[1-(BENZOYL)-PIPERIDIN-4-YLMETHYL]-PHENYL}-UREA DERIVATIVES AND RELATED COMPOUNDS AS INHIBITORS OF P38 KINASE AND/OR TNF INHIBITORS FOR THE TREATMENT OF INFLAMMATIONS AVENTIS PHARMA INC (US) 2006-12-20 EP claimed
EP-1660507-A2 PROTEASOME INHIBITORS AND METHODS OF USING THE SAME CEPHALON, INC. (US) 2006-05-31 EP claimed
US-20050107307-A1 Proteasome inhibitors and methods of using the same TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2005-05-19 US claimed
WO-2005021558-A2 PROTEASOME INHIBITORS AND METHODS OF USING THE SAME CEPHALON, INC. (US) 2005-03-10 WO claimed
WO-1998017646-A1 1-(4-PIPERDINYL)-PIPERIDINYLENE AS AGGREGATION INHIBITOR DR. KARL THOMAE GMBH (DE) 1998-04-30 WO claimed
EP-0023454-B1 PROCESS FOR THE PREPARATION OF 6,6-DIMETHYL-4-HYDROXY-3-OXABICYCLO(3.1.0)HEXAN-2-ONE AND ITS ETHERS OF ALL POSSIBLE STEREOISOMERIC FORMS ROUSSEL-UCLAF (FR) 1983-06-22 EP claimed
EP-4076730-A1 MULTI-FUNCTIONAL HYBRID MATERIAL BASED ON SEPIOLITE FOR ENVIRONMENTAL RECOVERY AND BIO-REMEDIATION Consiglio Nazionale Delle Ricerche (IT) 2022-10-26 EP disclosed
WO-2021124097-A1 MULTI-FUNCTIONAL HYBRID MATERIAL BASED ON SEPIOLITE FOR ENVIRONMENTAL RECOVERY AND BIO-REMEDIATION CONSIGLIO NAZIONALE DELLE RICERCHE (IT) 2021-06-24 WO disclosed
EP-0023454-B1 PROCESS FOR THE PREPARATION OF 6,6-DIMETHYL-4-HYDROXY-3-OXABICYCLO(3.1.0)HEXAN-2-ONE AND ITS ETHERS OF ALL POSSIBLE STEREOISOMERIC FORMS ROUSSEL-UCLAF (FR) 1983-06-22 EP disclosed
EP-0024241-A1 Sulphonated compounds comprising a lactone ring and the preparation of cyclopropane derivatives therefrom ROUSSEL-UCLAF (FR) 1981-02-25 EP disclosed
US-3936479-A 2-BENZAMIDO-BENZOPHENONES, UV STABILIZERS, PLASTICS SANDOZ LTD., (SANDOZ AG) (CH) 1976-02-03 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 (4 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-20090291918-A1 PROTEASOME INHIBITORS AND METHODS OF USING THE SAME PSMB11, PSMB5, PSMB6 TRPM8 4814/4885TRPA1 4791/4885EPHX1 2993/4885
US-20050107307-A1 Proteasome inhibitors and methods of using the same PSMB11, PSMB5, PSMB6 TRPM8 4814/4885TRPA1 4791/4885EPHX1 2993/4885
US-20070135465-A1 Fab I Inhibitor and Process for Preparing Same TFPI, TFPI2, FCGRT TRPM8 4603/4885TRPA1 4830/4885EPHX1 4222/4885
US-20110144033-A1 Proteasome Inhibitors and Methods of Using the Same PSMB11, PSMB5, PSMB6 TRPM8 4814/4885TRPA1 4791/4885EPHX1 2993/4885

“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.