SCHEMBL2500606

SCHEMBL2500606

CN[C@H]1CCN(C(=O)OC(C)(C)C)C1

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
EPHX1 P07099 1/20 0.57
USP30 Q70CQ3 6/20 0.50
ALDH1A1 P00352 3/20 0.50
HSD11B1 P28845 2/20 0.50
CYP2C9 P11712 1/20 0.50
MAPT P10636 2/20 0.49
NPC1 O15118 1/20 0.49
MAPK1 P28482 1/20 0.49
HTT P42858 1/20 0.49
RAB9A P51151 1/20 0.49
L3MBTL1 Q9Y468 1/20 0.49
HPGD P15428 1/20 0.49
RECQL P46063 1/20 0.47
PTPN2 P17706 1/20 0.46
PTPN1 P18031 1/20 0.46
PTPN6 P29350 1/20 0.46
USP2 O75604 1/20 0.45
SMN1; SMN2 Q16637 1/20 0.45
MEN1 O00255 1/20 0.45
KMT2A Q03164 1/20 0.45

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
SCHEMBL189361 1.00 EPHX1 (0.57) EPHX1USP30ALDH1A1HSD11B1CYP2C9
SCHEMBL671402 1.00 EPHX1 (0.57) EPHX1USP30ALDH1A1HSD11B1CYP2C9
Hydrochloric Acid SCHEMBL2500609 0.98 EPHX1 (0.56) EPHX1USP30ALDH1A1HSD11B1CYP2C9
Hydrochloric Acid SCHEMBL2495441 0.98 EPHX1 (0.56) EPHX1USP30ALDH1A1HSD11B1CYP2C9
SCHEMBL2026360 0.90 EPHX1 (0.55) EPHX1USP30ALDH1A1HSD11B1CYP2C9
SCHEMBL556321 0.90 EPHX1 (0.55) EPHX1USP30ALDH1A1HSD11B1CYP2C9
SCHEMBL2024838 0.90 EPHX1 (0.55) EPHX1USP30ALDH1A1HSD11B1CYP2C9
SCHEMBL215297 0.90 EPHX1 (0.65) EPHX1ALDH1A1MAPTNPC1MAPK1
SCHEMBL2069710 0.89 EPHX1 (0.57) EPHX1USP30ALDH1A1HSD11B1CYP2C9
SCHEMBL6758420 0.89 EPHX1 (0.57) EPHX1USP30ALDH1A1HSD11B1CYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2026085629-A1 SUBSTITUTED HETEROCYCLIC COMPOUNDS, COMPOSITIONS COMPRISING THEM AND USES THEREOF Université de Montréal (CA) 2026-04-30 WO disclosed
EP-4674484-A2 THIENOPYRROLE COMPOUNDS Gilead Sciences, Inc. (US) 2026-01-07 EP disclosed
US-20250388569-A1 HETEROCYCLIC COMPOUND FOR INHIBITING AND/OR INDUCING DEGRADATION OF KRAS PROTEIN ASTELLAS PHARMA INC. (JP) 2025-12-25 US disclosed
EP-4665458-A1 INHIBITING ALPHA V BETA8 INTEGRIN Morphic Therapeutic, Inc. (US) 2025-12-24 EP disclosed
EP-4139299-B1 KRAS G12D PROTEIN INHIBITORS TAIHO PHARMACEUTICAL CO LTD (JP) 2025-12-17 EP disclosed
EP-4656201-A2 RAS INHIBITORS Revolution Medicines, Inc. (US) 2025-12-03 EP disclosed
EP-4067344-B1 CYCLOALKYL UREA DERIVATIVE SUMITOMO PHARMA CO LTD (JP) 2025-11-26 EP disclosed
US-20250340548-A1 KRAS G12C INHIBITORS FRONTIER MEDICINES CORP (US) 2025-11-06 US disclosed
EP-4291562-B1 THIENOPYRROLE COMPOUNDS GILEAD SCIENCES INC (US) 2025-09-10 EP disclosed
US-12358910-B2 Heteroaromatic compounds as Vanin inhibitors BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2025-07-15 US disclosed
US-20090239928-A1 N-Pyrrolidin-3YL-Amide Derivatives As Serotonin and Noradrenalin Re-Uptake Inhibitors PFIZER INC. 2009-09-24 US disclosed
EP-2050735-A1 METHOD FOR PRODUCTION OF OPTICALLY ACTIVE 3-AMINO-NITROGENATED COMPOUND Kaneka Corporation (JP) 2009-04-22 EP disclosed
EP-1343503-B1 HETEROARYL UREA NEUROPEPTIDE Y Y5 RECEPTOR ANTAGONISTS SCHERING CORP (US) 2008-11-12 EP disclosed
WO-2008130569-A1 NOVEL PYRAZOLOPYRIMIDINES AS CYCLIN DEPENDENT KINASE INHIBITORS SCHERING CORPORATION (US) 2008-10-30 WO disclosed
US-7309704-B2 Heteroaryl urea neuropeptide Y Y5 receptor antagonists SCHERING CORPORATION (US) 2007-12-18 US disclosed
US-7309704-B2 Heteroaryl urea neuropeptide Y Y5 receptor antagonists SCHERING CORPORATION (US) 2007-12-18 US disclosed
US-20050176738-A1 Melanin-concentrating hormone receptor antagonists and compositions and methods related thereto NEUROCRINE BIOSCIENCES, INC. (US) 2005-08-11 US disclosed
US-20040147545-A1 Derivatives of oxazolidinones as antibacterial agents LABORATORIOS VITA, S.A. (ES) 2004-07-29 US disclosed
US-5866564-A STABILITY SANKYO COMPANY, LIMITED (JP) 1999-02-02 US disclosed
US-5712267-A Carbapenem derivatives, their preparation and their use as antibiotics SANKYO COMPANY,. LIMITED (JP) 1998-01-27 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 (6 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-12358910-B2 Heteroaromatic compounds as Vanin inhibitors VHL, FANCI, PAH EPHX1 1284/4885USP30 3167/4885ALDH1A1 543/4885
US-20090239928-A1 N-Pyrrolidin-3YL-Amide Derivatives As Serotonin and Noradrenalin Re-Uptake Inhibitors AOC3, AOC2, TPH2 EPHX1 677/4885USP30 3226/4885ALDH1A1 730/4885
US-20050176738-A1 Melanin-concentrating hormone receptor antagonists and compositions and methods related thereto MCHR1, MCHR2, MC1R EPHX1 515/4885USP30 1859/4885ALDH1A1 1368/4885
US-20250340548-A1 KRAS G12C INHIBITORS KRAS, NRAS, HRAS EPHX1 1898/4885USP30 1382/4885ALDH1A1 3319/4885
US-20250388569-A1 HETEROCYCLIC COMPOUND FOR INHIBITING AND/OR INDUCING DEGRADATION OF KRAS PROTEIN KRAS, NRAS, HRAS EPHX1 1897/4885USP30 2649/4885ALDH1A1 3855/4885
US-20040147545-A1 Derivatives of oxazolidinones as antibacterial agents OXA1L, Q6ZSR9, PGC EPHX1 2356/4885USP30 4108/4885ALDH1A1 1970/4885

“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.